RAI1
protein-coding gene in the species Homo sapiens
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RAI1
Summary
RAI1 is a gene[1].
Key Facts
- RAI1's instance of is recorded as gene[2].
- RAI1 is a type of protein-coding gene[3].
- RAI1's HomoloGene ID is recorded as 7508[4].
- RAI1's genomic start is recorded as 17584787[5].
- RAI1's genomic start is recorded as 17681458[6].
- RAI1's genomic end is recorded as 17811453[7].
- RAI1's genomic end is recorded as 17714767[8].
- RAI1's ortholog is recorded as Rai1[9].
- RAI1's ortholog is recorded as Rai1[10].
- RAI1's encodes is recorded as Retinoic acid induced 1[11].
- RAI1's found in taxon is recorded as Homo sapiens[12].
- RAI1's chromosome is recorded as human chromosome 17[13].
- RAI1's genetic association is recorded as Smith-Magenis syndrome[14].
- RAI1's strand orientation is recorded as forward strand[15].
- RAI1's exact match is recorded as http://identifiers.org/ncbigene/10743[16].
- RAI1's cytogenetic location is recorded as 17p11.2[17].
- RAI1's expressed in is recorded as retinal pigment epithelium[18].
- RAI1's expressed in is recorded as nipple[19].
- RAI1's expressed in is recorded as palpebral conjunctiva[20].
- RAI1's expressed in is recorded as urethra[21].
- RAI1's expressed in is recorded as pylorus[22].
- RAI1's expressed in is recorded as tibia[23].
- RAI1's expressed in is recorded as Brodmann area 23[24].
- RAI1's expressed in is recorded as cardia[25].
- RAI1's expressed in is recorded as human penis[26].