Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Immunogen sequence: SNYRQVTESK GVLRHMLRQH LAHGALPVAT VDRPDFYPPA YEESLEVEKQ SCPAEREASG IPPPLYTETG LEFQDGNDSH PEAPPSYRES IAGLVVTAIS EDAQRRGQEC
Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias. The C9orf71 gene product has been provisionally designated C9orf71 pending further characterization.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Transmembrane protein 252; transmembrane protein C9orf71; transmembrane protein C9orf71 homolog
Gene Aliases: C9orf71; E030010A14Rik; TMEM252
UniProt ID: (Human) Q8N6L7, (Mouse) Q8C353
Entrez Gene ID: (Human) 169693, (Mouse) 226040
If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Learn moreGet expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.
Contact tech support