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

FAM162A Gene

protein-coding   GIFtS: 52
GCID: GC03P122103

Family With Sequence Similarity 162, Member A

(Previous name: chromosome 3 open reading frame 28)
(Previous symbol: C3orf28)
  See related diseases
at  

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, 10fRNAdb, 12H-InvDB, 13NCBI, 14NONCODE, and/or 15RNAdb)
About This Section

Aliases
Family With Sequence Similarity 162, Member A1 2     E2-Induced Gene 5 Protein2 3
C3orf281 2 3 5     Chromosome 3 Open Reading Frame 281
E2IG52 3 5     HIF-1 Alpha-Responsive Proapoptotic Molecule2
Growth And Transformation-Dependent Protein2 3     Protein FAM162A2
HGTD-P2 3     

External Ids:    HGNC: 178651   Entrez Gene: 263552   Ensembl: ENSG000001140237   OMIM: 6080175   UniProtKB: Q96A263   

Export aliases for FAM162A gene to outside databases

Previous GC identifers: GC03P123587 GC03P119476


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

GeneCards Summary for FAM162A Gene: 
FAM162A (family with sequence similarity 162, member A) is a protein-coding gene. Diseases associated with FAM162A include hypoxia, and ischemia. GO annotations related to this gene include protein binding. An important paralog of this gene is FAM162B.

UniProtKB/Swiss-Prot: F162A_HUMAN, Q96A26
Function: Proposed to be involved in regulation of apoptosis; the exact mechanism may differ between cell
types/tissues. May be involved in hypoxia-induced cell death of transformed cells implicating cytochrome C
release and caspase activation (such as CASP9) and inducing mitochondrial permeability transition. May be
involved in hypoxia-induced cell death of neuronal cells probably by promoting release of AIFM1 from mitochondria
to cytoplasm and its translocation to the nucleus; however, the involvement of caspases has been reported
conflictingly




(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 73), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000003.11  NT_005612.16  NC_018914.2  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the FAM162A gene promoter:
         AML1a   STAT5A   CUTL1   Arnt   POU2F1   USF-1   FOXJ2 (long isoform)   POU2F1a   ARP-1   FOXJ2   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidFAM162A promoter sequence
   Search SABiosciences Chromatin IP Primers for FAM162A

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat FAM162A


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

Entrez Gene cytogenetic band: 3q21.1   Ensembl cytogenetic band:  3q21.1   HGNC cytogenetic band: 3q21.1

FAM162A Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
FAM162A gene location

GeneLoc information about chromosome 3         GeneLoc Exon Structure

GeneLoc location for GC03P122103:  view genomic region     (about GC identifiers)

Start:
122,103,023 bp from pter      End:
122,131,181 bp from pter
Size:
28,159 bases      Orientation:
plus strand

(According to UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE 1MOPED, 2PaxDb, and 3MAXQB 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 Cloud-Clone Corp.,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Cloud-Clone Corp., Ontologies according to Gene Ontology Consortium 01 Oct 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, LSBio, Abcam, and/or Cloud-Clone Corp.)
About This Section

UniProtKB/Swiss-Prot: F162A_HUMAN, Q96A26 (See protein sequence)
Recommended Name: Protein FAM162A  
Size: 154 amino acids; 17342 Da
Subunit: Interacts with HSP90AB1; HSP90AB1 is essential for FAM162A mitochondrial localization and pro-apoptotic
activity. Interacts with VDAC2; the interaction is probably involved in inducing mitochondrial permability
transition
Subcellular location: Membrane; Single-pass membrane protein (Potential). Mitochondrion
Sequence caution: Sequence=AAF09484.1; Type=Frameshift; Positions=147;
Secondary accessions: Q9NRN6 Q9UJX8

Explore the universe of human proteins at neXtProt for FAM162A: NX_Q96A26

Explore proteomics data for FAM162A at MOPED 

Post-translational modifications:

  • View modification sites using PhosphoSitePlus
  • View neXtProt modification sites for NX_Q96A26

  • FAM162A Protein expression data from MOPED1, PaxDb2 and MAXQB3 :    About this image 

    FAM162A Protein Expression
    REFSEQ proteins: NP_055182.3  
    ENSEMBL proteins: 
     ENSP00000232125   ENSP00000419088   ENSP00000419491  

    Human Recombinant Protein Products for FAM162A: 
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    Novus Biologicals FAM162A Protein
    Novus Biologicals FAM162A Lysate
    Browse Sino Biological Recombinant Proteins
    Browse Sino Biological Cell Lysates 
    Browse ProSpec Recombinant Proteins
    Cloud-Clone Corp. Proteins for FAM162A 

    Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005739mitochondrion IEA--
    GO:0016021integral to membrane IEA--

    FAM162A for ontologies           About GeneDecksing



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    Cloud-Clone Corp. ELISAs for FAM162A 
    Cloud-Clone Corp. CLIAs for FAM162A


    (According to HGNC, IUPHAR, InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section
    1 InterPro protein domain:
     IPR009432 DUF1075

    Graphical View of Domain Structure for InterPro Entry Q96A26

    ProtoNet protein and cluster: Q96A26

    UniProtKB/Swiss-Prot: F162A_HUMAN, Q96A26
    Similarity: Belongs to the UPF0389 family


    FAM162A for domains           About GeneDecksing


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013, inGenious Targeting Laboratory, genOway,
    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, Sirion Biotech, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, Vector BioLabs, and Sirion Biotech, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Oct 2013 via Entrez Gene.)
    About This Section

    Molecular Function:

         UniProtKB/Swiss-Prot Summary: F162A_HUMAN, Q96A26
    Function: Proposed to be involved in regulation of apoptosis; the exact mechanism may differ between cell
    types/tissues. May be involved in hypoxia-induced cell death of transformed cells implicating cytochrome C
    release and caspase activation (such as CASP9) and inducing mitochondrial permeability transition. May be
    involved in hypoxia-induced cell death of neuronal cells probably by promoting release of AIFM1 from mitochondria
    to cytoplasm and its translocation to the nucleus; however, the involvement of caspases has been reported
    conflictingly
    Induction: By 17-beta-estradiol. By hypoxia

         Gene Ontology (GO): 1 molecular function term (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005515protein binding IPI15082785
         
    FAM162A for ontologies           About GeneDecksing


    Animal Models:
       inGenious Targeting Laboratory - Custom generated mouse model solutions for FAM162A 
       inGenious Targeting Laboratory - Custom generated inducible mouse model solutions for FAM162A

       genOway customized KO model: permanent, tissue-specific or time-controlled inactivation for FAM162A 
       genOway customized Knockin model: humanization, point mutation, expression monitoring, etc. for FAM162A 

    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat FAM162A
    1 QIAGEN miScript miRNA Assays for microRNA that regulate FAM162A:
    hsa-miR-3658
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    Inhib. RNA
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    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Sino Biological, 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 Oct 2013 via Entrez Gene).
    About This Section



    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for FAM162A

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

    5/6 Interacting proteins for FAM162A (Q96A261, 2, 3 ENSP000004190884) via UniProtKB, MINT, STRING, and/or I2D (see all 6)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    HSP90AB1P082382, 3, ENSP000003258754MINT-2567397 MINT-2567472 MINT-2567511 I2D: score=1 STRING: ENSP00000325875
    HSP90AA1P079003, ENSP000003351534I2D: score=1 STRING: ENSP00000335153
    VDAC2P458801, ENSP000003616864EBI-6123466,EBI-354022 STRING: ENSP00000361686
    SQSTM1Q135013I2D: score=1 
    IKBKEENSP000003560874STRING: ENSP00000356087
    About this table

    Gene Ontology (GO): 5/6 biological process terms (GO ID links to tree view) (see all 6):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0006919activation of cysteine-type endopeptidase activity involved in apoptotic process IDA15082785
    GO:0006927transformed cell apoptotic process IDA15082785
    GO:0043065positive regulation of apoptotic process IDA15082785
    GO:0051402neuron apoptotic process IEA--
    GO:0071456cellular response to hypoxia IDA15082785

    FAM162A for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, Ligands according to IUPHAR, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for FAM162A (F162A)

    Search CenterWatch for drugs/clinical trials and news about FAM162A / F162A

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 236 Homo sapiens; Apr 25 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    Conferences by KenesGroup, 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, Sirion Biotech, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for FAM162A gene: 
    NM_014367.3  

    Unigene Cluster for FAM162A:

    Family with sequence similarity 162, member A
    Hs.584881  [show with all ESTs]
    Unigene Representative Sequence: AK125835
    3 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000232125 ENST00000477892(uc003eez.3) ENST00000469967(uc011bjq.1)

    miRNA
    Products:
         
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    1 QIAGEN miScript miRNA Assays for microRNA that regulate FAM162A:
    hsa-miR-3658
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    Inhib. RNA
    Products:
         
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    Clone
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat FAM162A
    Sirion Biotech Customized lentivirus for stable overexpression of FAM162A 
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    Primer
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    OriGene qPCR primer pairs and template standards for FAM162A
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat FAM162A
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat FAM162A

    Additional mRNA sequence: 

    AF107495.1 AF191020.1 AF201944.1 AK026030.1 AK125835.1 AK293994.1 BC010896.1 BC015060.1 

    9 DOTS entries:

    DT.418501  DT.418503  DT.100825396  DT.95117732  DT.100825400  DT.95117747  DT.120865950  DT.92430374 
    DT.99943747 

    24/263 AceView cDNA sequences (see all 263):

    CA413798 BF034502 BM980190 N64447 AI300894 AJ710750 BM761278 AI536726 
    BG057258 BQ937560 CB177903 BX644560 BM693062 CA941090 CA952819 BI827224 
    AI375600 AI127011 AA236720 AI075462 T66904 AI151271 BM674240 CR603838 

    GeneLoc Exon Structure

    3 Alternative Splicing Database (ASD) splice patterns (SP) for FAM162A    About this scheme

    ExUns: 1a · 1b ^ 2 ^ 3 ^ 4 ^ 5a · 5b ^ 6a · 6b
    SP1:                                      -               
    SP2:              -                       -               
    SP3:              -                                       


    ECgene alternative splicing isoforms for FAM162A

    (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

    FAM162A expression in normal human tissues (normalized intensities)      FAM162A embryonic expression: see
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS <intensity>2/3
    CGAP TAG: GTTATTGAGG
    FAM162A Expression
    About this image


    FAM162A expression in embryonic tissues and stem cells    About this table
    Data from LifeMap, the Embryonic Development and Stem Cells Database 
     5/1 selected tissues (see all 1) fully expand
     
     Uncategorized (Uncategorized)
             PureStem progenitor SK17

    See FAM162A Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for FAM162A

    SOURCE GeneReport for Unigene cluster: Hs.584881
        SABiosciences Custom PCR Arrays for FAM162A
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    In Situ
    Assay Products:
     

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for FAM162A

    (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 animals.

    Orthologs for FAM162A gene from 5/10 species (see all 10)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Fam162a1 , 5 family with sequence similarity 162, member A1, 5 83.55(n)1
    79.22(a)1
      16 (25.43 cM)5
    701861  NM_027342.11  NP_081618.11 
     360438445 
    chicken
    (Gallus gallus)
    Aves FAM162A1 family with sequence similarity 162, member A 61.07(n)
    54.74(a)
      418270  XM_416495.3  XP_416495.3 
    lizard
    (Anolis carolinensis)
    Reptilia FAM162A6
    Uncharacterized protein
    47(a)
    1 ↔ 1
    GL343473.1(100180-113447)
    zebrafish
    (Danio rerio)
    Actinopterygii wufb08c122 Transcribed sequence with weak similarity to protein more 75.35(n)    57076751 
    fruit fly
    (Drosophila melanogaster)
    Insecta CG92316
    --
    26(a)
    1 → many
    3L(19578193-19579070)


    ENSEMBL Gene Tree for FAM162A (if available)
    TreeFam Gene Tree for FAM162A (if available)

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for FAM162A gene
    FAM162B2  
    1 SIMAP similar gene for FAM162A using alignment to 3 protein entries:     F162A_HUMAN (see all proteins):
    FAM162B

    FAM162A for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, 4UniProtKB, 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

    10/498 SNPs in FAM162A are shown (see all 498)    About this table     
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 3 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs19619571,2
    C,F,O,A,H--122104122(+) TATCTG/AGTGTT 1 -- int121Minor allele frequency- A:0.37MN NS EA NA WA CSA 2416
    rs133178551,2
    C,F,H--122104234(+) ATGATT/ATCATT 1 -- int14Minor allele frequency- A:0.04EA NS NA 398
    rs1494560071,2
    C--122104350(+) AAAAAA/GGTTAA 1 -- int10--------
    rs729565331,2
    C,F--122104416(+) CTAATA/GCTGAG 1 -- int12Minor allele frequency- G:0.16WA 120
    rs783108831,2
    F--122104482(+) AAATAT/CATTTT 1 -- int11Minor allele frequency- C:0.01EA 120
    rs1125472711,2
    F--122104491(+) TTTGCG/ATCTCT 1 -- int12Minor allele frequency- A:0.33CSA 3
    rs1873266901,2
    --122104848(+) TGCCAA/GAAAAT 1 -- int10--------
    rs570860781,2
    C--122104982(+) TGAAAT/CGGAAG 1 -- int13Minor allele frequency- C:0.07NA EA 242
    rs1482101941,2
    C--122104987(+) TGGAAA/GAGTCA 1 -- int10--------
    rs98736841,2
    C--122105120(+) GCTCAA/GTGTGG 1 -- int16Minor allele frequency- G:0.40NA WA EA 364

    HapMap Linkage Disequilibrium report for FAM162A (122103023 - 122131181 bp)

    Structural Variations
         Database of Genomic Variants (DGV) 2 variations for FAM162A:    About this table     
    Variant IDTypeSubtypePubMed ID
    esv2660557CNV Deletion23128226
    nsv3973CNV Loss18451855

    SABiosciences Cancer Mutation PCR Assays
    SeqTarget long-range PCR primers for resequencing FAM162A
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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Conferences by KenesGroup, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section
    OMIM gene information: 608017    OMIM disorders: --

    5 diseases for FAM162A:    About MalaCards
    hypoxia    ischemia    adenoma    cervicitis
    neuronitis


    FAM162A for disorders           About GeneDecksing

    Genetic Association Database (GAD): FAM162A
    Human Genome Epidemiology (HuGE) Navigator: FAM162A (1 document)

    Export disorders for FAM162A 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 FAM162A gene, integrated from 9 sources (see all 19):
    (articles sorted by number of sources associating them with FAM162A)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Effects of estrogen on global gene expression: identification of novel targets of estrogen action. (PubMed id 11085516)1, 2, 3 Charpentier A.H.... Aldaz C.M. (2000)
    2. Genetic variants in nuclear-encoded mitochondrial gen es influence AIDS progression. (PubMed id 20877624)1, 4 Hendrickson S.L....O'Brien S.J. (2010)
    3. Interaction of pro-apoptotic protein HGTD-P with heat shock protein 90 is required for induction of mitochondrial apoptotic cascades. (PubMed id 16698020)1, 2 Kim J.Y....Park J.H. (2006)
    4. 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)
    5. Identification of the hypoxia-inducible factor 1 alpha-responsive HGTD-P gene as a mediator in the mitochondrial apoptotic pathway. (PubMed id 15082785)1, 2 Lee M.J....Park J.H. (2004)
    6. Proapoptotic role of human growth and transformation- dependent protein in the developing rat brain after hypoxia-ischemia. (PubMed id 19520982)1, 9 Qu Y....Mu D. (2009)
    7. Novel, gel-free proteomics approach identifies RNF5 an d JAMP as modulators of GPCR stability. (PubMed id 23798571)1 Roy S.J....Parent J.L. (2013)
    8. SGTA recognizes a noncanonical ubiquitin-like domain i n the Bag6-Ubl4A-Trc35 complex to promote endoplasmic reticulum-associated degra dation. (PubMed id 23246001)1 Xu Y....Ye Y. (2012)
    9. A census of human soluble protein complexes. (PubMed id 22939629)1 Havugimana P.C....Emili A. (2012)
    10. Methods for quantification of in vivo changes in prote in ubiquitination following proteasome and deubiquitinase inhibition. (PubMed id 22505724)1 Udeshi N.D....Carr S.A. (2012)

    (in PubMed, OMIM, and NCBI Bookshelf)
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    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 26355 HGNC: 17865 AceView: E2IG5 Ensembl:ENSG00000114023 euGenes: HUgn26355
    ECgene: FAM162A H-InvDB: FAM162A

    (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 FAM162A Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for FAM162A gene:
    Search GeneIP for patents involving FAM162A

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



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Cloud-Clone Corp., Thermo Fisher Scientific, LSBio, Gene Editing from DNA2.0 and Sirion Biotech, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Sirion Biotech, Cell lines from GenScript, and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences, In Situ Hybridization Assays from
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    GeneCards Homepage - Last full update: 23 Oct 2013 - Incrementals: 4 Nov 2013 , 7 Nov 2013 , 23 Jan 2014

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