IFT172
protein-coding gene in the species Homo sapiens
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IFT172
Summary
IFT172 is a gene[1].
Key Facts
- IFT172's instance of is recorded as gene[2].
- IFT172 is a type of protein-coding gene[3].
- IFT172's HomoloGene ID is recorded as 15202[4].
- IFT172's genomic start is recorded as 27667238[5].
- IFT172's genomic start is recorded as 27444377[6].
- IFT172's genomic end is recorded as 27712656[7].
- IFT172's genomic end is recorded as 27489805[8].
- IFT172's ortholog is recorded as Ift172[9].
- IFT172's ortholog is recorded as Ift172[10].
- IFT172's ortholog is recorded as Oseg2[11].
- IFT172's ortholog is recorded as osm-1[12].
- IFT172's ortholog is recorded as ift172[13].
- IFT172's encodes is recorded as Intraflagellar transport 172[14].
- IFT172's encodes is recorded as Intraflagellar transport protein 172 homolog[15].
- IFT172's found in taxon is recorded as Homo sapiens[16].
- IFT172's chromosome is recorded as human chromosome 2[17].
- IFT172's genetic association is recorded as short-rib thoracic dysplasia 10 with or without polydactyly[18].
- IFT172's genetic association is recorded as retinitis pigmentosa 71[19].
- IFT172's strand orientation is recorded as reverse strand[20].
- IFT172's exact match is recorded as http://identifiers.org/ncbigene/26160[21].
- IFT172's cytogenetic location is recorded as 2p23.3[22].
- IFT172's expressed in is recorded as right uterine tube[23].
- IFT172's expressed in is recorded as bronchial epithelial cell[24].
- IFT172's expressed in is recorded as left testis[25].
- IFT172's expressed in is recorded as right testis[26].