FAM168B
protein-coding gene in the species Homo sapiens
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Summary
FAM168B is a gene[1].
Key Facts
- FAM168B's instance of is recorded as gene[2].
- FAM168B is a type of protein-coding gene[3].
- FAM168B's HomoloGene ID is recorded as 18390[4].
- FAM168B's genomic start is recorded as 131047876[5].
- FAM168B's genomic start is recorded as 131805449[6].
- FAM168B's genomic end is recorded as 131093460[7].
- FAM168B's genomic end is recorded as 131851033[8].
- FAM168B's ortholog is recorded as Fam168b[9].
- FAM168B's ortholog is recorded as Fam168b[10].
- FAM168B's ortholog is recorded as fam168b[11].
- FAM168B's encodes is recorded as Family with sequence similarity 168 member B[12].
- FAM168B's found in taxon is recorded as Homo sapiens[13].
- FAM168B's chromosome is recorded as human chromosome 2[14].
- FAM168B's strand orientation is recorded as reverse strand[15].
- FAM168B's exact match is recorded as http://identifiers.org/ncbigene/130074[16].
- FAM168B's cytogenetic location is recorded as 2q21.1[17].
- FAM168B's expressed in is recorded as external globus pallidus[18].
- FAM168B's expressed in is recorded as cerebellar vermis[19].
- FAM168B's expressed in is recorded as lateral nuclear group of thalamus[20].
- FAM168B's expressed in is recorded as pons[21].
- FAM168B's expressed in is recorded as Brodmann area 46[22].
- FAM168B's expressed in is recorded as middle frontal gyrus[23].
- FAM168B's expressed in is recorded as parietal lobe[24].
- FAM168B's expressed in is recorded as postcentral gyrus[25].
- FAM168B's expressed in is recorded as superior vestibular nucleus[26].