Evidence Details for RRP8


Gene Symbol: | RRP8 ( KIAA0409 ) |
---|---|
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 |


>RRP8|23378|nucleotide
ATGTTCGAAGAGCCTGAGTGGGCCGAGGCGGCCCCAGTAGCCGCGGGCCTTGGGCCCGTAATCTCACGACCTCCGCCTGCGGCCTCCTCGCAAAACAAGGGCTCC
AAGCGCCGCCAGCTCTTGGCCACATTACGGGCCCTAGAGGCAGCATCTCTTTCCCAGCATCCCCCCAGCCTATGTATAAGTGACTCTGAGGAGGAGGAGGAGGAA
AGGAAGAAGAAATGCCCCAAAAAGGCATCATTTGCCAGTGCCTCTGCTGAAGTAGGGAAGAAAGGGAAGAAGAAATGTCAAAAACAGGGCCCACCTTGCAGTGAC
TCTGAGGAAGAAGTAGAAAGGAAGAAGAAATGCCACAAACAGGCTCTTGTTGGCAGTGACTCTGCTGAAGATGAGAAAAGAAAGAGGAAATGCCAGAAACATGCC
CCTATAAATTCAGCCCAGCACCTGGACAATGTTGACCAAACAGGTCCCAAAGCCTGGAAGGGTAGTACTACAAATGATCCACCAAAGCAAAGCCCTGGGTCCACT
TCCCCTAAACCCCCTCATACATTAAGCCGCAAGCAGTGGCGGAACCGGCAAAAGAATAAGAGAAGATGTAAGAACAAGTTTCAGCCACCTCAGGTGCCAGACCAG
GCCCCAGCTGAGGCCCCCACAGAGAAGACAGAGGTGTCTCCTGTTCCCAGGACAGACAGCCATGAGGCTCGGGCAGGGGCTTTGCGAGCCCGCATGGCACAGCGG
CTGGATGGGGCCCGATTTCGCTACCTCAATGAACAGTTGTACTCAGGGCCCAGCAGTGCTGCACAGCGTCTCTTCCAGGAAGACCCTGAGGCTTTTCTTCTCTAC
CACCGCGGCTTCCAGAGCCAAGTGAAGAAGTGGCCACTGCAGCCAGTGGACCGCATCGCCAGGGATCTTCGCCAGCGGCCTGCATCCCTAGTGGTGGCTGACTTC
GGCTGTGGGGATTGCCGCTTGGCTTCAAGTATCCGGAACCCTGTGCATTGCTTTGACTTGGCTTCTCTGGACCCTAGGGTCACTGTGTGTGACATGGCCCAGGTT
CCTCTGGAGGATGAGTCTGTGGATGTGGCTGTGTTTTGCCTTTCACTGATGGGAACCAACATCAGGGACTTCCTAGAGGAGGCAAATAGAGTACTGAAGCCAGGG
Show »
ATGTTCGAAGAGCCTGAGTGGGCCGAGGCGGCCCCAGTAGCCGCGGGCCTTGGGCCCGTAATCTCACGACCTCCGCCTGCGGCCTCCTCGCAAAACAAGGGCTCC
AAGCGCCGCCAGCTCTTGGCCACATTACGGGCCCTAGAGGCAGCATCTCTTTCCCAGCATCCCCCCAGCCTATGTATAAGTGACTCTGAGGAGGAGGAGGAGGAA
AGGAAGAAGAAATGCCCCAAAAAGGCATCATTTGCCAGTGCCTCTGCTGAAGTAGGGAAGAAAGGGAAGAAGAAATGTCAAAAACAGGGCCCACCTTGCAGTGAC
TCTGAGGAAGAAGTAGAAAGGAAGAAGAAATGCCACAAACAGGCTCTTGTTGGCAGTGACTCTGCTGAAGATGAGAAAAGAAAGAGGAAATGCCAGAAACATGCC
CCTATAAATTCAGCCCAGCACCTGGACAATGTTGACCAAACAGGTCCCAAAGCCTGGAAGGGTAGTACTACAAATGATCCACCAAAGCAAAGCCCTGGGTCCACT
TCCCCTAAACCCCCTCATACATTAAGCCGCAAGCAGTGGCGGAACCGGCAAAAGAATAAGAGAAGATGTAAGAACAAGTTTCAGCCACCTCAGGTGCCAGACCAG
GCCCCAGCTGAGGCCCCCACAGAGAAGACAGAGGTGTCTCCTGTTCCCAGGACAGACAGCCATGAGGCTCGGGCAGGGGCTTTGCGAGCCCGCATGGCACAGCGG
CTGGATGGGGCCCGATTTCGCTACCTCAATGAACAGTTGTACTCAGGGCCCAGCAGTGCTGCACAGCGTCTCTTCCAGGAAGACCCTGAGGCTTTTCTTCTCTAC
CACCGCGGCTTCCAGAGCCAAGTGAAGAAGTGGCCACTGCAGCCAGTGGACCGCATCGCCAGGGATCTTCGCCAGCGGCCTGCATCCCTAGTGGTGGCTGACTTC
GGCTGTGGGGATTGCCGCTTGGCTTCAAGTATCCGGAACCCTGTGCATTGCTTTGACTTGGCTTCTCTGGACCCTAGGGTCACTGTGTGTGACATGGCCCAGGTT
CCTCTGGAGGATGAGTCTGTGGATGTGGCTGTGTTTTGCCTTTCACTGATGGGAACCAACATCAGGGACTTCCTAGAGGAGGCAAATAGAGTACTGAAGCCAGGG
Show »
>RRP8|23378|protein
MFEEPEWAEAAPVAAGLGPVISRPPPAASSQNKGSKRRQLLATLRALEAASLSQHPPSLCISDSEEEEEERKKKCPKKASFASASAEVGKKGKKKCQKQGPPCSD
SEEEVERKKKCHKQALVGSDSAEDEKRKRKCQKHAPINSAQHLDNVDQTGPKAWKGSTTNDPPKQSPGSTSPKPPHTLSRKQWRNRQKNKRRCKNKFQPPQVPDQ
APAEAPTEKTEVSPVPRTDSHEARAGALRARMAQRLDGARFRYLNEQLYSGPSSAAQRLFQEDPEAFLLYHRGFQSQVKKWPLQPVDRIARDLRQRPASLVVADF
GCGDCRLASSIRNPVHCFDLASLDPRVTVCDMAQVPLEDESVDVAVFCLSLMGTNIRDFLEEANRVLKPGGLLKVAEVSSRFEDVRTFLRAVTKLGFKIVSKDLT
NSHFFLFDFQKTGPPLVGPKAQLSGLQLQPCLYKRR
Show »
MFEEPEWAEAAPVAAGLGPVISRPPPAASSQNKGSKRRQLLATLRALEAASLSQHPPSLCISDSEEEEEERKKKCPKKASFASASAEVGKKGKKKCQKQGPPCSD
SEEEVERKKKCHKQALVGSDSAEDEKRKRKCQKHAPINSAQHLDNVDQTGPKAWKGSTTNDPPKQSPGSTSPKPPHTLSRKQWRNRQKNKRRCKNKFQPPQVPDQ
APAEAPTEKTEVSPVPRTDSHEARAGALRARMAQRLDGARFRYLNEQLYSGPSSAAQRLFQEDPEAFLLYHRGFQSQVKKWPLQPVDRIARDLRQRPASLVVADF
GCGDCRLASSIRNPVHCFDLASLDPRVTVCDMAQVPLEDESVDVAVFCLSLMGTNIRDFLEEANRVLKPGGLLKVAEVSSRFEDVRTFLRAVTKLGFKIVSKDLT
NSHFFLFDFQKTGPPLVGPKAQLSGLQLQPCLYKRR
Show »


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 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (2) |














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. |






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.