FAM169B
protein-coding gene in the species Homo sapiens
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Summary
FAM169B is a pseudogene[1].
Key Facts
- FAM169B's instance of is recorded as pseudogene[2].
- FAM169B's subclass of is recorded as protein-coding gene[3].
- FAM169B's Entrez Gene ID is recorded as 283777[4].
- FAM169B's HGNC gene symbol is recorded as FAM169B[5].
- FAM169B's HGNC ID is recorded as 26835[6].
- FAM169B's HomoloGene ID is recorded as 89283[7].
- FAM169B's Ensembl gene ID is recorded as ENSG00000283597[8].
- FAM169B's RefSeq RNA ID is recorded as NM_182562[9].
- FAM169B's RefSeq RNA ID is recorded as NR_171054[10].
- FAM169B's genomic start is recorded as 98437162[11].
- FAM169B's genomic start is recorded as 98980391[12].
- FAM169B's genomic end is recorded as 98547728[13].
- FAM169B's genomic end is recorded as 99057611[14].
- FAM169B's encodes is recorded as Family with sequence similarity 169 member B[15].
- FAM169B's found in taxon is recorded as Homo sapiens[16].
- FAM169B's Ensembl transcript ID is recorded as ENST00000636796[17].
- FAM169B's Ensembl transcript ID is recorded as ENST00000637259[18].
- FAM169B's Ensembl transcript ID is recorded as ENST00000558256[19].
- FAM169B's chromosome is recorded as human chromosome 15[20].
- FAM169B's strand orientation is recorded as reverse strand[21].
- FAM169B's Google Knowledge Graph ID is recorded as /g/11gbldtbdj[22].
- FAM169B's exact match is recorded as http://identifiers.org/ncbigene/283777[23].
- FAM169B's UMLS CUI is recorded as C2681499[24].
- FAM169B's cytogenetic location is recorded as 15q26.3[25].