Evidence Details for C10orf68
Basic Information Top
| Gene Symbol: | C10orf68 ( FLJ13031,MGC149767,dJ1104A8.1 ) |
|---|---|
| Gene Full Name: | chromosome 10 open reading frame 68 |
| Band: | 10p11.22 |
| Quick Links | Entrez ID:79741; OMIM: NA; Uniprot ID:CJ068_HUMAN; ENSEMBL ID: ENSG00000150076; HGNC ID: |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>C10orf68|79741|nucleotide
ATGACTGAAGAACAAACTTACCAAGCAGCAGAAAAATCTCAAGCTCATAATGAAGTACCAAATGAAAGGCTTGTAGTTGAGCATCAAGAATCATTGTCAAAAACC
AAATTACAAATAAAGAAACAAGAAACTTCTACAGAGCAACCACTCACCACTCCTGATAAAGAACCAAATGAAAATCTTATACTTAGGCATCAAGACTCAATGTCA
AAATCAGAAATGCAAGTGAAGGAACAAAGAACTCTCAAAGGGCAAAGAATTATTACTCATGATGAAGAACCAGGCAAAAATCTTGTGCTTGAACATCAAGATTCA
GTGTCAAAACTGGAAATGCAAATTGAAAAAACCAAAAAACTTCCTAGAGAGAAAAGACATAGTACTCATGATGAAGAATCAGGTGAAAATCCTATGCTTAAACAT
CAAGATTCAGTGTCAAAAATCCAAGTGCAATTAGAGATTCAAGAAACTTCTGAAGGAGAAGGACGTAGCATACCAGATAAAAATTCTATGTTTGTTCATCAAGAT
TCAGTGTCAAAACTCCAAATGCAAGAAAAGAAAAAAATAACTCCTGGAAGGGAAAGGCGTAATACTCGTATTGTAGTACCAAATGAAAATGTGATTTCTGTTCAT
CAAGATTCAAAGTCAAAACTCCAAATGCAAGAAAAGAAACAAATAAATTCTGGAGTGGAAAGACACAAGACGTTTCCTTTAGAAATCAAAAAAAAGGATATATCA
CTTGAACATCTGTTGCCTGAGGAGAAAGTTTTATTATCAAGAAGCGAATCTCAAACGAAGAAACTTCAAGCTAAAGTAACTTCAAGAAAAAAGACTGATATAGAA
AGCTTGAGAGGTGCTTTGGGAAGACGCTTATTAAATGATGAATTCAAGACACAGTCAAAGAGTTTCCCTGGGCCTGATATAGAACAATTGACAGATGCATTTGGA
AGAGATATACTAAAGGATGAATTCAAGACACGATCAAAGAGTCTCCCTGAGACTGATGAACGATTGCATAGTACAACTGAGAGAGGTACAATAAATGATGCAATT
AAGACGCAGTTAAAGAGAAAGAGTTACCCTGAGACTGTCTTAAAACACTTGAAAGGTGTTAATGGAAAAGATATAATAAAGCATCTAATCAACATACAGTCAAAG
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ATGACTGAAGAACAAACTTACCAAGCAGCAGAAAAATCTCAAGCTCATAATGAAGTACCAAATGAAAGGCTTGTAGTTGAGCATCAAGAATCATTGTCAAAAACC
AAATTACAAATAAAGAAACAAGAAACTTCTACAGAGCAACCACTCACCACTCCTGATAAAGAACCAAATGAAAATCTTATACTTAGGCATCAAGACTCAATGTCA
AAATCAGAAATGCAAGTGAAGGAACAAAGAACTCTCAAAGGGCAAAGAATTATTACTCATGATGAAGAACCAGGCAAAAATCTTGTGCTTGAACATCAAGATTCA
GTGTCAAAACTGGAAATGCAAATTGAAAAAACCAAAAAACTTCCTAGAGAGAAAAGACATAGTACTCATGATGAAGAATCAGGTGAAAATCCTATGCTTAAACAT
CAAGATTCAGTGTCAAAAATCCAAGTGCAATTAGAGATTCAAGAAACTTCTGAAGGAGAAGGACGTAGCATACCAGATAAAAATTCTATGTTTGTTCATCAAGAT
TCAGTGTCAAAACTCCAAATGCAAGAAAAGAAAAAAATAACTCCTGGAAGGGAAAGGCGTAATACTCGTATTGTAGTACCAAATGAAAATGTGATTTCTGTTCAT
CAAGATTCAAAGTCAAAACTCCAAATGCAAGAAAAGAAACAAATAAATTCTGGAGTGGAAAGACACAAGACGTTTCCTTTAGAAATCAAAAAAAAGGATATATCA
CTTGAACATCTGTTGCCTGAGGAGAAAGTTTTATTATCAAGAAGCGAATCTCAAACGAAGAAACTTCAAGCTAAAGTAACTTCAAGAAAAAAGACTGATATAGAA
AGCTTGAGAGGTGCTTTGGGAAGACGCTTATTAAATGATGAATTCAAGACACAGTCAAAGAGTTTCCCTGGGCCTGATATAGAACAATTGACAGATGCATTTGGA
AGAGATATACTAAAGGATGAATTCAAGACACGATCAAAGAGTCTCCCTGAGACTGATGAACGATTGCATAGTACAACTGAGAGAGGTACAATAAATGATGCAATT
AAGACGCAGTTAAAGAGAAAGAGTTACCCTGAGACTGTCTTAAAACACTTGAAAGGTGTTAATGGAAAAGATATAATAAAGCATCTAATCAACATACAGTCAAAG
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>C10orf68|79741|protein
MTEEQTYQAAEKSQAHNEVPNERLVVEHQESLSKTKLQIKKQETSTEQPLTTPDKEPNENLILRHQDSMSKSEMQVKEQRTLKGQRIITHDEEPGKNLVLEHQDS
VSKLEMQIEKTKKLPREKRHSTHDEESGENPMLKHQDSVSKIQVQLEIQETSEGEGRSIPDKNSMFVHQDSVSKLQMQEKKKITPGRERRNTRIVVPNENVISVH
QDSKSKLQMQEKKQINSGVERHKTFPLEIKKKDISLEHLLPEEKVLLSRSESQTKKLQAKVTSRKKTDIESLRGALGRRLLNDEFKTQSKSFPGPDIEQLTDAFG
RDILKDEFKTRSKSLPETDERLHSTTERGTINDAIKTQLKRKSYPETVLKHLKGVNGKDIIKHLINIQSKSHGETDKNFFAYATGRGLMKESTTTQLKSHPETDK
EFLADAIGRGIIIGPITTQLKSHRETDKELLKDAIGRDIIKGPISAQLKSHQETDVEPLTNAIGSSKTIGEIKTQLRTHYDVNLFKNKDMSVQRQEGIFTRSITP
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MTEEQTYQAAEKSQAHNEVPNERLVVEHQESLSKTKLQIKKQETSTEQPLTTPDKEPNENLILRHQDSMSKSEMQVKEQRTLKGQRIITHDEEPGKNLVLEHQDS
VSKLEMQIEKTKKLPREKRHSTHDEESGENPMLKHQDSVSKIQVQLEIQETSEGEGRSIPDKNSMFVHQDSVSKLQMQEKKKITPGRERRNTRIVVPNENVISVH
QDSKSKLQMQEKKQINSGVERHKTFPLEIKKKDISLEHLLPEEKVLLSRSESQTKKLQAKVTSRKKTDIESLRGALGRRLLNDEFKTQSKSFPGPDIEQLTDAFG
RDILKDEFKTRSKSLPETDERLHSTTERGTINDAIKTQLKRKSYPETVLKHLKGVNGKDIIKHLINIQSKSHGETDKNFFAYATGRGLMKESTTTQLKSHPETDK
EFLADAIGRGIIIGPITTQLKSHRETDKELLKDAIGRDIIKGPISAQLKSHQETDVEPLTNAIGSSKTIGEIKTQLRTHYDVNLFKNKDMSVQRQEGIFTRSITP
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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 | 1 (1) | 0 (0) | 1 (3) | 0 (0) | 0 (0) | 0 (1) | 0 (0) | 0 (0) | 0 (0) | 6 (5) |
Syndromic Autism Gene TopGenome-Wide Association Studies (By Ethnic Group) Top Family Based Association Studies: 0
| Reference | Stage | Platform | #Families | Affecteds | Result | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| #Subjects (% Women) |
ADI-R | ADOS | Diagnosis | Age (range) |
IQ (range) |
|||||||
| No Evidence. | ||||||||||||
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) |
|||||
| MIXED/OTHERS | ||||||||||||
| Kuo PH, 2015_1 | Discovery | Affymetrix SNP array 6.0 | 597 (-) |  | | ASD | - - |
- | 1595 (-) |
- - | ||
CNV Studies TopLinkage Studies Top| 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 | - | - | - | - |
| Spence, 2006 | USA | microsatellite-based genomic screen | | | ASD | 133 | - | 133 | - | 280 | - | - |
| Lauritsen, 2006 | Faroe Islands | microsatellite-based genomic screen | | | autism | - | - | - | - | 12 | 44 | 56 |
Low Scale Association Studies (by Ethnic Group) TopLarge Scale Expression Studies TopNGS de novo Mutation Studies Top| Reference | Case Number | Family Number | de novo Number | Title |
|---|---|---|---|---|
| Tavassoli T, 2014 | 1 | 1 | 4 | De novo SCN2A splice site mutation in a boy with Autism spectrum disorder. |
NGS Mosaic SNV Studies TopNGS 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.