CYP2B7P cytochrome P450 family 2 subfamily B member 7, pseudogene [Homo sapiens (human)] - Gene

Summary

Official Symbol: CYP2B7Pprovided by HGNC
Official Full Name: cytochrome P450 family 2 subfamily B member 7, pseudogeneprovided by HGNC
Primary source: HGNC:HGNC:2616
See related: Ensembl:ENSG00000291083 AllianceGenome:HGNC:2616
Gene type: pseudo
RefSeq status: PROVISIONAL
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: CYP2B; CYP2B7; CYP2B7P1
Expression: Biased expression in lung (RPKM 25.4), liver (RPKM 15.7) and 3 other tissues See more
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Genomic context

Location:: 19q13.2

Exon count:: 9

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	19	NC_000019.10 (40924265..40950660)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	19	NC_060943.1 (43745020..43771413)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	19	NC_000019.9 (41430170..41456565)

Chromosome 19 - NC_000019.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Expression

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See details

Project title: Tissue-specific circular RNA induction during human fetal development
Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
BioProject: PRJNA270632
Publication: PMID 26076956
Analysis date: Mon Apr 2 22:54:59 2018

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

CYP2B6*29 represents a new mechanism of genetic variation at the CYP2B6 locus, underscoring the highly polymorphic nature of this isoenzyme.
Title: Partial deletion of CYP2B6 owing to unequal crossover with CYP2B7.

Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

GDB:434012 (e-PCR)
- UniSTS:157204

D19S815 (e-PCR)
- UniSTS:153880

D19S1089 (e-PCR)
- UniSTS:79643

D8S2279 (e-PCR)
- UniSTS:473907

RH11435 (e-PCR)
- UniSTS:49008

G35510 (e-PCR)
- UniSTS:44150

D11S3159 (e-PCR)
- UniSTS:152247

Other Names

cytochrome P450, family 2, subfamily B, polypeptide 7 pseudogene 1
cytochrome P450, family 2, subfamily B, polypeptide 7, pseudogene
cytochrome P450, subfamily IIB (phenobarbital-inducible), polypeptide 7

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.