Evidence Details for IGSF9B
Basic Information Top
Gene Symbol: | IGSF9B ( KIAA1030 ) |
---|---|
Gene Full Name: | immunoglobulin superfamily, member 9B |
Band: | 11q25 |
Quick Links | Entrez ID:22997; OMIM: NA; Uniprot ID:TUTLB_HUMAN; ENSEMBL ID: ENSG00000080854; HGNC ID: 32326 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>IGSF9B|22997|nucleotide
ATGATTTGGTATGTGGCCACTTTCATAGCAAGTGTGATCGGCACCCGAGGGCTTGCGGCTGAAGGCGCCCACGGCCTGCGAGAGGAGCCCGAGTTTGTGACGGCA
AGAGCTGGGGAGAGCGTGGTCCTGCGATGCGACGTGATCCACCCAGTGACGGGACAGCCCCCACCCTATGTCGTAGAGTGGTTCAAGTTCGGGGTCCCCATCCCT
ATCTTCATCAAGTTTGGCTACTACCCGCCGCACGTGGACCCTGAGTATGCAGGCCGGGCCAGTCTTCATGATAAGGCATCTCTGCGGCTGGAACAAGTTCGCTCT
GAGGACCAGGGCTGGTATGAGTGCAAAGTGCTCATGCTGGACCAGCAGTATGACACCTTCCACAATGGCAGCTGGGTCCACCTCACCATCAACGCCCCTCCCACC
TTTACAGAAACACCCCCCCAGTACATCGAGGCCAAGGAGGGTGGTAGTATCACCATGACCTGCACAGCTTTTGGGAACCCCAAGCCCATTGTCACCTGGCTCAAG
GAGGGGACGCTCCTCGGTGCTAGTGGGAAATACCAGGTGAGTGACGGCAGCCTGACAGTGACATCGGTCAGTCGGGAGGACAGAGGTGCCTACACCTGCCGAGCG
TACAGCATTCAGGGGGAGGCTGTCCACACGACTCACCTGCTTGTCCAAGGGCCCCCTTTCATCGTCTCCCCTCCTGAGAACATCACCGTCAACATCTCCCAGGAT
GCTCTGCTCACCTGCCGGGCAGAGGCGTATCCGGGCAACCTCACCTACACCTGGTACTGGCAGGACGAGAACGTCTACTTTCAGAACGACCTGAAGCTGAGGGTG
CGCATCCTAATCGATGGGACCCTGATCATCTTCCGGGTGAAGCCGGAGGACTCGGGGAAGTACACCTGTGTGCCCAGCAACAGCCTGGGGCGCTCCCCCTCCGCC
TCGGCGTACCTGACCGTGCAGTACCCAGCGCGTGTCCTCAACATGCCCCCTGTGATTTACGTGCCCGTGGGGATCCATGGCTACATCCGCTGCCCTGTGGACGCA
GAACCACCGGCCACCGTGGTCAAGTGGAACAAGGACGGCCGTCCCCTGCAGGTTGAGAAGAACCTCGGTTGGACCCTGATGGAGGATGGCTCCATTCGAATTGAG
Show »
ATGATTTGGTATGTGGCCACTTTCATAGCAAGTGTGATCGGCACCCGAGGGCTTGCGGCTGAAGGCGCCCACGGCCTGCGAGAGGAGCCCGAGTTTGTGACGGCA
AGAGCTGGGGAGAGCGTGGTCCTGCGATGCGACGTGATCCACCCAGTGACGGGACAGCCCCCACCCTATGTCGTAGAGTGGTTCAAGTTCGGGGTCCCCATCCCT
ATCTTCATCAAGTTTGGCTACTACCCGCCGCACGTGGACCCTGAGTATGCAGGCCGGGCCAGTCTTCATGATAAGGCATCTCTGCGGCTGGAACAAGTTCGCTCT
GAGGACCAGGGCTGGTATGAGTGCAAAGTGCTCATGCTGGACCAGCAGTATGACACCTTCCACAATGGCAGCTGGGTCCACCTCACCATCAACGCCCCTCCCACC
TTTACAGAAACACCCCCCCAGTACATCGAGGCCAAGGAGGGTGGTAGTATCACCATGACCTGCACAGCTTTTGGGAACCCCAAGCCCATTGTCACCTGGCTCAAG
GAGGGGACGCTCCTCGGTGCTAGTGGGAAATACCAGGTGAGTGACGGCAGCCTGACAGTGACATCGGTCAGTCGGGAGGACAGAGGTGCCTACACCTGCCGAGCG
TACAGCATTCAGGGGGAGGCTGTCCACACGACTCACCTGCTTGTCCAAGGGCCCCCTTTCATCGTCTCCCCTCCTGAGAACATCACCGTCAACATCTCCCAGGAT
GCTCTGCTCACCTGCCGGGCAGAGGCGTATCCGGGCAACCTCACCTACACCTGGTACTGGCAGGACGAGAACGTCTACTTTCAGAACGACCTGAAGCTGAGGGTG
CGCATCCTAATCGATGGGACCCTGATCATCTTCCGGGTGAAGCCGGAGGACTCGGGGAAGTACACCTGTGTGCCCAGCAACAGCCTGGGGCGCTCCCCCTCCGCC
TCGGCGTACCTGACCGTGCAGTACCCAGCGCGTGTCCTCAACATGCCCCCTGTGATTTACGTGCCCGTGGGGATCCATGGCTACATCCGCTGCCCTGTGGACGCA
GAACCACCGGCCACCGTGGTCAAGTGGAACAAGGACGGCCGTCCCCTGCAGGTTGAGAAGAACCTCGGTTGGACCCTGATGGAGGATGGCTCCATTCGAATTGAG
Show »
>IGSF9B|22997|protein
MIWYVATFIASVIGTRGLAAEGAHGLREEPEFVTARAGESVVLRCDVIHPVTGQPPPYVVEWFKFGVPIPIFIKFGYYPPHVDPEYAGRASLHDKASLRLEQVRS
EDQGWYECKVLMLDQQYDTFHNGSWVHLTINAPPTFTETPPQYIEAKEGGSITMTCTAFGNPKPIVTWLKEGTLLGASGKYQVSDGSLTVTSVSREDRGAYTCRA
YSIQGEAVHTTHLLVQGPPFIVSPPENITVNISQDALLTCRAEAYPGNLTYTWYWQDENVYFQNDLKLRVRILIDGTLIIFRVKPEDSGKYTCVPSNSLGRSPSA
SAYLTVQYPARVLNMPPVIYVPVGIHGYIRCPVDAEPPATVVKWNKDGRPLQVEKNLGWTLMEDGSIRIEEATEEALGTYTCVPYNTLGTMGQSAPARLVLKDPP
YFTVLPGWEYRQEAGRELLIPCAAAGDPFPVITWRKVGKPSRSKHSALPSGSLQFRALSKEDHGEWECVATNVVTSITASTHLTVIGTSPHAPGSVRVQVSMTTA
Show »
MIWYVATFIASVIGTRGLAAEGAHGLREEPEFVTARAGESVVLRCDVIHPVTGQPPPYVVEWFKFGVPIPIFIKFGYYPPHVDPEYAGRASLHDKASLRLEQVRS
EDQGWYECKVLMLDQQYDTFHNGSWVHLTINAPPTFTETPPQYIEAKEGGSITMTCTAFGNPKPIVTWLKEGTLLGASGKYQVSDGSLTVTSVSREDRGAYTCRA
YSIQGEAVHTTHLLVQGPPFIVSPPENITVNISQDALLTCRAEAYPGNLTYTWYWQDENVYFQNDLKLRVRILIDGTLIIFRVKPEDSGKYTCVPSNSLGRSPSA
SAYLTVQYPARVLNMPPVIYVPVGIHGYIRCPVDAEPPATVVKWNKDGRPLQVEKNLGWTLMEDGSIRIEEATEEALGTYTCVPYNTLGTMGQSAPARLVLKDPP
YFTVLPGWEYRQEAGRELLIPCAAAGDPFPVITWRKVGKPSRSKHSALPSGSLQFRALSKEDHGEWECVATNVVTSITASTHLTVIGTSPHAPGSVRVQVSMTTA
Show »
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) | 2 (3) | 0 (0) | 0 (0) | 0 (0) | 22 (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 | ||||||
Szatmari, 2007 | Europe, North America | SNP microarray | ASD | 1491 | - | - | - | - | - | 0 | ||
Zwaag, 2009 | - | SNP microarray | autism | - | - | - | - | 105 | 267 | 372 |
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 |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |
Yuen RK, 2016 | 200 | - | 301 | Genome-wide characteristics of de novo mutations in autism. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.