Evidence Details for NHLRC4
Basic Information Top
Gene Symbol: | NHLRC4 ( FLJ36208 ) |
---|---|
Gene Full Name: | NHL repeat containing 4 |
Band: | 16p13.3 |
Quick Links | Entrez ID:283948; OMIM: NA; Uniprot ID:NHLC4_HUMAN; ENSEMBL ID: ENSG00000161992; HGNC ID: 26700 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>NHLRC4|283948|nucleotide
ATGCTGGGTCTGGAGGGCCCCTGCTGGGTGGGCCCAGGGCCTGATGGGGGCCTTGCTGTGAGTGAGGAGTTTGGGGATGTGAGGCTGTTTGGCAGTGCCCGCCAA
CCCCTGGGCTCCCTGGGGGGCTGGACGGGGCACACTTTCGGCTGCCCAGCGGGCATCTGCTCCAACTCAGAGGGCAATGTTATTGTGGCAGACGAGCAGAGGCGC
CAGGTGACCCTGTTTCCCCGGGCTGGGCCACCCATCTGCCTGGTGTCAGAGGGGCTTGGGCAGCCCTTGGGAGTGGCCTGTGCACCCCAGGGCCAGCTCCTGGTG
GCTGATGCCAAGGACAACTCCATCAAGGTGTACCAGGGCCTCAAGGAGCTGGCCTGA
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ATGCTGGGTCTGGAGGGCCCCTGCTGGGTGGGCCCAGGGCCTGATGGGGGCCTTGCTGTGAGTGAGGAGTTTGGGGATGTGAGGCTGTTTGGCAGTGCCCGCCAA
CCCCTGGGCTCCCTGGGGGGCTGGACGGGGCACACTTTCGGCTGCCCAGCGGGCATCTGCTCCAACTCAGAGGGCAATGTTATTGTGGCAGACGAGCAGAGGCGC
CAGGTGACCCTGTTTCCCCGGGCTGGGCCACCCATCTGCCTGGTGTCAGAGGGGCTTGGGCAGCCCTTGGGAGTGGCCTGTGCACCCCAGGGCCAGCTCCTGGTG
GCTGATGCCAAGGACAACTCCATCAAGGTGTACCAGGGCCTCAAGGAGCTGGCCTGA
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>NHLRC4|283948|protein
MLGLEGPCWVGPGPDGGLAVSEEFGDVRLFGSARQPLGSLGGWTGHTFGCPAGICSNSEGNVIVADEQRRQVTLFPRAGPPICLVSEGLGQPLGVACAPQGQLLV
ADAKDNSIKVYQGLKELA
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MLGLEGPCWVGPGPDGGLAVSEEFGDVRLFGSARQPLGSLGGWTGHTFGCPAGICSNSEGNVIVADEQRRQVTLFPRAGPPICLVSEGLGQPLGVACAPQGQLLV
ADAKDNSIKVYQGLKELA
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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 (2) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 2 (5) |
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 | ||||||
Levy, 2011 | Simons Simplex Collection | aCGH | - | - | ASD | 915 | 915 | - | - | - | - | - |
Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
Linkage Studies Top
Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Buxbaum, 2004 | USA | microsatellite-based genomic screen | autism | 115 | - | 115 | - | - | - | - | ||
Lauritsen, 2006 | Faroe Islands | microsatellite-based genomic screen | autism | - | - | - | - | 12 | 44 | 56 |
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 |
---|---|---|---|---|
Chen R, 2017 | 107 | 116 | 128 | Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in aut |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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