FAM168A
protein-coding gene in the species Homo sapiens
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Summary
FAM168A is a gene[1].
Key Facts
- FAM168A's instance of is recorded as gene[2].
- FAM168A is a type of protein-coding gene[3].
- FAM168A's HomoloGene ID is recorded as 18702[4].
- FAM168A's genomic start is recorded as 73400487[5].
- FAM168A's genomic start is recorded as 73111532[6].
- FAM168A's genomic end is recorded as 73598189[7].
- FAM168A's genomic end is recorded as 73309234[8].
- FAM168A's ortholog is recorded as Fam168a[9].
- FAM168A's ortholog is recorded as Fam168a[10].
- FAM168A's ortholog is recorded as fam168a[11].
- FAM168A's encodes is recorded as Family with sequence similarity 168 member A[12].
- FAM168A's found in taxon is recorded as Homo sapiens[13].
- FAM168A's chromosome is recorded as human chromosome 11[14].
- FAM168A's strand orientation is recorded as reverse strand[15].
- FAM168A's exact match is recorded as http://identifiers.org/ncbigene/23201[16].
- FAM168A's cytogenetic location is recorded as 11q13.4[17].
- FAM168A's expressed in is recorded as ganglionic eminence[18].
- FAM168A's expressed in is recorded as external globus pallidus[19].
- FAM168A's expressed in is recorded as postcentral gyrus[20].
- FAM168A's expressed in is recorded as lateral nuclear group of thalamus[21].
- FAM168A's expressed in is recorded as prefrontal cortex[22].
- FAM168A's expressed in is recorded as primary visual cortex[23].
- FAM168A's expressed in is recorded as pons[24].
- FAM168A's expressed in is recorded as pars reticulata[25].
- FAM168A's expressed in is recorded as superior frontal gyrus[26].