Evidence Details for FAM157B


Gene Symbol: | FAM157B ( - ) |
---|---|
Gene Full Name: | family with sequence similarity 157, member B |
Band: | 9q34.3 |
Quick Links | Entrez ID:100132403; OMIM: NA; Uniprot ID:F157B_HUMAN; ENSEMBL ID: ; HGNC ID: 34080 |
Relate to Another Database: | SFARIGene; denovo-db |


>FAM157B|100132403|nucleotide
ATGGGGCCTTTGTTCACCACCATTCCTGGTGCCCATTCTGGTCCCATGCGTCCTCTGCCCAAGAAACACGTAGAACCCATGGCAGTGCGACAGCTGCTTCTTGGC
AACTCCACCATGATCAGGCACACTTGTCCCATGTCTGTCCCGTTGAGCCGGCAAGTCAAGGAAGTTGCTGCCCAGAAACCAAGTGAGGACATTTACAAGAACCGG
CAGCGGCGGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAACTGGATTTGCTTTTTCACCAGAGGATCCAGATTTCCCTGTGGCCTCGCAAACAAAAAAGA
AGGAAGACGGAGCAGCACAGTCATCCCTTTGTGAAAAAGGCATTCAGGTTCTCCGCCGGCCCTGGCTGCAGGCGGCCCTCATCTAACAAGATGCTTCGGTCCATG
GGTGGAGGACAAAGGCCTATGGGCTTGGGGAGCGAGTTCTTTCGTCTCCTACATGACCTTCATCTGCTCGCGTTTGCCACGAAGCGCATCTGGATCCACCGGAGG
GGCGAGGCCACAGCTCGACCGCGAGCACCTGAGCATCCTGCACCGCCTGCGACGGCCGTCAGGGGGCGCGATGCCGCCTCACAGAACCTCAAGCGGCGCCCGGGT
TCCGGCACAGACGGCCTGCGGCTCCAGGGGGCGGAGCCGAGCCGTCTCCTCAGGACCTACGCAGGAGGCGCCGTCATCCCTACAGGGACACCTGAGAGGGCCCAG
CCTCCTCCTCCTCAGGACCCACTCGGGAGACGCCGCTGGCTCTCTAGGAACACCTGGGGACCGTGGCCAGGGACGACCCAGCCTCCTTCTCCTCAGCTCCTCAGG
AACGACTGGGGAAGCTGTGGCTTCATGGTCCCCGAGGCTGCCCGAGGAAAGGTATTTCAGGACAGCCAGGAGGGGGCGCACATCCGCCGCGAAACTGTGAGCAAG
AGCGTCTGTGCTGAACCATGGCGCCACCAGAGGGCGCGCGATCCCGCCCCAACCAACTTCCCGCTGAAGTGCCAGAAGCAGCGAGGAGCTTCAACTTCCTCAGGG
CAGCACGGGGGTCGTGTTAATTTGGTGTTCTTCATTGATTCCCCAACAGTTATTGCTGTACCAGATTTGCAGTGTCCCACAAAATACTCCGGTATATTGTACTGA
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ATGGGGCCTTTGTTCACCACCATTCCTGGTGCCCATTCTGGTCCCATGCGTCCTCTGCCCAAGAAACACGTAGAACCCATGGCAGTGCGACAGCTGCTTCTTGGC
AACTCCACCATGATCAGGCACACTTGTCCCATGTCTGTCCCGTTGAGCCGGCAAGTCAAGGAAGTTGCTGCCCAGAAACCAAGTGAGGACATTTACAAGAACCGG
CAGCGGCGGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAACTGGATTTGCTTTTTCACCAGAGGATCCAGATTTCCCTGTGGCCTCGCAAACAAAAAAGA
AGGAAGACGGAGCAGCACAGTCATCCCTTTGTGAAAAAGGCATTCAGGTTCTCCGCCGGCCCTGGCTGCAGGCGGCCCTCATCTAACAAGATGCTTCGGTCCATG
GGTGGAGGACAAAGGCCTATGGGCTTGGGGAGCGAGTTCTTTCGTCTCCTACATGACCTTCATCTGCTCGCGTTTGCCACGAAGCGCATCTGGATCCACCGGAGG
GGCGAGGCCACAGCTCGACCGCGAGCACCTGAGCATCCTGCACCGCCTGCGACGGCCGTCAGGGGGCGCGATGCCGCCTCACAGAACCTCAAGCGGCGCCCGGGT
TCCGGCACAGACGGCCTGCGGCTCCAGGGGGCGGAGCCGAGCCGTCTCCTCAGGACCTACGCAGGAGGCGCCGTCATCCCTACAGGGACACCTGAGAGGGCCCAG
CCTCCTCCTCCTCAGGACCCACTCGGGAGACGCCGCTGGCTCTCTAGGAACACCTGGGGACCGTGGCCAGGGACGACCCAGCCTCCTTCTCCTCAGCTCCTCAGG
AACGACTGGGGAAGCTGTGGCTTCATGGTCCCCGAGGCTGCCCGAGGAAAGGTATTTCAGGACAGCCAGGAGGGGGCGCACATCCGCCGCGAAACTGTGAGCAAG
AGCGTCTGTGCTGAACCATGGCGCCACCAGAGGGCGCGCGATCCCGCCCCAACCAACTTCCCGCTGAAGTGCCAGAAGCAGCGAGGAGCTTCAACTTCCTCAGGG
CAGCACGGGGGTCGTGTTAATTTGGTGTTCTTCATTGATTCCCCAACAGTTATTGCTGTACCAGATTTGCAGTGTCCCACAAAATACTCCGGTATATTGTACTGA
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>FAM157B|100132403|protein
MGPLFTTIPGAHSGPMRPLPKKHVEPMAVRQLLLGNSTMIRHTCPMSVPLSRQVKEVAAQKPSEDIYKNRQRRQQQQQQQQQQQQLDLLFHQRIQISLWPRKQKR
RKTEQHSHPFVKKAFRFSAGPGCRRPSSNKMLRSMGGGQRPMGLGSEFFRLLHDLHLLAFATKRIWIHRRGEATARPRAPEHPAPPATAVRGRDAASQNLKRRPG
SGTDGLRLQGAEPSRLLRTYAGGAVIPTGTPERAQPPPPQDPLGRRRWLSRNTWGPWPGTTQPPSPQLLRNDWGSCGFMVPEAARGKVFQDSQEGAHIRRETVSK
SVCAEPWRHQRARDPAPTNFPLKCQKQRGASTSSGQHGGRVNLVFFIDSPTVIAVPDLQCPTKYSGILY
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MGPLFTTIPGAHSGPMRPLPKKHVEPMAVRQLLLGNSTMIRHTCPMSVPLSRQVKEVAAQKPSEDIYKNRQRRQQQQQQQQQQQQLDLLFHQRIQISLWPRKQKR
RKTEQHSHPFVKKAFRFSAGPGCRRPSSNKMLRSMGGGQRPMGLGSEFFRLLHDLHLLAFATKRIWIHRRGEATARPRAPEHPAPPATAVRGRDAASQNLKRRPG
SGTDGLRLQGAEPSRLLRTYAGGAVIPTGTPERAQPPPPQDPLGRRRWLSRNTWGPWPGTTQPPSPQLLRNDWGSCGFMVPEAARGKVFQDSQEGAHIRRETVSK
SVCAEPWRHQRARDPAPTNFPLKCQKQRGASTSSGQHGGRVNLVFFIDSPTVIAVPDLQCPTKYSGILY
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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 (1) | 1 (3) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 2 (4) |






Reference | Source | Method | ADI-R | ADOS | Diagnosis | Family | Individual | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Total | Simplex | Multiplex | Control | Affected | Control | Total | ||||||
Gregory, 2009 | USA | aCGH | ![]() | ![]() | ASD | - | - | - | - | 119 | 54 | 173 |


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 | - | - |












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