Evidence Details for FHAD1
Basic Information Top
| Gene Symbol: | FHAD1 ( DKFZp686G2134,DKFZp686P19183,FLJ31291,KIAA1937 ) |
|---|---|
| Gene Full Name: | forkhead-associated (FHA) phosphopeptide binding domain 1 |
| Band: | 1p36.21 |
| Quick Links | Entrez ID:114827; OMIM: NA; Uniprot ID:FHAD1_HUMAN; ENSEMBL ID: ENSG00000142621; HGNC ID: 29408 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>FHAD1|114827|nucleotide
ATGAAGGCCTATCTAAAGAGCGCAGAAGGCTTTTTTGTCCTAAATAAAAGTACCACAATTGGAAGGCATGAAAATTCAGACCTTGTTTTACAGTCTCCTGACATC
GACAACCACCATGCACTCATTGAATATAACGAGGCGGAGTGCAGCTTTGTTCTCCAGGACTTCAATTCCCGCAACGGCACGTTTGTCAACGAGTGCCACATTCAA
AACGTGGCTGTGAAGCTCATCCCTGGAGACATCCTGAGATTTGGGTCTGCAGGGCTGACCTATGAACTGGTCATTGAAAATCCACCTCCGGTCTCTTTCCCATGG
ATGAGGGGCCCAGCACCATGGCCAGGGCCACAGCCACCTCGTGCCACACAGCAGCCAAACCAGGCCCCCCCACCATCACATATCCCCTTCCACCAAGGTGTCCAG
CCAGCACCGATGCAAAGGAGCTGGTCCCAGGCCTTTCCCAGACCCACCGTGGTCCTGCCGGCCTCCCACAGGCGGCCTGTGAGCGCCAACAAGGAGATGTTCTCG
TTCGTGGTGGACGACGCCCGCAAGCCACCCGTCATCAAGCAAGTGTGGACCAATGCCATGAAACTGTCAGAAAAATCAGTGGCCGAGGGGATTCCTGGGGCAGTT
CCCCCTGCGGAGATTTATGTGGAGGAGGACTTGGCCCAGCAGGACAAGGATGAAATAATTCTGCTGCTGGGAAAAGAGGTCAGCCGTCTCTCAGATTATGAAATT
GAATCCAAATACAAAGACGTCATAATAGCAAACCTGCAGAATGAAGTGGCTGAGCTGAGTCAGAAGGTGTCAGAGACCACCACCTCCAGGCAGAATGAGAAGGAG
ATCTCGCAGAAGTGTCAGGTTCTGGATGAAGACATCGATGCCAAACAGAAAGAGATCCAGAGCTTGAAAAGCCAGATCAGTGCCCTACAGAAAGGCTACAGCAAG
GTGCTGTGCCAGACCCTGTCAGAGCGGAACTCAGAAATCACATCCCTGAAGAATGAGGGCGAGAACTTAAAGAGAGACAACGCTATCACATCAGGGATGGTGTCA
TCTTTGCAAAAAGACATATTAGCAAAGGATGAGCAAGTTCAACAACTAAAGGAAGAGGTCAGTCACCTAAAAAGTCAGAACAAGGACAAGGACCACCAGCTGGAA
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ATGAAGGCCTATCTAAAGAGCGCAGAAGGCTTTTTTGTCCTAAATAAAAGTACCACAATTGGAAGGCATGAAAATTCAGACCTTGTTTTACAGTCTCCTGACATC
GACAACCACCATGCACTCATTGAATATAACGAGGCGGAGTGCAGCTTTGTTCTCCAGGACTTCAATTCCCGCAACGGCACGTTTGTCAACGAGTGCCACATTCAA
AACGTGGCTGTGAAGCTCATCCCTGGAGACATCCTGAGATTTGGGTCTGCAGGGCTGACCTATGAACTGGTCATTGAAAATCCACCTCCGGTCTCTTTCCCATGG
ATGAGGGGCCCAGCACCATGGCCAGGGCCACAGCCACCTCGTGCCACACAGCAGCCAAACCAGGCCCCCCCACCATCACATATCCCCTTCCACCAAGGTGTCCAG
CCAGCACCGATGCAAAGGAGCTGGTCCCAGGCCTTTCCCAGACCCACCGTGGTCCTGCCGGCCTCCCACAGGCGGCCTGTGAGCGCCAACAAGGAGATGTTCTCG
TTCGTGGTGGACGACGCCCGCAAGCCACCCGTCATCAAGCAAGTGTGGACCAATGCCATGAAACTGTCAGAAAAATCAGTGGCCGAGGGGATTCCTGGGGCAGTT
CCCCCTGCGGAGATTTATGTGGAGGAGGACTTGGCCCAGCAGGACAAGGATGAAATAATTCTGCTGCTGGGAAAAGAGGTCAGCCGTCTCTCAGATTATGAAATT
GAATCCAAATACAAAGACGTCATAATAGCAAACCTGCAGAATGAAGTGGCTGAGCTGAGTCAGAAGGTGTCAGAGACCACCACCTCCAGGCAGAATGAGAAGGAG
ATCTCGCAGAAGTGTCAGGTTCTGGATGAAGACATCGATGCCAAACAGAAAGAGATCCAGAGCTTGAAAAGCCAGATCAGTGCCCTACAGAAAGGCTACAGCAAG
GTGCTGTGCCAGACCCTGTCAGAGCGGAACTCAGAAATCACATCCCTGAAGAATGAGGGCGAGAACTTAAAGAGAGACAACGCTATCACATCAGGGATGGTGTCA
TCTTTGCAAAAAGACATATTAGCAAAGGATGAGCAAGTTCAACAACTAAAGGAAGAGGTCAGTCACCTAAAAAGTCAGAACAAGGACAAGGACCACCAGCTGGAA
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>FHAD1|114827|protein
MKAYLKSAEGFFVLNKSTTIGRHENSDLVLQSPDIDNHHALIEYNEAECSFVLQDFNSRNGTFVNECHIQNVAVKLIPGDILRFGSAGLTYELVIENPPPVSFPW
MRGPAPWPGPQPPRATQQPNQAPPPSHIPFHQGVQPAPMQRSWSQAFPRPTVVLPASHRRPVSANKEMFSFVVDDARKPPVIKQVWTNAMKLSEKSVAEGIPGAV
PPAEIYVEEDLAQQDKDEIILLLGKEVSRLSDYEIESKYKDVIIANLQNEVAELSQKVSETTTSRQNEKEISQKCQVLDEDIDAKQKEIQSLKSQISALQKGYSK
VLCQTLSERNSEITSLKNEGENLKRDNAITSGMVSSLQKDILAKDEQVQQLKEEVSHLKSQNKDKDHQLEALGSRCSVLKEELKQEDAHRELREAQEKELKLCKT
QIQDMEKEMKKLRAELRKSCTEQSVISRTLREKSKVEEKLQEDSRRKLLQLQEMGNRESVIKINLERAVGQLEHFRSQVIKATYGRAKPFRDKPVTDQQLIEKIT
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MKAYLKSAEGFFVLNKSTTIGRHENSDLVLQSPDIDNHHALIEYNEAECSFVLQDFNSRNGTFVNECHIQNVAVKLIPGDILRFGSAGLTYELVIENPPPVSFPW
MRGPAPWPGPQPPRATQQPNQAPPPSHIPFHQGVQPAPMQRSWSQAFPRPTVVLPASHRRPVSANKEMFSFVVDDARKPPVIKQVWTNAMKLSEKSVAEGIPGAV
PPAEIYVEEDLAQQDKDEIILLLGKEVSRLSDYEIESKYKDVIIANLQNEVAELSQKVSETTTSRQNEKEISQKCQVLDEDIDAKQKEIQSLKSQISALQKGYSK
VLCQTLSERNSEITSLKNEGENLKRDNAITSGMVSSLQKDILAKDEQVQQLKEEVSHLKSQNKDKDHQLEALGSRCSVLKEELKQEDAHRELREAQEKELKLCKT
QIQDMEKEMKKLRAELRKSCTEQSVISRTLREKSKVEEKLQEDSRRKLLQLQEMGNRESVIKINLERAVGQLEHFRSQVIKATYGRAKPFRDKPVTDQQLIEKIT
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Evidence summary TopClick 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 (0) | 0 (0) | 0 (0) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 1 (1) |
Syndromic Autism Gene TopGenome-Wide Association Studies(By Ethnic Group) TopCNV Studies TopLinkage Studies TopLow Scale Association Studies (by Ethnic Group) TopLarge Scale Expression Studies Top Microarray Studies: 0
| Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| No Evidence. | ||||||||||||
Proteomics Studies:1
| Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
|---|---|---|---|---|---|---|---|---|---|
| Corbett, 2007_1 | USA | blood | liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS) | 69 (15.94%) |  | | ASD | 35 (17.14%) |
|
NGS de novo Mutation Studies TopNGS Mosaic SNV Studies TopNGS Other Studies Top Low Scale Gene Studies TopContact 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.