APTX Polyclonal Antibody, 20ul Tubes Diseases associated with HTR1F include

Diseases associated with HTR1F include migraine with or without aura 1

an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy

It may play an important role in hemopoietic differentiation

The PWWP2B protein is phosphorylated upon DNA damage

APTX Polyclonal Antibody, 20ul Tubes Diseases associated with HTR1F includeThis gene encodes a member of the histidine triad (HIT) superfamily. The encoded protein may play a role in single stranded DNA repair through its nucleotide binding activity and its diadenosine polyphosphate hydrolase activity. Mutations in this gene have been associated with ataxia ocular apraxia. Alternatively spliced transcript variants have been identified for this gene.