Homo sapiens (human): 112752
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Entry
112752 CDS
T01001
Symbol
IFT43, C14orf179, CED3, RP81, SRTD18
Name
(RefSeq) intraflagellar transport 43
KO
K19675
intraflagellar transport protein 43
Organism
hsa
Homo sapiens (human)
Disease
H00527
Retinitis pigmentosa
H00529
Cranioectodermal dysplasia
H02157
Short-rib thoracic dysplasia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
112752 (IFT43)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Intraflagellar transport (IFT) complex A
112752 (IFT43)
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GFIT
Motif
Pfam:
IFT43
Motif
Other DBs
NCBI-GeneID:
112752
NCBI-ProteinID:
NP_001096034
OMIM:
614068
HGNC:
29669
Ensembl:
ENSG00000119650
UniProt:
Q96FT9
Structure
PDB
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All DBs
Position
14:75985763..76084073
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AA seq
208 aa
AA seq
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MEDLLDLDEELRYSLATSRAKMGRRAQQESAQAENHLNGKNSSLTLTGETSSAKLPRCRQ
GGWAGDSVKASKFRRKASEEIEDFRLRPQSLNGSDYGGDIPIIPDLEEVQEEDFVLQVAA
PPSIQIKRVMTYRDLDNDLMKYSAIQTLDGEIDLKLLTKVLAPEHEVREDDVGWDWDHLF
TEVSSEVLTEWDPLQTEKEDPAGQARHT
NT seq
627 nt
NT seq
+upstream
nt +downstream
nt
atggaggatttgctcgacttggacgaggagcttcgctacagcttggctacctccagggcc
aagatgggtcgccgagctcaacaggagtcagcgcaggccgagaatcacctcaatggcaag
aattcctctttgactctgactggagagacttcctctgctaaattacctcgctgccgacag
ggaggctgggcaggtgattccgtgaaggcttcgaagtttaggaggaaggcttctgaagaa
atagaagatttccgcctcagaccacagagcctgaatggatcagattatggaggagatatt
cctatcattccggatctggaggaagtacaggaagaagactttgttttgcaggtggcagcc
cctcccagcatccagataaagcgggtgatgacctaccgtgacctggacaatgacctcatg
aagtactcagccattcagacactggatggggagatcgacctgaaactcctcaccaaagtg
ctcgcgccggagcacgaagtccgggaggatgatgtcggctgggactgggaccatctgttc
actgaggtgtcctcagaggtcctcactgagtgggacccactgcagacggagaaggaggac
cctgcggggcaggccaggcacacctga
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integrated database retrieval system