System Message

OKCancel
LOADING ...
Gene Symbol:
NCOR1
Entrez Gene ID
9611
Gene Name:
nuclear receptor corepressor 1
Gene Aliases
N-CoR, N-CoR1, PPP1R109, TRAC1, hN-CoR
Gene Chromosome Location
Chr.17: on Build GRCh38
UniGene
Hs.462323
Species:
Human
Primer Chromosome Location
Chr.17: 16164984-16165411 on Build GRCh38
Amplicon Length
428
Primer Sequences
Log in to view
Ampliseq ID's
Primer ID Hs00516353_CE
Primer 5'-tail Option
Purification
Primer Pair /FWD/REV
Synthesis Scale 25 nmol
Availability Made To Order
Catalog #'s A15629,A15630
Price (USD) USD 16.46,USD 16.46

Genomic Map

LOADING... Fetching data..
Back To Top

Assay Details

Gene Information


NCOR1
Accession Protein COSMIC ID Mutation AA
RefSeq NM_001190438.1 NP_001177367.1 - - -
NM_001190440.1 NP_001177369.1 4591259 c.571G>A p.E191K
6500675 c.559_569del11 p.V188fs*10
4897942 c.467C>T p.P156L
4767664 c.512C>T p.A171V
4860709 c.530C>G p.S177*
4907844 c.483G>A p.S161S
4593341 c.448G>A p.G150R
4858489 c.459T>C p.H153H
4590747 c.515C>T p.S172L
6945283 c.485G>T p.G162V
5773264 c.468A>G p.P156P
4547984 c.436G>A p.D146N
4816292 c.473C>T p.S158F
6928238 c.596_617del22 p.I199fs*79
7340274 c.485G>A p.G162E
4594688 c.447C>T p.F149F
4858518 c.436G>T p.D146Y
5226945 c.514delT p.S172fs*10
4590772 c.568C>T p.R190*
4548617 c.451G>A p.G151S
6919421 c.496G>T p.G166*
6056960 c.582A>T p.K194N
5005034 c.560G>A p.R187H
4594745 c.528C>T p.L176L
6967729 c.598C>T p.L200F
6913504 c.569G>A p.R190Q
4591234 c.534G>C p.K178N
4905740 c.460G>A p.E154K
6979205 c.559C>T p.R187C
4496242 c.470C>T p.S157F
6943824 c.587A>G p.E196G
5926972 c.439C>T p.P147S
6950017 c.530C>A p.S177*
7379155 c.608A>G p.K203R
5016557 c.436-2delA p.?
6080468 c.452G>A p.G151D
4595005 c.549G>A p.Q183Q
NM_006311.3 NP_006302.2 3773771 c.549G>A p.Q183Q
436099 c.514delT p.S172fs*10
3818895 c.473C>T p.S158F
3514568 c.460G>A p.E154K
6080467 c.452G>A p.G151D
704900 c.459T>C p.H153H
6950016 c.530C>A p.S177*
4129608 c.571G>A p.E191K
1686251 c.467C>T p.P156L
1630066 c.515C>T p.S172L
340462 c.494G>T p.C165F
3514569 c.436G>A p.D146N
4591233 c.534G>C p.K178N
704901 c.530C>G p.S177*
2739071 c.608A>G p.K203R
6500674 c.559_569del11 p.V188fs*10
4129609 c.568C>T p.R190*
6943823 c.587A>G p.E196G
124695 c.509A>G p.N170S
975884 c.442G>A p.A148T
5926971 c.439C>T p.P147S
5005033 c.560G>A p.R187H
6967728 c.598C>T p.L200F
3722726 c.450A>G p.G150G
249685 c.448G>A p.G150R
1520559 c.470C>T p.S157F
4548616 c.451G>A p.G151S
6919420 c.496G>T p.G166*
6928237 c.596_617del22 p.I199fs*79
4129610 c.528C>T p.L176L
5016556 c.436-2delA p.?
4064173 c.483G>A p.S161S
7340273 c.485G>A p.G162E
6913503 c.569G>A p.R190Q
4767663 c.512C>T p.A171V
6945282 c.485G>T p.G162V
6056959 c.582A>T p.K194N
6979204 c.559C>T p.R187C
704899 c.436G>T p.D146Y
4129611 c.447C>T p.F149F
5773263 c.468A>G p.P156P
XM_005256866.4 XP_005256923.1 - - -
XM_005256868.4 XP_005256925.1 - - -
XM_005256871.4 XP_005256928.1 - - -
XM_005256872.4 XP_005256929.1 - - -
XM_005256873.4 XP_005256930.1 - - -
XM_005256874.4 XP_005256931.1 - - -
XM_005256875.3 XP_005256932.1 - - -
XM_006721601.3 XP_006721664.1 - - -
XM_006721602.3 XP_006721665.1 - - -
XM_006721603.3 XP_006721666.1 - - -
XM_006721604.3 XP_006721667.1 - - -
XM_011524083.2 XP_011522385.1 - - -
XM_011524084.2 XP_011522386.1 - - -
XM_011524085.2 XP_011522387.1 - - -
XM_011524086.2 XP_011522388.1 - - -
XM_017025396.1 XP_016880885.1 - - -
XM_017025397.1 XP_016880886.1 - - -
XM_017025398.1 XP_016880887.1 - - -
XM_017025399.1 XP_016880888.1 - - -
XM_017025400.1 XP_016880889.1 - - -
XM_017025401.1 XP_016880890.1 - - -
XM_017025402.1 XP_016880891.1 - - -
XM_017025403.1 XP_016880892.1 - - -
XM_017025404.1 XP_016880893.1 - - -
XM_017025405.1 XP_016880894.1 - - -
XM_017025406.1 XP_016880895.1 - - -
XM_017025407.1 XP_016880896.1 - - -
XM_017025408.1 XP_016880897.1 - - -
XM_017025409.1 XP_016880898.1 - - -
XM_017025410.1 XP_016880899.1 - - -
XM_017025411.1 XP_016880900.1 - - -
XM_017025412.1 XP_016880901.1 - - -
XM_017025413.1 XP_016880902.1 - - -
XM_017025414.1 XP_016880903.1 - - -
XM_017025415.1 XP_016880904.1 - - -
XM_017025416.1 XP_016880905.1 - - -
XM_017025417.1 XP_016880906.1 - - -
XM_017025418.1 XP_016880907.1 - - -
XM_017025419.1 XP_016880908.1 - - -
XM_017025420.1 XP_016880909.1 - - -
GenBank AB028970.2 - - -
AF044209.1 AAC33550.1 - - -
AF087856.1 AAP97166.1 - - -
AF303586.1 AAO32942.1 - - -
AK307614.1 - - -
BC026028.1 - - -
BC035748.1 - - -
BC050594.2 AAH50594.1 - - -
BC056862.1 AAH56862.1 - - -
BC058511.1 AAH58511.1 - - -
BC068996.1 AAH68996.1 - - -
BC107772.1 AAI07773.1 - - -
BC142648.1 - - -
BC167431.1 - - -
ENST00000268712.0 - - -


Phenotype

MIM: 600849

Literature Links:

NCOR1 PubMed Links

SNP ID

rs778810900 rs748917951 rs747635891 rs767545851 rs74453660 rs1007943648 rs1015360732 rs757432309 rs748927292 rs755850300 rs750163298 rs775887208 rs370041911 rs755746636 rs765365064 rs200020868 rs768292710 rs755596876 rs780796530 rs754924127 rs993661460 rs201765279 rs367758096 rs77374546 rs76571303 rs764105818 rs746896731 rs763120484 rs752705846 rs777299498 rs200311165 rs777127113 rs78230791 rs762072050 rs533730138 rs769132482 rs753886331 rs758132759 rs758420075 rs113512856 rs76780359 rs755010261 rs772348807 rs751563085 rs117460600 rs200619126 rs952379999 rs767366178 rs764190554 rs796642927 rs199892481 rs761125618 rs779386592 rs751366596 rs777290475 rs780448158 rs1027843424 rs547433134 rs878955411 rs766597956 rs780886471 rs992220232 rs748595798 rs774344153 rs149251801 rs55844632 rs373497426 rs981060030 rs769218696 rs796602104 rs756042093 rs779837909 rs76375524 rs201706028 rs776750615 rs747360693 rs763556154 rs747557072 rs761714796 rs150910818 rs772418872 rs766116978 rs137862851 rs776894697

Submission count

NA

Allele Nomenclature



Chromosome Location

Chr.17: 16165038-16165038 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:

 Between 400-700 bp

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)

Format:

Each primer will be delivered in a single tube, dried-down

Quick Reference Guide

Primer Designer™ Tool Quick Reference




Back To Top

Related Products