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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.
Immunogen sequence: HPASGYVQGI NDLVTPFFVV FICEYIEAEE VDTVDVSGVP AEVLCNIEAD TYWCMSKLLD GIQDNYTFAQ PGIQMKVKML EELVSRIDEQ VHRHLDQHEV RYLQFAFRWM NNLLMREVPL RCTIRLWDTY QSE
Highest antigen sequence identity to the following orthologs: Mouse - 92%, Rat - 59%.
TBC1D22A (TBC1 domain family, member 22A), also known as C22orf4, is a 517 amino acid protein that contains one Rab-GAP TBC domain and is thought to function as a GTPase-activating protein for Rab family members. Multiple isoforms of TBC1D22A exist due to alternative splicing events. The gene encoding TBC1D22A maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: C22orf4; putative GTPase activator; unnamed protein product
Gene Aliases: C22orf4; HSC79E021
UniProt ID: (Human) Q8WUA7
Entrez Gene ID: (Human) 25771
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