Evidence Details for CCDC90B
Basic Information Top
| Gene Symbol: | CCDC90B ( MDS011,MDS025,MGC104239 ) |
|---|---|
| Gene Full Name: | coiled-coil domain containing 90B |
| Band: | 11q14.1 |
| Quick Links | Entrez ID:60492; OMIM: NA; Uniprot ID:CC90B_HUMAN; ENSEMBL ID: ENSG00000137500; HGNC ID: 28108 |
| Relate to Another Database: | SFARIGene; denovo-db |
Sequences Top>CCDC90B|60492|nucleotide
ATGAATAGTCGCCAGGCTTGGCGGCTCTTTCTCTCCCAAGGCAGAGGAGATCGTTGGGTTTCAAGGCCCCGCGGGCATTTCTCGCCGGCCCTGCGGAGAGAGTTC
TTCACTACCACAACCAAGGAGGGATATGATAGGCGGCCAGTGGATATAACTCCTTTAGAACAAAGGAAATTAACTTTTGATACCCATGCATTGGTTCAGGACTTG
GAAACTCATGGATTTGACAAAACACAAGCAGAAACAATTGTATCAGCGTTAACTGCTTTATCAAATGTCAGCCTGGATACTATCTATAAAGAGATGGTCACTCAA
GCTCAACAGGAAATAACAGTACAACAGCTAATGGCTCATTTGGATGCTATCAGGAAAGACATGGTCATCCTAGAGAAAAGTGAATTTGCAAATCTGAGAGCAGAG
AATGAGAAAATGAAAATTGAATTAGACCAAGTTAAGCAACAACTAATGCATGAAACCAGTCGAATCAGAGCAGATAATAAACTGGATATCAACTTAGAAAGGAGC
AGAGTAACAGATATGTTTACAGATCAAGAAAAGCAACTTATGGAAACAACTACAGAATTTACAAAAAAGGATACTCAAACCAAAAGTATTATTTCAGAGACCAGT
AATAAAATTGACGCTGAAATTGCTTCCTTAAAAACACTGATGGAATCTAACAAACTTGAGACAATTCGTTATCTTGCAGCTTCAGTGTTTACTTGCCTGGCAATA
GCATTGGGATTTTATAGATTCTGGAAGTAG
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ATGAATAGTCGCCAGGCTTGGCGGCTCTTTCTCTCCCAAGGCAGAGGAGATCGTTGGGTTTCAAGGCCCCGCGGGCATTTCTCGCCGGCCCTGCGGAGAGAGTTC
TTCACTACCACAACCAAGGAGGGATATGATAGGCGGCCAGTGGATATAACTCCTTTAGAACAAAGGAAATTAACTTTTGATACCCATGCATTGGTTCAGGACTTG
GAAACTCATGGATTTGACAAAACACAAGCAGAAACAATTGTATCAGCGTTAACTGCTTTATCAAATGTCAGCCTGGATACTATCTATAAAGAGATGGTCACTCAA
GCTCAACAGGAAATAACAGTACAACAGCTAATGGCTCATTTGGATGCTATCAGGAAAGACATGGTCATCCTAGAGAAAAGTGAATTTGCAAATCTGAGAGCAGAG
AATGAGAAAATGAAAATTGAATTAGACCAAGTTAAGCAACAACTAATGCATGAAACCAGTCGAATCAGAGCAGATAATAAACTGGATATCAACTTAGAAAGGAGC
AGAGTAACAGATATGTTTACAGATCAAGAAAAGCAACTTATGGAAACAACTACAGAATTTACAAAAAAGGATACTCAAACCAAAAGTATTATTTCAGAGACCAGT
AATAAAATTGACGCTGAAATTGCTTCCTTAAAAACACTGATGGAATCTAACAAACTTGAGACAATTCGTTATCTTGCAGCTTCAGTGTTTACTTGCCTGGCAATA
GCATTGGGATTTTATAGATTCTGGAAGTAG
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>CCDC90B|60492|protein
MNSRQAWRLFLSQGRGDRWVSRPRGHFSPALRREFFTTTTKEGYDRRPVDITPLEQRKLTFDTHALVQDLETHGFDKTQAETIVSALTALSNVSLDTIYKEMVTQ
AQQEITVQQLMAHLDAIRKDMVILEKSEFANLRAENEKMKIELDQVKQQLMHETSRIRADNKLDINLERSRVTDMFTDQEKQLMETTTEFTKKDTQTKSIISETS
NKIDAEIASLKTLMESNKLETIRYLAASVFTCLAIALGFYRFWK
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MNSRQAWRLFLSQGRGDRWVSRPRGHFSPALRREFFTTTTKEGYDRRPVDITPLEQRKLTFDTHALVQDLETHGFDKTQAETIVSALTALSNVSLDTIYKEMVTQ
AQQEITVQQLMAHLDAIRKDMVILEKSEFANLRAENEKMKIELDQVKQQLMHETSRIRADNKLDINLERSRVTDMFTDQEKQLMETTTEFTKKDTQTKSIISETS
NKIDAEIASLKTLMESNKLETIRYLAASVFTCLAIALGFYRFWK
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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 | 0 (0) | 0 (0) | 0 (0) | 0 (0) | 1 (1) | 0 (2) | 0 (0) | 0 (0) | 0 (0) | 1 (3) |
Syndromic Autism Gene TopGenome-Wide Association Studies(By Ethnic Group) TopCNV Studies TopLinkage Studies Top