Homo sapiens Gene: CISD2
Summary
InnateDB Gene IDBG-32295.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CISD2
Gene Name CDGSH iron sulfur domain 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000145354
Encoded Proteins
CDGSH iron sulfur domain 2
CDGSH iron sulfur domain 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is a zinc finger protein that localizes to the endoplasmic reticulum. The encoded protein binds an iron/sulfur cluster and may be involved in calcium homeostasis. Defects in this gene are a cause of Wolfram syndrome 2. [provided by RefSeq, Mar 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 4:102868978-102889242
Strand Forward strand
Band q24
Transcripts
ENST00000273986 ENSP00000273986
ENST00000503643 ENSP00000423716
ENST00000574446 ENSP00000458976
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 5 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0042803 protein homodimerization activity
GO:0044822 poly(A) RNA binding
GO:0046872 metal ion binding
GO:0051537 2 iron, 2 sulfur cluster binding
Biological Process
GO:0000422 mitochondrion degradation
GO:0010259 multicellular organismal aging
GO:0010506 regulation of autophagy
Cellular Component
GO:0005741 mitochondrial outer membrane
GO:0005783 endoplasmic reticulum
GO:0005789 endoplasmic reticulum membrane
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0043231 intracellular membrane-bounded organelle
GO:0043234 protein complex
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL I3L1N9
UniProt Splice Variant
Entrez Gene 493856
UniGene
RefSeq NM_001008388 XM_005263040
HUGO HGNC:24212
OMIM 611507
CCDS CCDS34040
HPRD 17413
IMGT
EMBL AC018797
GenPept
RNA Seq Atlas 493856