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Aliases for HNRNPA1 Gene

Aliases for HNRNPA1 Gene

  • Heterogeneous Nuclear Ribonucleoprotein A1 2 3 5
  • Single-Strand RNA-Binding Protein 3 4
  • Helix-Destabilizing Protein 3 4
  • HnRNP A1 3 4
  • HNRPA1 3 4
  • Putative Heterogeneous Nuclear Ribonucleoprotein A1-Like 3 3
  • Heterogeneous Nuclear Ribonucleoprotein Core Protein A1 3
  • Heterogeneous Nuclear Ribonucleoprotein A1B Protein 3
  • Heterogeneous Nuclear Ribonucleoprotein B2 Protein 3
  • Nuclear Ribonucleoprotein Particle A1 Protein 3
  • Single-Strand DNA-Binding Protein UP1 3
  • HnRNP Core Protein A1-Like 3 3
  • HnRNP Core Protein A1 4
  • HNRPA1L3 3
  • HnRNP-A1 3
  • IBMPFD3 3
  • ALS19 3
  • ALS20 3
  • UP 1 3

External Ids for HNRNPA1 Gene

Previous HGNC Symbols for HNRNPA1 Gene

  • HNRPA1

Previous GeneCards Identifiers for HNRNPA1 Gene

  • GC12P052961
  • GC12P054674
  • GC12P051713

Summaries for HNRNPA1 Gene

Entrez Gene Summary for HNRNPA1 Gene

  • This gene encodes a member of a family of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs), which are RNA-binding proteins that associate with pre-mRNAs in the nucleus and influence pre-mRNA processing, as well as other aspects of mRNA metabolism and transport. The protein encoded by this gene is one of the most abundant core proteins of hnRNP complexes and plays a key role in the regulation of alternative splicing. Mutations in this gene have been observed in individuals with amyotrophic lateral sclerosis 20. Multiple alternatively spliced transcript variants have been found. There are numerous pseudogenes of this gene distributed throughout the genome. [provided by RefSeq, Feb 2016]

GeneCards Summary for HNRNPA1 Gene

HNRNPA1 (Heterogeneous Nuclear Ribonucleoprotein A1) is a Protein Coding gene. Diseases associated with HNRNPA1 include Inclusion Body Myopathy Wtih Early-Onset Paget Disease Without Frontotemporal Dementia 3 and Amyotrophic Lateral Sclerosis 20. Among its related pathways are mRNA Splicing - Major Pathway and Gene Expression. GO annotations related to this gene include nucleic acid binding and RNA binding. An important paralog of this gene is HNRNPA1L2.

UniProtKB/Swiss-Prot for HNRNPA1 Gene

  • Involved in the packaging of pre-mRNA into hnRNP particles, transport of poly(A) mRNA from the nucleus to the cytoplasm and may modulate splice site selection.

  • (Microbial infection) May play a role in HCV RNA replication.

Gene Wiki entry for HNRNPA1 Gene

No data available for CIViC summary , Tocris Summary , PharmGKB "VIP" Summary , fRNAdb sequence ontologies and piRNA Summary for HNRNPA1 Gene

Genomics for HNRNPA1 Gene

Regulatory Elements for HNRNPA1 Gene

Enhancers for HNRNPA1 Gene
GeneHancer Identifier Enhancer Score Enhancer Sources Gene-Enhancer Score TSS distance (kb) Number of Genes Away Size (kb) Transcription Factor Binding Sites within enhancer Gene Targets for Enhancer
GH12G054291 1.9 FANTOM5 Ensembl ENCODE dbSUPER 27 +16.9 16919 11.8 HDGF PKNOX1 CREB3L1 ARNT ARID4B SIN3A YBX1 DMAP1 ZNF2 YY1 HNRNPA1 MAP3K12 ITGA5 RNU6-950P MIR148B GPR84 ZNF385A FLJ12825 GTSF1 AAAS
GH12G053971 2.1 FANTOM5 Ensembl ENCODE dbSUPER 6.5 -290.0 -289951 36.8 CREB3L1 AGO1 FEZF1 DMAP1 YY1 ZNF416 ZNF143 ZNF548 ZNF263 SP3 ZNF740 MAP3K12 ENSG00000258344 LOC100652999 HOXC8 HOXC5 SP1 HOTAIR CBX5 HOXC4
GH12G054323 1.4 Ensembl ENCODE 8.3 +47.7 47695 8.3 HDGF PKNOX1 FOXA2 MLX CREB3L1 ARNT ARID4B SIN3A DMAP1 ZNF2 HOXC8 HOXC9 ENSG00000258086 GPR84 HOXC5 HOXC6 HOXC4 ITGA5 HNRNPA1 GC12P054329
GH12G054367 1.6 Ensembl ENCODE dbSUPER 5.1 +90.1 90147 4.9 PKNOX1 ARNT AGO1 SIN3A ZNF2 ZNF143 DEK REST SMARCB1 ZNF592 MIR148B MAP3K12 CBX5 ENSG00000260470 ITGA5 GPR84 FLJ12825 ZNF385A HNRNPA1
GH12G053725 1.1 ENCODE 6.5 -553.3 -553315 3.1 HDGF PKNOX1 CREB3L1 ARNT ARID4B SIN3A FEZF1 ZNF2 ZBTB7B YY1 MAP3K12 ZNF740 HNRNPA1 LOC105369774 CALCOCO1
- Elite enhancer and/or Elite enhancer-gene association Download GeneHancer data dump

Enhancers around HNRNPA1 on UCSC Golden Path with GeneCards custom track

Promoters for HNRNPA1 Gene
Ensembl Regulatory Elements (ENSRs) TSS Distance (bp) Size (bp) Binding Sites for Transcription Factors within promoters
ENSR00000052331 307 4201 MLX CREB3L1 FEZF1 DMAP1 YY1 SLC30A9 ZNF143 ZNF263 SP3 NFYC

Genomic Location for HNRNPA1 Gene

Chromosome:
12
Start:
54,280,193 bp from pter
End:
54,287,088 bp from pter
Size:
6,896 bases
Orientation:
Plus strand

Genomic View for HNRNPA1 Gene

Genes around HNRNPA1 on UCSC Golden Path with GeneCards custom track

Cytogenetic band:
HNRNPA1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
Genomic Location for HNRNPA1 Gene
GeneLoc Logo Genomic Neighborhood Exon StructureGene Density

RefSeq DNA sequence for HNRNPA1 Gene

Proteins for HNRNPA1 Gene

  • Protein details for HNRNPA1 Gene (UniProtKB/Swiss-Prot)

    Protein Symbol:
    P09651-ROA1_HUMAN
    Recommended name:
    Heterogeneous nuclear ribonucleoprotein A1
    Protein Accession:
    P09651
    Secondary Accessions:
    • A8K4Z8
    • Q3MIB7
    • Q6PJZ7

    Protein attributes for HNRNPA1 Gene

    Size:
    372 amino acids
    Molecular mass:
    38747 Da
    Quaternary structure:
    • Identified in the spliceosome C complex (PubMed:11991638). Identified in a IGF2BP1-dependent mRNP granule complex containing untranslated mRNAs (PubMed:17289661). Interacts with SEPT6 (PubMed:17229681). Interacts with C9orf72 (PubMed:24549040). Interacts with KHDRBS1 (PubMed:17371836). Interacts with UBQLN2 (PubMed:25616961).
    • (Microbial infection) Interacts with HCV NS5B and with the 5-UTR and 3-UTR of HCV RNA.

    Three dimensional structures from OCA and Proteopedia for HNRNPA1 Gene

    Alternative splice isoforms for HNRNPA1 Gene

    UniProtKB/Swiss-Prot:

neXtProt entry for HNRNPA1 Gene

Post-translational modifications for HNRNPA1 Gene

  • Arg-194, Arg-206 and Arg-225 are dimethylated, probably to asymmetric dimethylarginine.
  • Sumoylated.
  • Ubiquitination at isoforms=3, 278 and posLast=350350
  • Modification sites at PhosphoSitePlus

Antibody Products

  • Cell Signaling Technology (CST) Antibodies for HNRNPA1 (hnRNP A1)
  • Cloud-Clone Corp. Antibodies for HNRNPA1

No data available for DME Specific Peptides for HNRNPA1 Gene

Domains & Families for HNRNPA1 Gene

Gene Families for HNRNPA1 Gene

Protein Domains for HNRNPA1 Gene

Graphical View of Domain Structure for InterPro Entry

genes like me logo Genes that share domains with HNRNPA1: view

No data available for UniProtKB/Swiss-Prot for HNRNPA1 Gene

Function for HNRNPA1 Gene

Molecular function for HNRNPA1 Gene

UniProtKB/Swiss-Prot Function:
Involved in the packaging of pre-mRNA into hnRNP particles, transport of poly(A) mRNA from the nucleus to the cytoplasm and may modulate splice site selection.
UniProtKB/Swiss-Prot Function:
(Microbial infection) May play a role in HCV RNA replication.

Gene Ontology (GO) - Molecular Function for HNRNPA1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0003676 nucleic acid binding IEA --
GO:0003697 single-stranded DNA binding IDA 8521471
GO:0003723 RNA binding IDA,TAS 22658674
GO:0003727 single-stranded RNA binding IC 8521471
GO:0005515 protein binding IPI 17229681
genes like me logo Genes that share ontologies with HNRNPA1: view
genes like me logo Genes that share phenotypes with HNRNPA1: view

Human Phenotype Ontology for HNRNPA1 Gene

HPO Id HPO Name Alternative Ids Definition Synonyms

Animal Model Products

CRISPR Products

miRNA for HNRNPA1 Gene

miRTarBase miRNAs that target HNRNPA1

Inhibitory RNA Products

Clone Products

Flow Cytometry Products

No data available for Enzyme Numbers (IUBMB) , Animal Models , Transcription Factor Targets and HOMER Transcription for HNRNPA1 Gene

Localization for HNRNPA1 Gene

Subcellular locations from UniProtKB/Swiss-Prot for HNRNPA1 Gene

Nucleus. Cytoplasm. Note=Localized in cytoplasmic mRNP granules containing untranslated mRNAs. Shuttles continuously between the nucleus and the cytoplasm along with mRNA. Component of ribonucleosomes (PubMed:17289661). {ECO:0000269 PubMed:17289661, ECO:0000269 PubMed:27694260}.
Cytoplasm. Note=(Microbial infection) In the course of viral infection, colocalizes with HCV NS5B at speckles in the cytoplasm in a HCV-replication dependent manner. {ECO:0000269 PubMed:17229681}.

Subcellular locations from

COMPARTMENTS
Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
COMPARTMENTS Subcellular localization image for HNRNPA1 gene
Compartment Confidence
extracellular 5
nucleus 5
cytosol 1

Gene Ontology (GO) - Cellular Components for HNRNPA1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0005634 nucleus IDA,IEA 23935072
GO:0005654 nucleoplasm TAS,IDA --
GO:0005681 spliceosomal complex IDA 9731529
GO:0005737 cytoplasm IDA 8521471
GO:0016020 membrane IDA 19946888
genes like me logo Genes that share ontologies with HNRNPA1: view

Pathways & Interactions for HNRNPA1 Gene

genes like me logo Genes that share pathways with HNRNPA1: view

Pathways by source for HNRNPA1 Gene

1 KEGG pathway for HNRNPA1 Gene
1 Qiagen pathway for HNRNPA1 Gene

SIGNOR curated interactions for HNRNPA1 Gene

Is inactivated by:

Gene Ontology (GO) - Biological Process for HNRNPA1 Gene

GO ID Qualified GO term Evidence PubMed IDs
GO:0000381 regulation of alternative mRNA splicing, via spliceosome IMP 25689357
GO:0000398 mRNA splicing, via spliceosome TAS --
GO:0006397 mRNA processing TAS 8521471
GO:0006405 RNA export from nucleus IC 8521471
GO:0006810 transport IEA --
genes like me logo Genes that share ontologies with HNRNPA1: view

Drugs & Compounds for HNRNPA1 Gene

(1) Drugs for HNRNPA1 Gene - From: Novoseek

Name Status Disease Links Group Role Mechanism of Action Clinical Trials
genes like me logo Genes that share compounds with HNRNPA1: view

Transcripts for HNRNPA1 Gene

Unigene Clusters for HNRNPA1 Gene

Heterogeneous nuclear ribonucleoprotein A1:
Representative Sequences:

CRISPR Products

Inhibitory RNA Products

Clone Products

Flow Cytometry Products

Alternative Splicing Database (ASD) splice patterns (SP) for HNRNPA1 Gene

ExUns: 1a · 1b ^ 2a · 2b · 2c ^ 3 ^ 4a · 4b ^ 5 ^ 6a · 6b ^ 7a · 7b ^ 8 ^ 9 ^ 10a · 10b ^ 11a · 11b ^ 12 ^ 13
SP1:
SP2:
SP3:
SP4: - - -
SP5:
SP6: -
SP7: - - - - - - - -
SP8:
SP9: - -

Relevant External Links for HNRNPA1 Gene

GeneLoc Exon Structure for
HNRNPA1
ECgene alternative splicing isoforms for
HNRNPA1

Expression for HNRNPA1 Gene

mRNA expression in normal human tissues from GTEx, Illumina, BioGPS, and CGAP SAGE for HNRNPA1 Gene

Protein differential expression in normal tissues from HIPED for HNRNPA1 Gene

This gene is overexpressed in Fetal gut (6.7) and Fetal ovary (6.5).

Integrated Proteomics: protein expression in normal tissues and cell lines from ProteomicsDB, PaxDb, MaxQB, and MOPED for HNRNPA1 Gene



Protein tissue co-expression partners for HNRNPA1 Gene

- Elite partner

NURSA nuclear receptor signaling pathways regulating expression of HNRNPA1 Gene:

HNRNPA1

SOURCE GeneReport for Unigene cluster for HNRNPA1 Gene:

Hs.546261

Evidence on tissue expression from TISSUES for HNRNPA1 Gene

  • Nervous system(5)
  • Eye(4.9)
  • Kidney(4.9)
  • Liver(4.9)
  • Lung(4.9)
  • Blood(4.8)
  • Intestine(4.7)
  • Skin(4.2)
  • Bone marrow(4)
  • Pancreas(4)
  • Muscle(3.9)
  • Heart(3.6)
  • Stomach(3.5)
  • Bone(3)
  • Spleen(2.3)

Phenotype-based relationships between genes and organs from Gene ORGANizer for HNRNPA1 Gene

Germ Layers:
  • ectoderm
  • endoderm
  • mesoderm
Systems:
  • cardiovascular
  • digestive
  • immune
  • nervous
  • respiratory
  • skeletal muscle
  • skeleton
  • urinary
Organs:
Head and neck:
  • brain
  • cerebellum
  • cranial nerve
  • ear
  • epiglottis
  • face
  • head
  • jaw
  • larynx
  • mandible
  • maxilla
  • mouth
  • neck
  • nose
  • pharynx
  • skull
  • tongue
  • vocal cord
Thorax:
  • bronchus
  • chest wall
  • clavicle
  • esophagus
  • heart
  • lung
  • rib
  • rib cage
  • scapula
  • sternum
  • trachea
Abdomen:
  • abdominal wall
  • biliary tract
  • kidney
  • liver
  • stomach
Pelvis:
  • pelvis
Limb:
  • ankle
  • arm
  • digit
  • elbow
  • femur
  • fibula
  • finger
  • foot
  • forearm
  • hand
  • hip
  • humerus
  • knee
  • lower limb
  • radius
  • shin
  • shoulder
  • thigh
  • tibia
  • toe
  • ulna
  • upper limb
  • wrist
General:
  • blood vessel
  • peripheral nerve
  • peripheral nervous system
  • spinal column
  • spinal cord
  • vertebrae
genes like me logo Genes that share expression patterns with HNRNPA1: view

Primer Products

No data available for mRNA expression in embryonic tissues and stem cells from LifeMap Discovery , mRNA differential expression in normal tissues and mRNA Expression by UniProt/SwissProt for HNRNPA1 Gene

Orthologs for HNRNPA1 Gene

This gene was present in the common ancestor of chordates.

Orthologs for HNRNPA1 Gene

Organism Taxonomy Gene Similarity Type Details
chimpanzee
(Pan troglodytes)
Mammalia HNRNPA1 34 35
  • 99.58 (n)
mouse
(Mus musculus)
Mammalia Hnrnpa1 35
  • 99 (a)
OneToOne
oppossum
(Monodelphis domestica)
Mammalia -- 35
  • 95 (a)
ManyToMany
-- 35
  • 86 (a)
ManyToMany
-- 35
  • 82 (a)
ManyToMany
cow
(Bos Taurus)
Mammalia HNRNPA1 34 35
  • 94.27 (n)
rat
(Rattus norvegicus)
Mammalia Hnrnpa1 34
  • 92.4 (n)
dog
(Canis familiaris)
Mammalia -- 35
  • 91 (a)
ManyToMany
-- 35
  • 88 (a)
ManyToMany
-- 35
  • 88 (a)
ManyToMany
-- 35
  • 86 (a)
ManyToMany
-- 35
  • 81 (a)
ManyToMany
-- 35
  • 81 (a)
ManyToMany
platypus
(Ornithorhynchus anatinus)
Mammalia -- 35
  • 90 (a)
OneToMany
chicken
(Gallus gallus)
Aves LOC100859627 34
  • 76.72 (n)
lizard
(Anolis carolinensis)
Reptilia -- 35
  • 87 (a)
OneToMany
African clawed frog
(Xenopus laevis)
Amphibia hnrpa1-prov 34
zebrafish
(Danio rerio)
Actinopterygii Dr.708 34
Species where no ortholog for HNRNPA1 was found in the sources mined by GeneCards:
  • A. gosspyii yeast (Ashbya gossypii)
  • Actinobacteria (Mycobacterium tuberculosis)
  • African malaria mosquito (Anopheles gambiae)
  • Alicante grape (Vitis vinifera)
  • alpha proteobacteria (Wolbachia pipientis)
  • amoeba (Dictyostelium discoideum)
  • Archea (Pyrococcus horikoshii)
  • baker's yeast (Saccharomyces cerevisiae)
  • barley (Hordeum vulgare)
  • beta proteobacteria (Neisseria meningitidis)
  • bread mold (Neurospora crassa)
  • Chromalveolata (Phytophthora infestans)
  • common water flea (Daphnia pulex)
  • corn (Zea mays)
  • E. coli (Escherichia coli)
  • filamentous fungi (Aspergillus nidulans)
  • Firmicute bacteria (Streptococcus pneumoniae)
  • fission yeast (Schizosaccharomyces pombe)
  • fruit fly (Drosophila melanogaster)
  • green algae (Chlamydomonas reinhardtii)
  • honey bee (Apis mellifera)
  • K. lactis yeast (Kluyveromyces lactis)
  • loblloly pine (Pinus taeda)
  • malaria parasite (Plasmodium falciparum)
  • medicago trunc (Medicago Truncatula)
  • moss (Physcomitrella patens)
  • orangutan (Pongo pygmaeus)
  • pig (Sus scrofa)
  • rainbow trout (Oncorhynchus mykiss)
  • rice (Oryza sativa)
  • rice blast fungus (Magnaporthe grisea)
  • schistosome parasite (Schistosoma mansoni)
  • sea anemone (Nematostella vectensis)
  • sea squirt (Ciona intestinalis)
  • sea squirt (Ciona savignyi)
  • sea urchin (Strongylocentrotus purpuratus)
  • sorghum (Sorghum bicolor)
  • soybean (Glycine max)
  • stem rust fungus (Puccinia graminis)
  • sugarcane (Saccharum officinarum)
  • thale cress (Arabidopsis thaliana)
  • tomato (Lycopersicon esculentum)
  • toxoplasmosis (Toxoplasma gondii)
  • Trichoplax (Trichoplax adhaerens)
  • tropical clawed frog (Silurana tropicalis)
  • wheat (Triticum aestivum)
  • worm (Caenorhabditis elegans)

Evolution for HNRNPA1 Gene

ENSEMBL:
Gene Tree for HNRNPA1 (if available)
TreeFam:
Gene Tree for HNRNPA1 (if available)

Paralogs for HNRNPA1 Gene

Pseudogenes.org Pseudogenes for HNRNPA1 Gene

genes like me logo Genes that share paralogs with HNRNPA1: view

Variants for HNRNPA1 Gene

Sequence variations from dbSNP and Humsavar for HNRNPA1 Gene

SNP ID Clin Chr 12 pos Sequence Context AA Info Type
rs397518452 Pathogenic, Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3 (IBMPFD3) [MIM:615424] 54,283,845(+) CAATG(A/T)TTTTG nc-transcript-variant, reference, missense
rs397518453 Pathogenic, Amyotrophic lateral sclerosis 20 (ALS20) [MIM:615426] 54,283,844(+) ACAAT(A/G)ATTTT nc-transcript-variant, reference, missense
rs397518454 Pathogenic, Amyotrophic lateral sclerosis 20 (ALS20) [MIM:615426] 54,283,860(+) TTACA(A/G)CAATC nc-transcript-variant, reference, missense
VAR_077531 Amyotrophic lateral sclerosis 20 (ALS20) [MIM:615426]
VAR_077533 Amyotrophic lateral sclerosis 20 (ALS20) [MIM:615426]

Structural Variations from Database of Genomic Variants (DGV) for HNRNPA1 Gene

Variant ID Type Subtype PubMed ID
esv25123 CNV loss 19812545
nsv1049160 CNV gain 25217958
nsv832420 CNV loss 17160897
nsv976627 CNV duplication 23825009

Variation tolerance for HNRNPA1 Gene

Residual Variation Intolerance Score: 33% of all genes are more intolerant (likely to be disease-causing)
Gene Damage Index Score: 1.28; 25.60% of all genes are more intolerant (likely to be disease-causing)

Relevant External Links for HNRNPA1 Gene

Human Gene Mutation Database (HGMD)
HNRNPA1
SNPedia medical, phenotypic, and genealogical associations of SNPs for
HNRNPA1

No data available for Polymorphic Variants from UniProtKB/Swiss-Prot for HNRNPA1 Gene

Disorders for HNRNPA1 Gene

MalaCards: The human disease database

(10) MalaCards diseases for HNRNPA1 Gene - From: OMIM, ClinVar, GeneTests, Orphanet, Swiss-Prot, DISEASES, and GeneCards

Disorder Aliases PubMed IDs
inclusion body myopathy wtih early-onset paget disease without frontotemporal dementia 3
  • inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3
amyotrophic lateral sclerosis 20
  • amyotrophic lateral sclerosis type 20
hnrnpa1-related amyotrophic lateral sclerosis
  • amyotrophic lateral sclerosis 20
amyotrophic lateral sclerosis 1
  • amyotrophic lateral sclerosis
lateral sclerosis
  • motor neuron disease
- elite association - COSMIC cancer census association via MalaCards

UniProtKB/Swiss-Prot

ROA1_HUMAN
  • Amyotrophic lateral sclerosis 20 (ALS20) [MIM:615426]: A neurodegenerative disorder affecting upper motor neurons in the brain and lower motor neurons in the brain stem and spinal cord, resulting in fatal paralysis. Sensory abnormalities are absent. The pathologic hallmarks of the disease include pallor of the corticospinal tract due to loss of motor neurons, presence of ubiquitin-positive inclusions within surviving motor neurons, and deposition of pathologic aggregates. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of the cases. {ECO:0000269 PubMed:23455423, ECO:0000269 PubMed:27694260}. Note=The disease is caused by mutations affecting the gene represented in this entry.
  • Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3 (IBMPFD3) [MIM:615424]: An autosomal dominant disease characterized by disabling muscle weakness clinically resembling to limb girdle muscular dystrophy, osteolytic bone lesions consistent with Paget disease, and premature frontotemporal dementia. Clinical features show incomplete penetrance. {ECO:0000269 PubMed:23455423}. Note=The disease is caused by mutations affecting the gene represented in this entry.

Relevant External Links for HNRNPA1

Genetic Association Database (GAD)
HNRNPA1
Human Genome Epidemiology (HuGE) Navigator
HNRNPA1
Atlas of Genetics and Cytogenetics in Oncology and Haematology:
HNRNPA1
genes like me logo Genes that share disorders with HNRNPA1: view

No data available for Genatlas for HNRNPA1 Gene

Publications for HNRNPA1 Gene

  1. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS. (PMID: 23455423) Kim H.J. … Taylor J.P. (Nature 2013) 2 3 4 64
  2. Assignment of the human heterogeneous nuclear ribonucleoprotein A1 gene (HNRPA1) to chromosome 12q13.1 by cDNA competitive in situ hybridization. (PMID: 1733858) Saccone S. … Della Valle G. (Genomics 1992) 2 3 22 64
  3. Alternative splicing in the human gene for the core protein A1 generates another hnRNP protein. (PMID: 1691095) Buvoli M. … Riva S. (EMBO J. 1990) 3 4 22 64
  4. Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS. (PMID: 27694260) Liu Q. … Zhang X. (Neurology 2016) 3 4 64
  5. ALS-linked mutations in ubiquilin-2 or hnRNPA1 reduce interaction between ubiquilin-2 and hnRNPA1. (PMID: 25616961) Gilpin K.M. … Monteiro M.J. (Hum. Mol. Genet. 2015) 3 4 64

Products for HNRNPA1 Gene

Sources for HNRNPA1 Gene

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