Evidence Details for MANBA
Basic Information Top
Gene Symbol: | MANBA ( MANB1 ) |
---|---|
Gene Full Name: | mannosidase, beta A, lysosomal |
Band: | 4q24 |
Quick Links | Entrez ID:4126; OMIM: 609489; Uniprot ID:MANBA_HUMAN; ENSEMBL ID: ENSG00000109323; HGNC ID: 6831 |
Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>MANBA|4126|nucleotide
ATGCGCCTCCACCTGCTCCTGCTGCTCGCGCTGTGCGGTGCAGGCACCACCGCCGCGGAGCTCAGTTACAGCTTGCGTGGCAACTGGAGCATCTGCAATGGGAAC
GGCTCGCTGGAGCTGCCCGGGGCGGTCCCTGGCTGCGTGCACAGCGCCTTGTTCCAGCAGGGCCTGATCCAGGATTCTTACTACAGATTTAATGACCTTAACTAC
AGATGGGTCTCTTTGGATAACTGGACCTATAGCAAAGAATTTAAAATCCCCTTTGAAATTAGCAAATGGCAAAAAGTAAATTTGATTCTTGAGGGAGTGGATACG
GTTTCAAAAATCCTGTTCAATGAAGTCACTATTGGGGAAACAGACAATATGTTCAATAGATATAGCTTTGATATTACCAACGTGGTCAGGGACGTGAACTCCATT
GAGCTGCGTTTCCAGTCAGCGGTGTTGTATGCAGCACAGCAGAGCAAAGCTCACACTCGCTACCAGGTTCCCCCAGACTGCCCTCCACTTGTGCAGAAGGGTGAA
TGCCATGTCAACTTTGTTCGGAAGGAGCAATGTTCCTTTAGTTGGGACTGGGGGCCTTCCTTTCCTACCCAGGGAATCTGGAAAGATGTTAGAATTGAAGCCTAT
AATATTTGTCACCTGAACTACTTCACATTTTCCCCAATATATGATAAGAGTGCCCAGGAGTGGAATCTGGAAATAGAGTCTACATTTGATGTTGTCAGCTCAAAG
CCAGTTGGTGGTCAAGTGATCGTAGCCATCCCTAAGTTGCAAACACAACAGACATACAGCATTGAACTTCAACCTGGGAAAAGGATTGTTGAGCTATTTGTGAAC
ATTAGCAAGAATATTACTGTAGAAACTTGGTGGCCTCATGGACATGGAAACCAGACTGGGTACAACATGACTGTTCTTTTTGAACTGGATGGAGGCTTAAATATT
GAAAAATCAGCTAAGGTTTATTTTAGGACAGTGGAACTTATAGAAGAGCCTATAAAAGGGTCTCCTGGTTTGAGTTTCTATTTCAAAATTAATGGATTTCCCATA
TTTCTAAAAGGCTCAAACTGGATCCCAGCAGATTCATTCCAGGACCGAGTAACCTCTGAGTTGTTACGGCTCCTTTTACAGTCTGTTGTGGATGCTAATATGAAT
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ATGCGCCTCCACCTGCTCCTGCTGCTCGCGCTGTGCGGTGCAGGCACCACCGCCGCGGAGCTCAGTTACAGCTTGCGTGGCAACTGGAGCATCTGCAATGGGAAC
GGCTCGCTGGAGCTGCCCGGGGCGGTCCCTGGCTGCGTGCACAGCGCCTTGTTCCAGCAGGGCCTGATCCAGGATTCTTACTACAGATTTAATGACCTTAACTAC
AGATGGGTCTCTTTGGATAACTGGACCTATAGCAAAGAATTTAAAATCCCCTTTGAAATTAGCAAATGGCAAAAAGTAAATTTGATTCTTGAGGGAGTGGATACG
GTTTCAAAAATCCTGTTCAATGAAGTCACTATTGGGGAAACAGACAATATGTTCAATAGATATAGCTTTGATATTACCAACGTGGTCAGGGACGTGAACTCCATT
GAGCTGCGTTTCCAGTCAGCGGTGTTGTATGCAGCACAGCAGAGCAAAGCTCACACTCGCTACCAGGTTCCCCCAGACTGCCCTCCACTTGTGCAGAAGGGTGAA
TGCCATGTCAACTTTGTTCGGAAGGAGCAATGTTCCTTTAGTTGGGACTGGGGGCCTTCCTTTCCTACCCAGGGAATCTGGAAAGATGTTAGAATTGAAGCCTAT
AATATTTGTCACCTGAACTACTTCACATTTTCCCCAATATATGATAAGAGTGCCCAGGAGTGGAATCTGGAAATAGAGTCTACATTTGATGTTGTCAGCTCAAAG
CCAGTTGGTGGTCAAGTGATCGTAGCCATCCCTAAGTTGCAAACACAACAGACATACAGCATTGAACTTCAACCTGGGAAAAGGATTGTTGAGCTATTTGTGAAC
ATTAGCAAGAATATTACTGTAGAAACTTGGTGGCCTCATGGACATGGAAACCAGACTGGGTACAACATGACTGTTCTTTTTGAACTGGATGGAGGCTTAAATATT
GAAAAATCAGCTAAGGTTTATTTTAGGACAGTGGAACTTATAGAAGAGCCTATAAAAGGGTCTCCTGGTTTGAGTTTCTATTTCAAAATTAATGGATTTCCCATA
TTTCTAAAAGGCTCAAACTGGATCCCAGCAGATTCATTCCAGGACCGAGTAACCTCTGAGTTGTTACGGCTCCTTTTACAGTCTGTTGTGGATGCTAATATGAAT
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>MANBA|4126|protein
MRLHLLLLLALCGAGTTAAELSYSLRGNWSICNGNGSLELPGAVPGCVHSALFQQGLIQDSYYRFNDLNYRWVSLDNWTYSKEFKIPFEISKWQKVNLILEGVDT
VSKILFNEVTIGETDNMFNRYSFDITNVVRDVNSIELRFQSAVLYAAQQSKAHTRYQVPPDCPPLVQKGECHVNFVRKEQCSFSWDWGPSFPTQGIWKDVRIEAY
NICHLNYFTFSPIYDKSAQEWNLEIESTFDVVSSKPVGGQVIVAIPKLQTQQTYSIELQPGKRIVELFVNISKNITVETWWPHGHGNQTGYNMTVLFELDGGLNI
EKSAKVYFRTVELIEEPIKGSPGLSFYFKINGFPIFLKGSNWIPADSFQDRVTSELLRLLLQSVVDANMNTLRVWGGGIYEQDEFYELCDELGIMVWQDFMFACA
LYPTDQGFLDSVTAEVAYQIKRLKSHPSIIIWSGNNENEEALMMNWYHISFTDRPIYIKDYVTLYVKNIRELVLAGDKSRPFITSSPTNGAETVAEAWVSQNPNS
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MRLHLLLLLALCGAGTTAAELSYSLRGNWSICNGNGSLELPGAVPGCVHSALFQQGLIQDSYYRFNDLNYRWVSLDNWTYSKEFKIPFEISKWQKVNLILEGVDT
VSKILFNEVTIGETDNMFNRYSFDITNVVRDVNSIELRFQSAVLYAAQQSKAHTRYQVPPDCPPLVQKGECHVNFVRKEQCSFSWDWGPSFPTQGIWKDVRIEAY
NICHLNYFTFSPIYDKSAQEWNLEIESTFDVVSSKPVGGQVIVAIPKLQTQQTYSIELQPGKRIVELFVNISKNITVETWWPHGHGNQTGYNMTVLFELDGGLNI
EKSAKVYFRTVELIEEPIKGSPGLSFYFKINGFPIFLKGSNWIPADSFQDRVTSELLRLLLQSVVDANMNTLRVWGGGIYEQDEFYELCDELGIMVWQDFMFACA
LYPTDQGFLDSVTAEVAYQIKRLKSHPSIIIWSGNNENEEALMMNWYHISFTDRPIYIKDYVTLYVKNIRELVLAGDKSRPFITSSPTNGAETVAEAWVSQNPNS
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Evidence summary Top
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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 (2) | 0 (0) | 0 (0) | 1 (2) | 0 (0) | 0 (0) | 0 (0) | 12 (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 | ||||||
Jacquemont, 2006 | France | aCGH | ASD | - | - | - | - | 29 | - | 29 |
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 | - | - | - | - | ||
Ylisaukko-oja, 2006 | USA, Finland | microsatellite-based genomic screen | ASD | 314 | - | 314 | - | - | - | - |
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 |
---|---|---|---|---|
De Rubeis S, 2014 | 2270 | - | 1702 | Synaptic, transcriptional and chromatin genes disrupted in autism |
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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