Evidence Details for FAM101B
Basic Information Top
| Gene Symbol: | FAM101B ( MGC45871 ) |
|---|---|
| Gene Full Name: | family with sequence similarity 101, member B |
| Band: | 17p13 |
| Quick Links | Entrez ID:359845; OMIM: NA; Uniprot ID:F101B_HUMAN; ENSEMBL ID: ENSG00000183688; HGNC ID: |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>FAM101B|359845|nucleotide
ATGGTGGGCCGGCTGAGCCTACAGGATGTGCCCGAGCTCGTGGACGCGAAGAAGAAGGGCGACGGCGTCCTGGACAGCCCGGACTCGGGGCTGCCCCCCAGCCCC
AGCCCCAGCCACTGGGGGCTCGCGGCGGGCGGAGGCGGCGGAGAGCGCGCGGCGGCACCGGGGACGCTGGAGCCCGACGCGGCGGCGGCGACCCCCGCGGCTCCG
AGTCCAGCGTCTCTCCCCCTGGCTCCCGGCTGTGCGCTGAGGCTTTGTCCCCTGTCCTTTGGCGAAGGAGTGGAGTTTGACCCCTTACCACCAAAGGAAGTAAGG
TACACCTCCTTGGTCAAGTACGACTCCGAGAGGCACTTCATCGACGACGTGCAGCTGCCCCTGGGCCTGGCGGTGGCCTCCTGCAGCCAGACGGTCACCTGTGTC
CCCAATGGCACGTGGCGCAACTACAAGGCCGAGGTGCGCTTCGAGCCACGCCACAGGCCCACCCGCTTCCTCAGTACCACCATCGTGTACCCCAAGTACCCCAAG
GCCGTCTACACCACCACCCTGGATTACAACTGCCGCAAGACGCTGAGGAGGTTTCTGTCCAGCGTGGAGCTCGAAGCCGCGGAGCTCCCGGGCAGCGACGACCTC
TCTGATGAATGCTGA
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ATGGTGGGCCGGCTGAGCCTACAGGATGTGCCCGAGCTCGTGGACGCGAAGAAGAAGGGCGACGGCGTCCTGGACAGCCCGGACTCGGGGCTGCCCCCCAGCCCC
AGCCCCAGCCACTGGGGGCTCGCGGCGGGCGGAGGCGGCGGAGAGCGCGCGGCGGCACCGGGGACGCTGGAGCCCGACGCGGCGGCGGCGACCCCCGCGGCTCCG
AGTCCAGCGTCTCTCCCCCTGGCTCCCGGCTGTGCGCTGAGGCTTTGTCCCCTGTCCTTTGGCGAAGGAGTGGAGTTTGACCCCTTACCACCAAAGGAAGTAAGG
TACACCTCCTTGGTCAAGTACGACTCCGAGAGGCACTTCATCGACGACGTGCAGCTGCCCCTGGGCCTGGCGGTGGCCTCCTGCAGCCAGACGGTCACCTGTGTC
CCCAATGGCACGTGGCGCAACTACAAGGCCGAGGTGCGCTTCGAGCCACGCCACAGGCCCACCCGCTTCCTCAGTACCACCATCGTGTACCCCAAGTACCCCAAG
GCCGTCTACACCACCACCCTGGATTACAACTGCCGCAAGACGCTGAGGAGGTTTCTGTCCAGCGTGGAGCTCGAAGCCGCGGAGCTCCCGGGCAGCGACGACCTC
TCTGATGAATGCTGA
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>FAM101B|359845|protein
MVGRLSLQDVPELVDAKKKGDGVLDSPDSGLPPSPSPSHWGLAAGGGGGERAAAPGTLEPDAAAATPAAPSPASLPLAPGCALRLCPLSFGEGVEFDPLPPKEVR
YTSLVKYDSERHFIDDVQLPLGLAVASCSQTVTCVPNGTWRNYKAEVRFEPRHRPTRFLSTTIVYPKYPKAVYTTTLDYNCRKTLRRFLSSVELEAAELPGSDDL
SDEC
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MVGRLSLQDVPELVDAKKKGDGVLDSPDSGLPPSPSPSHWGLAAGGGGGERAAAPGTLEPDAAAATPAAPSPASLPLAPGCALRLCPLSFGEGVEFDPLPPKEVR
YTSLVKYDSERHFIDDVQLPLGLAVASCSQTVTCVPNGTWRNYKAEVRFEPRHRPTRFLSTTIVYPKYPKAVYTTTLDYNCRKTLRRFLSSVELEAAELPGSDDL
SDEC
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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) | 1 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 3 (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 |
| Bremer, 2011 | - | aCGH |  | | ASD | - | - | - | - | 223 | - | 223 |
Linkage Studies TopLow Scale Association Studies (by Ethnic Group) TopLarge Scale Expression Studies Top Microarray Studies: 1
| Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ghahramani Seno, 2010_1 | Unknown | lymphoblastoid cell-line | 20 (35.00%) | | | - | AD | 22 (13.64%) |
1.22 | Up | 0.0157 | |
| ||||||||||||
Proteomics Studies:0
| Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
|---|---|---|---|---|---|---|---|---|---|
| No Evidence. | |||||||||
NGS de novo Mutation Studies TopNGS Mosaic SNV Studies TopNGS Other Studies Top Low Scale Gene Studies TopContact Us if you are an author of a study regarding this gene and do not find your study in this table or find errors in the representation of your study details.