Evidence Details for ARHGAP39
Basic Information Top
| Gene Symbol: | ARHGAP39 ( CrGAP,KIAA1688,Vilse ) |
|---|---|
| Gene Full Name: | Rho GTPase activating protein 39 |
| Band: | 8q24.3 |
| Quick Links | Entrez ID:80728; OMIM: NA; Uniprot ID:RHG39_HUMAN; ENSEMBL ID: ENSG00000147799; HGNC ID: 29351 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>ARHGAP39|80728|nucleotide
ATGTCCCAGACGCAGGACTACGAGTGCAGGAGCCATAATGTCGACCTGCCGGAGTCGAGGATTCCAGGGTCGAACACTCGGTTGGAGTGGGTGGAGATCATCGAA
CCGCGCACCCGCGAGCGCATGTACGCCAACCTGGTCACCGGTGAGTGCGTGTGGGACCCGCCGGCCGGCGTCCGCATCAAGCGCACCAGCGAGAACCAGTGGTGG
GAGCTGTTCGACCCCAACACGTCCCGCTTCTACTACTACAATGCCAGCACGCAGCGCACGGTGTGGCACCGGCCGCAGGGCTGCGACATCATCCCGCTGGCCAAG
CTGCAGACGCTGAAGCAGAACACGGAGTCCCCGCGCGCCTCGGCGGAGAGCAGCCCCGGGCGCGGCAGCAGCGTCAGCCGTGAGGGCAGCACCAGCTCCTCCCTG
GAGCCCGAGCCCGACACTGAGAAAGCGCAGGAGTTGCCAGCGAGGGCCGGGCGGCCCGCGGCGTTTGGGACAGTGAAGGAGGACAGCGGCAGCTCTTCACCACCA
GGAGTGTTCCTTGAGAAGGACTATGAGATTTACCGGGATTACAGTGCGGACGGCCAGCTTCTTCACTACAGGACCTCCTCGCTGCGGTGGAACTCGGGCGCCAAA
GAGCGCATGCTCATCAAGGTCGCTGATCGGGAGCCCAGCTTCCTCGCCGCCCAGGGCAATGGCTACGCCCCAGACGGCCCACCTGGGGTCCGCTCCCGCAGACCC
TCCGGCAGCCAGCACTCACCCAGCCTGCAGACCTTCGCCCCGGAGGCTGACGGCACCATCTTCTTCCCAGAGAGGAGGCCGTCACCCTTCCTGAAGAGGGCCGAG
CTCCCAGGGAGCAGCTCCCCGCTGCTGGCCCAGCCCCGAAAGCCCTCCGGGGACTCGCAGCCCTCCTCCCCGCGCTATGGCTATGAACCCCCGCTCTACGAGGAG
CCCCCAGTGGAGTACCAGGCCCCCATCTACGATGAGCCCCCCATGGACGTGCAATTCGAGGCTGGCGGGGGCTACCAGGCCGGCTCTCCCCAGCGGTCGCCGGGC
CGTAAGCCCCGGCCGTTCCTCCAGCCCAACAAGCAGGGCCCCCCCTCGCCCTGCCAGCAGCTGGTGCTCACCAAGCAGAAGTGTCCCGAGCGCTTCCTGAGCCTG
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ATGTCCCAGACGCAGGACTACGAGTGCAGGAGCCATAATGTCGACCTGCCGGAGTCGAGGATTCCAGGGTCGAACACTCGGTTGGAGTGGGTGGAGATCATCGAA
CCGCGCACCCGCGAGCGCATGTACGCCAACCTGGTCACCGGTGAGTGCGTGTGGGACCCGCCGGCCGGCGTCCGCATCAAGCGCACCAGCGAGAACCAGTGGTGG
GAGCTGTTCGACCCCAACACGTCCCGCTTCTACTACTACAATGCCAGCACGCAGCGCACGGTGTGGCACCGGCCGCAGGGCTGCGACATCATCCCGCTGGCCAAG
CTGCAGACGCTGAAGCAGAACACGGAGTCCCCGCGCGCCTCGGCGGAGAGCAGCCCCGGGCGCGGCAGCAGCGTCAGCCGTGAGGGCAGCACCAGCTCCTCCCTG
GAGCCCGAGCCCGACACTGAGAAAGCGCAGGAGTTGCCAGCGAGGGCCGGGCGGCCCGCGGCGTTTGGGACAGTGAAGGAGGACAGCGGCAGCTCTTCACCACCA
GGAGTGTTCCTTGAGAAGGACTATGAGATTTACCGGGATTACAGTGCGGACGGCCAGCTTCTTCACTACAGGACCTCCTCGCTGCGGTGGAACTCGGGCGCCAAA
GAGCGCATGCTCATCAAGGTCGCTGATCGGGAGCCCAGCTTCCTCGCCGCCCAGGGCAATGGCTACGCCCCAGACGGCCCACCTGGGGTCCGCTCCCGCAGACCC
TCCGGCAGCCAGCACTCACCCAGCCTGCAGACCTTCGCCCCGGAGGCTGACGGCACCATCTTCTTCCCAGAGAGGAGGCCGTCACCCTTCCTGAAGAGGGCCGAG
CTCCCAGGGAGCAGCTCCCCGCTGCTGGCCCAGCCCCGAAAGCCCTCCGGGGACTCGCAGCCCTCCTCCCCGCGCTATGGCTATGAACCCCCGCTCTACGAGGAG
CCCCCAGTGGAGTACCAGGCCCCCATCTACGATGAGCCCCCCATGGACGTGCAATTCGAGGCTGGCGGGGGCTACCAGGCCGGCTCTCCCCAGCGGTCGCCGGGC
CGTAAGCCCCGGCCGTTCCTCCAGCCCAACAAGCAGGGCCCCCCCTCGCCCTGCCAGCAGCTGGTGCTCACCAAGCAGAAGTGTCCCGAGCGCTTCCTGAGCCTG
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>ARHGAP39|80728|protein
MSQTQDYECRSHNVDLPESRIPGSNTRLEWVEIIEPRTRERMYANLVTGECVWDPPAGVRIKRTSENQWWELFDPNTSRFYYYNASTQRTVWHRPQGCDIIPLAK
LQTLKQNTESPRASAESSPGRGSSVSREGSTSSSLEPEPDTEKAQELPARAGRPAAFGTVKEDSGSSSPPGVFLEKDYEIYRDYSADGQLLHYRTSSLRWNSGAK
ERMLIKVADREPSFLAAQGNGYAPDGPPGVRSRRPSGSQHSPSLQTFAPEADGTIFFPERRPSPFLKRAELPGSSSPLLAQPRKPSGDSQPSSPRYGYEPPLYEE
PPVEYQAPIYDEPPMDVQFEAGGGYQAGSPQRSPGRKPRPFLQPNKQGPPSPCQQLVLTKQKCPERFLSLEYSPAGKEYVRQLVYVEQAGSSPKLRAGPRHKYAP
NPGGGSYSLQPSPCLLRDQRLGVKSGDYSTMEGPELRHSQPPTPLPQAQEDAMSWSSQQDTLSSTGYSPGTRKRKSRKPSLCQATSATPTEGPGDLLVEQPLAEE
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MSQTQDYECRSHNVDLPESRIPGSNTRLEWVEIIEPRTRERMYANLVTGECVWDPPAGVRIKRTSENQWWELFDPNTSRFYYYNASTQRTVWHRPQGCDIIPLAK
LQTLKQNTESPRASAESSPGRGSSVSREGSTSSSLEPEPDTEKAQELPARAGRPAAFGTVKEDSGSSSPPGVFLEKDYEIYRDYSADGQLLHYRTSSLRWNSGAK
ERMLIKVADREPSFLAAQGNGYAPDGPPGVRSRRPSGSQHSPSLQTFAPEADGTIFFPERRPSPFLKRAELPGSSSPLLAQPRKPSGDSQPSSPRYGYEPPLYEE
PPVEYQAPIYDEPPMDVQFEAGGGYQAGSPQRSPGRKPRPFLQPNKQGPPSPCQQLVLTKQKCPERFLSLEYSPAGKEYVRQLVYVEQAGSSPKLRAGPRHKYAP
NPGGGSYSLQPSPCLLRDQRLGVKSGDYSTMEGPELRHSQPPTPLPQAQEDAMSWSSQQDTLSSTGYSPGTRKRKSRKPSLCQATSATPTEGPGDLLVEQPLAEE
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Evidence summary Top
Click the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default.
| 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) | 0 (1) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 1 (2) |
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 | ||||||
| Levy, 2011 | Simons Simplex Collection | aCGH | - | - | ASD | 915 | 915 | - | - | - | - | - |
Linkage Studies Top

