KRT3
Protein in humans
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KRT3
Summary
KRT3 is a gene[1].
Key Facts
- KRT3's instance of is recorded as gene[2].
- KRT3 is a type of protein-coding gene[3].
- KRT3's genomic start is recorded as 52789685[4].
- KRT3's genomic start is recorded as 53183469[5].
- KRT3's genomic end is recorded as 52796117[6].
- KRT3's genomic end is recorded as 53189901[7].
- KRT3's encodes is recorded as keratin 3[8].
- KRT3's found in taxon is recorded as Homo sapiens[9].
- KRT3's chromosome is recorded as human chromosome 12[10].
- KRT3's genetic association is recorded as Meesmann corneal dystrophy[11].
- KRT3's strand orientation is recorded as reverse strand[12].
- KRT3's exact match is recorded as http://identifiers.org/ncbigene/3850[13].
- KRT3's cytogenetic location is recorded as 12q13.13[14].
- KRT3's expressed in is recorded as gums[15].
- KRT3's expressed in is recorded as skin of abdomen[16].
- KRT3's expressed in is recorded as vagina[17].
- KRT3's expressed in is recorded as skin of limb[18].
- KRT3's expressed in is recorded as skin of leg[19].
- KRT3's expressed in is recorded as tonsil[20].
- KRT3's expressed in is recorded as islet of Langerhans[21].
- KRT3's expressed in is recorded as cervix[22].
- KRT3's expressed in is recorded as salivary gland[23].
- KRT3's expressed in is recorded as right lobe of thyroid gland[24].