Evidence Details for STARD10
Basic Information Top
| Gene Symbol: | STARD10 ( MGC14401,NY-CO-28,PCTP2,SDCCAG28 ) |
|---|---|
| Gene Full Name: | StAR-related lipid transfer (START) domain containing 10 |
| Band: | 11q13 |
| Quick Links | Entrez ID:10809; OMIM: NA; Uniprot ID:PCTL_HUMAN; ENSEMBL ID: ENSG00000214530; HGNC ID: 10666 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top
>STARD10|10809|nucleotide
ATGGAGAAGCTGGCGGCCTCTACAGAGCCCCAAGGGCCTCGGCCGGTCCTGGGCCGTGAGAGTGTCCAGGTGCCCGATGACCAAGACTTTCGCAGCTTCCGGTCA
GAGTGTGAGGCTGAGGTGGGCTGGAACCTGACCTATAGCAGGGCTGGGGTGTCTGTCTGGGTGCAGGCTGTGGAGATGGATCGGACGCTGCACAAGATCAAGTGC
CGGATGGAGTGCTGTGATGTGCCAGCCGAGACACTCTACGACGTCCTACACGACATTGAGTACCGCAAGAAATGGGACAGCAACGTCATTGAGACTTTTGACATC
GCCCGCTTGACAGTCAACGCTGACGTGGGCTATTACTCCTGGAGGTGTCCCAAGCCCCTGAAGAACCGTGATGTCATCACCCTCCGCTCCTGGCTCCCCATGGGC
GCTGATTACATCATTATGAACTACTCAGTCAAACATCCCAAATACCCACCTCGGAAAGACTTGGTCCGAGCTGTGTCCATCCAGACGGGCTACCTCATCCAGAGC
ACAGGGCCCAAGAGCTGCGTCATCACCTACCTGGCCCAGGTGGACCCCAAAGGCTCCTTACCCAAGTGGGTGGTGAATAAATCTTCTCAGTTCCTGGCTCCCAAG
GCCATGAAGAAGATGTACAAGGCGTGCCTCAAGTACCCCGAGTGGAAACAGAAGCACCTGCCTCACTTCAAGCCGTGGCTGCACCCGGAGCAGAGCCCGTTGCCG
AGCCTGGCGCTGTCGGAGCTGTCGGTGCAGCATGCGGACTCACTGGAGAACATCGACGAGAGCGCGGTGGCCGAGAGCAGAGAGGAGCGGATGGGCGGCGCGGGC
GGCGAGGGCAGCGACGACGACACCTCGCTCACCTGA
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ATGGAGAAGCTGGCGGCCTCTACAGAGCCCCAAGGGCCTCGGCCGGTCCTGGGCCGTGAGAGTGTCCAGGTGCCCGATGACCAAGACTTTCGCAGCTTCCGGTCA
GAGTGTGAGGCTGAGGTGGGCTGGAACCTGACCTATAGCAGGGCTGGGGTGTCTGTCTGGGTGCAGGCTGTGGAGATGGATCGGACGCTGCACAAGATCAAGTGC
CGGATGGAGTGCTGTGATGTGCCAGCCGAGACACTCTACGACGTCCTACACGACATTGAGTACCGCAAGAAATGGGACAGCAACGTCATTGAGACTTTTGACATC
GCCCGCTTGACAGTCAACGCTGACGTGGGCTATTACTCCTGGAGGTGTCCCAAGCCCCTGAAGAACCGTGATGTCATCACCCTCCGCTCCTGGCTCCCCATGGGC
GCTGATTACATCATTATGAACTACTCAGTCAAACATCCCAAATACCCACCTCGGAAAGACTTGGTCCGAGCTGTGTCCATCCAGACGGGCTACCTCATCCAGAGC
ACAGGGCCCAAGAGCTGCGTCATCACCTACCTGGCCCAGGTGGACCCCAAAGGCTCCTTACCCAAGTGGGTGGTGAATAAATCTTCTCAGTTCCTGGCTCCCAAG
GCCATGAAGAAGATGTACAAGGCGTGCCTCAAGTACCCCGAGTGGAAACAGAAGCACCTGCCTCACTTCAAGCCGTGGCTGCACCCGGAGCAGAGCCCGTTGCCG
AGCCTGGCGCTGTCGGAGCTGTCGGTGCAGCATGCGGACTCACTGGAGAACATCGACGAGAGCGCGGTGGCCGAGAGCAGAGAGGAGCGGATGGGCGGCGCGGGC
GGCGAGGGCAGCGACGACGACACCTCGCTCACCTGA
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>STARD10|10809|protein
MEKLAASTEPQGPRPVLGRESVQVPDDQDFRSFRSECEAEVGWNLTYSRAGVSVWVQAVEMDRTLHKIKCRMECCDVPAETLYDVLHDIEYRKKWDSNVIETFDI
ARLTVNADVGYYSWRCPKPLKNRDVITLRSWLPMGADYIIMNYSVKHPKYPPRKDLVRAVSIQTGYLIQSTGPKSCVITYLAQVDPKGSLPKWVVNKSSQFLAPK
AMKKMYKACLKYPEWKQKHLPHFKPWLHPEQSPLPSLALSELSVQHADSLENIDESAVAESREERMGGAGGEGSDDDTSLT
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MEKLAASTEPQGPRPVLGRESVQVPDDQDFRSFRSECEAEVGWNLTYSRAGVSVWVQAVEMDRTLHKIKCRMECCDVPAETLYDVLHDIEYRKKWDSNVIETFDI
ARLTVNADVGYYSWRCPKPLKNRDVITLRSWLPMGADYIIMNYSVKHPKYPPRKDLVRAVSIQTGYLIQSTGPKSCVITYLAQVDPKGSLPKWVVNKSSQFLAPK
AMKKMYKACLKYPEWKQKHLPHFKPWLHPEQSPLPSLALSELSVQHADSLENIDESAVAESREERMGGAGGEGSDDDTSLT
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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) | 1 (1) | 0 (0) | 0 (0) | 1 (1) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 3 (3) |
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 | ||||||
| Berkel, 2010 | Canada | SNP microarray | ![]() | ![]() | ASD | - | - | - | - | 396 | 5023 | 5419 |
Linkage Studies Top
Low Scale Association Studies (by Ethnic Group) Top
Large Scale Expression Studies Top
Microarray Studies: 1
| Reference | Source | Tissue | #Subjects (% Women) |
ADI-R | ADOS | Endo- pheno | Diagnosis | Normal Controls (% Women) |
Fold Change | Up/ Down | P/Q value | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Voineagu, 2011_1 | Unknown | 16 frontal cortex(BA9) and 13 temporal cortex(BA41 | 16 (25.00%) | ![]() | ![]() | - | autism | 16 (6.25%) |
0.937946 | Down | 26.4019 | |
| ||||||||||||
Proteomics Studies:0
| Reference | Source | Tissue | Platform | #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Normal Controls(% Women) | |
|---|---|---|---|---|---|---|---|---|---|
| No Evidence. | |||||||||
NGS de novo Mutation Studies Top
| 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. |
NGS Mosaic SNV Studies Top
NGS Other Studies Top
Low Scale Gene Studies Top
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