QuickView for Wdr62 (gene)

Gene Symbol:

WDR62 Homo sapiens

Full name:

WD repeat domain 62

Synonyms:

C19orf14, MCPH2, WD repeat-containing protein 62, microcephaly, primary autosomal recessive 2, truncated WDR62

Genomic Location:

Chr 19: 41237623-41287852

Description:

This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and cognitive disability. Alternative splicing results in multiple transcript variants.

This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and cognitive disability. Alternative splicing results in multiple transcript variants.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus ,  Danio rerio

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

E2F1_Q4_01 ,  E2F4DP1_01 ,  AACTGAC_MIR223 ,  MYAATNNNNNNNGGC_UNKNOWN ,  TATAAA_TATA_01 ,  E2F_Q6 ,  E2F_Q4 ,  E2F1DP2_01 ,  E2F1DP1_01 ,  E2F_Q4_01 ,  E2F1DP1RB_01 ,  E2F_02 ,  IK3_01 ,  IK1_01 ,  E2F1_Q3 ,  E2F4DP2_01 ,  E2F_Q3_01 ,  E2F1_Q6 ,  SGCGSSAAA_E2F1DP2_01

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miRNA binding sites
(Source: TargetScan):

Predicted Gene Targets for miR-223

Cytogenetic Map:

19q13.12

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