AutismKB 2.0

Evidence Details for CUL7


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Basic Information Top
Gene Symbol:CUL7 ( KIAA0076,dJ20C7.5 )
Gene Full Name: cullin 7
Band: 6p21.1
Quick LinksEntrez ID:9820; OMIM: 609577; Uniprot ID:CUL7_HUMAN; ENSEMBL ID: ENSG00000044090; HGNC ID: 21024
Relate to Another Database: SFARIGene; denovo-db
Sequences Top
>CUL7|9820|nucleotide
ATGAGCCGTGGCTTTTGGCTGGCGGAGCCGCTGGCAGGGACCGGGCCCCACCCTGCCCCAGTGGCTGCCGACTCACGCGGGTGCAGCTCTGTTCCGCGGAGGCAC
GCCCCCTCCCGTCTCTCCGTCTCGACCCCCTCGCGGGGCCCAGGTGCCAGGATGGTGGGAGAACTCCGCTACAGGGAATTCAGGGTGCCCCTGGGGCCCGGCTTA
CATGCCTATCCTGATGAGCTGATCCGCCAGCGCGTGGGCCATGATGGGCATCCTGAGTACCAGATCCGTTGGCTCATCCTGCGGCGTGGCGATGAGGGGGACGGG
GGCTCTGGCCAAGTGGACTGCAAGGCTGAGCACATCCTGCTGTGGATGTCCAAGGATGAGATCTATGCCAACTGCCACAAGATGCTGGGCGAGGATGGCCAGGTC
ATCGGGCCCTCCCAGGAGTCTGCAGGGGAGGTTGGGGCCCTGGACAAATCTGTGCTGGAGGAGATGGAAACCGACGTGAAGTCCCTCATTCAGAGAGCCCTTCGG
CAGCTGGAGGAGTGTGTGGGCACTATCCCTCCTGCTCCTCTACTTCACACTGTCCACGTGCTCAGCGCCTATGCCAGCATTGAGCCCCTCACTGGAGTATTCAAG
GACCCAAGGGTCCTGGACTTGCTCATGCACATGTTGAGTAGTCCTGATTATCAGATTCGCTGGAGTGCAGGCCGGATGATACAAGCCCTGTCCTCCCATGACGCT
GGTGAGGGGCAGTGTGGGGAGGAAGGGAAAGCAGGAGAAGGGCTGGGTCGGCTCAGGGACTCACAGGACACTGTGGCAGGAGCCTCTGATCTCATCAGGACCCGG
ACTCAGATCCTTCTGTCACTGAGCCAACAAGAAGCCATTGAGAAACACCTGGATTTTGACAGCCGCTGTGCTCTGCTAGCACTGTTTGCACAGGCCACGCTCTCT
GAACACCCCATGTCTTTCGAGGGCATTCAGCTACCACAGGTCCCAGGAAGGGTGCTCTTCTCCCTGGTGAAGCGGTATTTGCATGTCACCTCGCTCCTGGATCAG
CTGAACGACAGTGCTGCGGAGCCAGGAGCCCAGAACACCTCTGCTCCTGAGGAGTTGAGTGGGGAGAGGGGTCAACTGGAGCTGGAGTTCAGTATGGCCATGGGC
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>CUL7|9820|protein
MSRGFWLAEPLAGTGPHPAPVAADSRGCSSVPRRHAPSRLSVSTPSRGPGARMVGELRYREFRVPLGPGLHAYPDELIRQRVGHDGHPEYQIRWLILRRGDEGDG
GSGQVDCKAEHILLWMSKDEIYANCHKMLGEDGQVIGPSQESAGEVGALDKSVLEEMETDVKSLIQRALRQLEECVGTIPPAPLLHTVHVLSAYASIEPLTGVFK
DPRVLDLLMHMLSSPDYQIRWSAGRMIQALSSHDAGEGQCGEEGKAGEGLGRLRDSQDTVAGASDLIRTRTQILLSLSQQEAIEKHLDFDSRCALLALFAQATLS
EHPMSFEGIQLPQVPGRVLFSLVKRYLHVTSLLDQLNDSAAEPGAQNTSAPEELSGERGQLELEFSMAMGTLISELVQAMRWDQASDRPRSSARSPGSIFQPQLA
DVSPGLPAAQAQPSFRRSRRFRPRSEFASGNTYALYVRDTLQPGMRVRMLDDYEEISAGDEGEFRQSNNGVPPVQVFWESTGRTYWVHWHMLEILGFEEDIEDMV
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Evidence summary Top

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Evidences Syndromic Gene GWAS CNV Linkage Association Expression NGS de novo NGS Mosaic NGS Other Low-Scale Gene Studies Total
Score (No. of Studies) No 0 (0) 1 (1) 0 (0) 0 (0) 0 (0) 0 (1) 0 (0) 0 (1) 0 (0) 2 (3)
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference Source Method ADI-R ADOS Diagnosis Family Individual
Total Simplex Multiplex Control Affected Control Total
Berkel, 2010 Canada SNP microarrayASD - - - - 396 5023 5419
Linkage Studies Top