Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.10: 46549574-46549303 on Build GRCh38 View in UCSC browser
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: GPRIN2
Entrez Gene ID: 9721
Gene Name: G protein regulated inducer of neurite outgrowth 2
Gene Aliases: GRIN2, KIAA0514
UniGene: Hs.523375
Gene Chromosome Location: Chr.10: 46543963-46556637 on Build GRCh38
Transcripts: NM_014696.3 XM_005277666.3 XM_011540388.2 XM_011540395.2 XM_011540400.2 XM_017016974.1 XM_017016975.1 XM_017016976.1 XM_017016977.1 XM_017016978.1 XM_017016979.1 XM_017016980.1 XM_017016981.1 XM_017016982.1 XM_017016983.1 XM_017016984.1 XM_017017029.1 XM_017017030.1 XM_017017031.1 XM_017017032.1 XM_017017033.1 XM_017017034.1 XM_017017038.1 XM_017017039.1 XM_017017040.1

Gene Symbol: LOC107984026
Entrez Gene ID: 107984026
Gene Name: arf-GAP with GTPase, ANK repeat and PH domain-containing protein 4-like
Gene Aliases: -
UniGene
Gene Chromosome Location: Chr.10: 46335552-46838268 on Build GRCh38
Transcripts: NM_014696.3 XM_005277666.3 XM_011540388.2 XM_011540395.2 XM_011540400.2 XM_017016974.1 XM_017016975.1 XM_017016976.1 XM_017016977.1 XM_017016978.1 XM_017016979.1 XM_017016980.1 XM_017016981.1 XM_017016982.1 XM_017016983.1 XM_017016984.1 XM_017017029.1 XM_017017030.1 XM_017017031.1 XM_017017032.1 XM_017017033.1 XM_017017034.1 XM_017017038.1 XM_017017039.1 XM_017017040.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
4014310	c.1182C>T	p.Y394Y	Chr.10: 46549555-46549555 on Build GRCh38
255923	c.1336C>T	p.R446C	Chr.10: 46549401-46549401 on Build GRCh38
4894477	c.1330C>T	p.L444L	Chr.10: 46549407-46549407 on Build GRCh38
3751795	c.1308A>G	p.P436P	Chr.10: 46549429-46549429 on Build GRCh38
4144708	c.1199T>C	p.L400P	Chr.10: 46549538-46549538 on Build GRCh38
6501482	c.1281C>T	p.S427S	Chr.10: 46549456-46549456 on Build GRCh38
3747186	c.1266C>T	p.P422P	Chr.10: 46549471-46549471 on Build GRCh38
6129665	c.1210G>A	p.G404S	Chr.10: 46549527-46549527 on Build GRCh38
4647183	c.1282C>T	p.L428L	Chr.10: 46549455-46549455 on Build GRCh38
1128052	c.1337G>A	p.R446H	Chr.10: 46549400-46549400 on Build GRCh38
1235914	c.1307C>T	p.P436L	Chr.10: 46549430-46549430 on Build GRCh38
1958326	c.1183G>A	p.G395R	Chr.10: 46549554-46549554 on Build GRCh38
6210501	c.1176G>A	p.E392E	Chr.10: 46549561-46549561 on Build GRCh38
3438025	c.1286C>T	p.S429F	Chr.10: 46549451-46549451 on Build GRCh38
6841541	c.1298G>A	p.R433Q	Chr.10: 46549439-46549439 on Build GRCh38
6837680	c.1349G>T	p.C450F	Chr.10: 46549388-46549388 on Build GRCh38
6852126	c.1365G>A	p.A455A	Chr.10: 46549372-46549372 on Build GRCh38
4392385	c.1329C>T	p.S443S	Chr.10: 46549408-46549408 on Build GRCh38
5370663	c.1194G>A	p.V398V	Chr.10: 46549543-46549543 on Build GRCh38
3751796	c.1359C>T	p.S453S	Chr.10: 46549378-46549378 on Build GRCh38
918371	c.1332G>A	p.L444L	Chr.10: 46549405-46549405 on Build GRCh38
4432432	c.1312C>T	p.R438W	Chr.10: 46549425-46549425 on Build GRCh38
918370	c.1206G>A	p.V402V	Chr.10: 46549531-46549531 on Build GRCh38
5482837	c.1191G>A	p.A397A	Chr.10: 46549546-46549546 on Build GRCh38
5458130	c.1181A>G	p.Y394C	Chr.10: 46549556-46549556 on Build GRCh38

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