Evidence Details for AP3B2
Basic Information Top
Gene Symbol: | AP3B2 ( DKFZp686D17136,NAPTB ) |
---|---|
Gene Full Name: | adaptor-related protein complex 3, beta 2 subunit |
Band: | 15q25.2 |
Quick Links | Entrez ID:8120; OMIM: 602166; Uniprot ID:AP3B2_HUMAN; ENSEMBL ID: ENSG00000103723; HGNC ID: 567 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>AP3B2|8120|nucleotide
ATGTCGGCCGCCCCCGCCTACAGCGAAGACAAGGGCGGCTCCGCTGGCCCCGGGGAGCCCGAGTACGGCCACGACCCCGCGAGCGGCGGCATCTTCTCCTCCGAC
TACAAGCGGCATGATGACCTGAAGGAGATGCTGGACACCAACAAGGATTCTCTCAAGCTGGAGGCCATGAAGAGGATTGTGGCGATGATTGCCCGAGGAAAGAAT
GCTTCAGACCTGTTTCCCGCGGTGGTGAAGAACGTGGCCTGTAAGAACATAGAGGTGAAGAAGCTTGTCTATGTGTACCTGGTACGCTACGCTGAGGAGCAGCAA
GACCTGGCCCTGCTGTCCATCTCCACCTTCCAACGTGGCCTAAAGGATCCCAACCAGCTGATTCGTGCCAGTGCCCTCCGTGTCCTCTCTAGCATCCGTGTGCCC
ATCATAGTGCCCATCATGATGCTAGCTATCAAGGAAGCCGCCTCGGACATGTCACCCTATGTGCGGAAAACAGCTGCCCACGCCATCCCTAAACTCTACAGTTTG
GACTCTGACCAGAAGGATCAGCTGATAGAAGTCATTGAGAAGCTTCTGGCTGACAAGACCACGCTGGTGGCGGGCAGTGTGGTGATGGCCTTTGAGGAGGTCTGC
CCGGAGCGCATCGACCTGATTCACAAAAACTACCGGAAACTCTGTAACCTGCTGATCGACGTGGAGGAGTGGGGCCAGGTGGTCATCATCAGCATGCTCACCCGC
TACGCCCGCACGCAGTTCCTGAGCCCCACCCAGAACGAATCCCTACTAGAGGAGAACGCGGAAAAAGCCTTCTACGGCTCAGAGGAGGACGAGGCCAAGGGCGCG
GGGTCTGAGGAGACGGCCGCCGCGGCCGCCCCCTCCCGAAAGCCCTATGTCATGGACCCCGACCACCGGCTGCTGCTGCGCAACACCAAACCCCTGCTGCAGAGC
CGCAGCGCCGCGGTGGTGATGGCGGTGGCGCAGCTCTACTTCCACCTGGCGCCCAAGGCGGAAGTGGGCGTCATCGCCAAGGCGCTGGTGCGCCTGCTGCGCAGC
CACAGTGAGGTGCAGTACGTTGTGCTCCAGAACGTGGCCACCATGTCCATCAAGCGCCGGGGTATGTTTGAGCCCTACCTGAAGAGCTTCTACATCAGGTCCACC
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ATGTCGGCCGCCCCCGCCTACAGCGAAGACAAGGGCGGCTCCGCTGGCCCCGGGGAGCCCGAGTACGGCCACGACCCCGCGAGCGGCGGCATCTTCTCCTCCGAC
TACAAGCGGCATGATGACCTGAAGGAGATGCTGGACACCAACAAGGATTCTCTCAAGCTGGAGGCCATGAAGAGGATTGTGGCGATGATTGCCCGAGGAAAGAAT
GCTTCAGACCTGTTTCCCGCGGTGGTGAAGAACGTGGCCTGTAAGAACATAGAGGTGAAGAAGCTTGTCTATGTGTACCTGGTACGCTACGCTGAGGAGCAGCAA
GACCTGGCCCTGCTGTCCATCTCCACCTTCCAACGTGGCCTAAAGGATCCCAACCAGCTGATTCGTGCCAGTGCCCTCCGTGTCCTCTCTAGCATCCGTGTGCCC
ATCATAGTGCCCATCATGATGCTAGCTATCAAGGAAGCCGCCTCGGACATGTCACCCTATGTGCGGAAAACAGCTGCCCACGCCATCCCTAAACTCTACAGTTTG
GACTCTGACCAGAAGGATCAGCTGATAGAAGTCATTGAGAAGCTTCTGGCTGACAAGACCACGCTGGTGGCGGGCAGTGTGGTGATGGCCTTTGAGGAGGTCTGC
CCGGAGCGCATCGACCTGATTCACAAAAACTACCGGAAACTCTGTAACCTGCTGATCGACGTGGAGGAGTGGGGCCAGGTGGTCATCATCAGCATGCTCACCCGC
TACGCCCGCACGCAGTTCCTGAGCCCCACCCAGAACGAATCCCTACTAGAGGAGAACGCGGAAAAAGCCTTCTACGGCTCAGAGGAGGACGAGGCCAAGGGCGCG
GGGTCTGAGGAGACGGCCGCCGCGGCCGCCCCCTCCCGAAAGCCCTATGTCATGGACCCCGACCACCGGCTGCTGCTGCGCAACACCAAACCCCTGCTGCAGAGC
CGCAGCGCCGCGGTGGTGATGGCGGTGGCGCAGCTCTACTTCCACCTGGCGCCCAAGGCGGAAGTGGGCGTCATCGCCAAGGCGCTGGTGCGCCTGCTGCGCAGC
CACAGTGAGGTGCAGTACGTTGTGCTCCAGAACGTGGCCACCATGTCCATCAAGCGCCGGGGTATGTTTGAGCCCTACCTGAAGAGCTTCTACATCAGGTCCACC
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>AP3B2|8120|protein
MSAAPAYSEDKGGSAGPGEPEYGHDPASGGIFSSDYKRHDDLKEMLDTNKDSLKLEAMKRIVAMIARGKNASDLFPAVVKNVACKNIEVKKLVYVYLVRYAEEQQ
DLALLSISTFQRGLKDPNQLIRASALRVLSSIRVPIIVPIMMLAIKEAASDMSPYVRKTAAHAIPKLYSLDSDQKDQLIEVIEKLLADKTTLVAGSVVMAFEEVC
PERIDLIHKNYRKLCNLLIDVEEWGQVVIISMLTRYARTQFLSPTQNESLLEENAEKAFYGSEEDEAKGAGSEETAAAAAPSRKPYVMDPDHRLLLRNTKPLLQS
RSAAVVMAVAQLYFHLAPKAEVGVIAKALVRLLRSHSEVQYVVLQNVATMSIKRRGMFEPYLKSFYIRSTDPTQIKILKLEVLTNLANETNIPTVLREFQTYIRS
MDKDFVAATIQAIGRCATNIGRVRDTCLNGLVQLLSNRDELVVAESVVVIKKLLQMQPAQHGEIIKHLAKLTDNIQVPMARASILWLIGEYCEHVPRIAPDVLRK
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MSAAPAYSEDKGGSAGPGEPEYGHDPASGGIFSSDYKRHDDLKEMLDTNKDSLKLEAMKRIVAMIARGKNASDLFPAVVKNVACKNIEVKKLVYVYLVRYAEEQQ
DLALLSISTFQRGLKDPNQLIRASALRVLSSIRVPIIVPIMMLAIKEAASDMSPYVRKTAAHAIPKLYSLDSDQKDQLIEVIEKLLADKTTLVAGSVVMAFEEVC
PERIDLIHKNYRKLCNLLIDVEEWGQVVIISMLTRYARTQFLSPTQNESLLEENAEKAFYGSEEDEAKGAGSEETAAAAAPSRKPYVMDPDHRLLLRNTKPLLQS
RSAAVVMAVAQLYFHLAPKAEVGVIAKALVRLLRSHSEVQYVVLQNVATMSIKRRGMFEPYLKSFYIRSTDPTQIKILKLEVLTNLANETNIPTVLREFQTYIRS
MDKDFVAATIQAIGRCATNIGRVRDTCLNGLVQLLSNRDELVVAESVVVIKKLLQMQPAQHGEIIKHLAKLTDNIQVPMARASILWLIGEYCEHVPRIAPDVLRK
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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) | 1 (2) | 0 (0) | 0 (0) | 0 (0) | 1 (2) | 0 (0) | 1 (1) | 0 (0) | 20 (5) |
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 | ||||||
Bonati, 2005 | - | FISH | autism | - | - | - | - | 1 | - | 1 | ||
Szatmari, 2007 | Europe, North America | SNP microarray | ASD | 1491 | - | - | - | - | - | 0 |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
O'Roak BJ, 2012 | 1703 | 209 | 242 | Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. |
Yuen RK, 2016 | 200 | - | 301 | Genome-wide characteristics of de novo mutations in autism. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | ||||||||
O'Roak BJ, 2012 | USA | Illumina HiSeq 2000 | - | - | ASD | - | - | - | 2446 | - |
Low Scale Gene Studies Top
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