Evidence Detail for HEY2
Basic Information
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| Gene Symbol: | HEY2 ( CHF1,GRIDLOCK,GRL,HERP1,HESR2,HRT2,MGC10720,bHLHb32 ) |
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| Gene Full Name: | hairy/enhancer-of-split related with YRPW motif 2 |
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| Band: | 6q21 |
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| Quick Links | Entrez ID:23493; OMIM: 604674; Uniprot ID:HEY2_HUMAN; ENSEMBL ID: ENSG00000135547 |
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>HEY2|23493|nucleotide
ATGAAGCGCCCCTGCGAGGAGACGACCTCCGAGAGCGACATGGACGAGACCATCGACGTGGGGAGCGAGAACAATTACTCGGGGCAAAGTACTAGCTCTGTGATT
AGATTGAATTCTCCAACAACAACATCTCAGATTATGGCAAGAAAGAAAAGGAGAGGGATTATAGAGAAAAGGCGTCGGGATCGGATAAATAACAGTTTATCTGAG
TTGAGAAGACTTGTGCCAACTGCTTTTGAAAAACAAGGATCTGCAAAGTTAGAAAAAGCTGAAATATTGCAAATGACAGTGGATCATTTGAAGATGCTTCAGGCA
ACAGGGGGTAAAGGCTACTTTGACGCACACGCTCTTGCCATGGACTTCATGAGCATAGGATTCCGAGAGTGCCTAACAGAAGTTGCGCGGTACCTGAGCTCCGTG
GAAGGCCTGGACTCCTCGGATCCGCTGCGGGTGCGGCTTGTGTCTCATCTCAGCACTTGCGCCACCCAGCGGGAGGCGGCGGCCATGACATCCTCCATGGCCCAC
CACCATCATCCGCTCCACCCGCATCACTGGGCCGCCGCCTTCCACCACCTGCCCGCAGCCCTGCTCCAGCCCAACGGCCTCCATGCCTCAGAGTCAACCCCTTGT
CGCCTCTCCACAACTTCAGAAGTGCCTCCTGCCCACGGCTCTGCTCTCCTCACGGCCACGTTTGCCCATGCGGATTCAGCCCTCCGAATGCCATCCACGGGCAGC
GTCGCCCCCTGCGTGCCACCTCTCTCCACCTCTCTCTTGTCCCTCTCTGCCACCGTCCACGCCGCAGCCGCAGCAGCCACCGCGGCTGCACACAGCTTCCCTCTG
TCCTTCGCGGGGGCATTCCCCATGCTTCCCCCAAACGCAGCAGCAGCAGTGGCCGCGGCCACAGCCATCAGCCCGCCCTTGTCAGTATCAGCCACGTCCAGTCCT
CAGCAGACCAGCAGTGGAACAAACAATAAACCTTACCGACCCTGGGGGACAGAAGTTGGAGCTTTTTAA
« Hide>HEY2|23493|protein
MKRPCEETTSESDMDETIDVGSENNYSGQSTSSVIRLNSPTTTSQIMARKKRRGIIEKRRRDRINNSLSELRRLVPTAFEKQGSAKLEKAEILQMTVDHLKMLQA
TGGKGYFDAHALAMDFMSIGFRECLTEVARYLSSVEGLDSSDPLRVRLVSHLSTCATQREAAAMTSSMAHHHHPLHPHHWAAAFHHLPAALLQPNGLHASESTPC
RLSTTSEVPPAHGSALLTATFAHADSALRMPSTGSVAPCVPPLSTSLLSLSATVHAAAAAATAAAHSFPLSFAGAFPMLPPNAAAAVAAATAISPPLSVSATSSP
QQTSSGTNNKPYRPWGTEVGAF
« Hide Evidence Statistic
TopClick the link of the category-specific score to view different category of evidences. The categories without any evidences are hidden by default. 
Syndromic Autism Gene
TopLow Scale Association Studies (by Ethnic Group)
Top Family Based Association Studies: 0
| Reference |
Population |
#SNPs/ #VNTRs |
#Families |
Affecteds |
Result |
#Subjects
(% Women) |
ADI-R |
ADOS |
Diagnosis |
Age
(range) |
IQ
(range) |
| No Evidence. |
Case Control Based Association Studies: 0
| Reference |
Population |
#SNPs/ #VNTRs |
ASD Cases |
Normal Controls |
Result |
#Subjects
(% Women) |
ADI-R |
ADOS |
Diagnosis |
Age
(range) |
IQ |
#Subjects
(% Women) |
Age
(range) |
| No Evidence. |
Genome-Wide Association Studies(By Ethnic Group)
Top Family Based Association Studies: 0
| Reference |
Stage |
#SNPs/ #VNTRs |
#Families |
Affecteds |
Result |
#Subjects
(% Women) |
ADI-R |
ADOS |
Diagnosis |
Age
(range) |
IQ
(range) |
| No Evidence. |
Case Control Based Association Studies: 0
| Reference |
Stage |
#SNPs/ #VNTRs |
ASD Cases |
Normal Controls |
Result |
#Subjects
(% Women) |
ADI-R |
ADOS |
Diagnosis |
Age
(range) |
IQ |
#Subjects
(% Women) |
Age
(range) |
| No Evidence. |
Other Low Scale Gene Studies
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| Reference |
Orangnism |
Tissue |
ADI-R |
ADOS |
Diagnosis |
Evidence Level |
Result |
| No Evidence. |
Large Scale Expression Studies
Top Microarray Studies: 2
Proteomics Studies:0
| Reference |
Population |
Tissue |
Platform |
#Subjects
(% Women) |
ADI-R |
ADOS |
Diagnosis |
Normal Controls(% Women) |
| No Evidence. |
CNV Studies
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| CNV Name |
Chr |
Band |
Gain/Loss |
Number of CNVs |
Evidence Type |
Reference |
| Case |
Control |
| No matched CNVs ! |
Linkage Studies
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| Linkage Name |
Band |
Chr |
Marker |
LOD |
NPL |
P_Value |
Reference |
| No Matched Linkage Regions ! |
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