FAM111B
protein-coding gene in the species Homo sapiens
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FAM111B
Summary
FAM111B is a gene[1].
Key Facts
- FAM111B's instance of is recorded as gene[2].
- FAM111B is a type of protein-coding gene[3].
- FAM111B's HomoloGene ID is recorded as 52377[4].
- FAM111B's genomic start is recorded as 59107185[5].
- FAM111B's genomic start is recorded as 58874658[6].
- FAM111B's genomic end is recorded as 58894883[7].
- FAM111B's genomic end is recorded as 59127412[8].
- FAM111B's encodes is recorded as Family with sequence similarity 111 member B[9].
- FAM111B's found in taxon is recorded as Homo sapiens[10].
- FAM111B's chromosome is recorded as human chromosome 11[11].
- FAM111B's genetic association is recorded as hereditary sclerosing poikiloderma with tendon and pulmonary involvement[12].
- FAM111B's strand orientation is recorded as forward strand[13].
- FAM111B's exact match is recorded as http://identifiers.org/ncbigene/374393[14].
- FAM111B's cytogenetic location is recorded as 11q12.1[15].
- FAM111B's expressed in is recorded as secondary oocyte[16].
- FAM111B's expressed in is recorded as buccal mucosa cell[17].
- FAM111B's expressed in is recorded as ganglionic eminence[18].
- FAM111B's expressed in is recorded as ventricular zone[19].
- FAM111B's expressed in is recorded as testicle[20].
- FAM111B's expressed in is recorded as rectum[21].
- FAM111B's expressed in is recorded as appendix[22].
- FAM111B's expressed in is recorded as stromal cell of endometrium[23].
- FAM111B's expressed in is recorded as mucosa of transverse colon[24].
- FAM111B's expressed in is recorded as lymph node[25].