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FIGURE: 1 / 3
Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
Antibody detects endogenous levels of total TMEM184B.
TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22; mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: C22orf5; CTA-447C4.2; putative MAPK-activating protein FM08; unnamed protein product
Gene Aliases: 2610507A11; 4732495E13Rik; C22orf5; FM08; HS5O6A; HSPC256; SLC51C2
UniProt ID: (Human) Q9Y519, (Mouse) Q8BG09
Entrez Gene ID: (Human) 25829, (Mouse) 223693
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