Type | Description |
---|---|
Definition | heterogeneous nuclear ribonucleoprotein R |
Date | Results | Publications |
---|---|---|
2020-09-12 16:04:00 | HnRNPR-CCNB1/CENPF axis contributes to gastric cancer proliferation and metastasis. | 31527303 |
2020-04-04 12:43:00 | Identification of the frequent presence of hnRNP R and hnRNP Q in frontotemporal lobar degeneration (FTLD)-FUS inclusions suggests a potential role for these hnRNPs in FTLD-FUS pathogenesis and supports the role of dysfunctional RNA metabolism in FTLD. | 30755280 |
2020-03-14 12:34:00 | HNRNPR Variants that Impair Homeobox Gene Expression causes Developmental Disorders. | 31079900 |
2017-08-05 12:49:00 | demonstrated that HNRNPR binds MHC class I mRNAs in their 3' untranslated regions and enhances their stability and their expression; regulation by HNRNPR modulates the cytotoxic activity of NK cell; conclude that HNRNPR acts as a general positive regulator of MHC class I expression | 27194785 |
2015-07-04 15:24:00 | SMN is involved in the axonal translocation of hnRNP R and hnRNP R-bound RNA/protein complexes. | 25338097 |
Type | IDs |
---|---|
Synonymous | HNRPR, hnRNP-R |
Gene |
UniProtKB-ID:
HNRPR_HUMAN,
Q6MZS5_HUMAN,
B4DMB1_HUMAN,
B4DT28_HUMAN,
B4DMD1_HUMAN,
Q0VGD6_HUMAN
UniprotKB:
O43390,
Q6MZS5,
B4DMB1,
B4DT28,
B4DMD1,
Q0VGD6
UniParc:
UPI00005A02CC,
UPI000006F30B,
UPI00001BDC25,
UPI00017A760F,
UPI0000DBE1A3,
UPI00017A7662,
UPI00005A02CD,
UPI000013454C,
UPI00015ADD09
EMBL:
AK297382,
AL109936,
AF000364,
BC110389,
AK297405,
DQ351905,
BC001449,
BX640912,
CH471134,
AK300029
Ensembl:
ENSG00000125944,
ENSG00000282958
KO:
hsa:10236
|
Nucleutide sequences |
EMBL-CDS:
AAH01449.1,
ABC73063.1,
AAC39540.1,
CAE45953.1,
BAG59823.1,
BAG61840.1,
EAW95040.1,
BAG59843.1,
AAI10390.1
Gene_ORFName:
hCG_38907
Ensembl_TRS:
ENST00000478691,
ENST00000634766,
ENST00000635150,
ENST00000634263,
ENST00000634713,
ENST00000374612,
ENST00000427764,
ENST00000302271,
ENST00000634634,
ENST00000374616,
ENST00000606561,
ENST00000635199
|
Protein sequencees |
Ensembl_PRO:
ENSP00000489275,
ENSP00000474437,
ENSP00000489252,
ENSP00000488941,
ENSP00000489371,
ENSP00000304405,
ENSP00000363741,
ENSP00000363745,
ENSP00000392799,
ENSP00000488945,
ENSP00000475760,
ENSP00000489386
RefSeq:
XP_011538776.1,
XP_011538773.1,
NP_005817.1,
XP_011538777.1,
NP_001284549.1,
XP_016855499.1,
NP_001284551.1,
XP_011538778.1,
XP_011538774.1,
XP_016855497.1,
NP_001095868.1,
XP_016855498.1,
NP_001095869.1,
NP_001284550.1,
XP_005245768.1,
NP_001095867.1,
XP_011538779.1
|
Others |
UniRef100:
UniRef100_Q0VGD6,
UniRef100_Q6MZS5,
UniRef100_O43390,
UniRef100_B4DMD1,
UniRef100_B4DT28,
UniRef100_B4DMB1
UniRef90:
UniRef90_M3V815,
UniRef90_B4DT28,
UniRef90_F6X1D1,
UniRef90_O43390,
UniRef90_B4DMD1
UniRef50:
UniRef50_Q6TGW7,
UniRef50_O60506
UniGene:
Hs.373763
CCDS:
CCDS232.1,
CCDS60020.1,
CCDS44085.1,
CCDS72727.1
|
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