Evidence Details for FAM168B
Basic Information Top
| Gene Symbol: | FAM168B ( MGC87527 ) |
|---|---|
| Gene Full Name: | family with sequence similarity 168, member B |
| Band: | 2q21.1 |
| Quick Links | Entrez ID:130074; OMIM: NA; Uniprot ID:F168B_HUMAN; ENSEMBL ID: ENSG00000152102; HGNC ID: 27016 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>FAM168B|130074|nucleotide
ATGAATCCTGTTTATAGTCCTGGATCTTCTGGGGTTCCCTATGCAAATGCCAAAGGAATTGGTTATCCAGCTGGTTTTCCCATGGGCTATGCAGCAGCAGCTCCT
GCCTATTCTCCTAACATGTATCCTGGAGCGAATCCTACCTTCCAAACAGGTTACACTCCTGGCACACCTTACAAAGTGTCCTGTTCCCCCACCAGCGGGGCTGTG
CCACCGTACTCCTCCTCCCCGAACCCCTACCAGACTGCCGTGTACCCTGTGCGAAGTGCCTACCCCCAGCAGAGCCCGTATGCACAGCAAGGCACGTACTACACA
CAGCCGCTGTATGCAGCACCTCCTCACGTCATCCACCACACCACGGTGGTGCAGCCCAACGGCATGCCTGCAACGGTGTACCCTGCTCCCATCCCCCCTCCTAGA
GGCAACGGGGTCACCATGGGCATGGTGGCTGGGACCACCATGGCCATGTCAGCAGGTACCCTGCTGACTGCTCACTCCCCAACTCCTGTCGCCCCCCACCCGGTC
ACTGTGCCCACGTACCGGGCCCCAGGAACGCCCACTTACAGCTATGTGCCCCCTCAGTGGTGA
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ATGAATCCTGTTTATAGTCCTGGATCTTCTGGGGTTCCCTATGCAAATGCCAAAGGAATTGGTTATCCAGCTGGTTTTCCCATGGGCTATGCAGCAGCAGCTCCT
GCCTATTCTCCTAACATGTATCCTGGAGCGAATCCTACCTTCCAAACAGGTTACACTCCTGGCACACCTTACAAAGTGTCCTGTTCCCCCACCAGCGGGGCTGTG
CCACCGTACTCCTCCTCCCCGAACCCCTACCAGACTGCCGTGTACCCTGTGCGAAGTGCCTACCCCCAGCAGAGCCCGTATGCACAGCAAGGCACGTACTACACA
CAGCCGCTGTATGCAGCACCTCCTCACGTCATCCACCACACCACGGTGGTGCAGCCCAACGGCATGCCTGCAACGGTGTACCCTGCTCCCATCCCCCCTCCTAGA
GGCAACGGGGTCACCATGGGCATGGTGGCTGGGACCACCATGGCCATGTCAGCAGGTACCCTGCTGACTGCTCACTCCCCAACTCCTGTCGCCCCCCACCCGGTC
ACTGTGCCCACGTACCGGGCCCCAGGAACGCCCACTTACAGCTATGTGCCCCCTCAGTGGTGA
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>FAM168B|130074|protein
MNPVYSPGSSGVPYANAKGIGYPAGFPMGYAAAAPAYSPNMYPGANPTFQTGYTPGTPYKVSCSPTSGAVPPYSSSPNPYQTAVYPVRSAYPQQSPYAQQGTYYT
QPLYAAPPHVIHHTTVVQPNGMPATVYPAPIPPPRGNGVTMGMVAGTTMAMSAGTLLTAHSPTPVAPHPVTVPTYRAPGTPTYSYVPPQW
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MNPVYSPGSSGVPYANAKGIGYPAGFPMGYAAAAPAYSPNMYPGANPTFQTGYTPGTPYKVSCSPTSGAVPPYSSSPNPYQTAVYPVRSAYPQQSPYAQQGTYYT
QPLYAAPPHVIHHTTVVQPNGMPATVYPAPIPPPRGNGVTMGMVAGTTMAMSAGTLLTAHSPTPVAPHPVTVPTYRAPGTPTYSYVPPQW
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Evidence summary TopClick 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) | 1 (2) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 2 (3) |
Syndromic Autism Gene TopGenome-Wide Association Studies(By Ethnic Group) TopCNV Studies Top| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Zwaag, 2009 | - | SNP microarray |  | | autism | - | - | - | - | 105 | 267 | 372 |
| Pinto, 2010 | - | SNP microarray, qPCR | | | ASD | - | - | - | - | 996 | 1287 | 2283 |
Linkage Studies Top