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ZFIN:cep290

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Contents

Species (Taxon ID) Danio rerio (zebrafish) (taxon:7955)
Gene Name(s) cep290
Protein Name(s) centrosomal protein 290,
External Links
ZFIN ZDB-GENE-041111-243

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0001654

eye development

ZFIN:ZDB-PUB-060517-14
PMID:16682973[1]

IMP: Inferred from Mutant Phenotype

ZFIN:ZDB-MRPHLNO-080428-2

P

From ZFIN

GO:0001654

eye development

ZFIN:ZDB-PUB-060517-14
PMID:16682973[1]

IMP: Inferred from Mutant Phenotype

ZFIN:ZDB-MRPHLNO-080428-3

P

From ZFIN

GO:0005634

nucleus

ZFIN:ZDB-PUB-020723-1

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0539

C

From ZFIN

GO:0005634

nucleus

ZFIN:ZDB-PUB-060517-14
PMID:16682973[1]

ISS: Inferred from Sequence or Structural Similarity

UniProtKB:O15078

C

From ZFIN

GO:0005737

cytoplasm

ZFIN:ZDB-PUB-020723-1

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0963

C

From ZFIN

GO:0005813

centrosome

ZFIN:ZDB-PUB-060517-14
PMID:16682973[1]

ISS: Inferred from Sequence or Structural Similarity

UniProtKB:O15078

C

From ZFIN

GO:0005856

cytoskeleton

ZFIN:ZDB-PUB-020723-1

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0206

C

From ZFIN

GO:0005932

microtubule basal body

ZFIN:ZDB-PUB-120306-2

IEA: Inferred from Electronic Annotation

UniProtKB-SubCell:SL-0087

C

From ZFIN

GO:0006810

transport

ZFIN:ZDB-PUB-020723-1

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0813

P

From ZFIN

GO:0007275

multicellular organismal development

ZFIN:ZDB-PUB-020723-1

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0217

P

From ZFIN

GO:0007369

gastrulation

ZFIN:ZDB-PUB-080311-9
PMID:18327255[2]

IGI: Inferred from Genetic Interaction

ZFIN:ZDB-MRPHLNO-080716-5
ZFIN:ZDB-MRPHLNO-080716-9

P

From ZFIN

GO:0015031

protein transport

ZFIN:ZDB-PUB-020723-1

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0653

P

From ZFIN

GO:0015031

protein transport

ZFIN:ZDB-PUB-110105-1

ISS: Inferred from Sequence or Structural Similarity

UniProtKB:Q6A078

P

From ZFIN

GO:0021549

cerebellum development

ZFIN:ZDB-PUB-060517-14
PMID:16682973[1]

IMP: Inferred from Mutant Phenotype

ZFIN:ZDB-MRPHLNO-080428-2

P

From ZFIN

GO:0030030

cell projection organization

ZFIN:ZDB-PUB-020723-1

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0970

P

From ZFIN

GO:0030916

otic vesicle formation

ZFIN:ZDB-PUB-060517-14
PMID:16682973[1]

IMP: Inferred from Mutant Phenotype

ZFIN:ZDB-MRPHLNO-080428-3

P

From ZFIN

GO:0042462

eye photoreceptor cell development

ZFIN:ZDB-PUB-060517-14
PMID:16682973[1]

IMP: Inferred from Mutant Phenotype

P

From ZFIN

GO:0042462

eye photoreceptor cell development

ZFIN:ZDB-PUB-110629-12
PMID:21685394[3]

IMP: Inferred from Mutant Phenotype

ZFIN:ZDB-MRPHLNO-110907-1

P

From ZFIN

GO:0042995

cell projection

ZFIN:ZDB-PUB-020723-1

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0966

C

From ZFIN

GO:0043010

camera-type eye development

ZFIN:ZDB-PUB-120327-10
PMID:22446187[4]

IGI: Inferred from Genetic Interaction

ZFIN:ZDB-MRPHLNO-060209-5
ZFIN:ZDB-MRPHLNO-110907-1

P

From ZFIN

GO:0048793

pronephros development

ZFIN:ZDB-PUB-060517-14
PMID:16682973[1]

IMP: Inferred from Mutant Phenotype

P

From ZFIN

GO:0048793

pronephros development

ZFIN:ZDB-PUB-080902-6
PMID:18723859[5]

IGI: Inferred from Genetic Interaction

ZFIN:ZDB-MRPHLNO-090324-1
ZFIN:ZDB-MRPHLNO-090324-2

P

From ZFIN

GO:0048793

pronephros development

ZFIN:ZDB-PUB-080902-6
PMID:18723859[5]

IMP: Inferred from Mutant Phenotype

ZFIN:ZDB-MRPHLNO-090324-2

P

From ZFIN

GO:0048839

inner ear development

ZFIN:ZDB-PUB-120327-10
PMID:22446187[4]

IGI: Inferred from Genetic Interaction

ZFIN:ZDB-MRPHLNO-060209-5
ZFIN:ZDB-MRPHLNO-110907-1

P

From ZFIN

GO:0060271

cilium morphogenesis

ZFIN:ZDB-PUB-110105-1

ISS: Inferred from Sequence or Structural Similarity

UniProtKB:Q6A078

P

From ZFIN


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 1.3 1.4 1.5 1.6 1.7 Sayer JA et al. (2006) The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nat Genet 38: 674-81 PubMed GONUTS page
  2. Leitch CC et al. (2008) Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome. Nat Genet 40: 443-8 PubMed GONUTS page
  3. Murga-Zamalloa CA et al. (2011) Accumulation of the Raf-1 kinase inhibitory protein (Rkip) is associated with Cep290-mediated photoreceptor degeneration in ciliopathies. J Biol Chem 286: 28276-86 PubMed GONUTS page
  4. 4.0 4.1 Rachel RA et al. (2012) Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis. J Clin Invest 122: 1233-45 PubMed GONUTS page
  5. 5.0 5.1 Schäfer T et al. (2008) Genetic and physical interaction between the NPHP5 and NPHP6 gene products. Hum Mol Genet 17: 3655-62 PubMed GONUTS page
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