RAPID: Resource of Primary Immunodeficiency Diseases

Last updated on May 20, 2013

THBD

mRNA IDs

Primary Information

NM_000361.2

Gene Symbol

THBD

Protein Name

thrombomodulin

Alternate Names

THRM

AHUS6

CD141

Gene Locus

20p11.2

Disease name	Characteristic / Associated features	Category	Inheritance type
Atypical hemolytic uremic syndrome 6	Microangiopathic hemolytic anemia; thrombocytopenia; acute renal failure; decreased serum complement C3; activation of the alternative complement pathway	Complement Deficiencies	Autosomal recessive / Autosomal dominant

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