Evidence Details for BEND3
Basic Information Top
Gene Symbol: | BEND3 ( KIAA1553,RP11-59I9.2 ) |
---|---|
Gene Full Name: | BEN domain containing 3 |
Band: | 6q21 |
Quick Links | Entrez ID:57673; OMIM: NA; Uniprot ID:BEND3_HUMAN; ENSEMBL ID: ENSG00000178409; HGNC ID: 23040 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>BEND3|57673|nucleotide
ATGAACTCAACTGAATTCACCGAAGATGTAGAAGAAGTTCTAAAAAGTATCACTGTGAAAGTGGAGACAGAGGCTGAAGATGCTGCTCTGGACTGCTCCGTGAAT
TCCAGGACTTCTGAGAAGCACTCTGTGGACAGCGTCCTCACTGCCCTGCAGGACTCCAGCAAACGAAAGCAGCTGGTCAGCGATGGCCTGCTAGACTCTGTCCCC
GGCGTGAAGAGGAGGCGGCTGATCCCCGAGGCTCTCCTAGCAGGCATGCGGAACCGTGAGAACAGCTCGCCCTGCCAAGGCAATGGTGAGCAGGCCGGCAGGGGC
AGGAGCCTGGGCAATGTGTGGCCTGGAGAGGAGGAGCCCTGCAACGATGCCACCACCCCTTCCTACAAGAAGCCTCTGTATGGCATCTCGCACAAGATCATGGAG
AAGAAGAATCCTCCCTCGGGGGACCTGCTAAACGTGTACGAGCTCTTTGAGAAGGCAAACGCCAGCAACAGCCCCTCGTCACTGCGGCTCCTGAATGAGCCACAG
AAGCGGGACTGTGGCAGCACCGGGGCAGGCACTGACAACGACCCCAACATCTACTTCCTGATCCAGAAGATGTTCTACATGCTGAACACCCTCACGTCCAACATG
TCCCAGCTGCACAGCAAGGTGGACCTGCTCTCCCTTGAGGTGAGCCGCATCAAGAAGCAGGTGAGCCCCACTGAGATGGTGGCCAAATTCCAGCCGCCCCCTGAG
TACCAGCTCACAGCCGCAGAGCTCAAGCAGATCGTGGACCAGAGCCTGTCAGGGGGGGACCTGGCCTGCCGCTTGCTGGTGCAGCTCTTCCCCGAGCTCTTCAGC
GACGTGGACTTCTCCCGGGGCTGCAGTGCCTGTGGCTTTGCGGCCAAGCGCAAGCTGGAGTCGCTGCACCTGCAGCTCATCCGCAACTATGTGGAGGTCTACTAC
CCCTCGGTGAAGGACACGGCTGTGTGGCAGGCCGAGTGCCTGCCCCAGCTGAACGACTTCTTCAGCCGCTTCTGGGCCCAGCGGGAAATGGAGGACAGCCAGCCC
AGCGGCCAGGTCGCCAGCTTCTTTGAGGCAGAGCAGGTGGACCCCGGCCACTTCCTGGACAACAAAGACCAGGAGGAGGCCCTGTCTCTTGACCGGAGCAGCACC
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ATGAACTCAACTGAATTCACCGAAGATGTAGAAGAAGTTCTAAAAAGTATCACTGTGAAAGTGGAGACAGAGGCTGAAGATGCTGCTCTGGACTGCTCCGTGAAT
TCCAGGACTTCTGAGAAGCACTCTGTGGACAGCGTCCTCACTGCCCTGCAGGACTCCAGCAAACGAAAGCAGCTGGTCAGCGATGGCCTGCTAGACTCTGTCCCC
GGCGTGAAGAGGAGGCGGCTGATCCCCGAGGCTCTCCTAGCAGGCATGCGGAACCGTGAGAACAGCTCGCCCTGCCAAGGCAATGGTGAGCAGGCCGGCAGGGGC
AGGAGCCTGGGCAATGTGTGGCCTGGAGAGGAGGAGCCCTGCAACGATGCCACCACCCCTTCCTACAAGAAGCCTCTGTATGGCATCTCGCACAAGATCATGGAG
AAGAAGAATCCTCCCTCGGGGGACCTGCTAAACGTGTACGAGCTCTTTGAGAAGGCAAACGCCAGCAACAGCCCCTCGTCACTGCGGCTCCTGAATGAGCCACAG
AAGCGGGACTGTGGCAGCACCGGGGCAGGCACTGACAACGACCCCAACATCTACTTCCTGATCCAGAAGATGTTCTACATGCTGAACACCCTCACGTCCAACATG
TCCCAGCTGCACAGCAAGGTGGACCTGCTCTCCCTTGAGGTGAGCCGCATCAAGAAGCAGGTGAGCCCCACTGAGATGGTGGCCAAATTCCAGCCGCCCCCTGAG
TACCAGCTCACAGCCGCAGAGCTCAAGCAGATCGTGGACCAGAGCCTGTCAGGGGGGGACCTGGCCTGCCGCTTGCTGGTGCAGCTCTTCCCCGAGCTCTTCAGC
GACGTGGACTTCTCCCGGGGCTGCAGTGCCTGTGGCTTTGCGGCCAAGCGCAAGCTGGAGTCGCTGCACCTGCAGCTCATCCGCAACTATGTGGAGGTCTACTAC
CCCTCGGTGAAGGACACGGCTGTGTGGCAGGCCGAGTGCCTGCCCCAGCTGAACGACTTCTTCAGCCGCTTCTGGGCCCAGCGGGAAATGGAGGACAGCCAGCCC
AGCGGCCAGGTCGCCAGCTTCTTTGAGGCAGAGCAGGTGGACCCCGGCCACTTCCTGGACAACAAAGACCAGGAGGAGGCCCTGTCTCTTGACCGGAGCAGCACC
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>BEND3|57673|protein
MNSTEFTEDVEEVLKSITVKVETEAEDAALDCSVNSRTSEKHSVDSVLTALQDSSKRKQLVSDGLLDSVPGVKRRRLIPEALLAGMRNRENSSPCQGNGEQAGRG
RSLGNVWPGEEEPCNDATTPSYKKPLYGISHKIMEKKNPPSGDLLNVYELFEKANASNSPSSLRLLNEPQKRDCGSTGAGTDNDPNIYFLIQKMFYMLNTLTSNM
SQLHSKVDLLSLEVSRIKKQVSPTEMVAKFQPPPEYQLTAAELKQIVDQSLSGGDLACRLLVQLFPELFSDVDFSRGCSACGFAAKRKLESLHLQLIRNYVEVYY
PSVKDTAVWQAECLPQLNDFFSRFWAQREMEDSQPSGQVASFFEAEQVDPGHFLDNKDQEEALSLDRSSTIASDHVVDTQDLTEFLDEASSPGEFAVFLLHRLFP
ELFDHRKLGEQYSCYGDGGKQELDPQRLQIIRNYTEIYFPDMQEEEAWLQQCAQRINDELEGLGLDAGSEGDPPRDDCYDSSSLPDDISVVKVEDSFEGERPGRR
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MNSTEFTEDVEEVLKSITVKVETEAEDAALDCSVNSRTSEKHSVDSVLTALQDSSKRKQLVSDGLLDSVPGVKRRRLIPEALLAGMRNRENSSPCQGNGEQAGRG
RSLGNVWPGEEEPCNDATTPSYKKPLYGISHKIMEKKNPPSGDLLNVYELFEKANASNSPSSLRLLNEPQKRDCGSTGAGTDNDPNIYFLIQKMFYMLNTLTSNM
SQLHSKVDLLSLEVSRIKKQVSPTEMVAKFQPPPEYQLTAAELKQIVDQSLSGGDLACRLLVQLFPELFSDVDFSRGCSACGFAAKRKLESLHLQLIRNYVEVYY
PSVKDTAVWQAECLPQLNDFFSRFWAQREMEDSQPSGQVASFFEAEQVDPGHFLDNKDQEEALSLDRSSTIASDHVVDTQDLTEFLDEASSPGEFAVFLLHRLFP
ELFDHRKLGEQYSCYGDGGKQELDPQRLQIIRNYTEIYFPDMQEEEAWLQQCAQRINDELEGLGLDAGSEGDPPRDDCYDSSSLPDDISVVKVEDSFEGERPGRR
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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) | 0 (0) | 1 (3) | 0 (0) | 0 (0) | 0 (0) | 10 (4) |
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 | ||||||
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 |
---|---|---|---|---|
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |
Takata A, 2018 | 262 | 262 | 322 | Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Di |
Fromer M, 2014 | - | - | 94 | De novo mutations in schizophrenia implicate synaptic networks. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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