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TTLL5 encodes a member of the tubulin tyrosine ligase like protein family. Additionally we are shipping Tubulin tyrosine Ligase-Like Family, Member 5 Antibodies (5) and and many more products for this protein.
this study has performed exome sequencing in 28 individuals with a similar disease phenotype and subsequently used a casecontrol approach to identify mutations in TTLL5 as a cause of recessive retinal dystrophy (show MERTK ELISA Kits).
This study indicates that a physiological function of STAMP in several settings is to modify cell growth rates in a manner that can be independent of steroid hormones.
STAMP is an important new, downstream component of GR action in both gene activation and gene repression.
study uncovers the pathogenic mechanism whereby absence of RPGR(ORF15 (show RPGR ELISA Kits)) glutamylation leads to retinal pathology in patients with TTLL5 gene mutations and connects these two genes into a common disease pathway.
STAMP appears to participate in a unique, tissue-selective TTLL-mediated pathway for alpha-tubulin (show TUBA4A ELISA Kits) polyglutamylation that is required for sperm maturation and motility and may be relevant for male fertility.
This gene encodes a member of the tubulin tyrosine ligase like protein family. This protein interacts with two glucocorticoid receptor coactivators, transcriptional intermediary factor 2 and steroid receptor coactivator 1. This protein may function as a coregulator of glucocorticoid receptor mediated gene induction and repression. This protein may also function as an alpha tubulin polyglutamylase.
tubulin polyglutamylase TTLL5
, tubulin tyrosine ligase-like family, member 5
, tubulin--tyrosine ligase-like protein 5
, SRC1 and TIF2 associated binding protein
, SRC1 and TIF2-associated modulatory protein
, tubulin tyrosine ligase like family 5