Dnajc30 DnaJ heat shock protein family (Hsp40) member C30 [Rattus norvegicus (Norway rat)] - Gene

Summary

Official Symbol: Dnajc30provided by RGD
Official Full Name: DnaJ heat shock protein family (Hsp40) member C30provided by RGD
Primary source: RGD:1595783
See related: Ensembl:ENSRNOG00000031721 AllianceGenome:RGD:1595783
Gene type: protein coding
RefSeq status: VALIDATED
Organism: Rattus norvegicus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Also known as: Wbscr18
Summary: Predicted to be involved in brain development and regulation of mitochondrial ATP synthesis coupled proton transport. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in Williams-Beuren syndrome and nuclear type mitochondrial complex I deficiency. Orthologous to human DNAJC30 (DnaJ heat shock protein family (Hsp40) member C30). [provided by Alliance of Genome Resources, Apr 2022]
Orthologs: human mouse all
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Genomic context

Location:: 12q12

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCr8 (GCF_036323735.1)	12	NC_086030.1 (27264861..27265940, complement)
RS_2023_06	previous assembly	mRatBN7.2 (GCF_015227675.2)	12	NC_051347.1 (21628319..21629398, complement)
106	previous assembly	Rnor_6.0 (GCF_000001895.5)	12	NC_005111.4 (24668398..24669464, complement)

Chromosome 12 - NC_086030.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Gene Ontology Provided by RGD

Process	Evidence Code	Pubs
involved_in brain development	ISO Inferred from Sequence Orthology more info
involved_in regulation of mitochondrial ATP synthesis coupled proton transport	ISO Inferred from Sequence Orthology more info

Component	Evidence Code	Pubs
located_in mitochondrial inner membrane	ISO Inferred from Sequence Orthology more info

General protein information

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Preferred Names: dnaJ homolog subfamily C member 30, mitochondrial

Names: DnaJ (Hsp40) homolog, subfamily C, member 30; Williams-Beuren syndrome chromosome region 18; dnaJ homolog subfamily C member 30

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)

NM_001109024.3 → NP_001102494.1 dnaJ homolog subfamily C member 30, mitochondrial

See identical proteins and their annotated locations for NP_001102494.1

Status: VALIDATED

Source sequence(s)

JAXUCZ010000012

UniProtKB/TrEMBL

A6J0F1, B2RYV0, M0R6A2

Related

ENSRNOP00000064946.1, ENSRNOT00000043393.4

Conserved Domains (2) summary

COG0484
Location:44 → 105

DnaJ; DnaJ-class molecular chaperone with C-terminal Zn finger domain [Posttranslational modification, protein turnover, chaperones]

pfam00226
Location:43 → 104

DnaJ; DnaJ domain