Evidence Detail for KLF7
Basic Information
Top
| Gene Symbol: | KLF7 ( UKLF ) |
|---|
| Gene Full Name: | Kruppel-like factor 7 (ubiquitous) |
|---|
| Band: | 2q32 |
|---|
| Quick Links | Entrez ID:8609; OMIM: 604865; Uniprot ID:KLF7_HUMAN; ENSEMBL ID: ENSG00000118263 |
|---|
>KLF7|8609|nucleotide
ATGGACGTGTTGGCTAGTTATAGTATATTCCAGGAGCTACAACTTGTCCACGACACCGGCTACTTCTCAGCTTTACCATCCCTGGAGGAGACCTGGCAGCAGACA
TGCCTTGAATTGGAACGCTACCTACAGACGGAGCCCCGGAGGATCTCAGAGACCTTTGGTGAGGACTTGGACTGTTTCCTCCACGCTTCCCCTCCCCCGTGCATT
GAGGAAAGCTTCCGTCGCTTAGACCCCCTGCTGCTCCCCGTGGAAGCGGCCATCTGTGAGAAGAGCTCGGCAGTGGACATCTTGCTCTCTCGGGACAAGTTGCTA
TCTGAGACCTGCCTCAGCCTCCAGCCGGCCAGCTCTTCTCTAGACAGCTACACAGCCGTCAACCAGGCCCAGCTCAACGCAGTGACCTCATTAACGCCCCCATCG
TCCCCTGAGCTCAGCCGCCATCTGGTCAAAACCTCACAAACTCTCTCTGCCGTGGATGGCACGGTGACGTTGAAACTGGTGGCCAAGAAGGCTGCTCTCAGCTCC
GTAAAGGTGGGAGGGGTCGCAACAGCTGCAGCAGCCGTGACGGCTGCGGGGGCCGTTAAGAGTGGACAGAGCGACAGTGACCAAGGAGGGCTAGGGGCTGAAGCA
TGTCCCGAAAACAAGAAGAGGGTTCACCGCTGTCAGTTTAACGGGTGCCGGAAAGTTTATACAAAAAGCTCCCACTTAAAGGCCCACCAGAGGACTCACACAGGT
GAGAAGCCTTATAAGTGCTCATGGGAGGGATGTGAGTGGCGTTTTGCACGAAGCGATGAGCTCACGAGGCACTACAGGAAACACACAGGTGCAAAGCCCTTCAAA
TGCAACCACTGCGACAGGTGTTTTTCCAGGTCTGACCATCTTGCCCTCCACATGAAGAGACATATCTAA
« Hide>KLF7|8609|protein
MDVLASYSIFQELQLVHDTGYFSALPSLEETWQQTCLELERYLQTEPRRISETFGEDLDCFLHASPPPCIEESFRRLDPLLLPVEAAICEKSSAVDILLSRDKLL
SETCLSLQPASSSLDSYTAVNQAQLNAVTSLTPPSSPELSRHLVKTSQTLSAVDGTVTLKLVAKKAALSSVKVGGVATAAAAVTAAGAVKSGQSDSDQGGLGAEA
CPENKKRVHRCQFNGCRKVYTKSSHLKAHQRTHTGEKPYKCSWEGCEWRFARSDELTRHYRKHTGAKPFKCNHCDRCFSRSDHLALHMKRHI
« 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: 1
| Reference |
Population |
Tissue |
#Subjects
(% Women) |
ADI-R |
ADOS |
Endo- pheno |
Diagnosis |
Normal Controls
(% Women) |
Fold Change |
Up/ Down |
P/Q value |
| Nishimura, 2007_1 |
America |
lymphoblastoid cell lines |
8
(-) |  | | autism with FMR1-FM | autism |
15
(-) |
1.26 |
Up |
0.0000059 | |
- Platform: Whole Human Genome Array G4112A (Agilent)
- ProbeSet: -
- RefSeq_ID/ EST: NM_003709
- GEO_ID: GSE7329
- Statistic Method: ANOVA by MeV3.1, PCA by GeneSpring GX7.3(Aligent), SAM and RankProd by Bioconductor packages
|
Proteomics Studies:0
| Reference |
Population |
Tissue |
Platform |
#Subjects
(% Women) |
ADI-R |
ADOS |
Diagnosis |
Normal Controls(% Women) |
| No Evidence. |
CNV Studies
Top
| CNV Name |
Chr |
Band |
Gain/Loss |
Number of CNVs |
Evidence Type |
Reference |
| Case |
Control |
| AutCNV0000262 |
2 |
2q33.3-35 |
loss |
1 |
- |
CNVs Only Present In Patients; |
Pescucci, 2003 |
Linkage Studies
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| Linkage Name |
Band |
Chr |
Marker |
LOD |
NPL |
P_Value |
Reference |
| No Matched Linkage Regions ! |
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.
