Type | Description |
---|---|
Definition | kinesin family member 16B |
Date | Results | Publications |
---|---|---|
2021-03-13 13:16:00 | Novel genetic variants in KIF16B and NEDD4L in the endosome-related genes are associated with nonsmall cell lung cancer survival. | 31618441 |
2019-05-25 10:56:00 | KIF16B mutation is associated with autosomal-recessive intellectual disability syndrome. | 29736960 |
2013-10-19 11:10:00 | The kinesin KIF16B mediates apical transcytosis of transferrin receptor in AP-1B-deficient epithelia. | 23749212 |
2013-01-26 10:49:00 | The tubule formations were dependent on microtubule interactions, and specifically controlled by Kif16b and dynein 1. | 22357949 |
2012-09-01 11:02:00 | genome-wide significance in genes involved in synaptic signaling (KIF16B; p = 1.27E-08) and neurodevelopment (PAX5; p = 3.58E-08). | 22449649 |
Type | IDs |
---|---|
Synonymous | C20orf23, KISC20ORF, SNX23 |
Gene |
UniProtKB-ID:
KI16B_HUMAN,
A0A140VK74_HUMAN,
A0A1B0GTU3_HUMAN
UniprotKB:
Q96L93,
A0A140VK74,
A0A1B0GTU3
UniParc:
UPI00003BF77C,
UPI0000206A61,
UPI00005B7380,
UPI00003BF77D,
UPI0000206A5A,
UPI00020B16EA
EMBL:
KF456837,
AL117376,
BX647572,
AY044654,
AK095322,
BC110317,
AB046810,
KF456843,
BC034984,
BC150261,
AL049794,
AY166853,
AK026698,
HM005614,
BX648426,
AK000142,
CH471133,
AL118509
Ensembl:
ENSG00000089177
KO:
hsa:55614
|
Nucleutide sequences |
EMBL-CDS:
AAI50262.1,
AAO17292.1,
BAB15530.1,
AAK98768.1,
AAH34984.2,
CAI46266.1,
AAI10318.1,
CAI46105.1,
BAA90971.1,
BAB13416.2,
EAX10290.1,
AEE61211.1
Ensembl_TRS:
ENST00000408042,
ENST00000354981,
ENST00000636835
|
Protein sequencees |
Ensembl_PRO:
ENSP00000384164,
ENSP00000347076,
ENSP00000489838
RefSeq:
NP_001186795.1,
XP_005260809.1,
XP_005260810.1,
XP_024307704.1,
NP_078980.3,
XP_005260808.1,
XP_006723651.1,
NP_001186794.1,
XP_016883415.1,
XP_005260812.1,
XP_005260807.1,
XP_005260811.1
|
Others |
UniRef100:
UniRef100_Q96L93,
UniRef100_A0A1B0GTU3
UniRef90:
UniRef90_A0A1B0GTU3,
UniRef90_Q96L93
UniRef50:
UniRef50_Q96L93,
UniRef50_Q96L93-5
UniGene:
Hs.101774
CCDS:
CCDS56178.1,
CCDS13122.1
|
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Refseq |
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