ROR2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 9[13]
- Cytogenetic location
- 9q22.31[17]
- Expressed in
- muscle layer of sigmoid colon, gastric mucosa, body of uterus, canal of the cervix, ectocervix, right ovary, gonad, left uterine tube, right auricle of heart, left ovary[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- brachydactyly type B1, autosomal recessive Robinow syndrome[14][15]
- HomoloGene ID
- 55831[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en BDB
en BDB1
en NTRKR2
en receptor tyrosine kinase like orphan receptor 2
en ROR2
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000169071
- Ensembl transcript ID
- ENST00000550066, ENST00000375708, ENST00000375715, ENST00000476440, ENST00000493846, ENST00000495386, ENST00000546883, ENST00000548585
- Entrez Gene ID
- 4920
- Exact match
- identifiers.org
- Freebase ID
- /m/0d8fh3
- HGNC ID
- 10257
- HGNC gene symbol
- ROR2
- Microsoft Academic ID (discontinued)
- 55326434
- OMIM ID
- 602337
- RefSeq RNA ID
- NM_004560, XM_005252008, XM_005252009, XM_006717121, NM_001318204, XM_017014762, XM_047423434, XM_047423435, XM_047423436, XM_047423437
- UMLS CUI
- C1366544
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