KEGG   Homo sapiens (human): 85478
Entry
85478             CDS       T01001                                 
Symbol
DRC2, CCDC65, CFAP250, FAP250, NYD-SP28
Name
(RefSeq) dynein regulatory complex subunit 2
  KO
K23728  dynein regulatory complex subunit 2
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]
    85478 (DRC2)
Cilium and associated proteins [BR:hsa03037]
 Motile cilia and associated proteins
  Nexin-dynein regulatory complex
   85478 (DRC2)
SSDB
Motif
Pfam: NYD-SP28
Other DBs
NCBI-GeneID: 85478
NCBI-ProteinID: NP_149115
OMIM: 611088
HGNC: 29937
Ensembl: ENSG00000139537
UniProt: Q8IXS2
Structure
Position
12:48904133..48921576
AA seq 484 aa
MPKKEKMAKTPLSDEKQLLLFQQKLLAEEEMAKKKERLLSQFLKDKLAKEEHNSALNLNK
INTQWRTVLREVKTRELHKDIEILSQTFERVVDCKDNVIKSLAKDLSEAEEQYAHALRSH
LHNVDQLLALQRHRLSLLEESYNMELEALTKEFETERKTIIDQHEKEIHYLQDIFMAMEQ
NYIDSEYESKLEFQSMWNDLKNMNLEEKHFLRLHLENRVEDLWRKFQDVLKNYTDATEDR
KAAFETLQVKDEKSSKEIEVQMKKIQKLQDAITISKGKIMIHSRESEDENRYIRNDKELV
LVQLRKLKAQRTQARAASQKNLVRLTLESNATLKALRKIVDKGEKILKLAEICRKFETEE
EKVLPFYSSVLTPKEQEGIQKNNLEELTEELTKVMVDYIGMENFWKRYNKVKLEQLSLQH
RRAQLLDINGKLREMLKQYLDGISVSDEVLSQLNPLFIVNYQSNLLQPLSIRIAHPGDKQ
HPTT
NT seq 1455 nt   +upstreamnt  +downstreamnt
atgcctaagaaagaaaaaatggccaagacgcccctgtccgatgagaagcagctgcttctg
tttcagcagaagttgctggcagaggaggagatggccaaaaagaaggagaggctcctcagc
cagttcttgaaggacaagctggccaaggaggaacacaacagtgctctgaaccttaataag
attaacacacagtggagaactgtccttcgggaagtcaagaccagagaacttcataaggac
attgagatcctcagccaaacatttgaacgagtggtggactgtaaggacaatgtcatcaag
tctttagctaaagacctgtccgaagccgaggagcagtacgcccatgccctgcgcagccac
ttgcacaatgttgaccagctcttggccctgcagaggcaccggctcagtctcctggaggaa
agttacaacatggagctggaagccctaaccaaggagtttgagacagaaaggaagacaatt
attgaccaacatgagaaagagattcactatctgcaagatatcttcatggccatggagcag
aactatatagattctgagtatgaaagcaagctggagttccagagcatgtggaatgatctc
aaaaacatgaatttagaagagaagcactttctaagactgcacctggagaacagagtagaa
gatctgtggagaaagttccaggatgtactcaagaattacactgatgccacagaggatcga
aaggctgcctttgagaccctgcaggtgaaggatgagaagagctccaaagagattgaagta
cagatgaaaaaaatacagaaactacaggatgccataactatttcaaaaggcaagatcatg
atacacagccgtgagagtgaagatgagaaccggtatatccgtaatgacaaggaattggtc
cttgtacaactgcgaaaacttaaggcccaaagaactcaggcccgggcagcatcccagaag
aacttagtcagactcaccctggaaagtaatgccaccctcaaggccctgagaaagattgtt
gataagggtgaaaagatccttaaacttgctgaaatatgtaggaaatttgaaaccgaagaa
gaaaaagtgctgcctttttattcatcagtattgactcctaaggagcaggaggggattcag
aagaataatctagaagagcttactgaggagctcaccaaggtgatggtggactacatagga
atggagaatttctggaaaaggtacaacaaagtgaaactggagcaactgagcctccaacat
agacgagcccagctgctagatatcaatgggaagctgcgggagatgctgaagcagtacttg
gatggcatctcagtgagtgacgaagtgctgagccagctcaacccactctttatagtcaac
tatcaaagcaacttactccagcccttgtccatacgtatagcccatccaggtgataaacaa
catccaaccacttaa

  All links  
Disease (2)   
   OMIM (2)   
Gene (9)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (18)   
   RefSeq(nuc) (2)   
   GenBank (8)   
   EMBL (8)   
3D Structure (1)   
   PDB (1)   
Protein domain (1)   
   Pfam (1)   
All databases (35)   

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