ROR1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[13]
- Cytogenetic location
- 1p31.3[16]
- Expressed in
- germinal epithelium, popliteal artery, tibial arteries, islet of Langerhans, right coronary artery, lower lobe of lung, saphenous vein, Descending thoracic aorta, sural nerve, buccal mucosa cell[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- autosomal recessive nonsyndromic deafness 108[14]
- HomoloGene ID
- 3675[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en dJ537F10.1
en NTRKR1
en receptor tyrosine kinase like orphan receptor 1
en receptor tyrosine kinase-like orphan receptor 1
en ROR1
🔖 Identifiers · 12
- OpenAlex ID
- C23440912
- Ensembl gene ID
- ENSG00000185483
- Ensembl transcript ID
- ENST00000371079, ENST00000371080, ENST00000482426
- Entrez Gene ID
- 4919
- Exact match
- identifiers.org
- Freebase ID
- /m/0dd8rj_
- HGNC ID
- 10256
- HGNC gene symbol
- ROR1
- Microsoft Academic ID (discontinued)
- 23440912
- OMIM ID
- 602336
- RefSeq RNA ID
- XM_011541526, NM_001083592, NM_005012, XM_017001376, XM_017001377
- UMLS CUI
- C1335633
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