CISD2 Back

CDGSH iron sulfur domain 2

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NCBI Description of CISD2
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. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

Community Annotation of CISD2 Add / Edit CISD2: Annotations

No community annotations yet for CISD2.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

CISD2 is highly significantly mutated in
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CISD2 is significantly mutated in
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CISD2 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


• Mutation list for CISD2