NTRK2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 9[13]
- Cytogenetic location
- 9q21.33[16]
- Expressed in
- optic nerve, external globus pallidus, Region I of hippocampus proper, internal globus pallidus, Epithelium of choroid plexus, superior vestibular nucleus, dorsal motor nucleus of vagus nerve, ventral tegmental area, postcentral gyrus, pars reticulata[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- obesity, Hyperphagia, and developmental delay[14]
- HomoloGene ID
- 4504[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en EIEE58
en GP145-TrkB
en neurotrophic receptor tyrosine kinase 2
en NTRK2
en OBHD
en trk-B
en TRKB
fa گیرنده تیروزین کیناز بی
ja トロポミオシン受容体キナーゼB
ja 脳由来神経栄養因子受容体
🔖 Identifiers · 14
- OpenAlex ID
- C97124661
- Image (Wikimedia Commons)
- Protein NTRK2 PDB 1hcf.png ↗
- CIViC gene ID
- 3984
- Ensembl gene ID
- ENSG00000148053
- Ensembl transcript ID
- ENST00000395882, ENST00000277120, ENST00000304053, ENST00000323115, ENST00000359847, ENST00000376208, ENST00000376213, ENST00000376214
- Entrez Gene ID
- 4915
- Exact match
- identifiers.org
- Freebase ID
- /m/0dfz6x
- HGNC ID
- 8032
- HGNC gene symbol
- NTRK2
- Microsoft Academic ID (discontinued)
- 2.9B (97.1M–2.9B, n=3)
- OMIM ID
- 600456
Show all 14 identifiers +2
- RefSeq RNA ID
- XM_011518720, NM_001007097, NM_001018064, NM_001018065, NM_001018066, NM_001291937, NM_006180, XM_005252001, XM_005252003, XM_005252004, XM_005252006, XM_005252007, XM_011518718, XM_017014751, XM_017014752, XM_017014753, XM_017014754, XM_017014755, XM_017014756, XM_017014757, XM_017014758, XM_017014759, XM_017014760, XM_017014761
- UMLS CUI
- C1334909
🔗 Connections
Expressed in 3
Chromosome 1
Found in taxon 1
Instance of 1
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Summary
NTRK2 is a gene[1].