1. Gene
  2. CISD1 - CDGSH iron sulfur domain 1 Gene

CISD1 - CDGSH iron sulfur domain 1 Gene

Homo sapiens

Also known as ZCD1; MDS029; C10orf70; mitoNEET

Gene ID: 55847 | Gene type: protein coding

About CISD1

Cytogenetic location: 10q21.1 Genomic coordinates (GRCh38): 10:58,269,162-58,289,586 (from NCBI)

This gene has 4 transcripts (splice variants), 227 orthologues and 2 paralogues. Ubiquitous expression in heart (RPKM 13.4), small intestine (RPKM 9.9) and 23 other tissues.

Summary

This gene encodes a protein with a CDGSH iron-sulfur domain and has been shown to bind a redox-active [2Fe-2S] cluster. The encoded protein has been localized to the outer membrane of mitochondria and is thought to play a role in regulation of oxidation. Genes encoding similar proteins are located on chromosomes 4 and 17, and a pseudogene of this gene is located on chromosome 2. [provided by RefSeq, Feb 2012]

CISD1 Products(1)

mRNA Protein Name
NM_018464.5 NP_060934.1 CDGSH iron-sulfur domain-containing protein 1

CISD1 Protein Structure

MitoNEET_N

MitoNEET_N: Iron-containing outer mitochondrial membrane protein N-terminus (12 - 40)

zf-CDGSH

zf-CDGSH: Iron-binding zinc finger CDGSH type (51 - 87)

  • 0
  • 100
  • 108 a.a.
Protein Preferred Names Protein Names

CDGSH iron-sulfur domain-containing protein 1

zinc finger CDGSH-type domain 1

Recombinant CISD1 Proteins

Cat. No. Product Name Accession Purity
HY-P76262 CISD1 Protein, Human (His) Q9NZ45/NP_060934.1 (K32-T108) ≥95%

Related Diseases

Diseases Alias
Wolfram Syndrome

Didmoad Syndrome

Didmoad

Diabetes Insipidus And Mellitus With Optic Atrophy And Deafness

Wfs

Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, And Deafness

Didmoadud

Diabetes Insipidus-Diabetes Mellitus-Optic Atrophy-Deafness Syndrome

Diabetes Insipidus-Diabetes Mellitus-Optic Atrophy-Hearing Loss Syndrome

Wolfram Syndrome 2

WFS2

Fanconi Anemia, Complementation Group D2

Fanconi Anemia Complementation Group D2

FANCD2

Fad2

Fa4

Fancd

Fanconi Pancytopenia Type 4

Fanconi Anemia, Complementation Group D

Fanconi Pancytopenia, Type 4

Facd

Fanconi Anemia Complementation Group D

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus CISD1 VGNC VGNC:27371
Rattus norvegicus CISD1 RGD RGD:1309529
Mus musculus CISD1 MGD MGI:1261855
Others CISD1 NCBI