TIM-1 Polyclonal Antibody, 20ul Polyclonal Antibody Preparation Mutations in this gene cause

Mutations in this gene cause syndromic microphthalmia 5 (MCOPS5) and combined pituitary hormone deficiency 6 (CPHD6)

have fewer positive charged residues that in other sodium channels

These variants encode different isoforms| which are differentially expressed and have different kinase activities

many proteins are phosphorylated directly by MPF or indirectly by kinases activated by MPF

TIM-1 Polyclonal Antibody, 20ul Polyclonal Antibody Preparation Mutations in this gene causeThe protein encoded by this gene is a membrane receptor for both human hepatitis A virus (HHAV) and TIMD4. The encoded protein may be involved in the moderation of asthma and allergic diseases. The reference genome represents an allele that retains a MTTVP amino acid segment that confers protection against atopy in HHAV seropositive individuals. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been