Product Details

Primer Sequences
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Primer Chromosome Location
Chr.10: 100167295-100167542 on Build GRCh38
Format
Each primer will be delivered in a single tube, dried-down
Quick Reference Guide
Primer Designer™ Tool Quick Reference
Ampliseq ID's

Gene Details

Gene Symbol
ERLIN1
Entrez Gene ID
10613
Gene Name
ER lipid raft associated 1
Gene Aliases
C10orf69, Erlin-1, KE04, KEO4, SPFH1, SPG62
UniGene
Hs.150087
Gene Chromosome Location
Chr.10: 100150090-100186057 on Build GRCh38
Transcripts
NM_001100626.1 NM_006459.3 XM_005269442.3 XM_017015541.1

Cosmic Detail

Cosmic ID Mutation AA Transcript Location
913876 c.548G>T p.R183I Chr.10: 100167363-100167363 on Build GRCh38
5006736 c.522A>C p.K174N Chr.10: 100167389-100167389 on Build GRCh38
6456772 c.508G>A p.V170M Chr.10: 100167403-100167403 on Build GRCh38
1251483 c.544A>T p.R182* Chr.10: 100167367-100167367 on Build GRCh38
7308108 c.533C>A p.P178Q Chr.10: 100167378-100167378 on Build GRCh38
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SNP Detail

SNP ID Chromosome Location
rs995856962 Chr.10: 100167513-100167513 on Build GRCh38
rs929764201 Chr.10: 100167399-100167399 on Build GRCh38
rs760011318 Chr.10: 100167393-100167394 on Build GRCh38
rs777022712 Chr.10: 100167375-100167381 on Build GRCh38
rs778227415 Chr.10: 100167376-100167376 on Build GRCh38
rs572770110 Chr.10: 100167481-100167481 on Build GRCh38
rs1037635784 Chr.10: 100167460-100167460 on Build GRCh38
rs771369980 Chr.10: 100167451-100167451 on Build GRCh38
rs368862199 Chr.10: 100167330-100167330 on Build GRCh38
rs898800773 Chr.10: 100167494-100167494 on Build GRCh38
rs1046948267 Chr.10: 100167516-100167516 on Build GRCh38
rs369000472 Chr.10: 100167332-100167332 on Build GRCh38
rs886295850 Chr.10: 100167374-100167374 on Build GRCh38
rs1005192831 Chr.10: 100167420-100167420 on Build GRCh38
rs772462235 Chr.10: 100167371-100167371 on Build GRCh38
rs748507681 Chr.10: 100167323-100167323 on Build GRCh38
rs59002242 Chr.10: 100167368-100167368 on Build GRCh38
rs747463145 Chr.10: 100167427-100167427 on Build GRCh38
rs371611939 Chr.10: 100167435-100167435 on Build GRCh38

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