OAT
protein-coding gene in the species Homo sapiens
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OAT
Summary
OAT is a gene[1].
Key Facts
- OAT's instance of is recorded as gene[2].
- OAT is a type of protein-coding gene[3].
- OAT's HomoloGene ID is recorded as 231[4].
- OAT's genomic start is recorded as 124397303[5].
- OAT's genomic start is recorded as 126085872[6].
- OAT's genomic end is recorded as 124418976[7].
- OAT's genomic end is recorded as 126107545[8].
- OAT's ortholog is recorded as Oat[9].
- OAT's ortholog is recorded as Oat[10].
- OAT's ortholog is recorded as CAR2[11].
- OAT's ortholog is recorded as oat[12].
- OAT's ortholog is recorded as Oat[13].
- OAT's ortholog is recorded as oatr-1[14].
- OAT's encodes is recorded as Ornithine aminotransferase[15].
- OAT's found in taxon is recorded as Homo sapiens[16].
- OAT's chromosome is recorded as human chromosome 10[17].
- OAT's genetic association is recorded as gyrate atrophy of the choroid[18].
- OAT's strand orientation is recorded as reverse strand[19].
- OAT's exact match is recorded as http://identifiers.org/ncbigene/4942[20].
- OAT's cytogenetic location is recorded as 10q26.13[21].
- OAT's expressed in is recorded as jejunal mucosa[22].
- OAT's expressed in is recorded as parotid gland[23].
- OAT's expressed in is recorded as duodenum[24].
- OAT's expressed in is recorded as secondary oocyte[25].
- OAT's expressed in is recorded as epithelium of nasopharynx[26].