Evidence Details for SLC22A11
Basic Information Top
Gene Symbol: | SLC22A11 ( MGC34282,OAT4,hOAT4 ) |
---|---|
Gene Full Name: | solute carrier family 22 (organic anion/urate transporter), member 11 |
Band: | 11q13.1 |
Quick Links | Entrez ID:55867; OMIM: 607097; Uniprot ID:S22AB_HUMAN; ENSEMBL ID: ENSG00000168065; HGNC ID: 18120 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>SLC22A11|55867|nucleotide
ATGGCGTTCTCGAAGCTCTTGGAGCAAGCCGGAGGCGTGGGCCTCTTCCAGACCCTGCAGGTGCTCACCTTCATCCTCCCCTGCCTCATGATACCTTCCCAGATG
CTCCTGGAGAACTTCTCAGCCGCCATCCCAGGCCACCGATGCTGGACACACATGCTGGACAATGGCTCTGCGGTTTCCACAAACATGACCCCCAAGGCCCTTCTG
ACCATCTCCATCCCGCCAGGCCCCAACCAGGGGCCCCACCAGTGCCGCCGCTTCCGCCAGCCACAGTGGCAGCTCTTGGACCCCAATGCCACGGCCACCAGCTGG
AGCGAAGCTGACACGGAGCCGTGTGTGGACGGCTGGGTCTATGACCGCAGCGTCTTCACCTCCACCATCGTGGCCAAGTGGGACCTGGTGTGCAGCTCCCAGGGC
TTGAAGCCCCTAAGCCAGTCCATCTTCATGTCCGGGATCCTGGTGGGCTCCTTTATCTGGGGCCTCCTCTCCTACCGGTTTGGGAGGAAGCCGATGCTGAGCTGG
TGCTGCCTGCAGTTGGCCGTGGCGGGCACCAGCACCATCTTCGCCCCAACATTCGTCATCTACTGCGGCCTGCGGTTCGTGGCCGCTTTTGGGATGGCCGGCATC
TTTCTGAGTTCACTGACACTGATGGTGGAGTGGACCACGACCAGCAGGAGGGCGGTCACCATGACGGTGGTGGGATGTGCCTTCAGCGCAGGCCAGGCGGCGCTG
GGCGGCCTGGCCTTTGCCCTGCGGGACTGGAGGACTCTCCAGCTGGCAGCATCAGTGCCCTTCTTTGCCATCTCCCTGATATCCTGGTGGCTGCCAGAATCCGCC
CGGTGGCTGATTATTAAGGGCAAACCAGACCAAGCACTTCAGGAGCTCAGAAAGGTGGCCAGGATAAATGGCCACAAGGAGGCCAAGAACCTGACCATAGAGGTG
CTGATGTCCAGCGTGAAGGAGGAGGTGGCCTCTGCAAAGGAGCCGCGGTCGGTGCTGGACCTGTTCTGCGTGCCCGTGCTCCGCTGGAGGAGCTGCGCCATGCTG
GTGGTGAATTTCTCTCTATTGATCTCCTACTATGGGCTGGTCTTCGACCTGCAGAGCCTGGGCCGTGACATCTTCCTCCTCCAGGCCCTCTTCGGGGCCGTGGAC
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ATGGCGTTCTCGAAGCTCTTGGAGCAAGCCGGAGGCGTGGGCCTCTTCCAGACCCTGCAGGTGCTCACCTTCATCCTCCCCTGCCTCATGATACCTTCCCAGATG
CTCCTGGAGAACTTCTCAGCCGCCATCCCAGGCCACCGATGCTGGACACACATGCTGGACAATGGCTCTGCGGTTTCCACAAACATGACCCCCAAGGCCCTTCTG
ACCATCTCCATCCCGCCAGGCCCCAACCAGGGGCCCCACCAGTGCCGCCGCTTCCGCCAGCCACAGTGGCAGCTCTTGGACCCCAATGCCACGGCCACCAGCTGG
AGCGAAGCTGACACGGAGCCGTGTGTGGACGGCTGGGTCTATGACCGCAGCGTCTTCACCTCCACCATCGTGGCCAAGTGGGACCTGGTGTGCAGCTCCCAGGGC
TTGAAGCCCCTAAGCCAGTCCATCTTCATGTCCGGGATCCTGGTGGGCTCCTTTATCTGGGGCCTCCTCTCCTACCGGTTTGGGAGGAAGCCGATGCTGAGCTGG
TGCTGCCTGCAGTTGGCCGTGGCGGGCACCAGCACCATCTTCGCCCCAACATTCGTCATCTACTGCGGCCTGCGGTTCGTGGCCGCTTTTGGGATGGCCGGCATC
TTTCTGAGTTCACTGACACTGATGGTGGAGTGGACCACGACCAGCAGGAGGGCGGTCACCATGACGGTGGTGGGATGTGCCTTCAGCGCAGGCCAGGCGGCGCTG
GGCGGCCTGGCCTTTGCCCTGCGGGACTGGAGGACTCTCCAGCTGGCAGCATCAGTGCCCTTCTTTGCCATCTCCCTGATATCCTGGTGGCTGCCAGAATCCGCC
CGGTGGCTGATTATTAAGGGCAAACCAGACCAAGCACTTCAGGAGCTCAGAAAGGTGGCCAGGATAAATGGCCACAAGGAGGCCAAGAACCTGACCATAGAGGTG
CTGATGTCCAGCGTGAAGGAGGAGGTGGCCTCTGCAAAGGAGCCGCGGTCGGTGCTGGACCTGTTCTGCGTGCCCGTGCTCCGCTGGAGGAGCTGCGCCATGCTG
GTGGTGAATTTCTCTCTATTGATCTCCTACTATGGGCTGGTCTTCGACCTGCAGAGCCTGGGCCGTGACATCTTCCTCCTCCAGGCCCTCTTCGGGGCCGTGGAC
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>SLC22A11|55867|protein
MAFSKLLEQAGGVGLFQTLQVLTFILPCLMIPSQMLLENFSAAIPGHRCWTHMLDNGSAVSTNMTPKALLTISIPPGPNQGPHQCRRFRQPQWQLLDPNATATSW
SEADTEPCVDGWVYDRSVFTSTIVAKWDLVCSSQGLKPLSQSIFMSGILVGSFIWGLLSYRFGRKPMLSWCCLQLAVAGTSTIFAPTFVIYCGLRFVAAFGMAGI
FLSSLTLMVEWTTTSRRAVTMTVVGCAFSAGQAALGGLAFALRDWRTLQLAASVPFFAISLISWWLPESARWLIIKGKPDQALQELRKVARINGHKEAKNLTIEV
LMSSVKEEVASAKEPRSVLDLFCVPVLRWRSCAMLVVNFSLLISYYGLVFDLQSLGRDIFLLQALFGAVDFLGRATTALLLSFLGRRTIQAGSQAMAGLAILANM
LVPQDLQTLRVVFAVLGKGCFGISLTCLTIYKAELFPTPVRMTADGILHTVGRLGAMMGPLILMSRQALPLLPPLLYGVISIASSLVVLFFLPETQGLPLPDTIQ
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MAFSKLLEQAGGVGLFQTLQVLTFILPCLMIPSQMLLENFSAAIPGHRCWTHMLDNGSAVSTNMTPKALLTISIPPGPNQGPHQCRRFRQPQWQLLDPNATATSW
SEADTEPCVDGWVYDRSVFTSTIVAKWDLVCSSQGLKPLSQSIFMSGILVGSFIWGLLSYRFGRKPMLSWCCLQLAVAGTSTIFAPTFVIYCGLRFVAAFGMAGI
FLSSLTLMVEWTTTSRRAVTMTVVGCAFSAGQAALGGLAFALRDWRTLQLAASVPFFAISLISWWLPESARWLIIKGKPDQALQELRKVARINGHKEAKNLTIEV
LMSSVKEEVASAKEPRSVLDLFCVPVLRWRSCAMLVVNFSLLISYYGLVFDLQSLGRDIFLLQALFGAVDFLGRATTALLLSFLGRRTIQAGSQAMAGLAILANM
LVPQDLQTLRVVFAVLGKGCFGISLTCLTIYKAELFPTPVRMTADGILHTVGRLGAMMGPLILMSRQALPLLPPLLYGVISIASSLVVLFFLPETQGLPLPDTIQ
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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 (0) | 0 (0) | 0 (0) | 0 (0) | (0) |
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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