CC2D2A
| Name | Synonyms | Full Name | RefSeq ID | Description (.pdf) | IGV-img (humangenome) | Sashimi-img (humangenome) | UCSC-img (humangenome) | IGV-img (batgenome) |
|---|---|---|---|---|---|---|---|---|
| CC2D2A | JBTS9, MKS6,KIAA1345, JBTS9 | coiled-coil and C2 domain containing 2A | NM_001080522 | NONE | ![]() |
Download all snapshots for IGV, UCSC and Sashimi (zip archive)
Description
This gene encodes a coiled-coil and calcium binding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joubert syndrome type 9. Alternative splicing results in multiple transcript variants.
This gene is not differentially expressed. %%%%%%%%%%%%%%%%%%%%%
Maximum read counts and DESeq normalized read counts for human and bat cell lines
| Source | Species | Mapping on | Mock3h | Mock7h | Mock23h | EBOV3h | EBOV7h | EBOV23h | MARV3h | MARV7h | MARV23h | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
Read_Max | H. sapiens | Genome | 42 | 40 | 42 | 43 | 46 | 47 | 42 | 61 | 39 | |
Read_Max | R. aegyptiacus | Transcriptome | 84 | 60 | 63 | 78 | 54 | 50 | 45 | 82 | 74 | |
Read_Max | R. aegyptiacus | Genome | 86 | 89 | 52 | 58 | 56 | 34 | 47 | 103 | 85 | |
DESeq | H. sapiens | Genome | 1002.59 | 988.24 | 898.51 | 999.1 | 1064.34 | 1248.49 | 942.24 | 914.66 | 1124.23 | |
DESeq | R. aegyptiacus | Transcriptome | 1029.33 | 900.52 | 1249.41 | 955.13 | 929.64 | 967.24 | 846.43 | 1040.37 | 1090.89 | |
DESeq | R. aegyptiacus | Genome | 1709.33 | 1554.3 | 1988.32 | 1615.52 | 1527.99 | 1661.79 | 1414.66 | 1646.95 | 1771.46 |
