Evidence Details for C9orf156
Basic Information Top
Gene Symbol: | C9orf156 ( HSPC219,NAP1 ) |
---|---|
Gene Full Name: | chromosome 9 open reading frame 156 |
Band: | 9q22.33 |
Quick Links | Entrez ID:51531; OMIM: NA; Uniprot ID:NAP1_HUMAN; ENSEMBL ID: ENSG00000136932; HGNC ID: |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>C9orf156|51531|nucleotide
ATGCGCGGCTTGGAGGAGTCGGGGCCTCGGCCTACAGCGACCCCGTGCGGCTGCGTTAAGCCGGCTCTGGAGACAGGGAATCTTTTAACTGAGCCAGTCGGCTAC
TTGGAATCTTGTTTCTCGGCCAAGAATGGTACTCCAAGACAGCCATCCATTTGTAGCTATTCTCGAGCCTGTTTGAGGATTAGAAAGAGGATCTTTAATAATCCT
GAACATTCCTTGATGGGCCTAGAACAGTTTTCTCATGTTTGGATTTTGTTTGTTTTTCACAAAAATGGTCATTTGAGCTGTAAGGCAAAAGTGCAGCCTCCTAGG
CTGAATGGTGCAAAGACTGGAGTTTTTTCCACAAGGAGCCCTCATCGTCCCAATGCAATAGGACTGACCCTGGCCAAGCTGGAAAAGGTAGAAGGTGGAGCTATA
TACCTTTCTGGAATTGACATGATACATGGCACACCCGTACTAGACATCAAGCCCTACATAGCTGAGTATGACTCACCGCAAAATGTGATGGAGCCTTTAGCAGAC
TTTAATTTACAGAATAACCAACATACACCAAACACTGTGTCCCAGTCTGACAGCAAGACTGACAGCTGTGACCAGCGACAGCTCTCAGGGTGTGATGAGCCACAA
CCCCACCATAGCACTAAGAGGAAACCTAAATGTCCTGAAGACAGAACTTCAGAAGAAAACTACCTGACACACAGTGACACAGCCAGAATTCAGCAAGCATTTCCT
ATGCACAGGGAGATAGCAGTGGATTTTGGTTTGGAATCAAGACGTGATCAGAGTTCCAGCGTGGCAGAAGAACAAATTGGCCCATATTGCCCAGAGAAGAGCTTT
TCAGAGAAAGGTACAGACAAGAAGCTAGAAAGAGTGGAAGGAGCAGCAGTCTTGCAAGGAAGCAGGGCAGAGACACAGCCCATGGCCCCTCACTGCCCTGCTGGA
AGGGCTGATGGAGCTCCCCGCAGCGTGGTTCCTGCCTGGGTGACAGAGGCTCCTGTGGCCACTTTAGAAGTGCGGTTTACTCCTCATGCCGAGATGGACCTTGGG
CAGCTCAGTTCACAAGATGTTGGTCAGGCGTCATTTAAATATTTTCAGTCAGCAGAGGAAGCAAAGCGTGCCATTGAGGCTGTGCTGTCAGCGGATCCTCGGTCT
Show »
ATGCGCGGCTTGGAGGAGTCGGGGCCTCGGCCTACAGCGACCCCGTGCGGCTGCGTTAAGCCGGCTCTGGAGACAGGGAATCTTTTAACTGAGCCAGTCGGCTAC
TTGGAATCTTGTTTCTCGGCCAAGAATGGTACTCCAAGACAGCCATCCATTTGTAGCTATTCTCGAGCCTGTTTGAGGATTAGAAAGAGGATCTTTAATAATCCT
GAACATTCCTTGATGGGCCTAGAACAGTTTTCTCATGTTTGGATTTTGTTTGTTTTTCACAAAAATGGTCATTTGAGCTGTAAGGCAAAAGTGCAGCCTCCTAGG
CTGAATGGTGCAAAGACTGGAGTTTTTTCCACAAGGAGCCCTCATCGTCCCAATGCAATAGGACTGACCCTGGCCAAGCTGGAAAAGGTAGAAGGTGGAGCTATA
TACCTTTCTGGAATTGACATGATACATGGCACACCCGTACTAGACATCAAGCCCTACATAGCTGAGTATGACTCACCGCAAAATGTGATGGAGCCTTTAGCAGAC
TTTAATTTACAGAATAACCAACATACACCAAACACTGTGTCCCAGTCTGACAGCAAGACTGACAGCTGTGACCAGCGACAGCTCTCAGGGTGTGATGAGCCACAA
CCCCACCATAGCACTAAGAGGAAACCTAAATGTCCTGAAGACAGAACTTCAGAAGAAAACTACCTGACACACAGTGACACAGCCAGAATTCAGCAAGCATTTCCT
ATGCACAGGGAGATAGCAGTGGATTTTGGTTTGGAATCAAGACGTGATCAGAGTTCCAGCGTGGCAGAAGAACAAATTGGCCCATATTGCCCAGAGAAGAGCTTT
TCAGAGAAAGGTACAGACAAGAAGCTAGAAAGAGTGGAAGGAGCAGCAGTCTTGCAAGGAAGCAGGGCAGAGACACAGCCCATGGCCCCTCACTGCCCTGCTGGA
AGGGCTGATGGAGCTCCCCGCAGCGTGGTTCCTGCCTGGGTGACAGAGGCTCCTGTGGCCACTTTAGAAGTGCGGTTTACTCCTCATGCCGAGATGGACCTTGGG
CAGCTCAGTTCACAAGATGTTGGTCAGGCGTCATTTAAATATTTTCAGTCAGCAGAGGAAGCAAAGCGTGCCATTGAGGCTGTGCTGTCAGCGGATCCTCGGTCT
Show »
>C9orf156|51531|protein
MRGLEESGPRPTATPCGCVKPALETGNLLTEPVGYLESCFSAKNGTPRQPSICSYSRACLRIRKRIFNNPEHSLMGLEQFSHVWILFVFHKNGHLSCKAKVQPPR
LNGAKTGVFSTRSPHRPNAIGLTLAKLEKVEGGAIYLSGIDMIHGTPVLDIKPYIAEYDSPQNVMEPLADFNLQNNQHTPNTVSQSDSKTDSCDQRQLSGCDEPQ
PHHSTKRKPKCPEDRTSEENYLTHSDTARIQQAFPMHREIAVDFGLESRRDQSSSVAEEQIGPYCPEKSFSEKGTDKKLERVEGAAVLQGSRAETQPMAPHCPAG
RADGAPRSVVPAWVTEAPVATLEVRFTPHAEMDLGQLSSQDVGQASFKYFQSAEEAKRAIEAVLSADPRSVYRRKLCQDRLFYFTVDIAHVTCWFGDGFAEVLRI
KPASEPVHMTGPVGSLVSLGS
Show »
MRGLEESGPRPTATPCGCVKPALETGNLLTEPVGYLESCFSAKNGTPRQPSICSYSRACLRIRKRIFNNPEHSLMGLEQFSHVWILFVFHKNGHLSCKAKVQPPR
LNGAKTGVFSTRSPHRPNAIGLTLAKLEKVEGGAIYLSGIDMIHGTPVLDIKPYIAEYDSPQNVMEPLADFNLQNNQHTPNTVSQSDSKTDSCDQRQLSGCDEPQ
PHHSTKRKPKCPEDRTSEENYLTHSDTARIQQAFPMHREIAVDFGLESRRDQSSSVAEEQIGPYCPEKSFSEKGTDKKLERVEGAAVLQGSRAETQPMAPHCPAG
RADGAPRSVVPAWVTEAPVATLEVRFTPHAEMDLGQLSSQDVGQASFKYFQSAEEAKRAIEAVLSADPRSVYRRKLCQDRLFYFTVDIAHVTCWFGDGFAEVLRI
KPASEPVHMTGPVGSLVSLGS
Show »
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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (1) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
NGS de novo Mutation Studies Top
Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
Contact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.