Evidence Details for LCN10
Basic Information Top
Gene Symbol: | LCN10 ( - ) |
---|---|
Gene Full Name: | lipocalin 10 |
Band: | 9q34.3 |
Quick Links | Entrez ID:414332; OMIM: 612904; Uniprot ID:LCN10_HUMAN; ENSEMBL ID: ENSG00000187922; HGNC ID: 20892 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>LCN10|414332|nucleotide
ATGAGGCAGGGGCTGCTGGTGCTGGCGCTGGTGCTGGTGCTGGTGCTAGTGCTGGCTGCAGGGTCCCAGGTGCAGGAGTGGTACCCCAGGGAGTCCCACGCCCTC
AACTGGAACAAGTTTTCAGGGTTCTGGTACATTCTGGCCACTGCCACTGATGCCCAGGGATTCTTGCCGGCCAGGGACAAGAGGAAGCTGGGGGCGTCCGTGGTA
AAGGTGAACAAAGTGGGCCAGCTCCGCGTGCTCCTCGCCTTCAGACGGTTGAAGGGGTGCCAGTCCCAGGAGGTGATCCTGAGGAAAGACGGGAAGAAGCCGGTG
TTTGGGAACGCCTGTGCATACGCGGCGGGCCCGAGGGAAGGACAGGAGGGAGTGAAAGGGGTGAAGGCCTTCCACGTGCTGTCCACTGACTACAGCTACGGCTTG
GTCTACCTCCGCCTGGGGCGTGCAACCCAAAACTACAAGAACCTGCTGCTCTTCCATAGGCAGAATGTTTCGAGCTTCCAGAGTCTGAAGGAATTCATGGACGCT
TGTGACATTCTGGGGCTCTCCAAGGCCGCCGTCATCCTCCCGAAAGACGCGTCCCGTACACACACCATCCTGCCATGA
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ATGAGGCAGGGGCTGCTGGTGCTGGCGCTGGTGCTGGTGCTGGTGCTAGTGCTGGCTGCAGGGTCCCAGGTGCAGGAGTGGTACCCCAGGGAGTCCCACGCCCTC
AACTGGAACAAGTTTTCAGGGTTCTGGTACATTCTGGCCACTGCCACTGATGCCCAGGGATTCTTGCCGGCCAGGGACAAGAGGAAGCTGGGGGCGTCCGTGGTA
AAGGTGAACAAAGTGGGCCAGCTCCGCGTGCTCCTCGCCTTCAGACGGTTGAAGGGGTGCCAGTCCCAGGAGGTGATCCTGAGGAAAGACGGGAAGAAGCCGGTG
TTTGGGAACGCCTGTGCATACGCGGCGGGCCCGAGGGAAGGACAGGAGGGAGTGAAAGGGGTGAAGGCCTTCCACGTGCTGTCCACTGACTACAGCTACGGCTTG
GTCTACCTCCGCCTGGGGCGTGCAACCCAAAACTACAAGAACCTGCTGCTCTTCCATAGGCAGAATGTTTCGAGCTTCCAGAGTCTGAAGGAATTCATGGACGCT
TGTGACATTCTGGGGCTCTCCAAGGCCGCCGTCATCCTCCCGAAAGACGCGTCCCGTACACACACCATCCTGCCATGA
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>LCN10|414332|protein
MRQGLLVLALVLVLVLVLAAGSQVQEWYPRESHALNWNKFSGFWYILATATDAQGFLPARDKRKLGASVVKVNKVGQLRVLLAFRRLKGCQSQEVILRKDGKKPV
FGNACAYAAGPREGQEGVKGVKAFHVLSTDYSYGLVYLRLGRATQNYKNLLLFHRQNVSSFQSLKEFMDACDILGLSKAAVILPKDASRTHTILP
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MRQGLLVLALVLVLVLVLAAGSQVQEWYPRESHALNWNKFSGFWYILATATDAQGFLPARDKRKLGASVVKVNKVGQLRVLLAFRRLKGCQSQEVILRKDGKKPV
FGNACAYAAGPREGQEGVKGVKAFHVLSTDYSYGLVYLRLGRATQNYKNLLLFHRQNVSSFQSLKEFMDACDILGLSKAAVILPKDASRTHTILP
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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 (2) | 1 (3) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 2 (6) |
Syndromic Autism Gene Top
Genome-Wide Association Studies(By Ethnic Group) Top
CNV Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Gregory, 2009 | USA | aCGH | ASD | - | - | - | - | 119 | 54 | 173 | ||
Pinto, 2010 | - | SNP microarray, qPCR | ASD | - | - | - | - | 996 | 1287 | 2283 |
Linkage Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Monaco, 2001 | - | microsatellite-based genomic screen | PDD | 152 | - | 152 | - | - | - | - | ||
Buxbaum, 2001 | USA | microsatellite-based genomic screen | autism, PDD, Asperger syndrome | 35 | - | 35 | - | - | - | - | ||
Lamb, 2005 | - | microsatellite-based genomic screen | autism | 207 | - | 207 | - | 420 | - | - |
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 |
---|---|---|---|---|
Sanders SJ, 2012 | - | 238 | 172 | De novo mutations revealed by whole-exome sequencing are strongly associated with autism. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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