Evidence Details for HNRNPUL2
Basic Information Top
Gene Symbol: | HNRNPUL2 ( DKFZp762N1910,HNRPUL2 ) |
---|---|
Gene Full Name: | heterogeneous nuclear ribonucleoprotein U-like 2 |
Band: | 11q12.3 |
Quick Links | Entrez ID:221092; OMIM: NA; Uniprot ID:HNRL2_HUMAN; ENSEMBL ID: ENSG00000214753; HGNC ID: 25451 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>HNRNPUL2|221092|nucleotide
ATGGAGGTGAAGCGGCTGAAAGTGACCGAGCTGCGGTCGGAGCTGCAGCGGCGGGGCCTGGACTCGCGCGGCCTCAAGGTGGATCTGGCGCAGCGGCTGCAGGAG
GCGCTGGACGCCGAGATGCTCGAGGACGAGGCCGGCGGCGGCGGGGCCGGGCCCGGCGGGGCCTGCAAGGCGGAGCCTCGGCCTGTGGCCGCGTCGGGCGGCGGC
CCGGGCGGGGACGAGGAGGAGGACGAAGAGGAGGAGGAGGAGGACGAGGAGGCGCTGCTTGAGGACGAGGACGAGGAGCCACCCCCTGCTCAAGCCTTGGGTCAG
GCCGCGCAGCCGCCGCCGGAGCCCCCGGAGGCGGCAGCCATGGAGGCCGCGGCCGAGCCAGATGCTTCCGAGAAGCCGGCGGAGGCCACGGCCGGGTCAGGCGGG
GTAAATGGTGGCGAAGAGCAGGGCCTCGGCAAGAGGGAGGAAGACGAACCCGAGGAGCGGAGCGGGGACGAGACGCCGGGATCCGAGGTGCCGGGTGACAAGGCC
GCCGAGGAACAGGGAGATGACCAGGATAGTGAAAAGTCAAAACCAGCAGGCTCAGATGGTGAGCGGCGGGGGGTAAAGAGACAGCGGGATGAGAAGGATGAACAT
GGCCGAGCTTACTATGAATTCCGAGAGGAGGCTTACCACAGCCGCTCAAAGTCTCCACTGCCTCCTGAAGAAGAGGCAAAAGATGAGGAGGAGGATCAAACTCTT
GTGAACCTGGACACGTATACCTCGGATCTGCATTTTCAAGTGAGCAAAGACCGCTATGGAGGGCAGCCACTTTTCTCAGAGAAGTTCCCCACCCTTTGGTCTGGG
GCAAGGAGTACTTACGGAGTGACAAAGGGAAAAGTCTGCTTTGAGGCAAAGGTAACCCAGAATCTCCCAATGAAAGAAGGCTGCACAGAGGTCTCTCTCCTTCGA
GTTGGGTGGTCTGTTGATTTTTCCCGTCCACAGCTTGGTGAAGATGAATTCTCTTACGGTTTCGATGGACGAGGACTCAAGGCAGAAAATGGACAATTTGAGGAA
TTTGGCCAGACTTTTGGGGAGAATGATGTTATTGGCTGCTTTGCTAATTTTGAGACTGAAGAAGTAGAACTTTCCTTCTCCAAGAATGGAGAAGACCTAGGTGTG
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ATGGAGGTGAAGCGGCTGAAAGTGACCGAGCTGCGGTCGGAGCTGCAGCGGCGGGGCCTGGACTCGCGCGGCCTCAAGGTGGATCTGGCGCAGCGGCTGCAGGAG
GCGCTGGACGCCGAGATGCTCGAGGACGAGGCCGGCGGCGGCGGGGCCGGGCCCGGCGGGGCCTGCAAGGCGGAGCCTCGGCCTGTGGCCGCGTCGGGCGGCGGC
CCGGGCGGGGACGAGGAGGAGGACGAAGAGGAGGAGGAGGAGGACGAGGAGGCGCTGCTTGAGGACGAGGACGAGGAGCCACCCCCTGCTCAAGCCTTGGGTCAG
GCCGCGCAGCCGCCGCCGGAGCCCCCGGAGGCGGCAGCCATGGAGGCCGCGGCCGAGCCAGATGCTTCCGAGAAGCCGGCGGAGGCCACGGCCGGGTCAGGCGGG
GTAAATGGTGGCGAAGAGCAGGGCCTCGGCAAGAGGGAGGAAGACGAACCCGAGGAGCGGAGCGGGGACGAGACGCCGGGATCCGAGGTGCCGGGTGACAAGGCC
GCCGAGGAACAGGGAGATGACCAGGATAGTGAAAAGTCAAAACCAGCAGGCTCAGATGGTGAGCGGCGGGGGGTAAAGAGACAGCGGGATGAGAAGGATGAACAT
GGCCGAGCTTACTATGAATTCCGAGAGGAGGCTTACCACAGCCGCTCAAAGTCTCCACTGCCTCCTGAAGAAGAGGCAAAAGATGAGGAGGAGGATCAAACTCTT
GTGAACCTGGACACGTATACCTCGGATCTGCATTTTCAAGTGAGCAAAGACCGCTATGGAGGGCAGCCACTTTTCTCAGAGAAGTTCCCCACCCTTTGGTCTGGG
GCAAGGAGTACTTACGGAGTGACAAAGGGAAAAGTCTGCTTTGAGGCAAAGGTAACCCAGAATCTCCCAATGAAAGAAGGCTGCACAGAGGTCTCTCTCCTTCGA
GTTGGGTGGTCTGTTGATTTTTCCCGTCCACAGCTTGGTGAAGATGAATTCTCTTACGGTTTCGATGGACGAGGACTCAAGGCAGAAAATGGACAATTTGAGGAA
TTTGGCCAGACTTTTGGGGAGAATGATGTTATTGGCTGCTTTGCTAATTTTGAGACTGAAGAAGTAGAACTTTCCTTCTCCAAGAATGGAGAAGACCTAGGTGTG
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>HNRNPUL2|221092|protein
MEVKRLKVTELRSELQRRGLDSRGLKVDLAQRLQEALDAEMLEDEAGGGGAGPGGACKAEPRPVAASGGGPGGDEEEDEEEEEEDEEALLEDEDEEPPPAQALGQ
AAQPPPEPPEAAAMEAAAEPDASEKPAEATAGSGGVNGGEEQGLGKREEDEPEERSGDETPGSEVPGDKAAEEQGDDQDSEKSKPAGSDGERRGVKRQRDEKDEH
GRAYYEFREEAYHSRSKSPLPPEEEAKDEEEDQTLVNLDTYTSDLHFQVSKDRYGGQPLFSEKFPTLWSGARSTYGVTKGKVCFEAKVTQNLPMKEGCTEVSLLR
VGWSVDFSRPQLGEDEFSYGFDGRGLKAENGQFEEFGQTFGENDVIGCFANFETEEVELSFSKNGEDLGVAFWISKDSLADRALLPHVLCKNCVVELNFGQKEEP
FFPPPEEFVFIHAVPVEERVRTAVPPKTIEECEVILMVGLPGSGKTQWALKYAKENPEKRYNVLGAETVLNQMRMKGLEEPEMDPKSRDLLVQQASQCLSKLVQI
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MEVKRLKVTELRSELQRRGLDSRGLKVDLAQRLQEALDAEMLEDEAGGGGAGPGGACKAEPRPVAASGGGPGGDEEEDEEEEEEDEEALLEDEDEEPPPAQALGQ
AAQPPPEPPEAAAMEAAAEPDASEKPAEATAGSGGVNGGEEQGLGKREEDEPEERSGDETPGSEVPGDKAAEEQGDDQDSEKSKPAGSDGERRGVKRQRDEKDEH
GRAYYEFREEAYHSRSKSPLPPEEEAKDEEEDQTLVNLDTYTSDLHFQVSKDRYGGQPLFSEKFPTLWSGARSTYGVTKGKVCFEAKVTQNLPMKEGCTEVSLLR
VGWSVDFSRPQLGEDEFSYGFDGRGLKAENGQFEEFGQTFGENDVIGCFANFETEEVELSFSKNGEDLGVAFWISKDSLADRALLPHVLCKNCVVELNFGQKEEP
FFPPPEEFVFIHAVPVEERVRTAVPPKTIEECEVILMVGLPGSGKTQWALKYAKENPEKRYNVLGAETVLNQMRMKGLEEPEMDPKSRDLLVQQASQCLSKLVQI
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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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