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See other LOC100128494 CNV Assays ›
Gene Symbol
LOC100128494
Assay Reference Genome
Location

Chr.11:72018303 on build GRCh38
Cytoband
11q13.4
Assay ID Hs00353754_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 100128494

Gene Name:

 uncharacterized LOC100128494

Gene Aliases:

 -

Location:

 Chr.11:72014291-72020910 on Build GRCh38

Assay Gene Location:

 Overlaps Exon 2 - Intron 2
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC100128494 NR_104178.1
AK126629.1

Target Gene Details

Entrez Gene ID:

 4926

Gene Name:

 nuclear mitotic apparatus protein 1

Gene Aliases:

 NMP-22, NUMA

Location:

 Chr.11:72002864-72080693 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 20 - Exon 21
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
NUMA1 NM_001286561.1 NP_001273490.1
NM_006185.3 NP_006176.2
NR_104476.1
XM_006718564.1 XP_006718627.1
XM_011545054.1 XP_011543356.1
XM_011545055.1 XP_011543357.1
XM_011545056.2 XP_011543358.1
XM_011545057.2 XP_011543359.1
XM_011545058.1 XP_011543360.1
XM_011545059.2 XP_011543361.1
XM_011545060.2 XP_011543362.1
XM_011545061.2 XP_011543363.1
XM_011545062.2 XP_011543364.1
XM_011545063.2 XP_011543365.1
XM_011545064.1 XP_011543366.1
XM_011545065.1 XP_011543367.1
XM_011545066.1 XP_011543368.1
XM_017017830.1 XP_016873319.1
XM_017017831.1 XP_016873320.1
AB210007.1
AK290509.1
AK307577.1
AK309041.1
BC004165.2 AAH04165.1
BC027493.1
BC043499.1 AAH43499.1
BC103765.1 AAI03766.1
Z11583.1 CAA77669.1
Z11584.1 CAA77670.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv428262 Chr.11:71652593 - 72093009 on Build GRCh38 Gain+Loss LRTOMT ALG1L9P MIR3165 LOC100128494 LOC100129216 ZNF705E FAM86C1 RNF121 IL18BP NUMA1 DEFB108B LOC100133315

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More Information


Additional Information:

For this assay, SNP(s) [rs113691033] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Set Membership:

 Intragenic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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