KEGG   Homo sapiens (human): 219854
Entry
219854            CDS       T01001                                 
Symbol
TMEM218, JBTS39
Name
(RefSeq) transmembrane protein 218
  KO
K26674  transmembrane protein 218
Organism
hsa  Homo sapiens (human)
Disease
H00530  Joubert syndrome and related disorders
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    219854 (TMEM218)
Cilium and associated proteins [BR:hsa03037]
 Primary cilia and associated proteins
  MKS complex
   219854 (TMEM218)
SSDB
Other DBs
NCBI-GeneID: 219854
NCBI-ProteinID: NP_001074015
OMIM: 619285
HGNC: 27344
Ensembl: ENSG00000150433
UniProt: A2RU14
Position
11:complement(125094389..125111626)
AA seq 115 aa
MAGTVLGVGAGVFILALLWVAVLLLCVLLSRASGAARFSVIFLFFGAVIITSVLLLFPRA
GEFPAPEVEVKIVDDFFIGRYVLLAFLSAIFLGGLFLVLIHYVLEPIYAKPLHSY
NT seq 348 nt   +upstreamnt  +downstreamnt
atggctggcactgtgctcggagtcggtgcgggcgtgttcatcttagccctgctctgggtg
gcagtgctgctgctgtgtgtgctgctgtccagagcctccggggcggcgaggttctctgtc
atttttttattcttcggtgctgtgatcatcacatcagttctgttgcttttcccgcgagct
ggtgaattcccagccccagaagtggaagttaagattgtggatgactttttcattggccgc
tatgtcctgctggctttccttagtgccatcttccttggaggcctcttcttggttttaatc
cattatgttctggagccgatctatgccaaaccactgcactcctactga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (7)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (52)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (50)   
DNA sequence (133)   
   RefSeq(nuc) (71)   
   GenBank (31)   
   EMBL (31)   
All databases (198)   

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