NCF1B

Summary

NCF1B is a pseudogene^[1].

Key Facts

• NCF1B's instance of is recorded as pseudogene^[2].
• NCF1B's subclass of is recorded as pseudogene^[3].
• NCF1B's Entrez Gene ID is recorded as 654816^[4].
• NCF1B's HGNC gene symbol is recorded as NCF1B^[5].
• NCF1B's HGNC ID is recorded as 32522^[6].
• NCF1B's Ensembl gene ID is recorded as ENSG00000182487^[7].
• NCF1B's RefSeq RNA ID is recorded as NR_003186^[8].
• NCF1B's genomic start is recorded as 73220624^[9].
• NCF1B's genomic start is recorded as 72634611^[10].
• NCF1B's genomic end is recorded as 73235945^[11].
• NCF1B's genomic end is recorded as 72649979^[12].
• NCF1B's found in taxon is recorded as Homo sapiens^[13].
• NCF1B's Ensembl transcript ID is recorded as ENST00000435988^[14].
• NCF1B's Ensembl transcript ID is recorded as ENST00000432102^[15].
• NCF1B's Ensembl transcript ID is recorded as ENST00000423083^[16].
• NCF1B's chromosome is recorded as human chromosome 7^[17].
• NCF1B's strand orientation is recorded as forward strand^[18].
• NCF1B's exact match is recorded as http://identifiers.org/ncbigene/654816^[19].
• NCF1B's UMLS CUI is recorded as C1826386^[20].
• NCF1B's cytogenetic location is recorded as 7q11.23^[21].