F13B
protein-coding gene in the species Homo sapiens
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F13B
Summary
F13B is a gene[1].
Key Facts
- F13B's instance of is recorded as gene[2].
- F13B is a type of protein-coding gene[3].
- F13B's HomoloGene ID is recorded as 1512[4].
- F13B's genomic start is recorded as 197008321[5].
- F13B's genomic start is recorded as 197038741[6].
- F13B's genomic end is recorded as 197036397[7].
- F13B's genomic end is recorded as 197067260[8].
- F13B's ortholog is recorded as F13b[9].
- F13B's encodes is recorded as Coagulation factor XIII B chain[10].
- F13B's found in taxon is recorded as Homo sapiens[11].
- F13B's chromosome is recorded as human chromosome 1[12].
- F13B's genetic association is recorded as erectile dysfunction[13].
- F13B's genetic association is recorded as factor Xiii, b subunit, deficiency of[14].
- F13B's strand orientation is recorded as reverse strand[15].
- F13B's exact match is recorded as http://identifiers.org/ncbigene/2165[16].
- F13B's cytogenetic location is recorded as 1q31.3[17].
- F13B's expressed in is recorded as right lobe of liver[18].
- F13B's expressed in is recorded as testicle[19].
- F13B's expressed in is recorded as jejunal mucosa[20].
- F13B's expressed in is recorded as duodenum[21].
- F13B's expressed in is recorded as gonad[22].
- F13B's expressed in is recorded as gallbladder[23].
- F13B's expressed in is recorded as skin of thigh[24].
- F13B's expressed in is recorded as Ventricular system of neuraxis[25].
- F13B's expressed in is recorded as ventricular zone[26].