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

