HNRNPA1

HNRNPA1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesHNRNPA1, ALS19, ALS20, HNRPA1, HNRPA1L3, IBMPFD3, hnRNP A1, hnRNP-A1, UP 1, heterogeneous nuclear ribonucleoprotein A1
External IDsOMIM: 164017; MGI: 104820; HomoloGene: 134664; GeneCards: HNRNPA1; OMA:HNRNPA1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

3178

15382

Ensembl

ENSG00000135486

ENSMUSG00000046434

UniProt

P09651

P49312

RefSeq (mRNA)

NM_002136
NM_031157

NM_001039129
NM_010447

RefSeq (protein)

NP_002127
NP_112420

NP_001034218
NP_034577

Location (UCSC)n/aChr 15: 103.15 – 103.16 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Heterogeneous nuclear ribonucleoprotein A1 is a protein that in humans is encoded by the HNRNPA1 gene. Mutations in hnRNP A1 are causative of amyotrophic lateral sclerosis and the syndrome multisystem proteinopathy.