Evidence Details for LRP11
Basic Information Top
Gene Symbol: | LRP11 ( FLJ14735,MANSC3,MGC39092,bA350J20.3 ) |
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Gene Full Name: | low density lipoprotein receptor-related protein 11 |
Band: | 6q25.1 |
Quick Links | Entrez ID:84918; OMIM: NA; Uniprot ID:LRP11_HUMAN; ENSEMBL ID: ENSG00000120256; HGNC ID: 16936 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>LRP11|84918|nucleotide
ATGGCCTCCGTCGCCCAGGAGAGCGCGGGCTCGCAGCGCCGGCTACCGCCGCGTCACGGGGCGCTGCGCGGGCTGCTACTGCTCTGCCTGTGGCTGCCAAGCGGC
CGTGCGGCCTTGCCGCCCGCGGCGCCGCTGTCCGAACTGCACGCGCAGCTGTCGGGCGTGGAGCAGCTGCTGGAGGAGTTCCGCCGGCAACTGCAGCAGGAGCGG
CCTCAGGAGGAGCTGGAGCTGGAGCTGCGCGCGGGCGGCGGCCCCCAGGAGGACTGCCCGGGCCCGGGCAGCGGCGGCTACAGCGCAATGCCTGACGCCATCATC
CGCACCAAGGACTCCCTGGCGGCGGGTGCCAGCTTCCTGCGGGCGCCGGCGGCCGTGCGGGGCTGGCGGCAATGCGTGGCGGCCTGCTGCTCCGAGCCGCGCTGC
TCCGTGGCCGTGGTGGAGCTGCCCCGGCGCCCCGCGCCCCCGGCAGCCGTGCTCGGCTGCTACCTCTTCAACTGCACGGCGCGCGGCCGCAACGTCTGCAAGTTC
GCGCTGCACAGCGGCTACAGCAGCTACAGCCTCAGCCGCGCGCCGGACGGCGCCGCCCTGGCCACCGCGCGCGCCTCGCCCCGGCAGGAAAAGGATGCGCCTCCA
CTTAGCAAGGCTGGGCAGGATGTGGTTCTGCATCTGCCCACAGACGGGGTGGTTCTAGACGGCCGCGAGAGCACAGATGACCACGCCATCGTCCAGTATGAGTGG
GCACTGCTGCAGGGGGACCCGTCAGTGGACATGAAGGTGCCTCAATCAGGAACCCTGAAGCTGTCCCACCTACAGGAGGGAACCTACACCTTCCAGCTGACCGTG
ACGGACACTGCCGGGCAGAGAAGCTCTGACAACGTGTCAGTGACAGTGCTTCGCGCAGCCTACTCCACAGGAGGATGTTTGCACACTTGCTCACGCTACCACTTC
TTCTGTGACGATGGCTGCTGCATTGACATCACGCTCGCCTGCGATGGAGTGCAGCAGTGTCCTGATGGGTCTGATGAAGACTTCTGCCAGAATCTGGGCCTGGAC
CGCAAGATGGTAACCCACACGGCAGCTAGTCCTGCCCTGCCAAGAACCACAGGGCCGAGTGAAGATGCAGGGGGTGACTCCTTGGTGGAAAAGTCTCAGAAAGCC
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ATGGCCTCCGTCGCCCAGGAGAGCGCGGGCTCGCAGCGCCGGCTACCGCCGCGTCACGGGGCGCTGCGCGGGCTGCTACTGCTCTGCCTGTGGCTGCCAAGCGGC
CGTGCGGCCTTGCCGCCCGCGGCGCCGCTGTCCGAACTGCACGCGCAGCTGTCGGGCGTGGAGCAGCTGCTGGAGGAGTTCCGCCGGCAACTGCAGCAGGAGCGG
CCTCAGGAGGAGCTGGAGCTGGAGCTGCGCGCGGGCGGCGGCCCCCAGGAGGACTGCCCGGGCCCGGGCAGCGGCGGCTACAGCGCAATGCCTGACGCCATCATC
CGCACCAAGGACTCCCTGGCGGCGGGTGCCAGCTTCCTGCGGGCGCCGGCGGCCGTGCGGGGCTGGCGGCAATGCGTGGCGGCCTGCTGCTCCGAGCCGCGCTGC
TCCGTGGCCGTGGTGGAGCTGCCCCGGCGCCCCGCGCCCCCGGCAGCCGTGCTCGGCTGCTACCTCTTCAACTGCACGGCGCGCGGCCGCAACGTCTGCAAGTTC
GCGCTGCACAGCGGCTACAGCAGCTACAGCCTCAGCCGCGCGCCGGACGGCGCCGCCCTGGCCACCGCGCGCGCCTCGCCCCGGCAGGAAAAGGATGCGCCTCCA
CTTAGCAAGGCTGGGCAGGATGTGGTTCTGCATCTGCCCACAGACGGGGTGGTTCTAGACGGCCGCGAGAGCACAGATGACCACGCCATCGTCCAGTATGAGTGG
GCACTGCTGCAGGGGGACCCGTCAGTGGACATGAAGGTGCCTCAATCAGGAACCCTGAAGCTGTCCCACCTACAGGAGGGAACCTACACCTTCCAGCTGACCGTG
ACGGACACTGCCGGGCAGAGAAGCTCTGACAACGTGTCAGTGACAGTGCTTCGCGCAGCCTACTCCACAGGAGGATGTTTGCACACTTGCTCACGCTACCACTTC
TTCTGTGACGATGGCTGCTGCATTGACATCACGCTCGCCTGCGATGGAGTGCAGCAGTGTCCTGATGGGTCTGATGAAGACTTCTGCCAGAATCTGGGCCTGGAC
CGCAAGATGGTAACCCACACGGCAGCTAGTCCTGCCCTGCCAAGAACCACAGGGCCGAGTGAAGATGCAGGGGGTGACTCCTTGGTGGAAAAGTCTCAGAAAGCC
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>LRP11|84918|protein
MASVAQESAGSQRRLPPRHGALRGLLLLCLWLPSGRAALPPAAPLSELHAQLSGVEQLLEEFRRQLQQERPQEELELELRAGGGPQEDCPGPGSGGYSAMPDAII
RTKDSLAAGASFLRAPAAVRGWRQCVAACCSEPRCSVAVVELPRRPAPPAAVLGCYLFNCTARGRNVCKFALHSGYSSYSLSRAPDGAALATARASPRQEKDAPP
LSKAGQDVVLHLPTDGVVLDGRESTDDHAIVQYEWALLQGDPSVDMKVPQSGTLKLSHLQEGTYTFQLTVTDTAGQRSSDNVSVTVLRAAYSTGGCLHTCSRYHF
FCDDGCCIDITLACDGVQQCPDGSDEDFCQNLGLDRKMVTHTAASPALPRTTGPSEDAGGDSLVEKSQKATAPNKPPALSNTEKRNHSAFWGPESQIIPVMPDSS
SSGKNRKEESYIFESKGDGGGGEHPAPETGAVLPLALGLAITALLLLMVACRLRLVKQKLKKARPITSEESDYLINGMYL
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MASVAQESAGSQRRLPPRHGALRGLLLLCLWLPSGRAALPPAAPLSELHAQLSGVEQLLEEFRRQLQQERPQEELELELRAGGGPQEDCPGPGSGGYSAMPDAII
RTKDSLAAGASFLRAPAAVRGWRQCVAACCSEPRCSVAVVELPRRPAPPAAVLGCYLFNCTARGRNVCKFALHSGYSSYSLSRAPDGAALATARASPRQEKDAPP
LSKAGQDVVLHLPTDGVVLDGRESTDDHAIVQYEWALLQGDPSVDMKVPQSGTLKLSHLQEGTYTFQLTVTDTAGQRSSDNVSVTVLRAAYSTGGCLHTCSRYHF
FCDDGCCIDITLACDGVQQCPDGSDEDFCQNLGLDRKMVTHTAASPALPRTTGPSEDAGGDSLVEKSQKATAPNKPPALSNTEKRNHSAFWGPESQIIPVMPDSS
SSGKNRKEESYIFESKGDGGGGEHPAPETGAVLPLALGLAITALLLLMVACRLRLVKQKLKKARPITSEESDYLINGMYL
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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
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