KEGG   Homo sapiens (human): 79645
Entry
79645             CDS       T01001                                 
Symbol
CLXN, CILD53, EFCAB1, ODAD5
Name
(RefSeq) calaxin
  KO
K27179  outer dynein arm-docking complex subunit 5
Organism
hsa  Homo sapiens (human)
Disease
H00564  Primary ciliary dyskinesia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    79645 (CLXN)
Cilium and associated proteins [BR:hsa03037]
 Motile cilia and associated proteins
  ODA docking complex
   79645 (CLXN)
SSDB
Motif
Pfam: EF-hand_7 EF-hand_1 EF-hand_6 EF-hand_5 EF-hand_8 Dockerin_1 DUF7809
Other DBs
NCBI-GeneID: 79645
NCBI-ProteinID: NP_078869
OMIM: 619564
HGNC: 25678
Ensembl: ENSG00000034239
UniProt: Q9HAE3
Structure
LinkDB
Position
8:complement(48710789..48735311)
AA seq 211 aa
MNRKKLQKLTDTLTKNCKHFNKFEVNCLIKLFYDLVGGVERQGLVVGLDRNAFRNILHVT
FGMTDDMIMDRVFRGFDKDNDGCVNVLEWIHGLSLFLRGSLEEKMKYCFEVFDLNGDGFI
SKEEMFHMLKNSLLKQPSEEDPDEGIKDLVEITLKKMDHDHDGKLSFADYELAVREETLL
LEAFGPCLPDPKSQMEFEAQVFKDPNEFNDM
NT seq 636 nt   +upstreamnt  +downstreamnt
atgaaccgcaagaaactgcagaagctgacggacaccttaaccaaaaattgcaagcatttt
aataaatttgaagtgaactgtcttataaagcttttttatgacttggtgggaggagtagag
aggcaaggtctggttgttggactggatcgtaatgcatttcgaaacatcctgcatgtgaca
tttggaatgacagatgacatgattatggacagagtattccgaggttttgataaagataat
gatggctgtgtaaatgtattggagtggattcatggattatcactgtttcttcgaggatct
ttggaagaaaaaatgaaatattgctttgaagtgtttgatttgaatggtgacggattcatt
tcaaaggaggaaatgtttcacatgttgaagaacagccttctcaaacagccatctgaggaa
gaccctgatgaaggaattaaagatttggttgaaataacactgaagaaaatggatcatgac
catgatgggaagctgtcttttgcagactatgaactggctgtgagagaagagactcttcta
ctggaggcctttgggccatgtcttcctgatccaaagagccagatggaatttgaagctcaa
gtattcaaagatccaaatgaattcaatgatatgtga

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