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C2CD5
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C2CD5
Description
C2 calcium dependent domain containing 5
Aliases
CDP138, KIAA0528
Gene Identifiers
mRNA Identifiers
RefSeq (mRNA)
NM_001286173.1; NM_001286174.2; NM_001286175.1; NM_001286176.1; NM_001286177.1; NM_014802.2; XM_005253538.2; XM_005253539.3; XM_006719170.2; XM_017020264.1; XM_017020265.1; XM_017020266.1; XM_017020267.1; XM_017020268.1; XM_017020269.1; XM_017020270.1; XM_017020271.1; XM_017020272.1; XM_017020273.1; XM_017020274.1; XM_017020275.1; XM_017020276.1; XM_017020277.1; XM_017020278.1; XM_017020279.1
Protein Identifiers
RefSeq (protein)
NP_001273102.1; NP_001273103.1; NP_001273104.1; NP_001273105.1; NP_001273106.1; NP_055617.1; XP_005253595.1; XP_005253596.1; XP_006719233.1; XP_016875753.1; XP_016875754.1; XP_016875755.1; XP_016875756.1; XP_016875757.1; XP_016875758.1; XP_016875759.1; XP_016875760.1; XP_016875761.1; XP_016875762.1; XP_016875763.1; XP_016875764.1; XP_016875765.1; XP_016875766.1; XP_016875767.1; XP_016875768.1
Uniprot ID
Ensembl protein ID
Protein Architecture
SMART
Disease Mapping
Druggability
- Candidate cancer driver
- Damaged in 356/7921 TCGA samples
- Damaged in 29/1291 cell lines
- Fewer loss of function mutations
- Equal damaging SNVs/indels
- Fewer structural variants