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LOADING
Gene Symbol:
ARID2
Entrez Gene ID
196528
Gene Name:
AT-rich interaction domain 2
Gene Aliases
BAF200, p200
Gene Chromosome Location
Chr.12: on Build GRCh38
UniGene
Hs.317304
Species:
Human
Primer Chromosome Location
Chr.12: 45817697-45817821 on Build GRCh38
View in UCSC browser
Amplicon Length
125
Primer Sequences
Log in to view
Ampliseq ID's
Primer ID
Hs00526937_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
ARID2
Accession
Protein
COSMIC ID
Mutation
AA
RefSeq
NM_152641.2
NP_689854.2
6914112
c.469G>C
p.D157H
1628602
c.551C>G
p.S184*
7325431
c.568G>A
p.V190I
265477
c.520G>T
p.D174Y
7329245
c.502G>T
p.G168*
5953323
c.487C>T
p.L163F
6969097
c.542_543delCT
p.L182fs*4
1676888
c.551C>A
p.S184*
268707
c.521A>G
p.D174G
4041980
c.484G>T
p.V162L
6890882
c.533A>C
p.N178T
7447833
c.540C>A
p.C180*
4041981
c.535G>A
p.V179I
4450131
c.457delA
p.N153fs*62
6986560
c.509C>G
p.P170R
6975423
c.502G>A
p.G168R
6072643
c.482T>A
p.L161*
274040
c.541A>G
p.T181A
159178
c.535G>T
p.V179L
4747142
c.527_546del20
p.N178fs*2
6253087
c.486G>T
p.V162V
693911
c.493C>T
p.L165L
4663265
c.479A>G
p.K160R
4633663
c.478A>G
p.K160E
XM_006719272.3
XP_006719335.1
-
-
-
GenBank
AK127872.1
BAC87171.1
-
-
-
AL832200.1
CAD91164.1
-
-
-
AY727870.2
AAU20329.2
-
-
-
CN419675.1
-
-
-
CR749833.1
CAH18689.1
-
-
-
DQ096628.1
-
-
-
ENST00000334344.0
-
-
-
Phenotype
MIM: 609539
Literature Links:
ARID2
PubMed Links
SNP ID
rs769017296
rs774797224
rs940745206
rs748418306
rs779533809
rs749833945
rs896638040
Submission count
NA
Allele Nomenclature
Chromosome Location
Chr.12: 45817743-45817743 on Build GRCh38
Allele Frequency
1000Genome
Applied Biosystems
®
HapMap
Global - Not Available
Caucasian - Not Available
CEPH (CEU) - Not Available
EAS - Not Available
African American - Not Available
YRI (Yoruba) - Not Available
SAS - Not Available
Chinese - Not Available
CHB (Han Chinese) - Not Available
AFR - Not Available
Japanese - Not Available
JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
Submission count
NA
Allele Nomenclature
Chromosome Location
Chr.12: 45817770-45817770 on Build GRCh38
Allele Frequency
1000Genome
Applied Biosystems
®
HapMap
Global - Not Available
Caucasian - Not Available
CEPH (CEU) - Not Available
EAS - Not Available
African American - Not Available
YRI (Yoruba) - Not Available
SAS - Not Available
Chinese - Not Available
CHB (Han Chinese) - Not Available
AFR - Not Available
Japanese - Not Available
JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
Submission count
NA
Allele Nomenclature
Chromosome Location
Chr.12: 45817764-45817764 on Build GRCh38
Allele Frequency
1000Genome
Applied Biosystems
®
HapMap
Global - Not Available
Caucasian - Not Available
CEPH (CEU) - Not Available
EAS - Not Available
African American - Not Available
YRI (Yoruba) - Not Available
SAS - Not Available
Chinese - Not Available
CHB (Han Chinese) - Not Available
AFR - Not Available
Japanese - Not Available
JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
Submission count
NA
Allele Nomenclature
Chromosome Location
Chr.12: 45817785-45817785 on Build GRCh38
Allele Frequency
1000Genome
Applied Biosystems
®
HapMap
Global - Not Available
Caucasian - Not Available
CEPH (CEU) - Not Available
EAS - Not Available
African American - Not Available
YRI (Yoruba) - Not Available
SAS - Not Available
Chinese - Not Available
CHB (Han Chinese) - Not Available
AFR - Not Available
Japanese - Not Available
JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
Submission count
NA
Allele Nomenclature
Chromosome Location
Chr.12: 45817725-45817725 on Build GRCh38
Allele Frequency
1000Genome
Applied Biosystems
®
HapMap
Global - Not Available
Caucasian - Not Available
CEPH (CEU) - Not Available
EAS - Not Available
African American - Not Available
YRI (Yoruba) - Not Available
SAS - Not Available
Chinese - Not Available
CHB (Han Chinese) - Not Available
AFR - Not Available
Japanese - Not Available
JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
Submission count
NA
Allele Nomenclature
Chromosome Location
Chr.12: 45817736-45817736 on Build GRCh38
Allele Frequency
1000Genome
Applied Biosystems
®
HapMap
Global - Not Available
Caucasian - Not Available
CEPH (CEU) - Not Available
EAS - Not Available
African American - Not Available
YRI (Yoruba) - Not Available
SAS - Not Available
Chinese - Not Available
CHB (Han Chinese) - Not Available
AFR - Not Available
Japanese - Not Available
JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
Submission count
NA
Allele Nomenclature
Chromosome Location
Chr.12: 45817786-45817786 on Build GRCh38
Allele Frequency
1000Genome
Applied Biosystems
®
HapMap
Global - Not Available
Caucasian - Not Available
CEPH (CEU) - Not Available
EAS - Not Available
African American - Not Available
YRI (Yoruba) - Not Available
SAS - Not Available
Chinese - Not Available
CHB (Han Chinese) - Not Available
AFR - Not Available
Japanese - Not Available
JPT (Japanese) - Not Available
EUR - Not Available
AMR - Not Available
Back To Top
More Information
Set Membership:
Less than 200 bp
Gene Ontology Categories:
Function(s)
Process(es)
nucleosome disassembly
transcription, DNA-templated
regulation of transcription, DNA-templated
negative regulation of cell proliferation
covalent chromatin modification
negative regulation of cell migration
DNA binding
protein binding
metal ion binding
Format:
Each primer will be delivered in a single tube, dried-down
Quick Reference Guide
Primer Designer
™
Tool Quick Reference
Back To Top
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git-commit: c531a7a49d92b854cb004d8acd820c41186dcba6
git-url: https://github.com/thermofisher/magellan-search
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