Evidence Details for MRPL18


Gene Symbol: | MRPL18 ( L18mt,MRP-L18 ) |
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Gene Full Name: | mitochondrial ribosomal protein L18 |
Band: | 6q25.3 |
Quick Links | Entrez ID:29074; OMIM: 611831; Uniprot ID:RM18_HUMAN; ENSEMBL ID: ENSG00000112110; HGNC ID: 14477 |
Relate to Another Database: | SFARIGene; denovo-db |


>MRPL18|29074|nucleotide
ATGGCGCTTCGGTCGCGGTTTTGGGGGTTGTTCTCGGTTTGCAGGAACCCTGGGTGCAGGTTCGCAGCCCTGTCAACCAGCTCCGAGCCGGCAGCGAAACCTGAA
GTGGACCCTGTGGAAAATGAAGCTGTCGCCCCAGAATTCACCAACCGGAACCCCCGGAACCTGGAGCTTTTATCTGTAGCCAGGAAAGAGCGGGGCTGGCGGACG
GTGTTTCCCTCCCGTGAGTTCTGGCACAGGTTGCGAGTTATAAGGACTCAGCATCATGTAGAAGCACTTGTGGAGCATCAGAATGGCAAGGTTGTGGTTTCGGCC
TCCACTCGTGAGTGGGCTATTAAAAAGCACCTTTATAGTACCAGAAATGTGGTGGCTTGTGAGAGTATAGGACGAGTGCTGGCACAGAGATGCTTAGAGGCGGGA
ATCAACTTCATGGTCTACCAACCAACCCCGTGGGAGGCAGCCTCAGACTCGATGAAACGACTACAAAGTGCCATGACAGAAGGTGGTGTGGTTCTACGGGAACCT
CAGAGAATCTATGAATAA
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ATGGCGCTTCGGTCGCGGTTTTGGGGGTTGTTCTCGGTTTGCAGGAACCCTGGGTGCAGGTTCGCAGCCCTGTCAACCAGCTCCGAGCCGGCAGCGAAACCTGAA
GTGGACCCTGTGGAAAATGAAGCTGTCGCCCCAGAATTCACCAACCGGAACCCCCGGAACCTGGAGCTTTTATCTGTAGCCAGGAAAGAGCGGGGCTGGCGGACG
GTGTTTCCCTCCCGTGAGTTCTGGCACAGGTTGCGAGTTATAAGGACTCAGCATCATGTAGAAGCACTTGTGGAGCATCAGAATGGCAAGGTTGTGGTTTCGGCC
TCCACTCGTGAGTGGGCTATTAAAAAGCACCTTTATAGTACCAGAAATGTGGTGGCTTGTGAGAGTATAGGACGAGTGCTGGCACAGAGATGCTTAGAGGCGGGA
ATCAACTTCATGGTCTACCAACCAACCCCGTGGGAGGCAGCCTCAGACTCGATGAAACGACTACAAAGTGCCATGACAGAAGGTGGTGTGGTTCTACGGGAACCT
CAGAGAATCTATGAATAA
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>MRPL18|29074|protein
MALRSRFWGLFSVCRNPGCRFAALSTSSEPAAKPEVDPVENEAVAPEFTNRNPRNLELLSVARKERGWRTVFPSREFWHRLRVIRTQHHVEALVEHQNGKVVVSA
STREWAIKKHLYSTRNVVACESIGRVLAQRCLEAGINFMVYQPTPWEAASDSMKRLQSAMTEGGVVLREPQRIYE
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MALRSRFWGLFSVCRNPGCRFAALSTSSEPAAKPEVDPVENEAVAPEFTNRNPRNLELLSVARKERGWRTVFPSREFWHRLRVIRTQHHVEALVEHQNGKVVVSA
STREWAIKKHLYSTRNVVACESIGRVLAQRCLEAGINFMVYQPTPWEAASDSMKRLQSAMTEGGVVLREPQRIYE
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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) |














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. |






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