Evidence Details for EAF1
Basic Information Top
Gene Symbol: | EAF1 ( - ) |
---|---|
Gene Full Name: | ELL associated factor 1 |
Band: | 3p25.1 |
Quick Links | Entrez ID:85403; OMIM: 608315; Uniprot ID:EAF1_HUMAN; ENSEMBL ID: ENSG00000144597; HGNC ID: 20907 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>EAF1|85403|nucleotide
ATGAATGGGACCGCAAACCCGCTGCTGGACCGCGAGGAACATTGCCTGAGGCTCGGGGAGAGCTTCGAGAAGCGGCCGCGGGCCTCCTTCCACACTATTCGTTAT
GATTTTAAACCAGCATCTATAGACACTTCCTGTGAAGGAGAGCTTCAAGTTGGCAAAGGAGATGAAGTCACAATTACACTGCCACATATCCCTGGATCCACACCA
CCCATGACTGTGTTCAAGGGGAACAAACGGCCTTACCAGAAAGACTGTGTGCTTATTATTAATCATGACACTGGTGAATATGTGCTGGAAAAACTCAGTAGCAGC
ATTCAGGTGAAGAAAACAAGAGCTGAGGGCAGCAGTAAAATCCAGGCCCGAATGGAACAGCAGCCCACTCGTCCTCCACAGACGTCACAGCCACCACCACCTCCA
CCACCTATGCCATTCAGAGCTCCAACGAAGCCTCCAGTTGGACCCAAAACTTCTCCCTTGAAAGATAACCCCTCACCTGAACCTCAGTTGGATGACATCAAAAGA
GAGCTGAGGGCTGAAGTTGACATTATTGAACAAATGAGCAGCAGCAGTGGGAGCAGCTCTTCAGACTCTGAGAGCTCTTCGGGAAGTGATGACGATAGCTCCAGC
AGTGGAGGCGAGGACAATGGCCCAGCCTCTCCTCCGCAGCCTTCACACCAGCAGCCCTACAACAGTAGGCCTGCCGTTGCCAATGGAACCAGCCGGCCACAAGGA
AGCAACCAGCTCATGAACACCCTCAGAAATGACTTGCAGTTGAGTGAGTCTGGCAGTGACAGTGATGACTAG
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ATGAATGGGACCGCAAACCCGCTGCTGGACCGCGAGGAACATTGCCTGAGGCTCGGGGAGAGCTTCGAGAAGCGGCCGCGGGCCTCCTTCCACACTATTCGTTAT
GATTTTAAACCAGCATCTATAGACACTTCCTGTGAAGGAGAGCTTCAAGTTGGCAAAGGAGATGAAGTCACAATTACACTGCCACATATCCCTGGATCCACACCA
CCCATGACTGTGTTCAAGGGGAACAAACGGCCTTACCAGAAAGACTGTGTGCTTATTATTAATCATGACACTGGTGAATATGTGCTGGAAAAACTCAGTAGCAGC
ATTCAGGTGAAGAAAACAAGAGCTGAGGGCAGCAGTAAAATCCAGGCCCGAATGGAACAGCAGCCCACTCGTCCTCCACAGACGTCACAGCCACCACCACCTCCA
CCACCTATGCCATTCAGAGCTCCAACGAAGCCTCCAGTTGGACCCAAAACTTCTCCCTTGAAAGATAACCCCTCACCTGAACCTCAGTTGGATGACATCAAAAGA
GAGCTGAGGGCTGAAGTTGACATTATTGAACAAATGAGCAGCAGCAGTGGGAGCAGCTCTTCAGACTCTGAGAGCTCTTCGGGAAGTGATGACGATAGCTCCAGC
AGTGGAGGCGAGGACAATGGCCCAGCCTCTCCTCCGCAGCCTTCACACCAGCAGCCCTACAACAGTAGGCCTGCCGTTGCCAATGGAACCAGCCGGCCACAAGGA
AGCAACCAGCTCATGAACACCCTCAGAAATGACTTGCAGTTGAGTGAGTCTGGCAGTGACAGTGATGACTAG
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>EAF1|85403|protein
MNGTANPLLDREEHCLRLGESFEKRPRASFHTIRYDFKPASIDTSCEGELQVGKGDEVTITLPHIPGSTPPMTVFKGNKRPYQKDCVLIINHDTGEYVLEKLSSS
IQVKKTRAEGSSKIQARMEQQPTRPPQTSQPPPPPPPMPFRAPTKPPVGPKTSPLKDNPSPEPQLDDIKRELRAEVDIIEQMSSSSGSSSSDSESSSGSDDDSSS
SGGEDNGPASPPQPSHQQPYNSRPAVANGTSRPQGSNQLMNTLRNDLQLSESGSDSDD
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MNGTANPLLDREEHCLRLGESFEKRPRASFHTIRYDFKPASIDTSCEGELQVGKGDEVTITLPHIPGSTPPMTVFKGNKRPYQKDCVLIINHDTGEYVLEKLSSS
IQVKKTRAEGSSKIQARMEQQPTRPPQTSQPPPPPPPMPFRAPTKPPVGPKTSPLKDNPSPEPQLDDIKRELRAEVDIIEQMSSSSGSSSSDSESSSGSDDDSSS
SGGEDNGPASPPQPSHQQPYNSRPAVANGTSRPQGSNQLMNTLRNDLQLSESGSDSDD
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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) | 1 (4) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 3 (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 | ||||||
Marshall, 2008 | - | SNP microarray | ASD | 427 | 238 | 189 | - | 427 | 500 | 927 | ||
Zwaag, 2009 | - | SNP microarray | autism | - | - | - | - | 105 | 267 | 372 | ||
Gai, 2011 | AGRE | SNP microarray | - | - | autism | - | - | - | - | 1224 | 3801 | 5025 |
Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
Microarray Studies: 1
Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Voineagu, 2011_1 | Unknown | 16 frontal cortex(BA9) and 13 temporal cortex(BA41 | 16 (25.00%) | - | autism | 16 (6.25%) |
0.890531 | Down | 4.9335 | |||
|
Proteomics Studies:0
Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
---|---|---|---|---|---|---|---|---|---|
No Evidence. |
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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