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LOADING
Gene Symbol:
GPRIN2
LOC107984026
Entrez Gene ID
9721
107984026
Gene Name:
G protein regulated inducer of neurite outgrowth 2
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 4-like
Gene Aliases
GRIN2, KIAA0514
-
Gene Chromosome Location
Chr.10: on Build GRCh38
Chr.10: on Build GRCh38
UniGene
Hs.523375
Species:
Human
Primer Chromosome Location
Chr.10: 46549822-46549551 on Build GRCh38
View in UCSC browser
Amplicon Length
272
Primer Sequences
Log in to view
Ampliseq ID's
Primer ID
Hs00642368_CE
Primer 5'-tail Option
Non-tailed
M13-tailed
Purification
Desalted
HPLC
Primer Pair /FWD/REV
Pair
Forward
Reverse
Synthesis Scale
25 nmol
Availability
Made To Order
Catalog #'s
A15629,A15630
Price
Add To Cart
Genomic Map
Assay Details
More Information
Genomic Map
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Assay Details
Gene Information
GPRIN2
Accession
Protein
COSMIC ID
Mutation
AA
RefSeq
NM_014696.3
NP_055511.2
4014309
c.1138C>T
p.R380W
3397139
c.1128G>A
p.P376P
3751794
c.987G>T
p.P329P
4144707
c.995C>A
p.A332D
1347901
c.1042G>T
p.V348L
1958317
c.1016C>T
p.A339V
1187936
c.925A>G
p.R309G
3438023
c.1063G>A
p.E355K
3438021
c.968C>G
p.A323G
4014307
c.1029G>A
p.A343A
6213340
c.1065A>G
p.E355E
1958322
c.1147C>T
p.R383*
6197573
c.964T>C
p.L322L
4651794
c.1112G>T
p.S371I
684245
c.1102C>G
p.L368V
1745806
c.1093G>C
p.E365Q
3867246
c.1116G>A
p.L372L
4573636
c.1114C>T
p.L372L
918368
c.1034G>A
p.C345Y
427581
c.983C>G
p.S328C
918366
c.1004C>A
p.A335D
379819
c.1131C>T
p.S377S
6674647
c.1044G>T
p.V348V
6674645
c.951C>T
p.T317T
4014310
c.1182C>T
p.Y394Y
3741663
c.962A>T
p.D321V
4933311
c.1128G>T
p.P376P
4014308
c.1125G>A
p.V375V
1560777
c.1017G>A
p.A339A
3397138
c.1068G>A
p.A356A
1347902
c.1089delC
p.P364fs*3
4144706
c.985C>G
p.P329A
1187937
c.1117G>C
p.E373Q
3438024
c.1153G>A
p.D385N
3931034
c.1033T>G
p.C345G
1958313
c.944C>T
p.T315I
3438022
c.1003G>A
p.A335T
4608316
c.1072G>T
p.A358S
5998870
c.961G>A
p.D321N
4014306
c.1007G>T
p.G336V
1958326
c.1183G>A
p.G395R
6210501
c.1176G>A
p.E392E
1208798
c.1076C>T
p.A359V
368473
c.1069C>T
p.P357S
1958320
c.1054C>T
p.P352S
6129666
c.1068G>T
p.A356A
189547
c.1056G>A
p.P352P
3438020
c.934G>A
p.D312N
3867245
c.998A>G
p.Q333R
918367
c.1021C>T
p.P341S
918365
c.987G>A
p.P329P
6674646
c.978G>T
p.E326D
918369
c.1127C>T
p.P376L
5458130
c.1181A>G
p.Y394C
XM_005277666.3
XP_005277723.1
-
-
-
XM_011540388.2
XP_011538690.1
-
-
-
XM_011540395.2
XP_011538697.1
-
-
-
XM_011540400.2
XP_011538702.1
-
-
-
XM_017016974.1
XP_016872463.1
-
-
-
XM_017016975.1
XP_016872464.1
-
-
-
XM_017016976.1
XP_016872465.1
-
-
-
XM_017016977.1
XP_016872466.1
-
-
-
XM_017016978.1
XP_016872467.1
-
-
-
XM_017016979.1
XP_016872468.1
-
-
-
XM_017016980.1
XP_016872469.1
-
-
-
XM_017016981.1
XP_016872470.1
-
-
-
XM_017016982.1
XP_016872471.1
-
-
-
XM_017016983.1
XP_016872472.1
-
-
-
XM_017016984.1
XP_016872473.1
-
-
-
GenBank
AB011086.1
BAA25440.2
-
-
-
BC011672.2
AAH11672.1
-
-
-
ENST00000374317.0
-
-
-
Phenotype
MIM: 611240
LOC107984026
Accession
Protein
COSMIC ID
Mutation
AA
RefSeq
XM_017017029.1
XP_016872518.1
-
-
-
XM_017017030.1
XP_016872519.1
-
-
-
XM_017017031.1
XP_016872520.1
-
-
-
XM_017017032.1
XP_016872521.1
-
-
-
XM_017017033.1
XP_016872522.1
-
-
-
XM_017017034.1
XP_016872523.1
-
-
-
XM_017017038.1
XP_016872527.1
-
-
-
XM_017017039.1
XP_016872528.1
-
-
-
XM_017017040.1
XP_016872529.1
-
-
-
Phenotype
Literature Links:
GPRIN2
PubMed Links
SNP ID
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More Information
Set Membership:
Between 200-400 bp
Gene Ontology Categories:
Process(es)
protein binding
Format:
Each primer will be delivered in a single tube, dried-down
Quick Reference Guide
Primer Designer
™
Tool Quick Reference
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Host server : magellan-search-5c7f9f6c68-89mxr:80/10.239.163.131:80.
git-commit: b16971a8df2afcd8df684aafbc9bf1e9f45e42d4
git-url: git@github.com:thermofisher/magellan-core.git
git-branch: origin/release/2.6.0-2024.04.15-1.0