FAM131C
protein-coding gene in the species Homo sapiens
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Summary
FAM131C is a gene[1].
Key Facts
- FAM131C's instance of is recorded as gene[2].
- FAM131C is a type of protein-coding gene[3].
- FAM131C's HomoloGene ID is recorded as 18806[4].
- FAM131C's genomic start is recorded as 16057769[5].
- FAM131C's genomic start is recorded as 16384264[6].
- FAM131C's genomic end is recorded as 16400127[7].
- FAM131C's genomic end is recorded as 16073651[8].
- FAM131C's ortholog is recorded as Fam131c[9].
- FAM131C's ortholog is recorded as Fam131c[10].
- FAM131C's ortholog is recorded as fam131c[11].
- FAM131C's encodes is recorded as Family with sequence similarity 131 member C[12].
- FAM131C's found in taxon is recorded as Homo sapiens[13].
- FAM131C's chromosome is recorded as human chromosome 1[14].
- FAM131C's strand orientation is recorded as reverse strand[15].
- FAM131C's exact match is recorded as http://identifiers.org/ncbigene/348487[16].
- FAM131C's cytogenetic location is recorded as 1p36.13[17].
- FAM131C's expressed in is recorded as cerebellar hemisphere[18].
- FAM131C's expressed in is recorded as right hemisphere of cerebellum[19].
- FAM131C's expressed in is recorded as C1 segment[20].
- FAM131C's expressed in is recorded as testicle[21].
- FAM131C's expressed in is recorded as substantia nigra[22].
- FAM131C's expressed in is recorded as apex of heart[23].
- FAM131C's expressed in is recorded as hypothalamus[24].
- FAM131C's expressed in is recorded as anterior cingulate cortex[25].
- FAM131C's expressed in is recorded as temporal lobe[26].