Evidence Details for C1orf174


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 |


>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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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) |






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 |










Reference | Case Number | Family Number | Mosaic Number | Title |
---|---|---|---|---|
Krupp DR, 2017 | - | 2264 | 247 | Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder |




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