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14 records found for search term Brwd3
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1354337BRWD3bromodomain and WD repeat domain containing 3The protein encoded by this gene contains a bromodomain and several WD repeats. It is thought to have a chromatin-modifying function, and may thus play a role in transcription. Mutations in this gene are associated with a spectrum of cognitive disabilities and X-linked macrocephaly. This gene is alsX8066950380809877Human124symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
1559445Brwd3bromodomain and WD repeat domain containing 3ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog); INTERACTS WITH 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine; bisphenol AX7784376677937240Rat81symbol , PhenoGengene, protein-coding, MODEL [RefSeq]
1623671Brwd3bromodomain and WD repeat domain containing 3Predicted to be involved in cytoskeleton organization; regulation of cell shape; and regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. Human ortholog(s) of this gene implicated in non-syndromic X-linked intellectual disability 93. Orthologous to human BRWD3X107779451107877965Mouse91symbol , PhenoGen , descriptiongene, protein-coding, VALIDATED [RefSeq]
9011920Brwd3bromodomain and WD repeat domain containing 3ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog)NW_004955529834459992259Chinchilla8symbolgene, protein-coding, MODEL [RefSeq]
11708229BRWD3bromodomain and WD repeat domain containing 3INVOLVED IN cytoskeleton organization (inferred); regulation of cell shape (inferred); regulation of transcription by RNA polymerase II (inferred); ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog); FOUND IN nucleus (inferred)X6971853269857507Bonobo13symbolgene, protein-coding, MODEL [RefSeq]
12092238BRWD3bromodomain and WD repeat domain containing 3ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog)X6200453662180260Dog12symbolgene, protein-coding, MODEL [RefSeq]
12546670Brwd3bromodomain and WD repeat domain containing 3INVOLVED IN cytoskeleton organization (inferred); regulation of cell shape (inferred); regulation of transcription by RNA polymerase II (inferred); ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog); FOUND IN nucleus (inferred)NW_00493654722361642354652Squirrel12symbolgene, protein-coding, MODEL [RefSeq]
14370323BRWD3Flysymbolgene, null
18931915Brwd3bromodomain and WD repeat domain containing 3INVOLVED IN cytoskeleton organization (inferred); regulation of cell shape (inferred); regulation of transcription by RNA polymerase II (inferred); ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog); FOUND IN nucleus (inferred)Naked Mole-Rat12symbolgene, protein-coding, MODEL [RefSeq]
625889073Brwd3bromodomain and WD repeat domain containing 3ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog)Black Rat8symbolgene, protein-coding, MODEL [RefSeq]
18509386BRWD3bromodomain and WD repeat domain containing 3INVOLVED IN cytoskeleton organization (inferred); regulation of cell shape (inferred); regulation of transcription by RNA polymerase II (inferred); ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog); FOUND IN nucleus (inferred)Green Monkey13symbolgene, protein-coding, MODEL [RefSeq]
14185423BRWD3bromodomain and WD repeat domain containing 3ASSOCIATED WITH autism spectrum disorder (ortholog); Developmental Disabilities (ortholog); genetic disease (ortholog)Pig12symbolgene, protein-coding, MODEL [RefSeq]
155231578brwd3Tropical Clawed Frogsymbolgene, null
155231577brwd3.LAfrican Clawed Frogsymbolgene, null