Type | Description |
---|---|
Definition | KIAA1217 |
Date | Results | Publications |
---|---|---|
2021-03-13 13:18:00 | KIAA1217: A novel candidate gene associated with isolated and syndromic vertebral malformations. | 32369272 |
2017-12-30 12:41:00 | Data suggest that the KIAA1217-RET-fusion gene is a promising target for lung cancer treatment. | 27150058 |
2012-02-04 10:32:00 | SKT is involved in the etiology of intervertebral disc degeneration among young adults. | 22107760 |
2010-06-30 22:05:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
2010-01-21 00:00:00 | Using tag SNPs, we examined the association in two independent Japanese case-control populations and found a significant association of lumbar herniation with SKT rs16924573 in the allele frequency model | 19338451 |
Type | IDs |
---|---|
Synonymous | ETL4, SKT |
Gene |
UniProtKB-ID:
SKT_HUMAN,
B7ZM29_HUMAN
UniprotKB:
Q5T5P2,
B7ZM29
UniParc:
UPI00003FECAE,
UPI000150AF22,
UPI00016277F2,
UPI0002065AA6,
UPI000189A92D,
UPI000155D4BA,
UPI000013EC2A,
UPI0000EE4160,
UPI0000140FD4,
UPI000150AF23
EMBL:
AL157473,
AL355977,
BX648451,
AL353583,
AL353650,
AL356477,
AC063961,
BC098577,
AL391499,
AB033043,
AL833280,
AL356113,
AK125675,
CH471072,
BC018764,
BX640796,
BC144227,
AL157781,
AL392104,
AB291616,
BC136521
Ensembl:
ENSG00000120549
KO:
hsa:56243
|
Nucleutide sequences |
EMBL-CDS:
BAA86531.2,
AAH18764.1,
EAW86124.1,
CAB75668.1,
AAI36522.1,
CAE45879.1,
BAF63529.1,
AAH98577.1,
BAC86241.1,
AAI44228.1
Ensembl_TRS:
ENST00000458595,
ENST00000396445,
ENST00000307544,
ENST00000376462,
ENST00000396446,
ENST00000376452,
ENST00000376451,
ENST00000376454,
ENST00000430453
|
Protein sequencees |
Ensembl_PRO:
ENSP00000379722,
ENSP00000365635,
ENSP00000392625,
ENSP00000389680,
ENSP00000365637,
ENSP00000302343,
ENSP00000379723,
ENSP00000365645,
ENSP00000365634
RefSeq:
XP_016871907.1,
XP_016871913.1,
XP_024303854.1,
XP_011517857.2,
NP_001091970.1,
XP_016871905.1,
XP_016871918.1,
XP_016871915.1,
XP_011517861.2,
XP_011517868.2,
XP_011517867.2,
XP_024303850.1,
XP_016871912.1,
XP_016871916.1,
XP_011517854.2,
NP_062536.2,
XP_024303853.1,
XP_005252573.1,
XP_016871908.1,
XP_011517866.1,
XP_011517860.2,
NP_001269697.1,
XP_024303852.1,
NP_001308610.1,
XP_016871910.1,
XP_011517864.2,
XP_016871911.1,
NP_001269699.1,
NP_001269696.1,
XP_016871909.1,
XP_016871906.1,
XP_016871914.1,
XP_024303851.1,
NP_001269698.1
|
Others |
UniRef100:
UniRef100_Q5T5P2,
UniRef100_B7ZM29
UniRef90:
UniRef90_Q5T5P2,
UniRef90_A0A2I3LR52
UniRef50:
UniRef50_Q5T5P2,
UniRef50_A0A2I3LR52
UniGene:
Hs.445885
CCDS:
CCDS60501.1,
CCDS31165.1,
CCDS60502.1,
CCDS41496.1,
CCDS60504.1,
CCDS60505.1
|
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Refseq |
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