FAM135B
protein-coding gene in the species Homo sapiens
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FAM135B
Summary
FAM135B is a gene[1].
Key Facts
- FAM135B's instance of is recorded as gene[2].
- FAM135B is a type of protein-coding gene[3].
- FAM135B's HomoloGene ID is recorded as 66605[4].
- FAM135B's genomic start is recorded as 138130023[5].
- FAM135B's genomic start is recorded as 139142266[6].
- FAM135B's genomic end is recorded as 139509065[7].
- FAM135B's genomic end is recorded as 138497261[8].
- FAM135B's ortholog is recorded as Fam135b[9].
- FAM135B's ortholog is recorded as Fam135b[10].
- FAM135B's encodes is recorded as Family with sequence similarity 135 member B[11].
- FAM135B's encodes is recorded as Protein FAM135B[12].
- FAM135B's found in taxon is recorded as Homo sapiens[13].
- FAM135B's chromosome is recorded as human chromosome 8[14].
- FAM135B's genetic association is recorded as periodontitis[15].
- FAM135B's strand orientation is recorded as reverse strand[16].
- FAM135B's exact match is recorded as http://identifiers.org/ncbigene/51059[17].
- FAM135B's cytogenetic location is recorded as 8q24.23[18].
- FAM135B's expressed in is recorded as left testis[19].
- FAM135B's expressed in is recorded as sperm[20].
- FAM135B's expressed in is recorded as right testis[21].
- FAM135B's expressed in is recorded as testicle[22].
- FAM135B's expressed in is recorded as cerebellar hemisphere[23].
- FAM135B's expressed in is recorded as right hemisphere of cerebellum[24].
- FAM135B's expressed in is recorded as gonad[25].
- FAM135B's expressed in is recorded as sural nerve[26].