Evidence Details for COL19A1


Gene Symbol: | COL19A1 ( COL9A1L,D6S228E ) |
---|---|
Gene Full Name: | collagen, type XIX, alpha 1 |
Band: | 6q13 |
Quick Links | Entrez ID:1310; OMIM: 120165; Uniprot ID:COJA1_HUMAN; ENSEMBL ID: ENSG00000082293; HGNC ID: 2196 |
Relate to Another Database: | SFARIGene; denovo-db |


>COL19A1|1310|nucleotide
ATGAGACTCACTGGCCCTTGGAAACTTTGGCTTTGGATGTCAATATTTCTGCTTCCTGCTTCCACTTCCGTGACCGTTAGGGACAAGACAGAAGAGTCATGCCCT
ATCCTGAGAATAGAGGGACATCAGCTGACATATGACAACATAAACAAACTTGAAGTTTCAGGTTTTGATCTAGGAGACAGCTTTTCTCTAAGACGTGCATTTTGT
GAAAGTGATAAAACCTGTTTCAAATTGGGAAGTGCACTTCTTATTAGAGACACTATTAAGATATTTCCCAAAGGCCTTCCTGAGGAGTACTCAGTAGCTGCCATG
TTTCGAGTACGAAGAAACGCCAAAAAGGAACGGTGGTTTCTGTGGCAGGTTTTAAACCAGCAGAATATTCCACAGATTTCTATAGTAGTTGATGGTGGAAAGAAG
GTGGTGGAATTTATGTTTCAAGCCACAGAGGGAGATGTGTTGAACTACATTTTTAGAAATCGAGAACTCCGTCCTTTGTTTGATCGTCAGTGGCACAAACTTGGC
ATTAGTATACAATCCCAGGTCATTTCACTTTATATGGATTGTAATTTAATTGCGAGGAGGCAGACTGATGAAAAGGACACTGTGGATTTCCATGGACGGACAGTT
ATTGCTACGCGAGCTTCAGATGGCAAGCCTGTGGATATTGAACTTCACCAACTTAAAATCTACTGCAGTGCAAACCTCATAGCTCAAGAAACATGTTGTGAAATA
TCAGATACTAAGTGCCCAGAGCAGGATGGCTTTGGAAATATTGCATCATCATGGGTAACTGCTCATGCCAGTAAAATGTCTTCATATCTGCCAGCAAAGCAGGAA
CTTAAAGACCAGTGCCAGTGCATTCCAAACAAGGGAGAAGCAGGATTACCAGGAGCTCCGGGTTCACCTGGGCAGAAAGGGCATAAAGGAGAGCCGGGTGAAAAT
GGTTTACATGGTGCTCCAGGATTCCCTGGTCAAAAGGGAGAGCAAGGTTTTGAAGGCAGCAAAGGAGAAACTGGTGAAAAGGGTGAACAAGGAGAAAAAGGAGAT
CCAGCTCTGGCTGGCCTTAATGGAGAAAATGGTTTGAAAGGTGACTTGGGTCCTCATGGTCCACCTGGCCCAAAAGGAGAAAAGGGAGATACAGGACCCCCAGGA
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ATGAGACTCACTGGCCCTTGGAAACTTTGGCTTTGGATGTCAATATTTCTGCTTCCTGCTTCCACTTCCGTGACCGTTAGGGACAAGACAGAAGAGTCATGCCCT
ATCCTGAGAATAGAGGGACATCAGCTGACATATGACAACATAAACAAACTTGAAGTTTCAGGTTTTGATCTAGGAGACAGCTTTTCTCTAAGACGTGCATTTTGT
GAAAGTGATAAAACCTGTTTCAAATTGGGAAGTGCACTTCTTATTAGAGACACTATTAAGATATTTCCCAAAGGCCTTCCTGAGGAGTACTCAGTAGCTGCCATG
TTTCGAGTACGAAGAAACGCCAAAAAGGAACGGTGGTTTCTGTGGCAGGTTTTAAACCAGCAGAATATTCCACAGATTTCTATAGTAGTTGATGGTGGAAAGAAG
GTGGTGGAATTTATGTTTCAAGCCACAGAGGGAGATGTGTTGAACTACATTTTTAGAAATCGAGAACTCCGTCCTTTGTTTGATCGTCAGTGGCACAAACTTGGC
ATTAGTATACAATCCCAGGTCATTTCACTTTATATGGATTGTAATTTAATTGCGAGGAGGCAGACTGATGAAAAGGACACTGTGGATTTCCATGGACGGACAGTT
ATTGCTACGCGAGCTTCAGATGGCAAGCCTGTGGATATTGAACTTCACCAACTTAAAATCTACTGCAGTGCAAACCTCATAGCTCAAGAAACATGTTGTGAAATA
TCAGATACTAAGTGCCCAGAGCAGGATGGCTTTGGAAATATTGCATCATCATGGGTAACTGCTCATGCCAGTAAAATGTCTTCATATCTGCCAGCAAAGCAGGAA
CTTAAAGACCAGTGCCAGTGCATTCCAAACAAGGGAGAAGCAGGATTACCAGGAGCTCCGGGTTCACCTGGGCAGAAAGGGCATAAAGGAGAGCCGGGTGAAAAT
GGTTTACATGGTGCTCCAGGATTCCCTGGTCAAAAGGGAGAGCAAGGTTTTGAAGGCAGCAAAGGAGAAACTGGTGAAAAGGGTGAACAAGGAGAAAAAGGAGAT
CCAGCTCTGGCTGGCCTTAATGGAGAAAATGGTTTGAAAGGTGACTTGGGTCCTCATGGTCCACCTGGCCCAAAAGGAGAAAAGGGAGATACAGGACCCCCAGGA
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>COL19A1|1310|protein
MRLTGPWKLWLWMSIFLLPASTSVTVRDKTEESCPILRIEGHQLTYDNINKLEVSGFDLGDSFSLRRAFCESDKTCFKLGSALLIRDTIKIFPKGLPEEYSVAAM
FRVRRNAKKERWFLWQVLNQQNIPQISIVVDGGKKVVEFMFQATEGDVLNYIFRNRELRPLFDRQWHKLGISIQSQVISLYMDCNLIARRQTDEKDTVDFHGRTV
IATRASDGKPVDIELHQLKIYCSANLIAQETCCEISDTKCPEQDGFGNIASSWVTAHASKMSSYLPAKQELKDQCQCIPNKGEAGLPGAPGSPGQKGHKGEPGEN
GLHGAPGFPGQKGEQGFEGSKGETGEKGEQGEKGDPALAGLNGENGLKGDLGPHGPPGPKGEKGDTGPPGPPALPGSLGIQGPQGPPGKEGQRGRRGKTGPPGKP
GPPGPPGPPGIQGIHQTLGGYYNKDNKGNDEHEAGGLKGDKGETGLPGFPGSVGPKGQKGEPGEPFTKGEKGDRGEPGVIGSQGVKGEPGDPGPPGLIGSPGLKG
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MRLTGPWKLWLWMSIFLLPASTSVTVRDKTEESCPILRIEGHQLTYDNINKLEVSGFDLGDSFSLRRAFCESDKTCFKLGSALLIRDTIKIFPKGLPEEYSVAAM
FRVRRNAKKERWFLWQVLNQQNIPQISIVVDGGKKVVEFMFQATEGDVLNYIFRNRELRPLFDRQWHKLGISIQSQVISLYMDCNLIARRQTDEKDTVDFHGRTV
IATRASDGKPVDIELHQLKIYCSANLIAQETCCEISDTKCPEQDGFGNIASSWVTAHASKMSSYLPAKQELKDQCQCIPNKGEAGLPGAPGSPGQKGHKGEPGEN
GLHGAPGFPGQKGEQGFEGSKGETGEKGEQGEKGDPALAGLNGENGLKGDLGPHGPPGPKGEKGDTGPPGPPALPGSLGIQGPQGPPGKEGQRGRRGKTGPPGKP
GPPGPPGPPGIQGIHQTLGGYYNKDNKGNDEHEAGGLKGDKGETGLPGFPGSVGPKGQKGEPGEPFTKGEKGDRGEPGVIGSQGVKGEPGDPGPPGLIGSPGLKG
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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 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 0 (2) |




Family Based Association Studies: 1
Reference | Stage | Platform | #Families | Affecteds | Result | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|
#Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ (range) |
||||||
CAUCASIAN | |||||||||||
Hussman, 2011_1 | Discovery | Illumina Infinium Human 1 M beadship | 597 | - (-) | ![]() | ![]() | ASD | - - |
- - |
Case Control Based Association Studies: 0
Reference | Stage | Platform | ASD Cases | Normal Controls | Result | |||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
#Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ | #Subjects (% Women) |
Age (range) |
|||||
No Evidence. |










Reference | Case Number | Family Number | de novo Number | Title |
---|---|---|---|---|
Iossifov I, 2014 | 2508 | - | 1194 | The contribution of de novo coding mutations to autism spectrum disorder. |






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