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Q96M63 Proteins with novel repeats
Uniprot ID:Q96M63
Gene name: CCDC114
Protein Family:ODA1/DCC2 family
Protein name: Coiled-coil domain-containing protein 114
Length : 670
Sequnce
>Q96M63 671 MEGERRAYSKEVHQRINKQLEEIRRLEEVRGDLQVQISAAQNQVKRLRDSQRLENMDRLLKGRAQVQAEIEELQEQTRALDKQIQEWETRIFTHSKNVRSPGFILDQKVKIRRRIRILENQLDRVTCHFDNQLVRNAALREELDLLRIDRNRYLNVDRKLKKEIHHLHHLVSTLILSSTSAYAVREEAKAKMGLLRERAEKEEAQSEMEAQVLQRQILHLEQLHHFLKLKNNDRQPDPDVLEKREKQAGEVAEGVWKTSQERLVLCYEDALNKLSQLMGESDPDLLVQKYLEIEERNFAEFNFINEQNLELEHVQEEIKEMQEALVSARASKDDQHLLQEQQQKVLQQRMDKVHSEAERLEARFQDVRGQLEKLKADIQLLFTKAHCDSSMIDDLLGVKTSMGDRDMGLFLSLIEKRLVELLTVQAFLHAQSFTSLADAALLVLGQSLEDLPKKMAPLQPPDTLEDPPGFEASDDYPMSREELLSQVEKLVELQEQAEAQRQKDLAAAAAKLDGTLSVDLASTQRAGSSTVLVPTRHPHAIPGSILSHKTSRDRGSLGHVTFGGLSSSTGHLPSHITHGDPNTGHVTFGSTSASSGGHVTFRPVSASSYLGSTGYVGSSRGGENTEGGVESGGTASDSSGGLGSSRDHVSSTGPASSTGPGSSTSKDSRG
Repeated Sequence regions
Length: 15 residues : 2 times from 584 to 611 :0.8333333333333334 region Length:28 GHVTFGSTSASS--G GHVTFRPVSASSYLG
Function
Probable component of the outer dynein arm complex required along the entire axoneme for tethering of outer dynein arms
Disease
"DISEASE: Ciliary dyskinesia, primary, 20 (CILD20) [MIM:615067]: A disorder characterized by abnormalities of motile cilia Respiratory infections leading to chronic inflammation and bronchiectasis are recurrent, due to defects in the respiratory cilia Patients may exhibit randomization of left-right body asymmetry and situs inversus, due to dysfunction of monocilia at the embryonic node Primary ciliary dyskinesia associated with situs inversus is referred to as Kartagener syndrome Unlike other forms of CILD characterized by reduced fertility, patients with CILD20 do not appear to be infertile Note=The disease is caused by mutations affecting the gene represented in this entry"