Evidence Details for C18orf8
Basic Information Top
| Gene Symbol: | C18orf8 ( FLJ23453,HsT2591,MIC1 ) |
|---|---|
| Gene Full Name: | chromosome 18 open reading frame 8 |
| Band: | 18q11.2 |
| Quick Links | Entrez ID:29919; OMIM: NA; Uniprot ID:MIC1_HUMAN; ENSEMBL ID: ENSG00000141452; HGNC ID: 24326 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C18orf8|29919|nucleotide
ATGGGCGAGGAGGACTACTATCTGGAGCTGTGCGAGCGGCCGGTGCAGTTCGAGAAGGCGAACCCTGTCAACTGCGTCTTCTTCGATGAGGCCAACAAGCAGGTT
TTTGCTGTTCGATCTGGTGGAGCTACTGGCGTGGTAGTTAAAGGCCCAGATGATAGGAATCCCATCTCATTTAGAATGGATGACAAAGGAGAAGTGAAGTGCATT
AAGTTTTCCTTAGAAAATAAGATATTGGCTGTTCAGAGGACCTCAAAGACTGTGGATTTTTGTAATTTTATCCCTGATAATTCCCAGCTGGAATACACACAGGAG
TGCAAGACTAAGAATGCCAACATTCTAGGATTCTGCTGGACTAGTTCAACTGAAATTGTCTTCATAACAGATCAAGGAATCGAATTTTACCAGGTATTACCAGAG
AAACGGAGTCTGAAACTCTTGAAGAGCCACAATCTCAATGTGAATTGGTACATGTACTGCCCCGAGAGCGCCGTGATCTTGCTGTCTACCACGGTCCTGGAGAAT
GTCCTGCAGCCTTTTCACTTTAGGGCTGGCACTATGTCGAAGCTGCCCAAATTTGAGATTGAATTACCAGCTGCGCCTAAGTCAACTAAACCCAGCCTTTCCGAA
AGAGACATCGCAATGGCTACCATATACGGGCAGCTGTATGTTCTCTTCTTGAGGCATCATTCTCGGACCTCCAACAGCACAGGAGCGGAGGTGGTCCTCTATCAT
CTACCACGAGAAGGTGCCTGTAAAAAGATGCACATATTGAAGTTAAATAGGACGGGAAAGTTTGCCCTGAACGTGGTGGACAACCTGGTAGTCGTGCATCATCAG
GATACAGAGACATCGGTAATATTCGATATCAAGTTACGGGGAGAGTTTGACGGCTCCGTTACCTTCCACCACCCCGTGCTTCCCGCTCGATCGATCCAGCCCTAT
CAGATCCCCATCACAGGTCCTGCTGCCGTGACCAGCCAGTCTCCTGTTCCATGTAAACTCTATTCTTCATCTTGGATTGTCTTTCAACCTGACATCATTATCAGC
GCAAGCCAAGGTTACCTCTGGAACCTCCAAGTGAAACTTGAGCCCATAGTAAATCTCTTACCAGACAAAGGAAGACTCATGGACTTTCTCCTCCAGAGAAAGGAA
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ATGGGCGAGGAGGACTACTATCTGGAGCTGTGCGAGCGGCCGGTGCAGTTCGAGAAGGCGAACCCTGTCAACTGCGTCTTCTTCGATGAGGCCAACAAGCAGGTT
TTTGCTGTTCGATCTGGTGGAGCTACTGGCGTGGTAGTTAAAGGCCCAGATGATAGGAATCCCATCTCATTTAGAATGGATGACAAAGGAGAAGTGAAGTGCATT
AAGTTTTCCTTAGAAAATAAGATATTGGCTGTTCAGAGGACCTCAAAGACTGTGGATTTTTGTAATTTTATCCCTGATAATTCCCAGCTGGAATACACACAGGAG
TGCAAGACTAAGAATGCCAACATTCTAGGATTCTGCTGGACTAGTTCAACTGAAATTGTCTTCATAACAGATCAAGGAATCGAATTTTACCAGGTATTACCAGAG
AAACGGAGTCTGAAACTCTTGAAGAGCCACAATCTCAATGTGAATTGGTACATGTACTGCCCCGAGAGCGCCGTGATCTTGCTGTCTACCACGGTCCTGGAGAAT
GTCCTGCAGCCTTTTCACTTTAGGGCTGGCACTATGTCGAAGCTGCCCAAATTTGAGATTGAATTACCAGCTGCGCCTAAGTCAACTAAACCCAGCCTTTCCGAA
AGAGACATCGCAATGGCTACCATATACGGGCAGCTGTATGTTCTCTTCTTGAGGCATCATTCTCGGACCTCCAACAGCACAGGAGCGGAGGTGGTCCTCTATCAT
CTACCACGAGAAGGTGCCTGTAAAAAGATGCACATATTGAAGTTAAATAGGACGGGAAAGTTTGCCCTGAACGTGGTGGACAACCTGGTAGTCGTGCATCATCAG
GATACAGAGACATCGGTAATATTCGATATCAAGTTACGGGGAGAGTTTGACGGCTCCGTTACCTTCCACCACCCCGTGCTTCCCGCTCGATCGATCCAGCCCTAT
CAGATCCCCATCACAGGTCCTGCTGCCGTGACCAGCCAGTCTCCTGTTCCATGTAAACTCTATTCTTCATCTTGGATTGTCTTTCAACCTGACATCATTATCAGC
GCAAGCCAAGGTTACCTCTGGAACCTCCAAGTGAAACTTGAGCCCATAGTAAATCTCTTACCAGACAAAGGAAGACTCATGGACTTTCTCCTCCAGAGAAAGGAA
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>C18orf8|29919|protein
MGEEDYYLELCERPVQFEKANPVNCVFFDEANKQVFAVRSGGATGVVVKGPDDRNPISFRMDDKGEVKCIKFSLENKILAVQRTSKTVDFCNFIPDNSQLEYTQE
CKTKNANILGFCWTSSTEIVFITDQGIEFYQVLPEKRSLKLLKSHNLNVNWYMYCPESAVILLSTTVLENVLQPFHFRAGTMSKLPKFEIELPAAPKSTKPSLSE
RDIAMATIYGQLYVLFLRHHSRTSNSTGAEVVLYHLPREGACKKMHILKLNRTGKFALNVVDNLVVVHHQDTETSVIFDIKLRGEFDGSVTFHHPVLPARSIQPY
QIPITGPAAVTSQSPVPCKLYSSSWIVFQPDIIISASQGYLWNLQVKLEPIVNLLPDKGRLMDFLLQRKECKMVILSVCSQMLSESDRASLPVIATVFDKLNHEY
KKYLDAEQSYAMAVEAGQSRSSPLLKRPVRTQAVLDQSDVYTHVLSAFVEKKEMPHKFVIAVLMEYIRSLNQFQIAVQHYLHELVIKTLVQHNLFYMLHQFLQYH
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MGEEDYYLELCERPVQFEKANPVNCVFFDEANKQVFAVRSGGATGVVVKGPDDRNPISFRMDDKGEVKCIKFSLENKILAVQRTSKTVDFCNFIPDNSQLEYTQE
CKTKNANILGFCWTSSTEIVFITDQGIEFYQVLPEKRSLKLLKSHNLNVNWYMYCPESAVILLSTTVLENVLQPFHFRAGTMSKLPKFEIELPAAPKSTKPSLSE
RDIAMATIYGQLYVLFLRHHSRTSNSTGAEVVLYHLPREGACKKMHILKLNRTGKFALNVVDNLVVVHHQDTETSVIFDIKLRGEFDGSVTFHHPVLPARSIQPY
QIPITGPAAVTSQSPVPCKLYSSSWIVFQPDIIISASQGYLWNLQVKLEPIVNLLPDKGRLMDFLLQRKECKMVILSVCSQMLSESDRASLPVIATVFDKLNHEY
KKYLDAEQSYAMAVEAGQSRSSPLLKRPVRTQAVLDQSDVYTHVLSAFVEKKEMPHKFVIAVLMEYIRSLNQFQIAVQHYLHELVIKTLVQHNLFYMLHQFLQYH
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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 (1) | 0 (0) | 0 (0) | 0 (1) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top

