Evidence Details for HEATR2
Basic Information Top
Gene Symbol: | HEATR2 ( FLJ20397,FLJ25564,FLJ31671,FLJ39381 ) |
---|---|
Gene Full Name: | HEAT repeat containing 2 |
Band: | 7p22.3 |
Quick Links | Entrez ID:54919; OMIM: NA; Uniprot ID:HEAT2_HUMAN; ENSEMBL ID: ENSG00000164818; HGNC ID: |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>HEATR2|54919|nucleotide
ATGGCGGCGCTGGGGGTGGCGGAGGCCGTGGCGGCCCCACACCCGGCTGAGGGGGCCGAGACGGCTGAGGCGGTGGAGCTGAGCCGCGCCCTGAGCCGCCTGCTG
CCGGGGCTGGAGGCCGACAGCAAGCCGGGCCGGCGGCGCGCCTTGGAGGCCCTGCGGCGCGCGCTGGAGGAGCCAGGCCCTGCCGCCGACCCCACCGCTTTCCAG
GGCCCCTGGGCGCGCCTACTGCTGCCGCGCTTGCTGCGCTGCCTGAGCGACCCCGCCGAGGGCTGCCGCGCGCTGGCAGTGCACCTGCTGGATCTGGGCCTGCGC
CGCGCCGCGCGGCCCCGCGATGCCCTGCCGCGCCTGCTGCCCGCGCTCGCCGCGCGCTTGGCCGGCCCCGTGCCCGCGCGCCGCCCGCCCGAGGCCTGTGAGGAG
CTGCGCCTGGCGCTTGTGCAGCTGCTGGGCCTGGCCGTGGACCTGTGCGGCGCCGCGCTCGCGCCCCACCTGGACGACGCTCTGCGCGCGCTGCGCTGCTCCCTG
CTCGACCCCTTCGCCGCCGTGCGCCGCGAGAGCTGCAGCTGCGCCGCCGCCCTGGCGCAGGCCACGCCCGACCACTTCCACATGCAGTCGGAGTCTCTGATCGGG
CCCCTGATGCAGACCATCTCCCACCAGCACTGGAAGGTCCGTGTGGCCGCCATTGAAGCCACAGGCGCAGTGATCCATTTTGGCAACGGGAAGTCCGTGGACGAC
GTGCTTTCCCATTTTGCTCAGCGACTGTTTGATGACGTCCCGCAGGTCCGGCGGGCGGTGGCCTCCGTGGTGGGCGGCTGGCTGCTGTGTCTGCGTGACCGTTAC
TCCTTCTTCCACAAGCTCATCCCTCTGCTGCTCAGTAGCCTCAACGACGAGGTGCCTGAGGTCAGGCAGCTGGCTGCCAGCCTCTGGGAGGACGTTGGCCTGCAG
TGGCAGAAGGAGAATGAGGAGGACCTGAAGGACAAGCTGGACTTTGCCCCTCCCACCCCACCCCATTACCCTCCACATGAGCGCCGCCCTGTGCTGGGCTGCCGG
GAGCTCGTCTTCAGGAACCTCTCCAAGATCCTCCCTGCCCTGTGCCACGACATCACCGACTGGGTGGTGGGGACCCGAGTGAAGTCGGCACAGCTGCTCCCAGTG
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ATGGCGGCGCTGGGGGTGGCGGAGGCCGTGGCGGCCCCACACCCGGCTGAGGGGGCCGAGACGGCTGAGGCGGTGGAGCTGAGCCGCGCCCTGAGCCGCCTGCTG
CCGGGGCTGGAGGCCGACAGCAAGCCGGGCCGGCGGCGCGCCTTGGAGGCCCTGCGGCGCGCGCTGGAGGAGCCAGGCCCTGCCGCCGACCCCACCGCTTTCCAG
GGCCCCTGGGCGCGCCTACTGCTGCCGCGCTTGCTGCGCTGCCTGAGCGACCCCGCCGAGGGCTGCCGCGCGCTGGCAGTGCACCTGCTGGATCTGGGCCTGCGC
CGCGCCGCGCGGCCCCGCGATGCCCTGCCGCGCCTGCTGCCCGCGCTCGCCGCGCGCTTGGCCGGCCCCGTGCCCGCGCGCCGCCCGCCCGAGGCCTGTGAGGAG
CTGCGCCTGGCGCTTGTGCAGCTGCTGGGCCTGGCCGTGGACCTGTGCGGCGCCGCGCTCGCGCCCCACCTGGACGACGCTCTGCGCGCGCTGCGCTGCTCCCTG
CTCGACCCCTTCGCCGCCGTGCGCCGCGAGAGCTGCAGCTGCGCCGCCGCCCTGGCGCAGGCCACGCCCGACCACTTCCACATGCAGTCGGAGTCTCTGATCGGG
CCCCTGATGCAGACCATCTCCCACCAGCACTGGAAGGTCCGTGTGGCCGCCATTGAAGCCACAGGCGCAGTGATCCATTTTGGCAACGGGAAGTCCGTGGACGAC
GTGCTTTCCCATTTTGCTCAGCGACTGTTTGATGACGTCCCGCAGGTCCGGCGGGCGGTGGCCTCCGTGGTGGGCGGCTGGCTGCTGTGTCTGCGTGACCGTTAC
TCCTTCTTCCACAAGCTCATCCCTCTGCTGCTCAGTAGCCTCAACGACGAGGTGCCTGAGGTCAGGCAGCTGGCTGCCAGCCTCTGGGAGGACGTTGGCCTGCAG
TGGCAGAAGGAGAATGAGGAGGACCTGAAGGACAAGCTGGACTTTGCCCCTCCCACCCCACCCCATTACCCTCCACATGAGCGCCGCCCTGTGCTGGGCTGCCGG
GAGCTCGTCTTCAGGAACCTCTCCAAGATCCTCCCTGCCCTGTGCCACGACATCACCGACTGGGTGGTGGGGACCCGAGTGAAGTCGGCACAGCTGCTCCCAGTG
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>HEATR2|54919|protein
MAALGVAEAVAAPHPAEGAETAEAVELSRALSRLLPGLEADSKPGRRRALEALRRALEEPGPAADPTAFQGPWARLLLPRLLRCLSDPAEGCRALAVHLLDLGLR
RAARPRDALPRLLPALAARLAGPVPARRPPEACEELRLALVQLLGLAVDLCGAALAPHLDDALRALRCSLLDPFAAVRRESCSCAAALAQATPDHFHMQSESLIG
PLMQTISHQHWKVRVAAIEATGAVIHFGNGKSVDDVLSHFAQRLFDDVPQVRRAVASVVGGWLLCLRDRYSFFHKLIPLLLSSLNDEVPEVRQLAASLWEDVGLQ
WQKENEEDLKDKLDFAPPTPPHYPPHERRPVLGCRELVFRNLSKILPALCHDITDWVVGTRVKSAQLLPVLLLHAEDHATQHLEVVLRTLFQACTDEEAAVVQSC
TRSAELVGTFVSPEVFLKLILSTLKKTPSASGLLVLASAMRGCPREALQPHLAAIATELAQAHICQASENDLYLERLLLCVQALVSVCHEDCGVASLQLLDVLLT
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MAALGVAEAVAAPHPAEGAETAEAVELSRALSRLLPGLEADSKPGRRRALEALRRALEEPGPAADPTAFQGPWARLLLPRLLRCLSDPAEGCRALAVHLLDLGLR
RAARPRDALPRLLPALAARLAGPVPARRPPEACEELRLALVQLLGLAVDLCGAALAPHLDDALRALRCSLLDPFAAVRRESCSCAAALAQATPDHFHMQSESLIG
PLMQTISHQHWKVRVAAIEATGAVIHFGNGKSVDDVLSHFAQRLFDDVPQVRRAVASVVGGWLLCLRDRYSFFHKLIPLLLSSLNDEVPEVRQLAASLWEDVGLQ
WQKENEEDLKDKLDFAPPTPPHYPPHERRPVLGCRELVFRNLSKILPALCHDITDWVVGTRVKSAQLLPVLLLHAEDHATQHLEVVLRTLFQACTDEEAAVVQSC
TRSAELVGTFVSPEVFLKLILSTLKKTPSASGLLVLASAMRGCPREALQPHLAAIATELAQAHICQASENDLYLERLLLCVQALVSVCHEDCGVASLQLLDVLLT
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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 (3) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (1) | 0 (0) | 0 (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 | ||||||
Christian, 2008 | USA | aCGH | ASD | 397 | 35 | 362 | - | 397 | 372 | 769 | ||
Gregory, 2009 | USA | aCGH | ASD | - | - | - | - | 119 | 54 | 173 | ||
Gai, 2011 | AGRE | SNP microarray | - | - | autism | - | - | - | - | 1224 | 3801 | 5025 |
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 |
---|---|---|---|---|
Takata A, 2018 | 262 | 262 | 322 | Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Di |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Reference | Source | Platform | ADI-R | ADOS | Diagnosis | Family | Affected | Validation Method | ||
---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | ||||||||
Cukier HN, 2014 | - | Illumina HiSeq 2000 | ASD | 40 | - | - | 100 | HumanExome BeadChip or Sanger sequencing |
Low Scale Gene Studies Top
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