Evidence Details for C7orf47
Basic Information Top
| Gene Symbol: | C7orf47 ( MGC22793 ) |
|---|---|
| Gene Full Name: | chromosome 7 open reading frame 47 |
| Band: | 7q22.1 |
| Quick Links | Entrez ID:221908; OMIM: NA; Uniprot ID:CG047_HUMAN; ENSEMBL ID: ENSG00000160813; HGNC ID: |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>C7orf47|221908|nucleotide
ATGATGATGGGTTGTGGGGAGTCAGAGCTGAAGTCGGCGGACGGGGAAGAAGCCGCGGCGGTCCCGGGGCCACCCCCGGAGCCCCAAGTCCCGCAACTCCGAGCC
CCAGTGCCCGAGCCCGGCCTGGACTTGAGCCTGAGCCCGCGGCCCGACAGCCCTCAGCCGCGGCACGGCAGCCCCGGGCGGCGGAAGGGGCGGGCGGAGCGGCGG
GGCGCGGCTCGGCAGCGGCGGCAGGTCCGCTTCCGCCTGACGCCGCCCTCCCCGGTGCGGTCCGAGCCGCAGCCTGCGGTGCCGCAGGAGCTGGAGATGCCCGTG
CTGAAGAGCAGCCTGGCCTTGGGCCTGGAGCTGCGGGCCGCAGCCGGGAGCCACTTTGATGCTGCGAAGGCCGTGGAGGAACAGCTGAGAAAGTCGTTCCAGATC
CGCTGCGGCCTGGAGGAGAGCGTGTCCGAGGGGCTGAACGTGCCGCGCTCCAAGCGGCTCTTCCGGGACCTGGTGAGCCTGCAGGTGCCGGAGGAACAGGTTCTG
AATGCCGCGCTCAGGGAGAAATTGGCTCTCCTGCCGCCACAGGCTCGAGCCCCGCACCCAAAGGAGCCACCTGGGCCTGGGCCAGACATGACCATCTTGTGTGAC
CCAGAAACGCTATTTTATGAATCTCCACACCTGACCCTGGACGGTCTGCCCCCTCTCCGACTTCAACTCCGGCCCCGCCCTTCAGAGGACACCTTCCTCATGCAC
CGGACACTGAGGCGATGGGAAGCGTAG
Show »
ATGATGATGGGTTGTGGGGAGTCAGAGCTGAAGTCGGCGGACGGGGAAGAAGCCGCGGCGGTCCCGGGGCCACCCCCGGAGCCCCAAGTCCCGCAACTCCGAGCC
CCAGTGCCCGAGCCCGGCCTGGACTTGAGCCTGAGCCCGCGGCCCGACAGCCCTCAGCCGCGGCACGGCAGCCCCGGGCGGCGGAAGGGGCGGGCGGAGCGGCGG
GGCGCGGCTCGGCAGCGGCGGCAGGTCCGCTTCCGCCTGACGCCGCCCTCCCCGGTGCGGTCCGAGCCGCAGCCTGCGGTGCCGCAGGAGCTGGAGATGCCCGTG
CTGAAGAGCAGCCTGGCCTTGGGCCTGGAGCTGCGGGCCGCAGCCGGGAGCCACTTTGATGCTGCGAAGGCCGTGGAGGAACAGCTGAGAAAGTCGTTCCAGATC
CGCTGCGGCCTGGAGGAGAGCGTGTCCGAGGGGCTGAACGTGCCGCGCTCCAAGCGGCTCTTCCGGGACCTGGTGAGCCTGCAGGTGCCGGAGGAACAGGTTCTG
AATGCCGCGCTCAGGGAGAAATTGGCTCTCCTGCCGCCACAGGCTCGAGCCCCGCACCCAAAGGAGCCACCTGGGCCTGGGCCAGACATGACCATCTTGTGTGAC
CCAGAAACGCTATTTTATGAATCTCCACACCTGACCCTGGACGGTCTGCCCCCTCTCCGACTTCAACTCCGGCCCCGCCCTTCAGAGGACACCTTCCTCATGCAC
CGGACACTGAGGCGATGGGAAGCGTAG
Show »
>C7orf47|221908|protein
MMMGCGESELKSADGEEAAAVPGPPPEPQVPQLRAPVPEPGLDLSLSPRPDSPQPRHGSPGRRKGRAERRGAARQRRQVRFRLTPPSPVRSEPQPAVPQELEMPV
LKSSLALGLELRAAAGSHFDAAKAVEEQLRKSFQIRCGLEESVSEGLNVPRSKRLFRDLVSLQVPEEQVLNAALREKLALLPPQARAPHPKEPPGPGPDMTILCD
PETLFYESPHLTLDGLPPLRLQLRPRPSEDTFLMHRTLRRWEA
Show »
MMMGCGESELKSADGEEAAAVPGPPPEPQVPQLRAPVPEPGLDLSLSPRPDSPQPRHGSPGRRKGRAERRGAARQRRQVRFRLTPPSPVRSEPQPAVPQELEMPV
LKSSLALGLELRAAAGSHFDAAKAVEEQLRKSFQIRCGLEESVSEGLNVPRSKRLFRDLVSLQVPEEQVLNAALREKLALLPPQARAPHPKEPPGPGPDMTILCD
PETLFYESPHLTLDGLPPLRLQLRPRPSEDTFLMHRTLRRWEA
Show »
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 (1) | 0 (0) | 0 (0) | 2 (2) |
Syndromic Autism Gene TopGenome-Wide Association Studies(By Ethnic Group) TopCNV Studies TopLinkage Studies Top