TTC8
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 14[14]
- Cytogenetic location
- 14q31.3[17]
- Expressed in
- left ovary, islet of Langerhans, right adrenal cortex, right uterine tube, pituitary gland, right ovary, anterior pituitary, left adrenal gland, left adrenal cortex, stromal cell of endometrium[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- retinitis pigmentosa 51[15]
- HomoloGene ID
- 14988[3]
- Strand orientation
- forward strand[16]
🏷️ Also known as
en BBS8
en RP51
en tetratricopeptide repeat domain 8
en TTC8
ar TTC٨
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000165533
- Ensembl transcript ID
- ENST00000622513, ENST00000338104, ENST00000346301, ENST00000354441, ENST00000380656, ENST00000553718, ENST00000554686, ENST00000555057, ENST00000556077, ENST00000556133, ENST00000556567, ENST00000556651, ENST00000557580
- Entrez Gene ID
- 123016
- Exact match
- identifiers.org
- Freebase ID
- /m/04my_xc
- HGNC ID
- 20087
- HGNC gene symbol
- TTC8
- Microsoft Academic ID (discontinued)
- 2781058271
- OMIM ID
- 608132
- RefSeq RNA ID
- NM_001288781, NM_001288782, NM_001288783, NM_144596, NM_198309, NM_198310, XM_011536433, XM_011536434, NM_001366535, NM_001366536, NR_159362
- UMLS CUI
- C1426673
🔗 Connections
Expressed in 3
Chromosome 1
Found in taxon 1
Instance of 1
Press Enter · cited answer in seconds