Evidence Details for C19orf22
Basic Information Top
| Gene Symbol: | C19orf22 ( MGC16353 ) |
|---|---|
| Gene Full Name: | chromosome 19 open reading frame 22 |
| Band: | 19p13.3 |
| Quick Links | Entrez ID:91300; OMIM: NA; Uniprot ID:CS022_HUMAN; ENSEMBL ID: ENSG00000198858; HGNC ID: |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>C19orf22|91300|nucleotide
ATGGTCGCGCTGGAGAACCCCGAGTGCGGCCCGGAGGCGGCGGAGGGCACCCCGGGCGGGCGGCGGCTGCTGCCCCTTCCCAGCTGCCTGCCTGCCCTAGCCAGC
TCCCAGGTGAAGAGACTCTCGGCTTCCAGGCGGAAACAGCACTTCATCAACCAGGCAGTGCGGAACTCAGACCTCGTGCCCAAGGCCAAGGGGCGGAAGAGCCTC
CAGCGCCTGGAGAACACCCAGTACCTCCTGACCCTGCTGGAGACAGACGGGGGCCTGCCTGGCCTGGAGGATGGGGACTTGGCACCCCCTGCATCACCAGGCATC
TTTGCCGAGGCCTGCAACAACGCCACCTATGTGGAGGTCTGGAACGATTTCATGAACCGCTCCGGGGAGGAGCAGGAGCGGGTTCTTCGCTACCTGGAGGATGAG
GGCAGGAGCAAGGCGCGGAGGAGGGGCCCTGGCCGTGGGGAGGACCGGAGGAGAGAGGACCCCGCCTATACACCCCGCGAGTGCTTCCAGCGCATCAGCCGGCGT
CTGCGAGCCGTCCTCAAGCGCAGCCGCATCCCCATGGAAACGCTGGAGACCTGGGAGGAGCGGCTGCTTCGGTTCTTCTCCGTGTCCCCCCAGGCCGTGTACACA
GCAATGCTAGACAACAGCTTCGAGAGGCTTCTGCTGCACGCTGTCTGCCAGTACATGGACCTCATCTCGGCCAGTGCTGACCTGGAGGGGAAGCGGCAGATGAAG
GTCAGTAATCGGCACCTGGATTTCCTGCCGCCGGGGCTGCTCCTGTCCGCCTACCTGGAGCAGCACAGCTGA
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ATGGTCGCGCTGGAGAACCCCGAGTGCGGCCCGGAGGCGGCGGAGGGCACCCCGGGCGGGCGGCGGCTGCTGCCCCTTCCCAGCTGCCTGCCTGCCCTAGCCAGC
TCCCAGGTGAAGAGACTCTCGGCTTCCAGGCGGAAACAGCACTTCATCAACCAGGCAGTGCGGAACTCAGACCTCGTGCCCAAGGCCAAGGGGCGGAAGAGCCTC
CAGCGCCTGGAGAACACCCAGTACCTCCTGACCCTGCTGGAGACAGACGGGGGCCTGCCTGGCCTGGAGGATGGGGACTTGGCACCCCCTGCATCACCAGGCATC
TTTGCCGAGGCCTGCAACAACGCCACCTATGTGGAGGTCTGGAACGATTTCATGAACCGCTCCGGGGAGGAGCAGGAGCGGGTTCTTCGCTACCTGGAGGATGAG
GGCAGGAGCAAGGCGCGGAGGAGGGGCCCTGGCCGTGGGGAGGACCGGAGGAGAGAGGACCCCGCCTATACACCCCGCGAGTGCTTCCAGCGCATCAGCCGGCGT
CTGCGAGCCGTCCTCAAGCGCAGCCGCATCCCCATGGAAACGCTGGAGACCTGGGAGGAGCGGCTGCTTCGGTTCTTCTCCGTGTCCCCCCAGGCCGTGTACACA
GCAATGCTAGACAACAGCTTCGAGAGGCTTCTGCTGCACGCTGTCTGCCAGTACATGGACCTCATCTCGGCCAGTGCTGACCTGGAGGGGAAGCGGCAGATGAAG
GTCAGTAATCGGCACCTGGATTTCCTGCCGCCGGGGCTGCTCCTGTCCGCCTACCTGGAGCAGCACAGCTGA
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>C19orf22|91300|protein
MVALENPECGPEAAEGTPGGRRLLPLPSCLPALASSQVKRLSASRRKQHFINQAVRNSDLVPKAKGRKSLQRLENTQYLLTLLETDGGLPGLEDGDLAPPASPGI
FAEACNNATYVEVWNDFMNRSGEEQERVLRYLEDEGRSKARRRGPGRGEDRRREDPAYTPRECFQRISRRLRAVLKRSRIPMETLETWEERLLRFFSVSPQAVYT
AMLDNSFERLLLHAVCQYMDLISASADLEGKRQMKVSNRHLDFLPPGLLLSAYLEQHS
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MVALENPECGPEAAEGTPGGRRLLPLPSCLPALASSQVKRLSASRRKQHFINQAVRNSDLVPKAKGRKSLQRLENTQYLLTLLETDGGLPGLEDGDLAPPASPGI
FAEACNNATYVEVWNDFMNRSGEEQERVLRYLEDEGRSKARRRGPGRGEDRRREDPAYTPRECFQRISRRLRAVLKRSRIPMETLETWEERLLRFFSVSPQAVYT
AMLDNSFERLLLHAVCQYMDLISASADLEGKRQMKVSNRHLDFLPPGLLLSAYLEQHS
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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) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 2 (2) |
Syndromic Autism Gene TopGenome-Wide Association Studies(By Ethnic Group) TopCNV Studies TopLinkage Studies Top