KRT12
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KRT12
Summary
KRT12 is a gene[1]. KRT12 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2]
Key Facts
- KRT12's instance of is recorded as gene[3].
- KRT12 is a type of protein-coding gene[4].
- KRT12's HomoloGene ID is recorded as 188[5].
- KRT12's genomic start is recorded as 39017555[6].
- KRT12's genomic start is recorded as 40861303[7].
- KRT12's genomic end is recorded as 39023462[8].
- KRT12's genomic end is recorded as 40867223[9].
- KRT12's ortholog is recorded as Krt12[10].
- KRT12's ortholog is recorded as Krt12[11].
- KRT12's encodes is recorded as keratin 12[12].
- KRT12's found in taxon is recorded as Homo sapiens[13].
- KRT12's chromosome is recorded as human chromosome 17[14].
- KRT12's genetic association is recorded as Meesmann corneal dystrophy[15].
- KRT12's strand orientation is recorded as reverse strand[16].
- KRT12's exact match is recorded as http://identifiers.org/ncbigene/3859[17].
- KRT12's cytogenetic location is recorded as 17q21.2[18].
- KRT12's expressed in is recorded as gonad[19].
- KRT12's expressed in is recorded as testicle[20].
- KRT12's expressed in is recorded as mucosa of transverse colon[21].
- KRT12's expressed in is recorded as eye[22].
- KRT12's expressed in is recorded as duodenum[23].
- KRT12's expressed in is recorded as skin of abdomen[24].
- KRT12's expressed in is recorded as rectum[25].
- KRT12's expressed in is recorded as skin of leg[26].
- KRT12's expressed in is recorded as vagina[27].
Why It Matters
KRT12 ranks in the top 2% of gene entities by monthly Wikipedia readership (9 views/month).[2]