Evidence Details for FAM124A
Basic Information Top
Gene Symbol: | FAM124A ( FLJ30707 ) |
---|---|
Gene Full Name: | family with sequence similarity 124A |
Band: | 13q14.3 |
Quick Links | Entrez ID:220108; OMIM: NA; Uniprot ID:F124A_HUMAN; ENSEMBL ID: ENSG00000150510; HGNC ID: 26413 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>FAM124A|220108|nucleotide
ATGGACCCAAAGGCGGGCGGCGGCGGCGAGGAGGACGACTGCGTGGACTCGGGCGCCGAGACCGGAGGGTCCGACTACAGCCACCTGTCCTCCACGAGCAATGGA
TTCTCCACCTGGCGGATGCCATGTTGCCTGTTCCTTTACTGTACACACGGTGACAAAGAAAAGGGAAGATGGAGCCTCCAGGTTGAACATACCTGGCCCTCAGGT
GAGCTTTCCGTTGAAGAGGCGCAGGACCCTTTCCTGGTCAGCATCCACATAATCGCAGACCCAGGGGAGTCCCAGCCCCTGCAGGAGGCCATCGACAACGTCCTG
GCGTGGATCCACCCCGACCTCCCGCTGTTCCGGGTGTCCGAGAGGCGGGCGTCCCGGCGGCGGCGGAAGCCCCCCAAGGGCGCTCAGCCAGCGCTGGCTGTGGTG
CTGTTCCTGCAGGAGGAGTACGGCGAAGAGCAGATCCTGCAGCTGCACCGCACACTGCAGCAGCCGCCCTGGCGCCACCACCACACCGAGCAGGTGCACGGCCGG
TTCCTGCCCTACCTGCCCTGCAGCCAGGACTTCTTCACGCTGGCCCCTGGGACGCCGCTTTGGGCCATCCGGCCCGTGCACTACGGCAAGGAAATCGTGCGCTTC
ACCGTCTACTGTCGCTACGACAACTATGCTGACAGCCTCAGGTTCTACCAGCTGATTCTCCGGAGGAACCCCAGCCAGAAGAAAGCGGACTTCTGCATCTTCCCT
ATTTTTTCCAACCTGGATGTGGACATCCAGTTCTCCCTGAAAAGACTGCCCTGTGACCAGTGCCCGGTGCCCACCGACTCCTCCGTGCTGGAGTTCCGAGTGAGG
GACATAGGCGAGCTCGTGCCTCTCCTGCCCAACCCTTGCAGCCCCATCAGCGAGGGGCGCTGGCAGACGGAGGACCATGATGGGAACAAGATCCTCCTACAGGCA
CAAAGGGTGCATAAGAAGTTTCCTAAACCTGGCAGAGTACATCATGCCTCCGAGAAGAAACGTCATTCCACTCCTTTGCCGAGCACTGCTGTACCAAGCCATACA
CCTGGCAGCAGCCAGCAGTCCCCGCTCAACAGTCCTCACCCGGGGCCCATCCGGACAGGCCTGCCTCCTGGGCACCAGCAGGAATTTGCCGGACGAGCCAACAGC
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ATGGACCCAAAGGCGGGCGGCGGCGGCGAGGAGGACGACTGCGTGGACTCGGGCGCCGAGACCGGAGGGTCCGACTACAGCCACCTGTCCTCCACGAGCAATGGA
TTCTCCACCTGGCGGATGCCATGTTGCCTGTTCCTTTACTGTACACACGGTGACAAAGAAAAGGGAAGATGGAGCCTCCAGGTTGAACATACCTGGCCCTCAGGT
GAGCTTTCCGTTGAAGAGGCGCAGGACCCTTTCCTGGTCAGCATCCACATAATCGCAGACCCAGGGGAGTCCCAGCCCCTGCAGGAGGCCATCGACAACGTCCTG
GCGTGGATCCACCCCGACCTCCCGCTGTTCCGGGTGTCCGAGAGGCGGGCGTCCCGGCGGCGGCGGAAGCCCCCCAAGGGCGCTCAGCCAGCGCTGGCTGTGGTG
CTGTTCCTGCAGGAGGAGTACGGCGAAGAGCAGATCCTGCAGCTGCACCGCACACTGCAGCAGCCGCCCTGGCGCCACCACCACACCGAGCAGGTGCACGGCCGG
TTCCTGCCCTACCTGCCCTGCAGCCAGGACTTCTTCACGCTGGCCCCTGGGACGCCGCTTTGGGCCATCCGGCCCGTGCACTACGGCAAGGAAATCGTGCGCTTC
ACCGTCTACTGTCGCTACGACAACTATGCTGACAGCCTCAGGTTCTACCAGCTGATTCTCCGGAGGAACCCCAGCCAGAAGAAAGCGGACTTCTGCATCTTCCCT
ATTTTTTCCAACCTGGATGTGGACATCCAGTTCTCCCTGAAAAGACTGCCCTGTGACCAGTGCCCGGTGCCCACCGACTCCTCCGTGCTGGAGTTCCGAGTGAGG
GACATAGGCGAGCTCGTGCCTCTCCTGCCCAACCCTTGCAGCCCCATCAGCGAGGGGCGCTGGCAGACGGAGGACCATGATGGGAACAAGATCCTCCTACAGGCA
CAAAGGGTGCATAAGAAGTTTCCTAAACCTGGCAGAGTACATCATGCCTCCGAGAAGAAACGTCATTCCACTCCTTTGCCGAGCACTGCTGTACCAAGCCATACA
CCTGGCAGCAGCCAGCAGTCCCCGCTCAACAGTCCTCACCCGGGGCCCATCCGGACAGGCCTGCCTCCTGGGCACCAGCAGGAATTTGCCGGACGAGCCAACAGC
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>FAM124A|220108|protein
MDPKAGGGGEEDDCVDSGAETGGSDYSHLSSTSNGFSTWRMPCCLFLYCTHGDKEKGRWSLQVEHTWPSGELSVEEAQDPFLVSIHIIADPGESQPLQEAIDNVL
AWIHPDLPLFRVSERRASRRRRKPPKGAQPALAVVLFLQEEYGEEQILQLHRTLQQPPWRHHHTEQVHGRFLPYLPCSQDFFTLAPGTPLWAIRPVHYGKEIVRF
TVYCRYDNYADSLRFYQLILRRNPSQKKADFCIFPIFSNLDVDIQFSLKRLPCDQCPVPTDSSVLEFRVRDIGELVPLLPNPCSPISEGRWQTEDHDGNKILLQA
QRVHKKFPKPGRVHHASEKKRHSTPLPSTAVPSHTPGSSQQSPLNSPHPGPIRTGLPPGHQQEFAGRANSTPNPPWSFQRSKSLFCLPTGGPSLASSAEPQWFSN
TGAPGHRASEWRHGHLLSIDDLEGAQETDVDTGLRLSSSDLSVVSAYSAPSRFCSTVETPLPSERCSSHWAAHKDSREGPLPTVSRVTTEASWASLPFFTKRSSS
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MDPKAGGGGEEDDCVDSGAETGGSDYSHLSSTSNGFSTWRMPCCLFLYCTHGDKEKGRWSLQVEHTWPSGELSVEEAQDPFLVSIHIIADPGESQPLQEAIDNVL
AWIHPDLPLFRVSERRASRRRRKPPKGAQPALAVVLFLQEEYGEEQILQLHRTLQQPPWRHHHTEQVHGRFLPYLPCSQDFFTLAPGTPLWAIRPVHYGKEIVRF
TVYCRYDNYADSLRFYQLILRRNPSQKKADFCIFPIFSNLDVDIQFSLKRLPCDQCPVPTDSSVLEFRVRDIGELVPLLPNPCSPISEGRWQTEDHDGNKILLQA
QRVHKKFPKPGRVHHASEKKRHSTPLPSTAVPSHTPGSSQQSPLNSPHPGPIRTGLPPGHQQEFAGRANSTPNPPWSFQRSKSLFCLPTGGPSLASSAEPQWFSN
TGAPGHRASEWRHGHLLSIDDLEGAQETDVDTGLRLSSSDLSVVSAYSAPSRFCSTVETPLPSERCSSHWAAHKDSREGPLPTVSRVTTEASWASLPFFTKRSSS
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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 (1) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 3 (2) |
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 | ||||||
Steele, 2001 | - | Chromosomal analysis of G-band | autism | - | - | - | - | 1 | - | 1 |
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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Kuwano, 2011_1 | Japan | ASD | 21 (19.05%) | - | autism | 21 (-) |
2.14 | Up | 0.00407 | |||
|
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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