Evidence Details for MYO16
Basic Information Top
| Gene Symbol: | MYO16 ( KIAA0865,MYR8,Myo16b ) |
|---|---|
| Gene Full Name: | myosin XVI |
| Band: | 13q33.3 |
| Quick Links | Entrez ID:23026; OMIM: NA; Uniprot ID:MYO16_HUMAN; ENSEMBL ID: ENSG00000041515; HGNC ID: 29822 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>MYO16|23026|nucleotide
ATGTCTCACTATCATTTTATCAAGTGCTGTTGCTTTCAGCTATGTAACGTTTTTCGATCCCATGAGATGGAAATCGACCAGTGCTTGCTAGAGTCCCTTCCCCTT
GGCCAACGGCAGCGTCTAGTGAAGCGCATGCGCTGTGAGCAAATCAAAGCCTACTATGAGCGCGAGAAGGCTTTTCAGAAGCAGGAAGGGTTCCTGAAAAGGCTG
AAGCATGCGAAGAATCCGAAAGTTCACTTCAACCTCACGGACATGCTACAGGACGCGATTATCCACCACAATGACAAAGAAGTGCTTCGGCTCCTGAAGGAGGGG
GCAGACCCCCACACCCTCGTCTCCTCGGGAGGGTCCCTGCTCCATCTGTGTGCTCGGTATGATAATGCCTTCATTGCAGAAATTCTGATTGACAGAGGAGTCAAC
GTCAACCACCAGGATGAAGACTTCTGGACGCCCATGCACATTGCCTGTGCCTGCGATAACCCTGATATTGTCCTGCTTCTTGTATTAGCTGGAGCCAATGTCCTT
CTCCAGGATGTGAATGGAAATATCCCATTAGATTATGCTGTAGAAGGGACAGAATCCAGCTCTATCCTGTTGACCTATCTGGATGAAAATGGAGTGGATTTGACC
TCACTGCGCCAGATGAAGCTTCAGAGACCAATGAGTATGTTAACAGATGTCAAACACTTCTTATCATCTGGAGGAAATGTCAATGAGAAAAACGATGAAGGAGTA
ACCCTGTTACACATGGCGTGTGCGAGTGGCTACAAGGAGGTGGTGTCTCTTATCCTGGAACATGGTGGAGACCTCAACATAGTAGATGATCAGTACTGGACTCCC
CTCCACTTGGCAGCCAAATATGGCCAGACAAATCTGGTGAAACTTCTCCTGATGCATCAGGCAAACCCACACCTCGTGAACTGTAATGAGGAGAAGGCGTCAGAT
ATTGCTGCCTCTGAGTTTATTGAGGAAATGCTGCTGAAAGCCGAAATTGCCTGGGAAGAAAAAATGAAAGAGCCTTTATCTGCTTCTACCTTAGCTCAAGAAGAG
CCCTATGAAGAGATCATTCACGATCTTCCCGTACTGTCGAGTAAGCTCAGTCCCCTGGTGTTACCAATTGCCAAGCAAGACAGTTTGTTGGAAAAAGACATTATG
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ATGTCTCACTATCATTTTATCAAGTGCTGTTGCTTTCAGCTATGTAACGTTTTTCGATCCCATGAGATGGAAATCGACCAGTGCTTGCTAGAGTCCCTTCCCCTT
GGCCAACGGCAGCGTCTAGTGAAGCGCATGCGCTGTGAGCAAATCAAAGCCTACTATGAGCGCGAGAAGGCTTTTCAGAAGCAGGAAGGGTTCCTGAAAAGGCTG
AAGCATGCGAAGAATCCGAAAGTTCACTTCAACCTCACGGACATGCTACAGGACGCGATTATCCACCACAATGACAAAGAAGTGCTTCGGCTCCTGAAGGAGGGG
GCAGACCCCCACACCCTCGTCTCCTCGGGAGGGTCCCTGCTCCATCTGTGTGCTCGGTATGATAATGCCTTCATTGCAGAAATTCTGATTGACAGAGGAGTCAAC
GTCAACCACCAGGATGAAGACTTCTGGACGCCCATGCACATTGCCTGTGCCTGCGATAACCCTGATATTGTCCTGCTTCTTGTATTAGCTGGAGCCAATGTCCTT
CTCCAGGATGTGAATGGAAATATCCCATTAGATTATGCTGTAGAAGGGACAGAATCCAGCTCTATCCTGTTGACCTATCTGGATGAAAATGGAGTGGATTTGACC
TCACTGCGCCAGATGAAGCTTCAGAGACCAATGAGTATGTTAACAGATGTCAAACACTTCTTATCATCTGGAGGAAATGTCAATGAGAAAAACGATGAAGGAGTA
ACCCTGTTACACATGGCGTGTGCGAGTGGCTACAAGGAGGTGGTGTCTCTTATCCTGGAACATGGTGGAGACCTCAACATAGTAGATGATCAGTACTGGACTCCC
CTCCACTTGGCAGCCAAATATGGCCAGACAAATCTGGTGAAACTTCTCCTGATGCATCAGGCAAACCCACACCTCGTGAACTGTAATGAGGAGAAGGCGTCAGAT
ATTGCTGCCTCTGAGTTTATTGAGGAAATGCTGCTGAAAGCCGAAATTGCCTGGGAAGAAAAAATGAAAGAGCCTTTATCTGCTTCTACCTTAGCTCAAGAAGAG
CCCTATGAAGAGATCATTCACGATCTTCCCGTACTGTCGAGTAAGCTCAGTCCCCTGGTGTTACCAATTGCCAAGCAAGACAGTTTGTTGGAAAAAGACATTATG
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>MYO16|23026|protein
MSHYHFIKCCCFQLCNVFRSHEMEIDQCLLESLPLGQRQRLVKRMRCEQIKAYYEREKAFQKQEGFLKRLKHAKNPKVHFNLTDMLQDAIIHHNDKEVLRLLKEG
ADPHTLVSSGGSLLHLCARYDNAFIAEILIDRGVNVNHQDEDFWTPMHIACACDNPDIVLLLVLAGANVLLQDVNGNIPLDYAVEGTESSSILLTYLDENGVDLT
SLRQMKLQRPMSMLTDVKHFLSSGGNVNEKNDEGVTLLHMACASGYKEVVSLILEHGGDLNIVDDQYWTPLHLAAKYGQTNLVKLLLMHQANPHLVNCNEEKASD
IAASEFIEEMLLKAEIAWEEKMKEPLSASTLAQEEPYEEIIHDLPVLSSKLSPLVLPIAKQDSLLEKDIMFKDATKGLCKQQSQDSIPENPMMSGSTKPEQVKLM
PPAPNDDLATLSELNDGSLLYEIQKRFGNNQIYTFIGDILLLVNPYKELPIYSSMVSQLYFSSSGKLCSSLPPHLFSCVERAFHQLFREQRPQCFILSGERGSGK
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MSHYHFIKCCCFQLCNVFRSHEMEIDQCLLESLPLGQRQRLVKRMRCEQIKAYYEREKAFQKQEGFLKRLKHAKNPKVHFNLTDMLQDAIIHHNDKEVLRLLKEG
ADPHTLVSSGGSLLHLCARYDNAFIAEILIDRGVNVNHQDEDFWTPMHIACACDNPDIVLLLVLAGANVLLQDVNGNIPLDYAVEGTESSSILLTYLDENGVDLT
SLRQMKLQRPMSMLTDVKHFLSSGGNVNEKNDEGVTLLHMACASGYKEVVSLILEHGGDLNIVDDQYWTPLHLAAKYGQTNLVKLLLMHQANPHLVNCNEEKASD
IAASEFIEEMLLKAEIAWEEKMKEPLSASTLAQEEPYEEIIHDLPVLSSKLSPLVLPIAKQDSLLEKDIMFKDATKGLCKQQSQDSIPENPMMSGSTKPEQVKLM
PPAPNDDLATLSELNDGSLLYEIQKRFGNNQIYTFIGDILLLVNPYKELPIYSSMVSQLYFSSSGKLCSSLPPHLFSCVERAFHQLFREQRPQCFILSGERGSGK
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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 | 2 (3) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 8 (4) |
Syndromic Autism Gene TopGenome-Wide Association Studies (By Ethnic Group) Top Family Based Association Studies: 2
| Reference | Stage | Platform | #Families | Affecteds | Result | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ (range) |
||||||
| CAUCASIAN | |||||||||||
| Wang, 2009_1 | Discovery | Illumina HumanHap550 BeadChip | 780 | 1299 (-) |  | | ASD | - - |
- - | ||
| Hussman, 2011_1 | Discovery | Illumina Infinium Human 1 M beadship | 597 | - (-) | |  | ASD | - - |
- - | ||
Case Control Based Association Studies: 1
| Reference | Stage | Platform | ASD Cases | Normal Controls | Result | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ | #Subjects (% Women) |
Age (range) |
|||||
| CAUCASIAN | ||||||||||||
| Wang, 2009_2 | Discovery | Illumina HumanHap550 BeadChip | 1204 (-) | | | ASD | 10.3±6.6 - |
10.9±6.7 | 6491 (-) |
8.8±5.4 - | ||
CNV Studies TopLinkage Studies TopLow Scale Association Studies (by Ethnic Group) TopLarge Scale Expression Studies TopNGS de novo Mutation Studies TopNGS Mosaic SNV Studies Top| Reference | Case Number | Family Number | Mosaic Number | Title |
|---|---|---|---|---|
| Dou Y, 2017 | - | 2361 | 230 | Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and |
NGS 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.