KRT222
protein-coding gene in the species Homo sapiens
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KRT222
Summary
KRT222 is a gene[1].
Key Facts
- KRT222's instance of is recorded as gene[2].
- KRT222 is a type of protein-coding gene[3].
- KRT222's HomoloGene ID is recorded as 17556[4].
- KRT222's genomic start is recorded as 40654665[5].
- KRT222's genomic start is recorded as 38785049[6].
- KRT222's genomic start is recorded as 38810917[7].
- KRT222's genomic end is recorded as 40665181[8].
- KRT222's genomic end is recorded as 38821393[9].
- KRT222's genomic end is recorded as 38821433[10].
- KRT222's ortholog is recorded as Krt222[11].
- KRT222's ortholog is recorded as Krt222[12].
- KRT222's ortholog is recorded as krt222[13].
- KRT222's encodes is recorded as Keratin 222[14].
- KRT222's found in taxon is recorded as Homo sapiens[15].
- KRT222's chromosome is recorded as human chromosome 17[16].
- KRT222's strand orientation is recorded as reverse strand[17].
- KRT222's exact match is recorded as http://identifiers.org/ncbigene/125113[18].
- KRT222's cytogenetic location is recorded as 17q21.2[19].
- KRT222's expressed in is recorded as lateral nuclear group of thalamus[20].
- KRT222's expressed in is recorded as Brodmann area 23[21].
- KRT222's expressed in is recorded as Brodmann area 46[22].
- KRT222's expressed in is recorded as primary visual cortex[23].
- KRT222's expressed in is recorded as Brodmann area 9[24].
- KRT222's expressed in is recorded as cerebellar cortex[25].
- KRT222's expressed in is recorded as cerebellar hemisphere[26].