CCDC114
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Official Full Name
coiled-coil domain containing 114 -
Synonyms
CCDC114;coiled-coil domain containing 114;26560;ENSG00000105479;19q13.33;FLJ32926;coiled-coil domain-containing protein 114;coiled-coil domain-containing protein 114
Recombinant Proteins
- Human
- Rat
- Zebrafish
- Mouse
- E.coli
- Wheat Germ
- Mammalian Cells
- HEK293
- In Vitro Cell Free System
- His
- GST
- His&Fc&Avi
- Myc&DDK
Involved Pathway
CCDC114 involved in several pathways and played different roles in them. We selected most pathways CCDC114 participated on our site, such as , which may be useful for your reference. Also, other proteins which involved in the same pathway with CCDC114 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
| Pathway Name | Pathway Related Protein |
|---|
Protein Function
CCDC114 has several biochemical functions, for example, molecular_function. Some of the functions are cooperated with other proteins, some of the functions could acted by CCDC114 itself. We selected most functions CCDC114 had, and list some proteins which have the same functions with CCDC114. You can find most of the proteins on our site.
| Function | Related Protein |
|---|---|
| molecular_function | ILVBL,CRESTIN,UAP1L1,PCED1B,LMAN2LB,SIRP-BETA,FAM69C,GM8660,PDDC1,GM4179 |
Interacting Protein
CCDC114 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with CCDC114 here. Most of them are supplied by our site. Hope this information will be useful for your research of CCDC114.
Resources
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References
- Hjeij, R; Onoufriadis, A; et al. CCDC151 Mutations Cause Primary Ciliary Dyskinesia by Disruption of the Outer Dynein Arm Docking Complex Formation. AMERICAN JOURNAL OF HUMAN GENETICS 95:257-274(2014).
- Hjeij, R; Lindstrand, A; et al. ARMC4 Mutations Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry. AMERICAN JOURNAL OF HUMAN GENETICS 93:357-367(2013).
