Evidence Details for C1orf174
Basic Information Top
| Gene Symbol: | C1orf174 ( RP13-531C17.2 ) |
|---|---|
| Gene Full Name: | chromosome 1 open reading frame 174 |
| Band: | 1p36.32 |
| Quick Links | Entrez ID:339448; OMIM: NA; Uniprot ID:CA174_HUMAN; ENSEMBL ID: ENSG00000198912; HGNC ID: 27915 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C1orf174|339448|nucleotide
ATGAGGAGCCGGAAGCTCACAGGTGCAGTGCGGTCTTCAGCGCGCTTGAAAGCACGAAGTTGTTCGGCAGCCAGGTTGGCCTCTGCCCAGGAAGTTGCTGGTTCC
ACGTCTGCCAAGACAGCATGTCTGACTTCCTCATCCCACAAAGCCACAGACACGCGAACGTCCAAGAAGTTCAAATGTGACAAAGGACATCTTGTGAAGTCAGAA
TTACAGAAGCTTGTCCCTAAGAATGACAGCGCTTCTTTGCCAAAAGTGACACCTGAGACCCCTTGTGAAAATGAGTTTGCTGAAGGCAGTGCCTTGCTTCCAGGC
AGCGAGGCTGGCGTTTCTGTGCAGCAGGGGGCTGCAAGTCTTCCTCTCGGTGGCTGCAGAGTTGTGAGTGACTCTCGCTTAGCAAAGACTAGAGATGGCCTGTCC
GTGCCAAAACACAGTGCCGGGTCCGGAGCAGAAGAATCCAACAGCAGCTCCACTGTGCAGAAGCAGAATGAGCCAGGGCTACAGACAGAGGATGTGCAGAAGCCA
CCACTTCAGATGGACAACAGCGTCTTTCTAGATGACGACAGCAATCAGCCAATGCCCGTGAGCCGGTTCTTTGGAAACGTTGAGCTCATGCAGGACCTCCCACCT
GCGTCTTCATCTTGTCCTTCAATGAGCAGACGAGAGTTCAGAAAAATGCATTTCAGAGCCAAAGATGATGATGATGACGACGACGATGATGCAGAAATGTAG
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ATGAGGAGCCGGAAGCTCACAGGTGCAGTGCGGTCTTCAGCGCGCTTGAAAGCACGAAGTTGTTCGGCAGCCAGGTTGGCCTCTGCCCAGGAAGTTGCTGGTTCC
ACGTCTGCCAAGACAGCATGTCTGACTTCCTCATCCCACAAAGCCACAGACACGCGAACGTCCAAGAAGTTCAAATGTGACAAAGGACATCTTGTGAAGTCAGAA
TTACAGAAGCTTGTCCCTAAGAATGACAGCGCTTCTTTGCCAAAAGTGACACCTGAGACCCCTTGTGAAAATGAGTTTGCTGAAGGCAGTGCCTTGCTTCCAGGC
AGCGAGGCTGGCGTTTCTGTGCAGCAGGGGGCTGCAAGTCTTCCTCTCGGTGGCTGCAGAGTTGTGAGTGACTCTCGCTTAGCAAAGACTAGAGATGGCCTGTCC
GTGCCAAAACACAGTGCCGGGTCCGGAGCAGAAGAATCCAACAGCAGCTCCACTGTGCAGAAGCAGAATGAGCCAGGGCTACAGACAGAGGATGTGCAGAAGCCA
CCACTTCAGATGGACAACAGCGTCTTTCTAGATGACGACAGCAATCAGCCAATGCCCGTGAGCCGGTTCTTTGGAAACGTTGAGCTCATGCAGGACCTCCCACCT
GCGTCTTCATCTTGTCCTTCAATGAGCAGACGAGAGTTCAGAAAAATGCATTTCAGAGCCAAAGATGATGATGATGACGACGACGATGATGCAGAAATGTAG
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>C1orf174|339448|protein
MRSRKLTGAVRSSARLKARSCSAARLASAQEVAGSTSAKTACLTSSSHKATDTRTSKKFKCDKGHLVKSELQKLVPKNDSASLPKVTPETPCENEFAEGSALLPG
SEAGVSVQQGAASLPLGGCRVVSDSRLAKTRDGLSVPKHSAGSGAEESNSSSTVQKQNEPGLQTEDVQKPPLQMDNSVFLDDDSNQPMPVSRFFGNVELMQDLPP
ASSSCPSMSRREFRKMHFRAKDDDDDDDDDAEM
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MRSRKLTGAVRSSARLKARSCSAARLASAQEVAGSTSAKTACLTSSSHKATDTRTSKKFKCDKGHLVKSELQKLVPKNDSASLPKVTPETPCENEFAEGSALLPG
SEAGVSVQQGAASLPLGGCRVVSDSRLAKTRDGLSVPKHSAGSGAEESNSSSTVQKQNEPGLQTEDVQKPPLQMDNSVFLDDDSNQPMPVSRFFGNVELMQDLPP
ASSSCPSMSRREFRKMHFRAKDDDDDDDDDAEM
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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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (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 | ||||||
| Gai, 2011 | AGRE | SNP microarray | - | - | autism | - | - | - | - | 1224 | 3801 | 5025 |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
| Reference | Case Number | Family Number | Mosaic Number | Title |
|---|---|---|---|---|
| Krupp DR, 2017 | - | 2264 | 247 | Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder |
NGS Other Studies Top
Low Scale Gene Studies Top
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