Evidence Details for RASL10B
Basic Information Top
Gene Symbol: | RASL10B ( MGC47540,RRP17,VTS58635 ) |
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Gene Full Name: | RAS-like, family 10, member B |
Band: | 17q12 |
Quick Links | Entrez ID:91608; OMIM: 612128; Uniprot ID:RSLAB_HUMAN; ENSEMBL ID: ENSG00000141150; HGNC ID: 30295 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>RASL10B|91608|nucleotide
ATGGTCTCCACCTACCGGGTGGCCGTGCTGGGGGCGCGAGGTGTGGGCAAGAGTGCCATCGTGCGCCAGTTCTTGTACAACGAGTTCAGCGAGGTCTGCGTCCCC
ACCACCGCCCGCCGCCTTTACCTGCCTGCTGTCGTCATGAACGGCCACGTGCACGACCTCCAGATCCTCGACTTTCCACCCATCAGCGCCTTCCCTGTCAATACG
CTCCAGGAGTGGGCAGACACCTGCTGCAGGGGACTCCGGAGTGTCCACGCCTACATCCTGGTCTACGACATCTGCTGCTTTGACAGCTTTGAGTACGTCAAGACC
ATCCGCCAGCAGATCCTGGAGACGAGGGTGATCGGAACCTCAGAGACGCCCATCATCATCGTGGGCAACAAGCGGGACCTGCAGCGCGGACGCGTGATCCCGCGC
TGGAACGTGTCGCACCTGGTACGCAAGACCTGGAAGTGCGGCTACGTGGAATGCTCGGCCAAGTACAACTGGCACATCCTGCTGCTCTTCAGCGAGCTGCTCAAG
AGCGTCGGCTGCGCCCGTTGCAAGCACGTGCACGCTGCCCTGCGCTTCCAGGGCGCGCTGCGCCGCAACCGCTGCGCCATCATGTGA
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ATGGTCTCCACCTACCGGGTGGCCGTGCTGGGGGCGCGAGGTGTGGGCAAGAGTGCCATCGTGCGCCAGTTCTTGTACAACGAGTTCAGCGAGGTCTGCGTCCCC
ACCACCGCCCGCCGCCTTTACCTGCCTGCTGTCGTCATGAACGGCCACGTGCACGACCTCCAGATCCTCGACTTTCCACCCATCAGCGCCTTCCCTGTCAATACG
CTCCAGGAGTGGGCAGACACCTGCTGCAGGGGACTCCGGAGTGTCCACGCCTACATCCTGGTCTACGACATCTGCTGCTTTGACAGCTTTGAGTACGTCAAGACC
ATCCGCCAGCAGATCCTGGAGACGAGGGTGATCGGAACCTCAGAGACGCCCATCATCATCGTGGGCAACAAGCGGGACCTGCAGCGCGGACGCGTGATCCCGCGC
TGGAACGTGTCGCACCTGGTACGCAAGACCTGGAAGTGCGGCTACGTGGAATGCTCGGCCAAGTACAACTGGCACATCCTGCTGCTCTTCAGCGAGCTGCTCAAG
AGCGTCGGCTGCGCCCGTTGCAAGCACGTGCACGCTGCCCTGCGCTTCCAGGGCGCGCTGCGCCGCAACCGCTGCGCCATCATGTGA
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>RASL10B|91608|protein
MVSTYRVAVLGARGVGKSAIVRQFLYNEFSEVCVPTTARRLYLPAVVMNGHVHDLQILDFPPISAFPVNTLQEWADTCCRGLRSVHAYILVYDICCFDSFEYVKT
IRQQILETRVIGTSETPIIIVGNKRDLQRGRVIPRWNVSHLVRKTWKCGYVECSAKYNWHILLLFSELLKSVGCARCKHVHAALRFQGALRRNRCAIM
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MVSTYRVAVLGARGVGKSAIVRQFLYNEFSEVCVPTTARRLYLPAVVMNGHVHDLQILDFPPISAFPVNTLQEWADTCCRGLRSVHAYILVYDICCFDSFEYVKT
IRQQILETRVIGTSETPIIIVGNKRDLQRGRVIPRWNVSHLVRKTWKCGYVECSAKYNWHILLLFSELLKSVGCARCKHVHAALRFQGALRRNRCAIM
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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) | 2 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 2 (2) |
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
Microarray Studies: 2
Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
---|---|---|---|---|---|---|---|---|---|---|---|---|
Nishimura, 2007_1 | America | lymphoblastoid cell lines | 8 (-) | autism with FMR1-FM | autism | 15 (-) |
0.88 | Down | 0.000000012 | |||
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Nishimura, 2007_2 | America | lymphoblastoid cell lines | 7 (-) | autism with dup(15q) | autism | 15 (-) |
0.84 | Down | 0.000000012 | |||
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Proteomics Studies:0
Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
---|---|---|---|---|---|---|---|---|---|
No Evidence. |
NGS de novo Mutation Studies Top
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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