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See other SLC25A19 CNV Assays ›
Gene Symbol
SLC25A19
Assay Reference Genome
Location

Chr.17:75286704 on build GRCh38
Cytoband
17q25.1
Assay ID Hs02752734_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 60386

Gene Name:

 solute carrier family 25 member 19

Gene Aliases:

 DNC, MCPHA, MUP1, THMD3, THMD4, TPC

Location:

 Chr.17:75272980-75289957 on Build GRCh38

Assay Gene Location:

 Within Exon 4
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC25A19 NM_001126121.1 3 285 NP_001119593.1
NM_001126122.1 2 195 NP_001119594.1
NM_021734.4 3 269 NP_068380.3
XM_005257559.3 3 907 XP_005257616.1
XM_005257560.2 3 461 XP_005257617.1
XM_005257561.3 3 797 XP_005257618.1
XM_005257562.2 3 444 XP_005257619.1
XM_006722007.2 3 317 XP_006722070.1
XM_011525098.1 3 777 XP_011523400.1
XM_017024926.1 2 859 XP_016880415.1
XM_017024927.1 XP_016880416.1
XM_017024928.1 3 793 XP_016880417.1
AF182404.1 1 61 AAG16903.1
AJ251857.1 1 99 CAC27560.1
AK075239.1 4 291 BAC11492.1
AK097882.1 1 971
AK225881.1 1 98
AL833387.1 3 236 CAI46136.1
AY346372.1 1 61 AAQ54327.1
BC001075.2 3 197 AAH01075.1
BC005120.1 3 197 AAH05120.1
BM455504.1
BU177306.1 2 154
DA605220.1 3 250
DB482052.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv510727 Chr.17:75260216 - 75331456 on Build GRCh38 Deletion GRB2 LOC100287042 MIF4GD GGA3 MRPS7 SLC25A19
nsv1066312 Chr.17:75260266 - 75323694 on Build GRCh38 Gain GRB2 LOC100287042 MIF4GD GGA3 MRPS7 SLC25A19
nsv576027 Chr.17:75249939 - 75750289 on Build GRCh38 Gain SMIM5 GRB2 MIF4GD ITGB4 GGA3 MRPS7 TSEN54 SMIM6 SLC25A19 MIR3678 LOC100287042 TMEM94 CASKIN2 MIR6785 SAP30BP MYO15B RECQL5 LLGL2

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More Information


Additional Information:

For this assay, SNP(s) [rs546901072] 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 Exonic DGV Variation

Panther Classification:

Molecular Function -

mitochondrial carrier protein

Gene Ontology Categories:

Function(s) Process(es)


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