Evidence Details for RRP8
Basic Information Top
Gene Symbol: | RRP8 ( KIAA0409 ) |
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Gene Full Name: | ribosomal RNA processing 8, methyltransferase, homolog (yeast) |
Band: | 11p15.4 |
Quick Links | Entrez ID:23378; OMIM: NA; Uniprot ID:RRP8_HUMAN; ENSEMBL ID: ENSG00000132275; HGNC ID: 29030 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>RRP8|23378|nucleotide
ATGTTCGAAGAGCCTGAGTGGGCCGAGGCGGCCCCAGTAGCCGCGGGCCTTGGGCCCGTAATCTCACGACCTCCGCCTGCGGCCTCCTCGCAAAACAAGGGCTCC
AAGCGCCGCCAGCTCTTGGCCACATTACGGGCCCTAGAGGCAGCATCTCTTTCCCAGCATCCCCCCAGCCTATGTATAAGTGACTCTGAGGAGGAGGAGGAGGAA
AGGAAGAAGAAATGCCCCAAAAAGGCATCATTTGCCAGTGCCTCTGCTGAAGTAGGGAAGAAAGGGAAGAAGAAATGTCAAAAACAGGGCCCACCTTGCAGTGAC
TCTGAGGAAGAAGTAGAAAGGAAGAAGAAATGCCACAAACAGGCTCTTGTTGGCAGTGACTCTGCTGAAGATGAGAAAAGAAAGAGGAAATGCCAGAAACATGCC
CCTATAAATTCAGCCCAGCACCTGGACAATGTTGACCAAACAGGTCCCAAAGCCTGGAAGGGTAGTACTACAAATGATCCACCAAAGCAAAGCCCTGGGTCCACT
TCCCCTAAACCCCCTCATACATTAAGCCGCAAGCAGTGGCGGAACCGGCAAAAGAATAAGAGAAGATGTAAGAACAAGTTTCAGCCACCTCAGGTGCCAGACCAG
GCCCCAGCTGAGGCCCCCACAGAGAAGACAGAGGTGTCTCCTGTTCCCAGGACAGACAGCCATGAGGCTCGGGCAGGGGCTTTGCGAGCCCGCATGGCACAGCGG
CTGGATGGGGCCCGATTTCGCTACCTCAATGAACAGTTGTACTCAGGGCCCAGCAGTGCTGCACAGCGTCTCTTCCAGGAAGACCCTGAGGCTTTTCTTCTCTAC
CACCGCGGCTTCCAGAGCCAAGTGAAGAAGTGGCCACTGCAGCCAGTGGACCGCATCGCCAGGGATCTTCGCCAGCGGCCTGCATCCCTAGTGGTGGCTGACTTC
GGCTGTGGGGATTGCCGCTTGGCTTCAAGTATCCGGAACCCTGTGCATTGCTTTGACTTGGCTTCTCTGGACCCTAGGGTCACTGTGTGTGACATGGCCCAGGTT
CCTCTGGAGGATGAGTCTGTGGATGTGGCTGTGTTTTGCCTTTCACTGATGGGAACCAACATCAGGGACTTCCTAGAGGAGGCAAATAGAGTACTGAAGCCAGGG
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ATGTTCGAAGAGCCTGAGTGGGCCGAGGCGGCCCCAGTAGCCGCGGGCCTTGGGCCCGTAATCTCACGACCTCCGCCTGCGGCCTCCTCGCAAAACAAGGGCTCC
AAGCGCCGCCAGCTCTTGGCCACATTACGGGCCCTAGAGGCAGCATCTCTTTCCCAGCATCCCCCCAGCCTATGTATAAGTGACTCTGAGGAGGAGGAGGAGGAA
AGGAAGAAGAAATGCCCCAAAAAGGCATCATTTGCCAGTGCCTCTGCTGAAGTAGGGAAGAAAGGGAAGAAGAAATGTCAAAAACAGGGCCCACCTTGCAGTGAC
TCTGAGGAAGAAGTAGAAAGGAAGAAGAAATGCCACAAACAGGCTCTTGTTGGCAGTGACTCTGCTGAAGATGAGAAAAGAAAGAGGAAATGCCAGAAACATGCC
CCTATAAATTCAGCCCAGCACCTGGACAATGTTGACCAAACAGGTCCCAAAGCCTGGAAGGGTAGTACTACAAATGATCCACCAAAGCAAAGCCCTGGGTCCACT
TCCCCTAAACCCCCTCATACATTAAGCCGCAAGCAGTGGCGGAACCGGCAAAAGAATAAGAGAAGATGTAAGAACAAGTTTCAGCCACCTCAGGTGCCAGACCAG
GCCCCAGCTGAGGCCCCCACAGAGAAGACAGAGGTGTCTCCTGTTCCCAGGACAGACAGCCATGAGGCTCGGGCAGGGGCTTTGCGAGCCCGCATGGCACAGCGG
CTGGATGGGGCCCGATTTCGCTACCTCAATGAACAGTTGTACTCAGGGCCCAGCAGTGCTGCACAGCGTCTCTTCCAGGAAGACCCTGAGGCTTTTCTTCTCTAC
CACCGCGGCTTCCAGAGCCAAGTGAAGAAGTGGCCACTGCAGCCAGTGGACCGCATCGCCAGGGATCTTCGCCAGCGGCCTGCATCCCTAGTGGTGGCTGACTTC
GGCTGTGGGGATTGCCGCTTGGCTTCAAGTATCCGGAACCCTGTGCATTGCTTTGACTTGGCTTCTCTGGACCCTAGGGTCACTGTGTGTGACATGGCCCAGGTT
CCTCTGGAGGATGAGTCTGTGGATGTGGCTGTGTTTTGCCTTTCACTGATGGGAACCAACATCAGGGACTTCCTAGAGGAGGCAAATAGAGTACTGAAGCCAGGG
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>RRP8|23378|protein
MFEEPEWAEAAPVAAGLGPVISRPPPAASSQNKGSKRRQLLATLRALEAASLSQHPPSLCISDSEEEEEERKKKCPKKASFASASAEVGKKGKKKCQKQGPPCSD
SEEEVERKKKCHKQALVGSDSAEDEKRKRKCQKHAPINSAQHLDNVDQTGPKAWKGSTTNDPPKQSPGSTSPKPPHTLSRKQWRNRQKNKRRCKNKFQPPQVPDQ
APAEAPTEKTEVSPVPRTDSHEARAGALRARMAQRLDGARFRYLNEQLYSGPSSAAQRLFQEDPEAFLLYHRGFQSQVKKWPLQPVDRIARDLRQRPASLVVADF
GCGDCRLASSIRNPVHCFDLASLDPRVTVCDMAQVPLEDESVDVAVFCLSLMGTNIRDFLEEANRVLKPGGLLKVAEVSSRFEDVRTFLRAVTKLGFKIVSKDLT
NSHFFLFDFQKTGPPLVGPKAQLSGLQLQPCLYKRR
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MFEEPEWAEAAPVAAGLGPVISRPPPAASSQNKGSKRRQLLATLRALEAASLSQHPPSLCISDSEEEEEERKKKCPKKASFASASAEVGKKGKKKCQKQGPPCSD
SEEEVERKKKCHKQALVGSDSAEDEKRKRKCQKHAPINSAQHLDNVDQTGPKAWKGSTTNDPPKQSPGSTSPKPPHTLSRKQWRNRQKNKRRCKNKFQPPQVPDQ
APAEAPTEKTEVSPVPRTDSHEARAGALRARMAQRLDGARFRYLNEQLYSGPSSAAQRLFQEDPEAFLLYHRGFQSQVKKWPLQPVDRIARDLRQRPASLVVADF
GCGDCRLASSIRNPVHCFDLASLDPRVTVCDMAQVPLEDESVDVAVFCLSLMGTNIRDFLEEANRVLKPGGLLKVAEVSSRFEDVRTFLRAVTKLGFKIVSKDLT
NSHFFLFDFQKTGPPLVGPKAQLSGLQLQPCLYKRR
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Evidence summary Top
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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 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (2) |
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 |
---|---|---|---|---|
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |
Yuen RK, 2016 | 200 | - | 301 | Genome-wide characteristics of de novo mutations in autism. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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