Type | Description |
---|---|
Definition | intraflagellar transport 88 |
Date | Results | Publications |
---|---|---|
2020-10-24 13:55:00 | IFT88 controls NuMA enrichment at k-fibers minus-ends to facilitate their re-anchoring into mitotic spindles. | 31312011 |
2020-05-16 12:29:00 | The Intraflagellar IFT88 Is Disrupted in Cystic Fibrosis. | 31891309 |
2020-05-02 10:09:00 | Significant association was found between IFT88 rs9509311 and rs2497490 and Nonsyndromic cleft lip with or without cleft palate (NSCLP) in non-Hispanic white families (p = .004 and .005), while nominal associations were found for rs7998361 and rs9509307 (p < .05). Pairwise association analyses also showed nominal associations between NSCLP in both NHW and Hispanic data sets (p < .05). | 30953423 |
2019-09-07 10:03:00 | TCTN2 Depletion-Induced IFT88 Lumen Leakage and Ciliary Weakening | 29866362 |
2019-03-30 11:52:00 | These observations suggest that the rare and unique combination of IFT88 alleles observed in this study provide insight into the physiological role of IFT88 in humans and the likely mechanism underlying retinal pathology in the pedigree with inherited retinal degeneration | 29978320 |
Type | IDs |
---|---|
Synonymous | D13S1056E, DAF19, TG737, TTC10, hTg737 |
Gene |
UniProtKB-ID:
IFT88_HUMAN,
A0A140VJL7_HUMAN,
B3KX42_HUMAN
UniprotKB:
Q13099,
A0A140VJL7,
B3KX42
UniParc:
UPI00001616F5,
UPI0001F4E01D,
UPI00004A275E,
UPI0000160108
EMBL:
BC030776,
HM005406,
CH471075,
AK126668,
AK300769,
AL161772,
U20362,
AL590096
Ensembl:
ENSG00000032742
KO:
hsa:8100
|
Nucleutide sequences |
EMBL-CDS:
BAG62434.1,
AAA86720.1,
EAX08272.1,
AAH30776.2,
AEE61004.1,
BAG54354.1
Ensembl_TRS:
ENST00000351808,
ENST00000319980
|
Protein sequencees |
Ensembl_PRO:
ENSP00000261632,
ENSP00000323580
RefSeq:
NP_001340499.1,
XP_016876251.1,
XP_016876247.1,
XP_016876257.1,
XP_016876248.1,
XP_016876262.1,
NP_783195.2,
NP_001340501.1,
XP_016876265.1,
NP_001340506.1,
NP_006522.2,
NP_001340503.1,
NP_001340500.1,
NP_001340498.1,
XP_006719933.1,
NP_001340504.1,
NP_001340508.1,
NP_001340505.1,
XP_016876252.1,
NP_001340495.1,
XP_011533545.1,
NP_001340502.1,
XP_016876264.1,
XP_024305183.1,
NP_001340496.1,
NP_001305420.1,
XP_024305179.1,
XP_024305180.1,
NP_001340494.1,
XP_024305181.1,
XP_016876246.1,
NP_001340497.1,
NP_001305422.1,
NP_001340507.1,
XP_024305182.1
|
Others |
UniRef100:
UniRef100_Q13099,
UniRef100_B3KX42
UniRef90:
UniRef90_Q13099,
UniRef90_B3KX42
UniRef50:
UniRef50_Q13099
UniGene:
Hs.187376
CCDS:
CCDS31945.1,
CCDS31944.1
|
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Refseq |
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