Type | Description |
---|---|
Definition | protein tyrosine phosphatase receptor type N2 |
Date | Results | Publications |
---|---|---|
2020-10-03 12:54:00 | The association of genetically controlled CpG methylation (cg158269415) of protein tyrosine phosphatase, receptor type N2 (PTPRN2) with childhood obesity. | 30890718 |
2017-08-26 11:26:00 | Copy-number variations are enriched for PTPRN2 and other neurodevelopmental genes in children with developmental coordination disorder. | 27489308 |
2017-05-20 10:50:00 | Haplotype-dependent allele-specific methylation of PTPRN2 gene is associated with neurological disorders. | 27153397 |
2016-05-07 10:23:00 | Reduction in plasma membrane PI(4,5)P2 abundance by PTPRN2 and PLCbeta1 releases the PI(4,5)P2-binding protein cofilin from its inactive membrane-associated state into the cytoplasm where it mediates actin turnover dynamics. | 26620550 |
2015-12-05 11:52:00 | Data indicate the X-ray structure of the mature ectodomain of mature ectodomain of phogrin/IA-2beta (PTPRN2) (ME phogrin) at pH 7.4 and 4.6. | 25421040 |
Type | IDs |
---|---|
Synonymous | IA-2beta, IAR, ICAAR, PTPRP, R-PTP-N2 |
Gene |
UniProtKB-ID:
PTPR2_HUMAN,
E7EM83_HUMAN,
I6L9F8_HUMAN
UniprotKB:
Q92932,
E7EM83,
I6L9F8
UniParc:
UPI000002E7C7,
UPI00001AFFA3,
UPI00001AF931,
UPI00003782EB,
UPI00018814AD,
UPI00017BE7A9
EMBL:
AC011899,
KF458646,
AB002385,
AC005481,
AC093662,
AF007555,
U66702,
KF510999,
BC034040,
AC093856,
AC006003,
U81561,
AC078942,
AC019043,
Y08569,
AC125243,
AC006372,
KF510998,
BC071570
Ensembl:
ENSG00000155093
KO:
hsa:5799
|
Nucleutide sequences |
EMBL-CDS:
AAH34040.1,
AAB68603.1,
CAA69880.1,
AAB63600.1,
AAC50742.1,
BAA20841.2,
AAH71570.1
Ensembl_TRS:
ENST00000389418,
ENST00000389416,
ENST00000389413,
ENST00000409483
|
Protein sequencees |
Ensembl_PRO:
ENSP00000374067,
ENSP00000374064,
ENSP00000374069,
ENSP00000387114
RefSeq:
NP_570858.2,
NP_570857.2,
XP_011514750.1,
XP_011514748.1,
NP_002838.2,
XP_016867965.1,
XP_011514751.1,
XP_016867964.1,
NP_001295197.1,
XP_011514749.1,
NP_001295196.1
|
Others |
UniRef100:
UniRef100_I6L9F8,
UniRef100_E7EM83,
UniRef100_Q92932
UniRef90:
UniRef90_I6L9F8,
UniRef90_Q92932,
UniRef90_Q92932-2
UniRef50:
UniRef50_I6L9F8,
UniRef50_Q92932
UniGene:
Hs.490789
CCDS:
CCDS5947.1,
CCDS5948.1,
CCDS5949.1
|
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