Evidence Details for FAM189A1
Basic Information Top
| Gene Symbol: | FAM189A1 ( FLJ61121,KIAA0574,TMEM228 ) |
|---|---|
| Gene Full Name: | family with sequence similarity 189, member A1 |
| Band: | 15q13.1 |
| Quick Links | Entrez ID:23359; OMIM: NA; Uniprot ID:F1891_HUMAN; ENSEMBL ID: ENSG00000104059; HGNC ID: 29075 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>FAM189A1|23359|nucleotide
ATGCCTCCGGCCGGCGGCCCCCGAGCGCCGCGTCCCGCCGCGCTGCCCCGCAGCCTGTCCCGCCTGCGCGAGTGCCCGGGCCGCTCCCGCATCGTGCTGGCGCTC
GGGGCCACGCAGATGGCGCTCGGATGCCTCATCGTGGCAGTCAGCTTCGCCGCGCTGGCGCTCACCACCTCGGCCCGCGTCCGCCACTCCTGCCCCTTCTGGGCA
GGCTTCTCGGTGCTGCTGTCGGGACTCATAGGTGTCGTCTCCTGGAAGAGGCCTCTCTCCCTTGTGATAACCTTTTTCATGCTGCTTTCTGCAGTGTGTGTAATG
CTGAATTTGGCTGGTTCAATTCTCTCTTGTCAGAATGCTCAGCTAGTCAACTCCCTAGAAGGCTGCCAGTTGATTAAGTTTGACAGTGTGGAGGTGTGTGTCTGC
TGTGAGCTGCAGCACCAGTCGTCCGGCTGCAGCAACCTCGGGGAGACGCTGAAGCTGAACCCGCTGCAGGAGAACTGCAACGCTGTGAGGCTGACCTTGAAGGAT
CTCCTCTTCAGCGTGTGTGCCCTCAACGTCCTGTCCACTATCGTGTGTGCGCTGGCCACAGCCATGTGCTGTATGCAGATGGTCTCCTCCGATGTCCTGCAGATG
TTCCTTCCGCAGAGGTCACATCCTGCCAACCCCACCTGCGTGACTCCTCACGGCACCGTTCTCCACCAGACCCTGGATTTCGACGAGTTCATCCCCCCACTCCCG
CCTCCACCCTATTACCCCCCAGAGTACACCTGCACACCGTCCACTGAGGCCCAGAGGGGCCTCCACCTGGACTTTGCTCCGTCTCCATTCGGCACTTTGTATGAC
GTGGCCATCAATAGCCCCGGCCTGCTCTATCCTGCTGAGCTCCCCCCTCCGTACGAGGCGGTGGTGGGCCAGCCCCCTGCCAGCCAGGTTACAAGTATAGGTCAG
CAGGTGGCCGAGTCCAGCTCCGGGGACCCAAACACCAGTGCTGGCTTCAGCACTCCAGTACCAGCTGACAGCACAAGCCTCCTGGTGTCCGAGGGCACTGCTACG
CCAGGTTCCAGCCCATCCCCCGATGGCCCTGTGGGCGCCCCAGCACCCTCCGAACCTGCCCTTCCCCCTGGCCATGTGTCTCCAGAGGATCCTGGCATGGGCTCA
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ATGCCTCCGGCCGGCGGCCCCCGAGCGCCGCGTCCCGCCGCGCTGCCCCGCAGCCTGTCCCGCCTGCGCGAGTGCCCGGGCCGCTCCCGCATCGTGCTGGCGCTC
GGGGCCACGCAGATGGCGCTCGGATGCCTCATCGTGGCAGTCAGCTTCGCCGCGCTGGCGCTCACCACCTCGGCCCGCGTCCGCCACTCCTGCCCCTTCTGGGCA
GGCTTCTCGGTGCTGCTGTCGGGACTCATAGGTGTCGTCTCCTGGAAGAGGCCTCTCTCCCTTGTGATAACCTTTTTCATGCTGCTTTCTGCAGTGTGTGTAATG
CTGAATTTGGCTGGTTCAATTCTCTCTTGTCAGAATGCTCAGCTAGTCAACTCCCTAGAAGGCTGCCAGTTGATTAAGTTTGACAGTGTGGAGGTGTGTGTCTGC
TGTGAGCTGCAGCACCAGTCGTCCGGCTGCAGCAACCTCGGGGAGACGCTGAAGCTGAACCCGCTGCAGGAGAACTGCAACGCTGTGAGGCTGACCTTGAAGGAT
CTCCTCTTCAGCGTGTGTGCCCTCAACGTCCTGTCCACTATCGTGTGTGCGCTGGCCACAGCCATGTGCTGTATGCAGATGGTCTCCTCCGATGTCCTGCAGATG
TTCCTTCCGCAGAGGTCACATCCTGCCAACCCCACCTGCGTGACTCCTCACGGCACCGTTCTCCACCAGACCCTGGATTTCGACGAGTTCATCCCCCCACTCCCG
CCTCCACCCTATTACCCCCCAGAGTACACCTGCACACCGTCCACTGAGGCCCAGAGGGGCCTCCACCTGGACTTTGCTCCGTCTCCATTCGGCACTTTGTATGAC
GTGGCCATCAATAGCCCCGGCCTGCTCTATCCTGCTGAGCTCCCCCCTCCGTACGAGGCGGTGGTGGGCCAGCCCCCTGCCAGCCAGGTTACAAGTATAGGTCAG
CAGGTGGCCGAGTCCAGCTCCGGGGACCCAAACACCAGTGCTGGCTTCAGCACTCCAGTACCAGCTGACAGCACAAGCCTCCTGGTGTCCGAGGGCACTGCTACG
CCAGGTTCCAGCCCATCCCCCGATGGCCCTGTGGGCGCCCCAGCACCCTCCGAACCTGCCCTTCCCCCTGGCCATGTGTCTCCAGAGGATCCTGGCATGGGCTCA
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>FAM189A1|23359|protein
MPPAGGPRAPRPAALPRSLSRLRECPGRSRIVLALGATQMALGCLIVAVSFAALALTTSARVRHSCPFWAGFSVLLSGLIGVVSWKRPLSLVITFFMLLSAVCVM
LNLAGSILSCQNAQLVNSLEGCQLIKFDSVEVCVCCELQHQSSGCSNLGETLKLNPLQENCNAVRLTLKDLLFSVCALNVLSTIVCALATAMCCMQMVSSDVLQM
FLPQRSHPANPTCVTPHGTVLHQTLDFDEFIPPLPPPPYYPPEYTCTPSTEAQRGLHLDFAPSPFGTLYDVAINSPGLLYPAELPPPYEAVVGQPPASQVTSIGQ
QVAESSSGDPNTSAGFSTPVPADSTSLLVSEGTATPGSSPSPDGPVGAPAPSEPALPPGHVSPEDPGMGSQVQPGPGRVSRSTSDPTLCTSSMAGDASSHRPSCS
QDLEAGLSEAVPGSASMSRSATAACRAQLSPAGDPDTWKTDQRPTPEPFPATSKERPRSLVDSKAYADARVLVAKFLEHSHCALPTEAQHMVGAMRLAVTNEERL
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MPPAGGPRAPRPAALPRSLSRLRECPGRSRIVLALGATQMALGCLIVAVSFAALALTTSARVRHSCPFWAGFSVLLSGLIGVVSWKRPLSLVITFFMLLSAVCVM
LNLAGSILSCQNAQLVNSLEGCQLIKFDSVEVCVCCELQHQSSGCSNLGETLKLNPLQENCNAVRLTLKDLLFSVCALNVLSTIVCALATAMCCMQMVSSDVLQM
FLPQRSHPANPTCVTPHGTVLHQTLDFDEFIPPLPPPPYYPPEYTCTPSTEAQRGLHLDFAPSPFGTLYDVAINSPGLLYPAELPPPYEAVVGQPPASQVTSIGQ
QVAESSSGDPNTSAGFSTPVPADSTSLLVSEGTATPGSSPSPDGPVGAPAPSEPALPPGHVSPEDPGMGSQVQPGPGRVSRSTSDPTLCTSSMAGDASSHRPSCS
QDLEAGLSEAVPGSASMSRSATAACRAQLSPAGDPDTWKTDQRPTPEPFPATSKERPRSLVDSKAYADARVLVAKFLEHSHCALPTEAQHMVGAMRLAVTNEERL
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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) | 2 (19) | 1 (1) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 6 (21) |
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 | ||||||
| Wolpert, 2000 | - | STS mapping | ![]() | ![]() | autism | 3 | - | 3 | - | 3 | - | 3 |
| Wassink, 2001 | USA | Chromosomal analysis of G-band | ![]() | ![]() | autism | - | - | - | - | 278 | - | 278 |
| Silva, 2002 | - | FISH | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 |
| Keller, 2003 | USA | FISH | ![]() | ![]() | ASD | - | - | - | - | 2 | - | 2 |
| Mann, 2004 | - | STS mapping | ![]() | ![]() | PDD-NOS | - | - | - | - | 2 | - | 2 |
| Bolton, 2004 | UK | STS mapping | ![]() | ![]() | ASD | - | - | - | - | 181 | 40 | 221 |
| Sahoo, 2005 | USA | aCGH | ![]() | ![]() | autism | - | - | - | - | 9 | - | 9 |
| Jacquemont, 2006 | France | aCGH | ![]() | ![]() | ASD | - | - | - | - | 29 | - | 29 |
| Kwasnicka-Crawford, 2007 | - | STS mapping | ![]() | ![]() | autism | - | - | - | - | 1 | - | 1 |
| Sebat, 2007 | USA | aCGH | ![]() | ![]() | autism | 165 | 118 | 47 | 99 | 195 | 196 | 391 |
| Wassink, 2007 | USA | FISH | ![]() | ![]() | PDD | - | - | - | - | 104 | - | 104 |
| Marshall, 2008 | - | SNP microarray | ![]() | ![]() | ASD | 427 | 238 | 189 | - | 427 | 500 | 927 |
| Christian, 2008 | USA | aCGH | ![]() | ![]() | ASD | 397 | 35 | 362 | - | 397 | 372 | 769 |
| Weiss, 2008 | USA, Ireland | aCGH, SNP microarray | ![]() | ![]() | ASD | 751 | - | - | - | 2252 | 23502 | 25754 |
| Gregory, 2009 | USA | aCGH | ![]() | ![]() | ASD | - | - | - | - | 119 | 54 | 173 |
| Bremer, 2009 | - | aCGH | ![]() | ![]() | ASD | - | - | - | - | 148 | - | 148 |
| Pinto, 2010 | - | SNP microarray, qPCR | ![]() | ![]() | ASD | - | - | - | - | 996 | 1287 | 2283 |
| Sanders, 2011 | Simons Simplex Collection | SNP microarray | - | - | ASD | 1127 | 1127 | - | - | - | - | - |
| Gai, 2011 | AGRE | SNP microarray | - | - | autism | - | - | - | - | 1224 | 3801 | 5025 |
Linkage Studies Top
| Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
| Allen-Brady, 2010 | USA | SNP-based genomic screen | ![]() | ![]() | ASD | 40 | - | 40 | - | 192 | 461 | 653 |
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 |
|---|---|---|---|---|
| Yuen RK, 2016 | 200 | - | 301 | Genome-wide characteristics of de novo mutations in autism. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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