IFT172
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 2[14]
- Cytogenetic location
- 2p23.3[18]
- Encodes
- Intraflagellar transport 172, Intraflagellar transport protein 172 homolog[11][12]
- Expressed in
- right uterine tube, bronchial epithelial cell, left testis, right testis, olfactory zone of nasal mucosa, anterior pituitary, left ovary, right ovary, right hemisphere of cerebellum, rectum[19][20][21][22][23][24]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- short-rib thoracic dysplasia 10 with or without polydactyly, retinitis pigmentosa 71[15][16]
- HomoloGene ID
- 15202[3]
- Strand orientation
- reverse strand[17]
🏷️ Also known as
en BBS20
en IFT172
en intraflagellar transport 172
en NPHP17
en osm-1
en RP71
en SLB
en SRTD10
en wim
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000138002
- Ensembl transcript ID
- ENST00000511842, ENST00000260570, ENST00000359466, ENST00000416524, ENST00000420854, ENST00000443889, ENST00000450564, ENST00000463613, ENST00000475476, ENST00000475909, ENST00000476264, ENST00000476693, ENST00000479419, ENST00000480892, ENST00000489492, ENST00000494163, ENST00000507184, ENST00000509128, ENST00000676300, ENST00000675729, ENST00000676101, ENST00000675410, ENST00000675963, ENST00000674824, ENST00000676119, ENST00000674594, ENST00000674932, ENST00000675728, ENST00000675690, ENST00000675925, ENST00000675618, ENST00000675757, ENST00000675826, ENST00000674701
- Entrez Gene ID
- 26160
- Exact match
- identifiers.org
- Google Knowledge Graph ID
- /g/11fy_4rd07
- HGNC ID
- 30391
- HGNC gene symbol
- IFT172
- OMIM ID
- 607386
- RefSeq RNA ID
- XM_011532760, NM_015662, XM_005264254, XM_006711986, XM_006711987, XM_011532758, XM_011532759, XM_047443900, XM_047443901, XM_047443902, XM_047443903, XM_047443904
- UMLS CUI
- C1825575
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