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CYP4F29P cytochrome P450 family 4 subfamily F member 29, pseudogene [ Homo sapiens (human) ]

Gene ID: 54055, updated on 11-Jun-2021

Summary

Official Symbol
CYP4F29Pprovided by HGNC
Official Full Name
cytochrome P450 family 4 subfamily F member 29, pseudogeneprovided by HGNC
Primary source
HGNC:HGNC:2647
See related
Ensembl:ENSG00000228314
Gene type
pseudo
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
C21orf15; CYP4F3LP; 4F-se4[6:7:8]; CYP4F-se4[6:7:8]
Expression
Biased expression in esophagus (RPKM 8.9), testis (RPKM 2.3) and 7 other tissues See more
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Genomic context

See CYP4F29P in Genome Data Viewer
Location:
21q11.2
Exon count:
6
Annotation release Status Assembly Chr Location
109.20210514 current GRCh38.p13 (GCF_000001405.39) 21 NC_000021.9 (13843133..13848364, complement)
105.20201022 previous assembly GRCh37.p13 (GCF_000001405.25) 21 NC_000021.8 (15215454..15220685, complement)

Chromosome 21 - NC_000021.9Genomic Context describing neighboring genes Neighboring gene calponin 2 pseudogene 7 Neighboring gene zinc finger protein 114 pseudogene 1 Neighboring gene ankyrin repeat domain 18B pseudogene Neighboring gene sorting nexin 18 pseudogene 13

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

General gene information

Other Names

  • cytochrome P450 pseudogene
  • cytochrome P450, family 4, subfamily F, polypeptide 29, pseudogene
  • cytochrome P450, family 4, subfamily F, polypeptide 3-like pseudogene
  • cytochrome P450, subfamily IVF, polypeptide 3-like pseudogene

Clone Names

  • DKFZp686M2227

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.

RNA

  1. NR_026755.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AY040090, CA415229
    Related
    ENST00000428301.1

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.20210514

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000021.9 Reference GRCh38.p13 Primary Assembly

    Range
    13843133..13848364 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NG_000927.2: Suppressed sequence

    Description
    NG_000927.2: This RefSeq was permanently suppressed because it is now thought that this gene is a transcribed pseudogene.
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