Homo sapiens (human): 11020
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ras
Roc
Arf
nSTAND3
AAA_18
TniB
Motif
Other DBs
NCBI-GeneID:
11020
NCBI-ProteinID:
NP_001171172
OMIM:
615870
HGNC:
18626
Ensembl:
ENSG00000100360
UniProt:
Q9BW83
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All DBs
Position
22:complement(36758211..36776119)
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AA seq
186 aa
AA seq
DB search
MVKLAAKCILAGDPAVGKTALAQIFRSDGAHFQKSYTLTTGMDLVVKTVPVPDTGDSVEL
FIFDSAGKELFSEMLDKLWESPNVLCLVYDVTNEESFNNCSKWLEKARSQAPGISLPGVL
VGNKTDLAGRRAVDSAEARAWALGQGLECFETSVKEMENFEAPFHCLAKQFHQLYREKVE
VFRALA
NT seq
561 nt
NT seq
+upstream
nt +downstream
nt
atggtgaagctggcagccaaatgcatcctggcaggagacccagcagtgggcaagaccgcc
ctggcacagatcttccgcagtgatggagcccatttccagaaaagctacaccctgacaaca
ggaatggatttggtggtgaagacagtgccagttcctgacacgggagacagtgtggaactc
ttcatttttgactctgctggcaaggagctgttttcggaaatgctggataaattgtgggag
agtcccaatgtcttatgtctcgtctatgatgtgaccaatgaagaatccttcaacaactgc
agcaagtggctggagaaggctcggtcacaggctccaggcatctctctcccaggtgtttta
gttgggaacaagacagacctggccggcagacgagcagtggactcagctgaggcccgggca
tgggcgctgggccagggcctggaatgttttgaaacatccgtgaaagagatggaaaacttc
gaagcccctttccactgccttgccaagcagttccaccagctgtaccgggagaaggtggag
gttttccgggccctggcatga
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integrated database retrieval system