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C21ORF29


Official Full Name
thrombospondin type laminin G domain and EAR repeats
Organism
Homo sapiens
Gene ID
54084
Background
This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
Synonyms
TSPEAR; DFNB98; ECTD14; STHAG10; TSP-EAR; C21orf29

Cat.No. Product Name Price
SHG121231 shRNA set against Human C21orf29(NM_144991.2) Inquiry
SHH242954 shRNA set against Human ATP6AP1L (NM_001017971.1) Inquiry
SHH242958 shRNA set against Mouse ATP6AP1L (NM_001145879.1) Inquiry
SHH436452 shRNA set against Human TSPEAR (NM_144991.2) Inquiry
Cat.No. Product Name Price
CDCR317975 Human TSPEAR ORF Clone(NM_144991.2) Inquiry
CDFG008790 Human TSPEAR cDNA Clone(NM_144991.2) Inquiry
CDFG019768 Mouse Atp6ap1l cDNA Clone(NM_001145879.1) Inquiry
CDFH001472 Human ATP6AP1L cDNA Clone(NM_001017971.1) Inquiry
MiUTR1H-01341 TSPEAR miRNA 3'UTR clone Inquiry
MiUTR1H-05865 ATP6AP1L miRNA 3'UTR clone Inquiry
CDCB190592 Rabbit TSPEAR ORF clone (XM_008252306.1) Inquiry
CDCB194042 Rabbit ATP6AP1L ORF clone (XM_008261898.1) Inquiry
CDCG000495 Rat ATP6AP1L ORF clone(NM_001191843.1) Inquiry
CDCR031914 Human ATP6AP1L ORF clone (NM_001017971.1) Inquiry
CDCR031916 Mouse Atp6ap1l ORF clone (NM_001145879.1) Inquiry
CDCS419870 Human TSPEAR ORF Clone (BC021197) Inquiry
CDCS419871 Human TSPEAR ORF Clone (BC115415) Inquiry
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