Evidence Details for FAM134A
Basic Information Top
Gene Symbol: | FAM134A ( C2orf17,DKFZp686C2379,MGC3035 ) |
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Gene Full Name: | family with sequence similarity 134, member A |
Band: | 2q35 |
Quick Links | Entrez ID:79137; OMIM: NA; Uniprot ID:F134A_HUMAN; ENSEMBL ID: ENSG00000144567; HGNC ID: |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>FAM134A|79137|nucleotide
ATGGCGAGCGGCGGTGGCGGGGGTAACACTGGCGCGGGTGGGGGGCCGGGGATGGGCCTGAGCCTGGGCCTGGGTCTGGGTCTGAGCCTAGGCATGAGTGAGGCC
ACCAGTGAGGCAGAGGAGGAGGCGGCCACGGCCGAGGCGGTGGGACGCCTGGCCACGACGCTGTGGCTGCGGCTCCGCGGCTGGGAGGCGGTGCTGGCGGCGGCG
CAGCGGTTGCTGGTGTGGGAGAAGCCGCTGCACAGCCTGGTCACGGCGGCCGCGCTCAACGGCCTCTTCTGGTTGCTGTCTTCCTCGTCCCTCCGGCCCTTCTTC
CTACTCAGCGTCTCACTTTTGGCCTATTTTCTGCTGGATCTCTGGCAGCCTCGCTTTCTCCCTGACGTTTCAGCATCATCCCCAGAGGAGCCACACTCTGACAGT
GAGGGTGCGGGGTCAGGCGCCCGGCCGCACCTGCTGAGTGTGCCCGAGTTGTGCAGATACCTGGCTGAGAGCTGGCTCACCTTCCAGATTCACCTGCAGGAGCTG
CTGCAGTACAAGAGGCAGAATCCAGCTCAGTTCTGCGTTCGAGTCTGCTCTGGCTGTGCTGTGTTGGCTGTGTTGGGACACTATGTTCCAGGGATTATGATTTCC
TACATTGTCTTGTTGAGTATCCTGCTGTGGCCCCTGGTGGTTTATCATGAGCTGATCCAGAGGATGTACACTCGCCTGGAGCCCCTGCTCATGCAGCTGGACTAC
AGCATGAAGGCAGAAGCCAATGCCCTGCATCACAAACACGACAAGAGGAAGCGTCAGGGGAAGAATGCACCCCCAGGAGGTGATGAGCCACTGGCAGAGACAGAG
AGTGAAAGCGAGGCAGAGCTGGCTGGCTTCTCCCCAGTGGTGGATGTGAAGAAAACAGCATTGGCCTTGGCCATTACAGACTCAGAGCTGTCAGATGAGGAGGCT
TCTATCTTGGAGAGTGGTGGCTTCTCCGTATCCCGGGCCACAACTCCGCAGCTGACTGATGTCTCCGAGGATTTGGACCAGCAGAGCCTGCCAAGTGAACCAGAG
GAGACCCTAAGCCGGGACCTAGGGGAGGGAGAGGAGGGAGAGCTGGCCCCTCCCGAAGACCTACTAGGCCGTCCTCAAGCTCTGTCAAGGCAAGCCCTGGACTCG
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ATGGCGAGCGGCGGTGGCGGGGGTAACACTGGCGCGGGTGGGGGGCCGGGGATGGGCCTGAGCCTGGGCCTGGGTCTGGGTCTGAGCCTAGGCATGAGTGAGGCC
ACCAGTGAGGCAGAGGAGGAGGCGGCCACGGCCGAGGCGGTGGGACGCCTGGCCACGACGCTGTGGCTGCGGCTCCGCGGCTGGGAGGCGGTGCTGGCGGCGGCG
CAGCGGTTGCTGGTGTGGGAGAAGCCGCTGCACAGCCTGGTCACGGCGGCCGCGCTCAACGGCCTCTTCTGGTTGCTGTCTTCCTCGTCCCTCCGGCCCTTCTTC
CTACTCAGCGTCTCACTTTTGGCCTATTTTCTGCTGGATCTCTGGCAGCCTCGCTTTCTCCCTGACGTTTCAGCATCATCCCCAGAGGAGCCACACTCTGACAGT
GAGGGTGCGGGGTCAGGCGCCCGGCCGCACCTGCTGAGTGTGCCCGAGTTGTGCAGATACCTGGCTGAGAGCTGGCTCACCTTCCAGATTCACCTGCAGGAGCTG
CTGCAGTACAAGAGGCAGAATCCAGCTCAGTTCTGCGTTCGAGTCTGCTCTGGCTGTGCTGTGTTGGCTGTGTTGGGACACTATGTTCCAGGGATTATGATTTCC
TACATTGTCTTGTTGAGTATCCTGCTGTGGCCCCTGGTGGTTTATCATGAGCTGATCCAGAGGATGTACACTCGCCTGGAGCCCCTGCTCATGCAGCTGGACTAC
AGCATGAAGGCAGAAGCCAATGCCCTGCATCACAAACACGACAAGAGGAAGCGTCAGGGGAAGAATGCACCCCCAGGAGGTGATGAGCCACTGGCAGAGACAGAG
AGTGAAAGCGAGGCAGAGCTGGCTGGCTTCTCCCCAGTGGTGGATGTGAAGAAAACAGCATTGGCCTTGGCCATTACAGACTCAGAGCTGTCAGATGAGGAGGCT
TCTATCTTGGAGAGTGGTGGCTTCTCCGTATCCCGGGCCACAACTCCGCAGCTGACTGATGTCTCCGAGGATTTGGACCAGCAGAGCCTGCCAAGTGAACCAGAG
GAGACCCTAAGCCGGGACCTAGGGGAGGGAGAGGAGGGAGAGCTGGCCCCTCCCGAAGACCTACTAGGCCGTCCTCAAGCTCTGTCAAGGCAAGCCCTGGACTCG
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>FAM134A|79137|protein
MASGGGGGNTGAGGGPGMGLSLGLGLGLSLGMSEATSEAEEEAATAEAVGRLATTLWLRLRGWEAVLAAAQRLLVWEKPLHSLVTAAALNGLFWLLSSSSLRPFF
LLSVSLLAYFLLDLWQPRFLPDVSASSPEEPHSDSEGAGSGARPHLLSVPELCRYLAESWLTFQIHLQELLQYKRQNPAQFCVRVCSGCAVLAVLGHYVPGIMIS
YIVLLSILLWPLVVYHELIQRMYTRLEPLLMQLDYSMKAEANALHHKHDKRKRQGKNAPPGGDEPLAETESESEAELAGFSPVVDVKKTALALAITDSELSDEEA
SILESGGFSVSRATTPQLTDVSEDLDQQSLPSEPEETLSRDLGEGEEGELAPPEDLLGRPQALSRQALDSEEEEEDVAAKETLLRLSSPLHFVNTHFNGAGSPPD
GVKCSPGGPVETLSPETVSGGLTALPGTLSPPLCLVGSDPAPSPSILPPVPQDSPQPLPAPEEEEALTTEDFELLDQGELEQLNAELGLEPETPPKPPDAPPLGP
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MASGGGGGNTGAGGGPGMGLSLGLGLGLSLGMSEATSEAEEEAATAEAVGRLATTLWLRLRGWEAVLAAAQRLLVWEKPLHSLVTAAALNGLFWLLSSSSLRPFF
LLSVSLLAYFLLDLWQPRFLPDVSASSPEEPHSDSEGAGSGARPHLLSVPELCRYLAESWLTFQIHLQELLQYKRQNPAQFCVRVCSGCAVLAVLGHYVPGIMIS
YIVLLSILLWPLVVYHELIQRMYTRLEPLLMQLDYSMKAEANALHHKHDKRKRQGKNAPPGGDEPLAETESESEAELAGFSPVVDVKKTALALAITDSELSDEEA
SILESGGFSVSRATTPQLTDVSEDLDQQSLPSEPEETLSRDLGEGEEGELAPPEDLLGRPQALSRQALDSEEEEEDVAAKETLLRLSSPLHFVNTHFNGAGSPPD
GVKCSPGGPVETLSPETVSGGLTALPGTLSPPLCLVGSDPAPSPSILPPVPQDSPQPLPAPEEEEALTTEDFELLDQGELEQLNAELGLEPETPPKPPDAPPLGP
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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) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | (0) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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