KEGG   Homo sapiens (human): 11020
Entry
11020             CDS       T01001                                 
Symbol
IFT27, BBS19, CFAP156, FAP156, RABL4, RAYL
Name
(RefSeq) intraflagellar transport 27
  KO
K07934  intraflagellar transport protein 27
Organism
hsa  Homo sapiens (human)
Disease
H00418  Bardet-Biedl syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   03037 Cilium and associated proteins [BR:hsa03037]
    11020 (IFT27)
   04031 GTP-binding proteins [BR:hsa04031]
    11020 (IFT27)
Cilium and associated proteins [BR:hsa03037]
 Primary cilia and associated proteins
  Intraflagellar transport (IFT) complex B1
   11020 (IFT27)
GTP-binding proteins [BR:hsa04031]
 Small (monomeric) G-proteins
  Rho Family
   Others
    11020 (IFT27)
SSDB
Motif
Pfam: Ras Roc Arf nSTAND3 AAA_18 TniB
Other DBs
NCBI-GeneID: 11020
NCBI-ProteinID: NP_001171172
OMIM: 615870
HGNC: 18626
Ensembl: ENSG00000100360
UniProt: Q9BW83
Position
22:complement(36758211..36776119)
AA seq 186 aa
MVKLAAKCILAGDPAVGKTALAQIFRSDGAHFQKSYTLTTGMDLVVKTVPVPDTGDSVEL
FIFDSAGKELFSEMLDKLWESPNVLCLVYDVTNEESFNNCSKWLEKARSQAPGISLPGVL
VGNKTDLAGRRAVDSAEARAWALGQGLECFETSVKEMENFEAPFHCLAKQFHQLYREKVE
VFRALA
NT seq 561 nt   +upstreamnt  +downstreamnt
atggtgaagctggcagccaaatgcatcctggcaggagacccagcagtgggcaagaccgcc
ctggcacagatcttccgcagtgatggagcccatttccagaaaagctacaccctgacaaca
ggaatggatttggtggtgaagacagtgccagttcctgacacgggagacagtgtggaactc
ttcatttttgactctgctggcaaggagctgttttcggaaatgctggataaattgtgggag
agtcccaatgtcttatgtctcgtctatgatgtgaccaatgaagaatccttcaacaactgc
agcaagtggctggagaaggctcggtcacaggctccaggcatctctctcccaggtgtttta
gttgggaacaagacagacctggccggcagacgagcagtggactcagctgaggcccgggca
tgggcgctgggccagggcctggaatgttttgaaacatccgtgaaagagatggaaaacttc
gaagcccctttccactgccttgccaagcagttccaccagctgtaccgggagaaggtggag
gttttccgggccctggcatga

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