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CHCHD4 coiled-coil-helix-coiled-coil-helix domain containing 4 [ Homo sapiens (human) ]

Gene ID: 131474, updated on 5-Mar-2024

Summary

Official Symbol
CHCHD4provided by HGNC
Official Full Name
coiled-coil-helix-coiled-coil-helix domain containing 4provided by HGNC
Primary source
HGNC:HGNC:26467
See related
Ensembl:ENSG00000163528 MIM:611077; AllianceGenome:HGNC:26467
Gene type
protein coding
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
MIA40; TIMM40
Summary
CHCHD4, a component of human mitochondria, belongs to a protein family whose members share 6 highly conserved cysteine residues constituting a -CXC-CX(9)C-CX(9)C- motif in the C terminus (Hofmann et al., 2005 [PubMed 16185709]).[supplied by OMIM, Mar 2008]
Expression
Ubiquitous expression in kidney (RPKM 8.0), duodenum (RPKM 6.4) and 25 other tissues See more
Orthologs
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Genomic context

See CHCHD4 in Genome Data Viewer
Location:
3p25.1
Exon count:
4
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (14112077..14124870, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (14114022..14126815, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (14153577..14166370, complement)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene tetrapeptide repeat homeobox like (pseudogene) Neighboring gene uncharacterized LOC112268445 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_64840 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr3:14098805-14100004 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:14106267-14106839 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19495 Neighboring gene vomeronasal 1 receptor 21 pseudogene Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr3:14163053-14163787 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr3:14163788-14164523 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19496 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14088 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:14165995-14166729 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:14166730-14167464 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:14185247-14185934 Neighboring gene transmembrane protein 43 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 19499 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr3:14190053-14190737 Neighboring gene H3K27ac hESC enhancer GRCh37_chr3:14192355-14192855 Neighboring gene XPC antisense RNA 1 Neighboring gene XPC complex subunit, DNA damage recognition and repair factor

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

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Clone Names

  • FLJ31709

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
enables protein-disulfide reductase activity IBA
Inferred from Biological aspect of Ancestor
more info
 
enables protein-disulfide reductase activity IDA
Inferred from Direct Assay
more info
PubMed 
enables protein-disulfide reductase activity IMP
Inferred from Mutant Phenotype
more info
PubMed 
Component Evidence Code Pubs
is_active_in mitochondrial intermembrane space IBA
Inferred from Biological aspect of Ancestor
more info
 
located_in mitochondrial intermembrane space IDA
Inferred from Direct Assay
more info
PubMed 
located_in mitochondrion IDA
Inferred from Direct Assay
more info
PubMed 

General protein information

Preferred Names
mitochondrial intermembrane space import and assembly protein 40
Names
coiled-coil-helix-coiled-coil-helix domain-containing protein 4
translocase of inner mitochondrial membrane 40 homolog

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.

mRNA and Protein(s)

  1. NM_001098502.2NP_001091972.1  mitochondrial intermembrane space import and assembly protein 40 isoform 1

    See identical proteins and their annotated locations for NP_001091972.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (1) is the predominant transcript. It does not contain an N-terminal, cleavable mitochondrial target sequence, yet experimental studies have determined that the encoded protein (isoform 1) is found within the intermembrane space of the mitochondrion.
    Source sequence(s)
    BC017082, BC033775, DB452249, DB501565
    Consensus CDS
    CCDS43054.1
    UniProtKB/Swiss-Prot
    A8K3Z9, Q8N4Q1, Q96AI2, Q96MY6
    Related
    ENSP00000380122.3, ENST00000396914.4
    Conserved Domains (1) summary
    pfam06747
    Location:64100
    CHCH; CHCH domain
  2. NM_144636.3NP_653237.1  mitochondrial intermembrane space import and assembly protein 40 isoform 2

    See identical proteins and their annotated locations for NP_653237.1

    Status: VALIDATED

    Description
    Transcript Variant: This variant (2) contains an alternate segment for the 5' coding region and uses a downstream start codon, compared to variant 1. Variant 2 is found at a much lower frequency than variant 1. The predicted protein (isoform 2) is longer and has a distinct and longer N-terminus, compared to isoform 1.
    Source sequence(s)
    AK056271, BC017082, DB452249
    Consensus CDS
    CCDS2617.1
    Related
    ENSP00000295767.5, ENST00000295767.9
    Conserved Domains (1) summary
    pfam06747
    Location:77113
    CHCH; CHCH domain

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    14112077..14124870 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    14114022..14126815 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)