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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

INHA Gene

protein-coding   GIFtS: 65
GCID: GC02P220433

inhibin, alpha

 Explore 99 diseases affiliated with
INHA via our new
 Human Malady Compendium 
Biological research products
for INHA
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Inhibin, Alpha1 2
A-Inhibin Subunit2
Inhibin Alpha Chain2

External Ids:    HGNC: 60651   Entrez Gene: 36232   Ensembl: ENSG000001239997   OMIM: 1473805   UniProtKB: P051113   

Export aliases for INHA gene to outside databases

Previous GC identifers: GC02P218459 GC02P219158 GC02P220400 GC02P220639 GC02P220262 GC02P220145 GC02P212289


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for INHA:
This gene encodes the alpha subunit of inhibins A and B protein complexes. These complexes negatively regulate follicle
stimulating hormone secretion from the pituitary gland. Inhibins have also been implicated in regulating numerous
cellular processes including cell proliferation, apoptosis, immune response and hormone secretion.(provided by RefSeq,
Dec 2010)

UniProtKB/Swiss-Prot: INHA_HUMAN, P05111
Function: Inhibins and activins inhibit and activate, respectively, the secretion of follitropin by the pituitary
gland. Inhibins/activins are involved in regulating a number of diverse functions such as hypothalamic and pituitary
hormone secretion, gonadal hormone secretion, germ cell development and maturation, erythroid differentiation, insulin
secretion, nerve cell survival, embryonic axial development or bone growth, depending on their subunit composition.
Inhibins appear to oppose the functions of activins

Gene Wiki entry for INHA


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000002.11  NC_018913.1  NT_005403.17  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the INHA gene promoter:
         GR   Pax-5   GATA-6   p53   GR-alpha   GATA-2   E47   GATA-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidINHA promoter sequence
   Search SABiosciences Chromatin IP Primers for INHA

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat INHA


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 2q33-q36   Ensembl cytogenetic band:  2q35   HGNC cytogenetic band: 2q33-qter

INHA Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
INHA gene location

GeneLoc information about chromosome 2         GeneLoc Exon Structure

GeneLoc location for GC02P220433:  view genomic region     (about GC identifiers)

Start:
220,433,884 bp from pter      End:
220,440,435 bp from pter
Size:
6,552 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: INHA_HUMAN, P05111 (See protein sequence)
Recommended Name: Inhibin alpha chain precursor  
Size: 366 amino acids; 39670 Da
Subunit: Dimeric, linked by one or more disulfide bonds. Inhibin A is a dimer of alpha and beta-A. Inhibin B is a dimer
of alpha and beta-B
Subcellular location: Secreted
Secondary accessions: A8K8H5

Explore the universe of human proteins at neXtProt for INHA: NX_P05111

Post-translational modifications:

  • Proteolytic processing yields a number of bioactive forms. The 20/23 kDa forms consist solely of the mature alpha
  • chain, the 26/29 kDa forms consist of the most N-terminal propeptide linked through a disulfide bond to the mature
    alpha chain, the 50/53 kDa forms encompass the entire proprotein. Each type can be furthermore either mono- or
    diglycosylated, causing the mass difference1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_P05111

  • INHA Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_002182.1  
    ENSEMBL proteins: 
     ENSP00000243786  

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    ProSpec Recombinant Protein for INHA
    Uscn Proteins for INHA

    Gene Ontology (GO): 5/7 cellular component terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001750photoreceptor outer segment IEA--
    GO:0001917photoreceptor inner segment IEA--
    GO:0005576extracellular region TAS12456957
    GO:0005615extracellular space ----
    GO:0034673inhibin-betaglycan-ActRII complex IDA10746731


    INHA for ontologies           About GeneDecksing



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    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    INHA for domains           About GeneDecksing

    4 InterPro domains/families:
     IPR002405 Inhibin_asu
     IPR017175 Inhibin_asu_subgr
     IPR001839 TGF-b_C
     IPR017948 TGFb_CS

    Graphical View of Domain Structure for InterPro Entry P05111

    ProtoNet protein and cluster: P05111

    2 Blocks protein families:
    IPB001839 Transforming growth factor beta (TGFb)
    IPB002405 Inhibin alpha chain signature


    UniProtKB/Swiss-Prot: INHA_HUMAN, P05111
    Similarity: Belongs to the TGF-beta family


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: INHA_HUMAN, P05111
    Function: Inhibins and activins inhibit and activate, respectively, the secretion of follitropin by the pituitary
    gland. Inhibins/activins are involved in regulating a number of diverse functions such as hypothalamic and pituitary
    hormone secretion, gonadal hormone secretion, germ cell development and maturation, erythroid differentiation, insulin
    secretion, nerve cell survival, embryonic axial development or bone growth, depending on their subunit composition.
    Inhibins appear to oppose the functions of activins

         Genatlas biochemistry entry for INHA:
    inhibin,alpha subunit,18kDa,dimerizing with INHBA or INHBB,TGFB superfamily member,to form inhibitin A or B
    respectively,inhibitors of FSH secretion,homodimerizing to form activing A stimulator of FSH secretion and involved in
    embryonic axis development or heterodimerizing with INHBB or INHA to form activin AB or inhibitin B,respectively

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    SwitchGear 3'UTR luciferase reporter plasmidINHA 3' UTR sequence
    Inhib. RNA
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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for INHA

    Gene Ontology (GO): 5/7 molecular function terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005102receptor binding IPI9032295
    GO:0005125cytokine activity TAS12456957
    GO:0005179hormone activity TAS12456957
    GO:0005515contributes to protein binding IPI10746731
    GO:0008083growth factor activity TAS12324653


    INHA for ontologies           About GeneDecksing


    1 GenomeRNAi human phenotype for INHA:
     Decreased cell number and incr 

    Animal Models:
         Mouse knock-out Inhatm1Bay for INHA
         13 MGI mutant phenotypes (inferred from 1 allele(MGI details for Inha):
     cardiovascular system  digestive/alimentary  endocrine/exocrine gland  growth/size  hematopoietic system 
     homeostasis/metabolism  immune system  liver/biliary system  mortality/aging  normal 
     reproductive system  skeleton  tumorigenesis 

    INHA for phenotypes           About GeneDecksing


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Signal transduction Activin A signaling regulation
    Signal transduction Activin A signaling regulation1.00
    Signal transduction_Activin A signaling regulation0.96
    2Ovarian Infertility Genes
    Ovarian Infertility Genes1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    1 EMD Millipore Pathway for INHA
        Signal transduction Activin A signaling regulation


    1 GeneGo (Thomson Reuters) Pathway for INHA
        Signal transduction Activin A signaling regulation

    1 BioSystems Pathway for INHA 
        Ovarian Infertility Genes



    INHA for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for INHA

    STRING Interaction Network Preview (showing 5 interactants - click image to see 9)

    5/9 Interacting proteins for INHA (P051113 ENSP000002437864) via UniProtKB, MINT, STRING, and/or I2D (see all 9)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    FSTP198833, ENSP000002567594I2D: score=1 STRING: ENSP00000256759
    TGFBR3Q031673, ENSP000002123554I2D: score=1 STRING: ENSP00000212355
    ACVR2AP270373, ENSP000002414164I2D: score=1 STRING: ENSP00000241416
    INHBAP084763, ENSP000002422084I2D: score=1 STRING: ENSP00000242208
    INHBBP095293, ENSP000002952284I2D: score=1 STRING: ENSP00000295228
    About this table

    Gene Ontology (GO): 5/22 biological process terms (GO ID links to tree view) (see all 22):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0001501skeletal system development TAS10865214
    GO:0001541ovarian follicle development NAS9166111
    GO:0006917induction of apoptosis IDA8267637
    GO:0007050cell cycle arrest TAS12456957
    GO:0007165signal transduction TAS3267209


    INHA for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    INHA for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for INHA
    10/34 Novoseek chemical compound relationships for INHA gene (see all 34)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    isoniazid 89 119 15854436 (5), 12543676 (4), 14974741 (3), 7599116 (3) (see all 74)
    manganese(iii) pyrophosphate 80.4 1 11948876 (1)
    rifampicin 77.5 48 19893355 (3), 18560033 (2), 19172878 (2), 17897230 (2) (see all 30)
    ethionamide 76.1 10 19861006 (3), 7599116 (2), 14638486 (1), 19486070 (1) (see all 6)
    progesterone 61.5 51 8080927 (6), 12783698 (3), 16580171 (3), 16831355 (3) (see all 24)
    ethambutol 60.1 3 9494673 (1), 16870753 (1), 17360809 (1)
    streptomycin 57.1 6 9494673 (1), 11601331 (1), 16249627 (1), 11796356 (1)
    ribonucleic acid 55.8 7 8886632 (2), 1955539 (2), 1892206 (1), 11710435 (1) (see all 5)
    pyrazinamide 49.5 2 9494673 (1), 17360809 (1)
    testosterone 46.3 15 2307118 (4), 7608253 (2), 10569979 (1), 16429274 (1) (see all 11)

    Search CenterWatch for drugs/clinical trials and news about INHA 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for INHA gene: 
    NM_002191.3  

    Unigene Cluster for INHA:

    Inhibin, alpha
    Hs.407506  [show with all ESTs]
    Unigene Representative Sequence: BC039076
    2 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000489456 ENST00000243786(uc002vmk.2)

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    Additional cDNA sequence: 

    BC006391.2 BC039076.1 BT006954.1 M13144.1 M13981.1 

    5 DOTS entries:

    DT.411686  DT.97823930  DT.97824402  DT.101961551  DT.91819820 

    24/55 AceView cDNA sequences (see all 55):

    NM_002191 AI919290 BQ013783 M13981 BT006954 AW235196 CR617999 BC006391 
    BM711366 M13144 AU134634 BF312530 BI826892 BM670529 BI829338 AL540575 
    AU155550 BM546385 AI807888 BI520936 BM700412 AI351176 T29423 BE552259 

    GeneLoc Exon Structure


    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    INHA expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: GTGGTTGTGG

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    INHA expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    4 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    EyeInner Nuclear LayerMature Rod Bipolar CellsBipolar, Retina
    OvaryOvary InterstitiumOvary
    Skeletal MuscleExtraocular MusclesSkeletal Muscle
    TestisSeminiferous TubulesTestis
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization

    See INHA Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for INHA

    SOURCE GeneReport for Unigene cluster: Hs.407506

    UniProtKB/Swiss-Prot: INHA_HUMAN, P05111
    Tissue specificity: Originally found in ovary (granulosa cells) and testis (Sertoli cells), but widely distributed in
    many tissues including brain and placenta. In adrenal cortex expression is limited to the zona reticularis and the
    innermost zona fasciculata in the normal gland, extending centripetally into the zona fasciculata in hyperplasia. Also
    found in adrenocortical tumors. Also expressed in prostate epithelium of benign prostatic hyperplasia, in regions of
    basal cell hyperplasia and in nonmalignant regions of high grade prostate cancer. Only circulating inhibin B is found
    in male, whereas circulating inhibins A and B are found in female

        SABiosciences Expression via Pathway-Focused PCR Arrays including INHA (see all 8): 
              Growth Factors in human mouse rat
              Cell Cycle in human mouse rat
              TGFB/BMP Signaling Pathway in human mouse rat
              Common Cytokines in human mouse rat
              Apoptosis 384HT in human mouse rat

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    QIAGEN QuantiFast Probe-based Assays in human, mouse, rat INHA
    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for INHA

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for INHA gene from 4/11 species (see all 11)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Inha1 , 5 inhibin alpha1, 5 82.5(n)1
    79.72(a)1
      1 (39.16 cM)5
    163221  NM_010564.41  NP_034694.31 
     755070775 
    chicken
    (Gallus gallus)
    Aves INHA1 inhibin, alpha 63.1(n)
    55.66(a)
      424197  NM_001031257.1  NP_001026428.1 
    lizard
    (Anolis carolinensis)
    Reptilia INHA6
    --
    49(a)
    1 ↔ 1
    1(94519299-94523134)
    zebrafish
    (Danio rerio)
    Actinopterygii inha1 inhibin, alpha 50.15(n)
    38.77(a)
      570520  NM_001045204.1  NP_001038669.1 


    ENSEMBL Gene Tree for INHA (if available)
    TreeFam Gene Tree for INHA (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
      --

    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/131 NCBI SNPs in INHA are shown (see all 131    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 2 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs1116479131,2
    C,--212289728(+) GTGTGT/AGAGAG 3 -- us2k11Minor allele frequency- A:0.50CSA 2
    rs729596671,2
    C,--212289734(+) GAGAGT/AGTGTG 3 -- us2k11Minor allele frequency- A:0.50CSA 2
    rs746871371,2
    C,F,--212289901(+) ATAAGG/ACTCAT 3 -- us2k11Minor allele frequency- A:0.04WA 118
    rs1175444741,2
    C,F,--212290514(+) AGCAAT/CAGGCC 3 -- us2k11Minor allele frequency- C:0.06EA 120
    rs124642501,2
    C,H,--212290656(+) AGACCA/GGGGGT 3 -- us2k10--------
    rs1862081,2
    H--212290697(+) CCCTTC/TCTGCC 3 -- us2k14Minor allele frequency- T:0.00NS EA 418
    rs621916161,2
    --212290794(+) ATACAG/TGCAAA 3 -- us2k12Minor allele frequency- T:0.04NA 122
    rs1433772001,2
    --220436681(+) GTGTC-/TGTGTGT 4 -- us2k10--------
    rs800383851,2
    C,--220436694(+) GTGTGA/TGTGAG 4 -- us2k10--------
    rs730891261,2
    C,,--220436696(+) GTGTGT/AGAGAG 4 -- us2k11Minor allele frequency- A:0.50CSA 2

    HapMap Linkage Disequilibrium report for INHA (220433884 - 220440435 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for INHA: --
    Human Gene Mutation Database (HGMD): INHA

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    INHA for disorders           About GeneDecksing

    OMIM gene information: 147380    OMIM disorders: --

    20/99 diseases for INHA (see all 99):    About MalaCards
    von hippel-lindau disease    sex cord-gonadal stromal tumor    sertoli-leydig cell tumor    peutz-jeghers syndrome
    mixed epithelial stromal tumour    multidrug-resistant tuberculosis    leydig cell tumor    parovarian cyst
    gestational trophoblastic neoplasm    fallopian tube adenocarcinoma    androgen insensitivity syndrome    renal clear cell carcinoma
    epithelioid trophoblastic tumor    polycystic ovary syndrome    sertoli cell tumor    granular cell tumor
    pre-eclampsia    adenofibroma    placental abruption    serous cystadenoma

    9 diseases from the University of Copenhagen DISEASES database for INHA:
    Epithelioid trophoblastic tumor     Sex cord-gonadal stromal tumor     Premature ovarian failure     Parovarian cyst
    Sertoli cell tumor     Leydig cell tumor     Granular cell tumor     Fallopian tube adenocarcinoma
    Testicular cancer

    10/80 Novoseek disease relationships for INHA gene (see all 80)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    sex cord-stromal tumor 87.5 19 11192074 (3), 10747314 (2), 15256111 (2), 15381902 (1) (see all 11)
    granulosa cell tumor 86.6 20 17609358 (4), 9190962 (3), 10843483 (3), 19115695 (2) (see all 12)
    sertoli cell tumor 84.3 5 19255517 (1), 15363041 (1), 11971979 (1)
    sertoli-leydig cell tumor 82.6 3 9475192 (1), 20158943 (1), 12502966 (1)
    trophoblastic tumor 82.5 3 11603223 (2), 10202672 (1)
    tuberculosis 76.1 146 15854436 (4), 11802940 (4), 8684371 (3), 20200152 (3) (see all 85)
    trophoblastic tumor placental site 75 3 11603223 (2), 10202672 (1)
    thecoma 72.4 1 20198651 (1)
    adenoma adrenocortical 70 12 12910679 (4), 11556749 (2), 15256108 (1), 15970011 (1) (see all 6)
    stromal tumors 69.3 5 15059165 (3), 11192073 (1)

    Genetic Association Database (GAD): INHA
    Human Genome Epidemiology (HuGE) Navigator: INHA (35 documents)
    Tumor Gene Database (TGDB): INHA

    Export disorders for INHA gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for INHA gene, integrated from 9 sources (see all 510):
    (articles sorted by number of sources associating them with INHA)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. INHA promoter polymorphisms are associated with premature ovarian failure. (PubMed id 16390856)1, 4, 9 Harris S.E....Shelling A.N. (2005)
    2. Loss of the expression and localization of inhibin alpha-subunit in high grade prostate cancer. (PubMed id 9506758)1, 2, 9 Mellor S.L....Risbridger G.P. (1998)
    3. Controversial role of inhibin alpha-subunit gene in the aetiology of premature ovarian failure. (PubMed id 16396934)1, 4 Sundblad V....Dain L. (2006)
    4. Mutational analysis of the inhibin alpha gene in preeclamptic women. (PubMed id 15816368)1, 4 Ciarmela P....Petraglia F. (2005)
    5. [The use of DNA analysis for diagnostics of hereditary premature ovarian failure] (PubMed id 16161415)1, 4 Livshyts' H.B....Sudoma I.A. (2005)
    6. G769A variation of inhibin alpha-gene in korean women with premature ovarian failure. (PubMed id 15227735)1, 4 Jeong H.J....Cha K.Y. (2004)
    7. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    8. Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure. (PubMed id 12093833)1, 4 Marozzi A....Ginelli E. (2002)
    9. Inhibin: a candidate gene for premature ovarian failure. (PubMed id 11098038)1, 2 Shelling A.N....Winship I.M. (2000)
    10. Characterization and determination of the biological activities of noncleavable high molecular weight forms of inhibin A and activin A. (PubMed id 8885240)1, 2 Mason A.J.... Sullivan J. (1996)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
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    Aliases
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 3623 HGNC: 6065 AceView: INHA Ensembl:ENSG00000123999 euGenes: HUgn3623
    ECgene: INHA H-InvDB: INHA

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for INHA Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for INHA Genetics and Cytogenetics in Oncology and Haematology
    Wikipedia http://en.wikipedia.org/wiki/Inhibin

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for INHA gene:
    Search GeneIP for patents involving INHA

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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