4 sources retrieved Β· Most recent: April 2026 Β· Index updated 15 days ago
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14PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITYβ Experimental GO Evidenceβ Swiss-Prot Reviewed
protein bindingcell morphogenesiscell motilitycytoplasmsialadenitismixed connective tissue diseasemale infertilitymale reproductive organ cancer
LRATD1 (LRAT domain containing 1) is a substrate protein of N-Myristoyltransferases (NMTs) identified through interactome analysis 1. The protein is predicted to play a role in cell morphology and motility based on functional annotations, though direct experimental evidence of its specific molecular function is limited. LRATD1 contains an LRAT domain and functions as a substrate for NMT1/2-mediated N-terminal myristoylation 1, a post-translational modification that typically regulates protein localization and function. The myristoylation of LRATD1 suggests involvement in cellular processes requiring membrane association or protein-protein interactions. While no disease-specific studies directly examine LRATD1, its identification as an NMT substrate places it within the broader context of PTM regulation affecting cell biology. The clinical significance of LRATD1 remains to be established, as functional studies characterizing its role in normal physiology and disease pathogenesis have not been reported in available literature. Further investigation is needed to elucidate LRATD1's specific cellular functions and potential involvement in disease processes.
1
LRATD1 was identified as a previously unknown substrate protein of human NMT1/2 through interactome data mining; demonstrates that NMT enzymes catalyze N-terminal myristoylation
PMID: 34956690β Limited data available β This gene has 1 indexed publication. Summary and analysis may be incomplete.
mixed connective tissue diseaseOpen Targets
male infertilityOpen Targets
male reproductive organ cancerOpen Targets
ocular hypotensionOpen Targets
multiple sclerosisOpen Targets
ankylosing spondylitisOpen Targets
metabolic diseaseOpen Targets
color vision disorderOpen Targets
Abnormality of the integumentOpen Targets
ovarian neoplasmOpen Targets
Parkinson diseaseOpen Targets
pituitary gland diseaseOpen Targets
pyogenic granulomaOpen Targets
mental or behavioural disorderOpen Targets
No pathogenic variants reported on ClinVar for this gene.