RBM19
protein-coding gene in the species Homo sapiens
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Summary
RBM19 is a gene[1]. RBM19 ranks in the top 2% of gene entities by monthly Wikipedia readership (6 views/month).[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 7158[4]
- Genomic start: 113816738[5], 114254543[6]
- Genomic end: 114404176[7], 113966325[8]
- Ortholog: Rbm19[9], MRD1[10], CG3335[11], rbd-1[12]
- Encodes: RNA binding motif protein 19[13]
- Found in taxon: Homo sapiens[14]
- Chromosome: human chromosome 12[15]
- Genetic association: amyotrophic lateral sclerosis[16]
- Strand orientation: reverse strand[17]
- Exact match: http://identifiers.org/ncbigene/9904[18]
- Cytogenetic location: 12q24.13-q24.21[19]
- Expressed in: sural nerve[20], left lobe of thyroid gland[21], right lobe of thyroid gland[22], right uterine tube[23], left ovary[24], apex of heart[25], right ovary[26], left adrenal cortex[27], right adrenal cortex[28], body of uterus[29]
Why It Matters
RBM19 is known by 4 alternative names across languages and contexts.[30]