IFT140
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 16[13]
- Cytogenetic location
- 16p13.3[16]
- Expressed in
- right uterine tube, right lobe of thyroid gland, left lobe of thyroid gland, left testis, right testis, ventricular zone, anterior pituitary, stromal cell of endometrium, olfactory zone of nasal mucosa, bronchial epithelial cell[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- short-rib thoracic dysplasia 9 with or without polydactyly[14]
- HomoloGene ID
- 40979[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en c305C8.4
en c380F5.1
en gs114
en IFT140
en intraflagellar transport 140
en MZSDS
en RP80
en SRTD9
en WDTC2
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000187535
- Ensembl transcript ID
- ENST00000569812, ENST00000361339, ENST00000397417, ENST00000426508, ENST00000439987, ENST00000561954, ENST00000565298, ENST00000566052, ENST00000566818, ENST00000568837, ENST00000569646
- Entrez Gene ID
- 9742
- Exact match
- identifiers.org
- Freebase ID
- /m/0vpv7ks
- HGNC ID
- 29077
- HGNC gene symbol
- IFT140
- OMIM ID
- 614620
- RefSeq RNA ID
- XM_011522772, NM_014714, XM_005255725, XM_005255726, XM_006720990, XM_006720991, XM_006720992, XM_011522766, XM_011522767, XM_011522769, XM_011522771, XM_017023910, XM_017023911
- UMLS CUI
- C1825574
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