Mks1 - MKS transition zone complex subunit 1 Gene

Rattus norvegicus

Gene ID: 287612 | Gene type: protein coding

About Mks1

Summary

Predicted to be involved in branching morphogenesis of an epithelial tube and cilium assembly. Predicted to act upstream of or within several processes, including chordate embryonic development; plasma membrane bounded cell projection organization; and regulation of signal transduction. Predicted to be located in several cellular components, including ciliary transition zone; cytoplasm; and microtubule organizing center. Predicted to be part of MKS complex. Human ortholog(s) of this gene implicated in Bardet-Biedl syndrome; Bardet-Biedl syndrome 13; Joubert syndrome 28; and Meckel syndrome 1. Orthologous to human MKS1 (MKS transition zone complex subunit 1). [provided by Alliance of Genome Resources, Apr 2022]

Mks1 Products(1)

mRNA	Protein	Name
NM_001034917.2	NP_001030089.2	tectonic-like complex member MKS1

Protein Preferred Names

Protein Names

tectonic-like complex member MKS1

Meckel syndrome type 1 protein homolog

Meckel syndrome, type 1

meckel syndrome type 1 protein homolog

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS08482	MKS1 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Mks1	NCBI	NCBI:54903

Name
Email *

	Sorry, but the email address you supplied was invalid.