FAM131B
protein-coding gene in the species Homo sapiens
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Summary
FAM131B is a gene[1].
Key Facts
- FAM131B's instance of is recorded as gene[2].
- FAM131B is a type of protein-coding gene[3].
- FAM131B's HomoloGene ID is recorded as 8797[4].
- FAM131B's genomic start is recorded as 143353400[5].
- FAM131B's genomic start is recorded as 143050493[6].
- FAM131B's genomic end is recorded as 143362770[7].
- FAM131B's genomic end is recorded as 143059863[8].
- FAM131B's ortholog is recorded as Fam131b[9].
- FAM131B's ortholog is recorded as Fam131b[10].
- FAM131B's encodes is recorded as Family with sequence similarity 131 member B[11].
- FAM131B's found in taxon is recorded as Homo sapiens[12].
- FAM131B's chromosome is recorded as human chromosome 7[13].
- FAM131B's strand orientation is recorded as reverse strand[14].
- FAM131B's exact match is recorded as http://identifiers.org/ncbigene/9715[15].
- FAM131B's cytogenetic location is recorded as 7q34[16].
- FAM131B's expressed in is recorded as right hemisphere of cerebellum[17].
- FAM131B's expressed in is recorded as C1 segment[18].
- FAM131B's expressed in is recorded as prefrontal cortex[19].
- FAM131B's expressed in is recorded as right frontal lobe[20].
- FAM131B's expressed in is recorded as ganglionic eminence[21].
- FAM131B's expressed in is recorded as Brodmann area 9[22].
- FAM131B's expressed in is recorded as primary visual cortex[23].
- FAM131B's expressed in is recorded as endothelial cell[24].
- FAM131B's expressed in is recorded as internal globus pallidus[25].
- FAM131B's expressed in is recorded as middle temporal gyrus[26].