1. Gene
  2. CIAO1 - cytosolic iron-sulfur assembly component 1 Gene

CIAO1 - cytosolic iron-sulfur assembly component 1 Gene

Homo sapiens

Also known as CIA1; WDR39

Gene ID: 9391 | Gene type: protein coding

About CIAO1

Cytogenetic location: 2q11.2 Genomic coordinates (GRCh38): 2:96,266,225-96,274,173 (from NCBI)

This gene has 4 transcripts (splice variants) and 202 orthologues. Ubiquitous expression in adrenal (RPKM 18.1), kidney (RPKM 17.3) and 25 other tissues.

Summary

Involved in iron-sulfur cluster assembly and protein maturation by iron-sulfur cluster transfer. Located in cytoplasm. Part of CIA complex and MMXD complex. [provided by Alliance of Genome Resources, Apr 2022]

CIAO1 Products(1)

mRNA Protein Name
NM_004804.3 NP_004795.1 probable cytosolic iron-sulfur protein assembly protein CIAO1
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
Biological Process GO Annotation Evidence Reference Source
involved in iron-sulfur cluster assembly IGI
IGI: Inferred from genetic interaction
17937914 GOA
involved in iron-sulfur cluster assembly IMP
IMP: Inferred from mutant phenotype
23891004 GOA
involved in protein maturation by iron-sulfur cluster transfer IMP
IMP: Inferred from mutant phenotype
23891004 GOA
Cellular Component GO Annotation Evidence Reference Source
part of MMXD complex IDA
IDA: Inferred from direct assay
20797633 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
23585563 GOA
part of cytosolic [4Fe-4S] assembly targeting complex IDA
IDA: Inferred from direct assay
22678361 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CIAO1 Protein Structure

WD40

WD40: WD domain, G-beta repeat (17 - 43)

WD40

WD40: WD domain, G-beta repeat (50 - 89)

WD40

WD40: WD domain, G-beta repeat (96 - 133)

WD40

WD40: WD domain, G-beta repeat (141 - 177)

WD40

WD40: WD domain, G-beta repeat (184 - 221)

WD40

WD40: WD domain, G-beta repeat (241 - 279)

WD40

WD40: WD domain, G-beta repeat (299 - 332)

  • 0
  • 100
  • 200
  • 300
  • 339 a.a.
Protein Preferred Names Protein Names

probable cytosolic iron-sulfur protein assembly protein CIAO1

WD repeat domain 39

CIAO1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CIAO1 O76071 MMS19 Homo sapiens Q96T76-8
Y2H Array
25416956
Intra
CIAO1 O76071 MMS19 Homo sapiens Q96T76-8
Y2H Prey Pooling
25416956
Intra
CIAO1 O76071 MMS19 Homo sapiens Q96T76
Anti Bait CoIP
17353931
Intra
CIAO1 O76071 MMS19 Homo sapiens Q96T76
Anti Tag CoIP
28178521
Intra
CIAO1 O76071 MMS19 Homo sapiens Q96T76
TAP
24981860
Intra
CIAO1 O76071 SLC4A7 Homo sapiens Q9Y6M7
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 SLC4A7 Homo sapiens Q9Y6M7
Validated Y2H
32296183
Intra
CIAO1 O76071 SLC4A7 Homo sapiens Q9Y6M7
Y2H Array
32296183
Intra
CIAO1 O76071 SHISA6 Homo sapiens Q6ZSJ9
Y2H Array
32296183
Intra
CIAO1 O76071 SHISA6 Homo sapiens Q6ZSJ9
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 SHISA6 Homo sapiens Q6ZSJ9
Validated Y2H
32296183
Intra
CIAO1 O76071 ANKRD55 Homo sapiens Q3KP44
Validated Y2H
32296183
Intra
CIAO1 O76071 ANKRD55 Homo sapiens Q3KP44
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 ANKRD55 Homo sapiens Q3KP44
Y2H Array
32296183
Intra
CIAO1 O76071 MEOX2 Homo sapiens Q6FHY5
Y2H Array
32296183
Intra
CIAO1 O76071 MEOX2 Homo sapiens Q6FHY5
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 MEOX2 Homo sapiens Q6FHY5
Validated Y2H
32296183
Intra
CIAO1 O76071 C19orf2 Homo sapiens Q6NX55
Y2H Array
32296183
Intra
CIAO1 O76071 C19orf2 Homo sapiens Q6NX55
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 C19orf2 Homo sapiens Q6NX55
Validated Y2H
32296183
Intra
CIAO1 O76071 HAUS3 Homo sapiens Q68CZ6
Y2H Array
32296183
Intra
CIAO1 O76071 HAUS3 Homo sapiens Q68CZ6
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 HAUS3 Homo sapiens Q68CZ6
Validated Y2H
32296183
Intra
CIAO1 O76071 MEOX1 Homo sapiens P50221
Y2H Array
25416956
Intra
CIAO1 O76071 TOP3B Homo sapiens O95985
Validated Y2H
32296183
Intra
CIAO1 O76071 TCP10L Homo sapiens Q8TDR4
Validated Y2H
32296183
Intra
CIAO1 O76071 TCP10L Homo sapiens Q8TDR4
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 TCP10L Homo sapiens Q8TDR4
Y2H Array
32296183
Intra
CIAO1 O76071 ERCC2 Homo sapiens P18074
Anti Tag CoIP
23585563
Intra
CIAO1 O76071 RGS2 Homo sapiens P41220
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 RGS2 Homo sapiens P41220
Validated Y2H
32296183
Intra
CIAO1 O76071 RGS2 Homo sapiens P41220
Y2H Array
32296183
Intra
CIAO1 O76071 CIAO2B Homo sapiens Q9Y3D0
Y2H Array
32296183
Intra
CIAO1 O76071 CIAO2B Homo sapiens Q9Y3D0
Anti Tag CoIP
28178521
Intra
CIAO1 O76071 CIAO2B Homo sapiens Q9Y3D0
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 CIAO2B Homo sapiens Q9Y3D0
TAP
24981860
Intra
CIAO1 O76071 CIAO2B Homo sapiens Q9Y3D0
Y2H Pooling
16189514
Intra
CIAO1 O76071 CIAO2B Homo sapiens Q9Y3D0
Validated Y2H
32296183
Intra
CIAO1 O76071 CIAO2B Homo sapiens Q9Y3D0
Y2H Array
25416956
Intra
CIAO1 O76071 SF1 Homo sapiens Q15637
Y2H Prey Pooling
25416956
Intra
CIAO1 O76071 SF1 Homo sapiens Q15637
Validated Y2H
25416956
Intra
CIAO1 O76071 CIAO2A Homo sapiens Q9H5X1
Y2H Prey Pooling
25416956
Intra
CIAO1 O76071 CIAO2A Homo sapiens Q9H5X1
Y2H Prey Pooling
32296183
Intra
CIAO1 O76071 CIAO2A Homo sapiens Q9H5X1
Validated Y2H
32296183
Intra
CIAO1 O76071 CIAO2A Homo sapiens Q9H5X1
Y2H Array
25416956
Intra
CIAO1 O76071 CIAO2A Homo sapiens Q9H5X1
Y2H Array
32296183
Intra
CIAO1 O76071 CIAO2A Homo sapiens Q9H5X1
TAP
24981860
Intra
CIAO1 O76071 CIAO2A Homo sapiens Q9H5X1
Y2H Pooling
16189514
Intra
CIAO1 O76071 CIAO2A Homo sapiens Q9H5X1
GMS
32222833
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 6

Mitochondrial Dna Deletion Syndrome With Progressive Myopathy

PEOA6

Autosomal Dominant Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions 6

Dna2-Related Mitochondrial Dna Deletion Syndrome

Mitochondrial Dna Deletion Syndrome With Limb-Girdle Weakness

Mtdna Deletion Syndrome With Limb-Girdle Weakness

Mtdna Deletion Syndrome With Progressive Myopathy

Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 6

Progressive External Ophthalmoplegia, Autosomal Dominant 6

Autosomal Dominant Progressive External Ophthalmoplegia 6

Progressive External Ophthalmoplegia Autosomal Dominant 6

Ophthalmoplegia, External, Progressive, With Mitochondrial Dna Deletions, Autosomal Dominant, Type 6

Xeroderma Pigmentosum, Complementation Group D

Xeroderma Pigmentosum, Group D

Xpdc

Xeroderma Pigmentosum Iv

XPD

Xeroderma Pigmentosum Group D

Xeroderma Pigmentosum Viii

Xp Group D

Xp Group H

Xp4

Xp8

Xph

Xp, Group D

Xp4 Xeroderma Pigmentosum Viii, Formerly

Xp8, Formerly

Xp, Group H, Formerly

Xph, Formerly

Xeroderma Pigmentosum Complementation Group D

XP-D

Xp-D/Cs

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
Mus musculus CIAO1 MGD MGI:1346998
Canis familiaris CIAO1 VGNC VGNC:39263
Felis catus CIAO1 VGNC VGNC:80065
Rattus norvegicus CIAO1 RGD RGD:1307285
Macaca mulatta CIAO1 VGNC VGNC:70950
Bos taurus CIAO1 VGNC VGNC:27356
Others CIAO1 NCBI