TNNI2 Chromosome 11

Troponin I2, fast skeletal type
18 variants 18 Health Risk

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What This Gene Does
This gene encodes a fast-twitch skeletal muscle protein, a member of the troponin I gene family, and a component of the troponin complex including troponin T, troponin C and troponin I subunits. The troponin complex, along with tropomyosin, is responsible for the calcium-dependent regulation of striated muscle contraction. Mouse studies show that this component is also present in vascular smooth muscle and may play a role in regulation of smooth muscle function. In addition to muscle tissues, this protein is found in corneal epithelium, cartilage where it is an inhibitor of angiogenesis to inhibit tumor growth and metastasis, and mammary gland where it functions as a co-activator of estrogen receptor-related receptor alpha. This protein also suppresses tumor growth in human ovarian carcinoma. Mutations in this gene cause myopathy and distal arthrogryposis type 2B. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2009]
Gene Info
Gene Group
Troponin complex subunits
Locus Type
gene with protein product
Location
11p15.5
Ensembl
ENSG00000130598
Associated Conditions (7)
TNNI2-related disorder
Distal arthrogryposis type 2B1
Inborn genetic diseases
Calcaneovalgus deformity
Congenital finger flexion contractures
Ulnar deviation of the wrist
Distal arthrogryposis
Key Variants
All Variants (18)
RSID Category Clinical Significance Conditions
RS141400587 Health Risk Conflicting classifications of pathogenicity TNNI2-related disorder, TNNI2-related disorder
RS143863270 Health Risk Conflicting classifications of pathogenicity
RS1847180082 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS200110633 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201133081 Health Risk Conflicting classifications of pathogenicity Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS376294428 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1057519093 Health Risk Likely pathogenic
RS1589797083 Health Risk Likely pathogenic Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS1847181948 Health Risk Likely pathogenic Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS2133035336 Health Risk Likely pathogenic
RS2493967150 Health Risk Likely pathogenic Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS2493967214 Health Risk Likely pathogenic Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS104894311 Health Risk Pathogenic Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS104894312 Health Risk Pathogenic Distal arthrogryposis type 2B1, Calcaneovalgus deformity, Congenital finger flexion contractures
RS1589797063 Health Risk Pathogenic Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS199474800 Health Risk Pathogenic Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
RS199474801 Health Risk Pathogenic/Likely pathogenic Distal arthrogryposis type 2B1, TNNI2-related disorder, Distal arthrogryposis type 2B1
RS797046046 Health Risk Pathogenic/Likely pathogenic Distal arthrogryposis type 2B1, Distal arthrogryposis type 2B1
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