Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.9: 105617952-105618181 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: FKTN
Entrez Gene ID: 2218
Gene Name: fukutin
Gene Aliases: CMD1X, FCMD, LGMD2M, MDDGA4, MDDGB4, MDDGC4
UniGene: Hs.55777
Gene Chromosome Location: Chr.9: 105558117-105655950 on Build GRCh38
Transcripts: NM_001079802.1 NM_001198963.1 NM_006731.2 XM_006717014.2 XM_011518368.2 XM_011518369.2 XM_011518370.2 XM_011518371.2 XM_011518373.2 XM_011518374.2 XM_011518375.2 XM_011518376.2 XM_011518378.2 XM_011518379.2 XM_011518381.2 XM_011518387.2 XM_011518389.2 XM_011518390.2 XM_011518391.2 XM_017014462.1 XM_017014463.1 XM_017014464.1 XM_017014465.1 XM_017014466.1 XM_017014467.1 XM_017014468.1 XM_017014469.1 XM_017014470.1 XM_017014471.1 XM_017014472.1 XM_017014473.1 XM_017014474.1 XM_017014475.1 XM_017014476.1 XM_017014477.1 XM_017014478.1 XM_017014479.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
5467555	c.919C>T	p.R307*	Chr.9: 105617967-105617967 on Build GRCh38
1103574	c.949G>T	p.D317Y	Chr.9: 105617997-105617997 on Build GRCh38
3652621	c.1006C>T	p.Q336*	Chr.9: 105618054-105618054 on Build GRCh38
6366241	c.976G>T	p.D326Y	Chr.9: 105618024-105618024 on Build GRCh38
4163187	c.1026C>A	p.L342L	Chr.9: 105618074-105618074 on Build GRCh38
5692242	c.911G>T	p.G304V	Chr.9: 105617959-105617959 on Build GRCh38
6854936	c.954T>C	p.V318V	Chr.9: 105618002-105618002 on Build GRCh38
3847266	c.112C>T	p.P38S	Chr.9: 105618070-105618070 on Build GRCh38
373734	c.1009G>T	p.D337Y	Chr.9: 105618057-105618057 on Build GRCh38
6487578	c.1044G>A	p.K348K	Chr.9: 105618092-105618092 on Build GRCh38
7225990	c.943A>G	p.S315G	Chr.9: 105617991-105617991 on Build GRCh38
3168197	c.955delG	p.D319fs*2	Chr.9: 105618003-105618003 on Build GRCh38
7368343	c.943A>T	p.S315C	Chr.9: 105617991-105617991 on Build GRCh38
3847265	c.1022C>T	p.P341L	Chr.9: 105618070-105618070 on Build GRCh38
325354	c.929A>G	p.N310S	Chr.9: 105617977-105617977 on Build GRCh38
6854937	c.44T>C	p.V15A	Chr.9: 105618002-105618002 on Build GRCh38
7447724	c.938C>T	p.P313L	Chr.9: 105617986-105617986 on Build GRCh38
6114475	c.949G>C	p.D317H	Chr.9: 105617997-105617997 on Build GRCh38
7447725	c.28C>T	p.P10S	Chr.9: 105617986-105617986 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs774410536	Chr.9: 105618023-105618023 on Build GRCh38
rs75946934	Chr.9: 105618150-105618150 on Build GRCh38
rs777297548	Chr.9: 105618121-105618124 on Build GRCh38
rs1018122957	Chr.9: 105618026-105618026 on Build GRCh38
rs750787127	Chr.9: 105618085-105618085 on Build GRCh38
rs992936408	Chr.9: 105618148-105618148 on Build GRCh38
rs748169818	Chr.9: 105618135-105618135 on Build GRCh38
rs764441249	Chr.9: 105618070-105618070 on Build GRCh38
rs146967918	Chr.9: 105618071-105618071 on Build GRCh38
rs200801909	Chr.9: 105618109-105618109 on Build GRCh38
rs780980837	Chr.9: 105618130-105618130 on Build GRCh38
rs915268305	Chr.9: 105618134-105618134 on Build GRCh38
rs752721354	Chr.9: 105618057-105618057 on Build GRCh38
rs17309806	Chr.9: 105618074-105618074 on Build GRCh38
rs746456728	Chr.9: 105618116-105618116 on Build GRCh38
rs769691253	Chr.9: 105618020-105618020 on Build GRCh38
rs951073727	Chr.9: 105618145-105618145 on Build GRCh38
rs141120187	Chr.9: 105618000-105618000 on Build GRCh38
rs886044385	Chr.9: 105618069-105618069 on Build GRCh38
rs759791267	Chr.9: 105618025-105618025 on Build GRCh38
rs773018262	Chr.9: 105618138-105618138 on Build GRCh38
rs970907026	Chr.9: 105617990-105617990 on Build GRCh38
rs924159503	Chr.9: 105618053-105618053 on Build GRCh38
rs768352058	Chr.9: 105618129-105618129 on Build GRCh38
rs118064041	Chr.9: 105618136-105618136 on Build GRCh38
rs767753943	Chr.9: 105618028-105618028 on Build GRCh38
rs760756067	Chr.9: 105618058-105618058 on Build GRCh38
rs532960237	Chr.9: 105618151-105618151 on Build GRCh38
rs751122944	Chr.9: 105618063-105618063 on Build GRCh38

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