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HUMAN:WDR62

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Species (Taxon ID) Homo sapiens (Human). (9606)
Gene Name(s) WDR62 (synonyms: C19orf14)
Protein Name(s) WD repeat-containing protein 62
External Links
UniProt O43379
EMBL AK090617
BX647726
AL133651
AD000813
AC004144
BC017261
BC058939
CCDS CCDS33001.1
CCDS46059.1
PIR T01437
RefSeq NP_001077430.1
NP_775907.4
UniGene Hs.116244
ProteinModelPortal O43379
SMR O43379
BioGrid 129863
IntAct O43379
MINT MINT-1376343
STRING 9606.ENSP00000384792
PhosphoSite O43379
MaxQB O43379
PaxDb O43379
PRIDE O43379
DNASU 284403
Ensembl ENST00000270301
ENST00000401500
ENST00000587391
GeneID 284403
KEGG hsa:284403
UCSC uc002odb.2
uc002odc.2
uc002odd.2
CTD 284403
GeneCards GC19P036545
GeneReviews WDR62
HGNC HGNC:24502
HPA CAB046468
HPA043255
HPA043639
MIM 604317
613583
neXtProt NX_O43379
Orphanet 2512
PharmGKB PA134963627
eggNOG COG2319
GeneTree ENSGT00770000120572
HOGENOM HOG000010231
HOVERGEN HBG108669
InParanoid O43379
OMA LASTFLW
OrthoDB EOG74N5FW
PhylomeDB O43379
TreeFam TF323254
SignaLink O43379
ChiTaRS WDR62
GeneWiki WDR62
GenomeRNAi 284403
NextBio 94836
PRO PR:O43379
Proteomes UP000005640
Bgee O43379
CleanEx HS_WDR62
ExpressionAtlas O43379
Genevestigator O43379
GO GO:0005737
GO:0005634
GO:0000922
GO:0021987
GO:0022008
Gene3D 2.130.10.10
InterPro IPR011047
IPR015943
IPR001680
IPR017986
Pfam PF00400
SMART SM00320
SUPFAM SSF50978
SSF50998
PROSITE PS50082
PS50294

Annotations

Qualifier GO ID GO term name Reference ECO ID ECO term name with/from Aspect Extension Notes Status
GO:0042803

protein homodimerization activity

PMID:23341463[1]

ECO:0000314

F

Figure 1B.

complete
CACAO 6451

part_of

GO:0005813

centrosome

PMID:26297806[2]

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

involved_in

GO:0007099

centriole replication

PMID:26297806[2]

ECO:0000315

mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

involved_in

GO:0022008

neurogenesis

PMID:20890278[3]

ECO:0000315

mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

involved_in

GO:0021987

cerebral cortex development

PMID:20729831[4]

ECO:0000315

mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

part_of

GO:0005634

nucleus

PMID:20729831[4]

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

part_of

GO:0000922

spindle pole

PMID:20890279[5]

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

part_of

GO:0000922

spindle pole

PMID:20890278[3]

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

involved_in

GO:0022008

neurogenesis

PMID:21873635[6]

ECO:0000318

biological aspect of ancestor evidence used in manual assertion

PANTHER:PTN001871421
UniProtKB:O43379

P

Seeded From UniProt

complete

involved_in

GO:0007052

mitotic spindle organization

PMID:21873635[6]

ECO:0000318

biological aspect of ancestor evidence used in manual assertion

PANTHER:PTN001871421
UniProtKB:O43379

P

Seeded From UniProt

complete

part_of

GO:0005634

nucleus

PMID:21873635[6]

ECO:0000318

biological aspect of ancestor evidence used in manual assertion

PANTHER:PTN001871421
UniProtKB:O43379

C

Seeded From UniProt

complete

part_of

GO:0000922

spindle pole

PMID:21873635[6]

ECO:0000318

biological aspect of ancestor evidence used in manual assertion

PANTHER:PTN001871421
UniProtKB:O43379

C

Seeded From UniProt

complete

involved_in

GO:0007052

mitotic spindle organization

PMID:24388750[7]

ECO:0000315

mutant phenotype evidence used in manual assertion

P

Seeded From UniProt

complete

part_of

GO:0005829

cytosol

GO_REF:0000052

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

part_of

GO:0005815

microtubule organizing center

GO_REF:0000052

ECO:0000314

direct assay evidence used in manual assertion

C

Seeded From UniProt

complete

involved_in

GO:0007399

nervous system development

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-0524

P

Seeded From UniProt

complete

part_of

GO:0005737

cytoplasm

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-0963

C

Seeded From UniProt

complete

part_of

GO:0005634

nucleus

GO_REF:0000037
GO_REF:0000039

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-0539
UniProtKB-SubCell:SL-0191

C

Seeded From UniProt

complete

part_of

GO:0005856

cytoskeleton

GO_REF:0000037

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-KW:KW-0206

C

Seeded From UniProt

complete

part_of

GO:0005814

centriole

GO_REF:0000039

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-SubCell:SL-0046

C

Seeded From UniProt

complete

part_of

GO:0000922

spindle pole

GO_REF:0000039

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-SubCell:SL-0448

C

Seeded From UniProt

complete

part_of

GO:0005815

microtubule organizing center

GO_REF:0000039

ECO:0000322

imported manually asserted information used in automatic assertion

UniProtKB-SubCell:SL-0048

C

Seeded From UniProt

complete

Notes

References

See Help:References for how to manage references in GONUTS.

  1. Cohen-Katsenelson, K et al. (2013) Identification and analysis of a novel dimerization domain shared by various members of c-Jun N-terminal kinase (JNK) scaffold proteins. J. Biol. Chem. 288 7294-304 PubMed GONUTS page
  2. 2.0 2.1 Kodani, A et al. (2015) Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication. Elife 4 PubMed GONUTS page
  3. 3.0 3.1 Yu, TW et al. (2010) Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Nat. Genet. 42 1015-20 PubMed GONUTS page
  4. 4.0 4.1 Bilgüvar, K et al. (2010) Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature 467 207-10 PubMed GONUTS page
  5. Nicholas, AK et al. (2010) WDR62 is associated with the spindle pole and is mutated in human microcephaly. Nat. Genet. 42 1010-4 PubMed GONUTS page
  6. 6.0 6.1 6.2 6.3 Gaudet, P et al. (2011) Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Brief. Bioinformatics 12 449-62 PubMed GONUTS page
  7. Xu, D et al. (2014) Microcephaly-associated protein WDR62 regulates neurogenesis through JNK1 in the developing neocortex. Cell Rep 6 104-16 PubMed GONUTS page