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TMEM67


Official Full Name
transmembrane protein 67
Organism
Homo sapiens
Gene ID
91147
Background
The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq, Nov 2008]
Synonyms
MKS3; JBTS6; NPHP11; TNEM67; MECKELIN

Cat.No. Product Name Price
SHH430876 shRNA set against Human TMEM67 (NM_153704.5) Inquiry
SHH430880 shRNA set against Mouse TMEM67 (NM_177861.4) Inquiry
SHH430884 shRNA set against Rat TMEM67 (NM_001107916.2) Inquiry
Cat.No. Product Name Price
CDFG010193 Human TMEM67 cDNA Clone(NM_153704.5) Inquiry
CDFH019909 Human TMEM67 cDNA Clone(NM_001142301.1) Inquiry
CDFL014020 Mouse Tmem67 cDNA Clone(NM_177861.4) Inquiry
CDFR007561 Rat Tmem67 cDNA Clone(NM_001107916.2) Inquiry
MiUTR3H-10872 TMEM67 miRNA 3'UTR clone Inquiry
MiUTR3H-10873 TMEM67 miRNA 3'UTR clone Inquiry
CDCB184561 Rabbit TMEM67 ORF clone (XM_008255733.1) Inquiry
CDCH092890 human TMEM67 ORF clone (NM_001142301.1) Inquiry
CDCR274454 Mouse Tmem67 ORF Clone(NM_177861.4) Inquiry
CDCR320959 Human TMEM67 ORF Clone(NM_153704.5) Inquiry
CDCR374584 Rat Tmem67 ORF Clone(NM_001107916.2) Inquiry
CDCS408248 Human TMEM67 ORF Clone (BC032835) Inquiry
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