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Details of TPM3 gene in Homo sapiens
IDs | |||||||||
---|---|---|---|---|---|---|---|---|---|
Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| TPM3 | --- | P06753 | TPM3_HUMAN | 7170 | ENSG00000143549 | Tropomyosin alpha-3 chain | SPROT |
Disease | |||||||||
---|---|---|---|---|---|---|---|---|---|
Disease | OMIM id | ||||||||
Nemaline myopathy 1 (NEM1) [MIM:609284]: A form of nemaline myopathy with autosomal dominant or recessive inheritance. Nemaline myopathies are muscular disorders characterized by muscle weakness of varying severity and onset, and abnormal thread-like or rod-shaped structures in muscle fibers on histologic examination. Autosomal dominant nemaline myopathy type 1 is characterized by a moderate phenotype with onset between birth and early second decade of life. Weakness is diffuse and symmetric with slow progression often with need for a wheelchair in adulthood. The autosomal recessive form has onset at birth with moderate-to-severe hypotonia and diffuse weakness. In the most severe cases, death can occur before 2 years. Less severe cases have delayed major motor milestones, and these patients may walk, but often need a wheelchair before 10 years. Note=The disease is caused by mutations affecting the gene represented in this entry. | 609284 | Thyroid papillary carcinoma (TPC) [MIM:188550]: A common tumor of the thyroid that typically arises as an irregular, solid or cystic mass from otherwise normal thyroid tissue. Papillary carcinomas are malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. Note=The disease is caused by mutations affecting the gene represented in this entry. A chromosomal aberration involving TPM3 is found in thyroid papillary carcinomas. A rearrangement with NTRK1 generates the TRK fusion transcript by fusing the amino end of isoform 2 of TPM3 to the 3'-end of NTRK1. | 188550 |
Phenotypes
Abnormal appendicular skeleton morphology, Abnormal axial skeleton morphology, Abnormal facial shape, Abnormality of body weight, Abnormality of connective tissue, Abnormality of eye movement, Abnormality of facial musculature, Abnormality of facial soft tissue, Abnormality of head and neck, Abnormality of higher mental function, Abnormality of joint mobility, Abnormality of limb bone morphology, Abnormality of muscle fibers, Abnormality of muscle morphology, Abnormality of muscle physiology, Abnormality of pelvic girdle bone morphology, Abnormality of prenatal development or birth, Abnormality of skeletal morphology, Abnormality of skeletal muscle fiber size, Abnormality of the abdomen, Abnormality of the abdominal organs, Abnormality of the brainstem, Abnormality of the cardiovascular system, Abnormality of the central nervous system, Abnormality of the cranial nerves, Abnormality of the curvature of the vertebral column, Abnormality of the esophagus, Abnormality of the eye, Abnormality of the face, Abnormality of the foot, Abnormality of the gastrointestinal tract, Abnormality of the head, Abnormality of the heart, Abnormality of the hip bone, Abnormality of the hip joint, Abnormality of the joints of the lower limbs, Abnormality of the larynx, Abnormality of the lower limb, Abnormality of the lung, Abnormality of the motor neurons, Abnormality of the mouth, Abnormality of the musculature, Abnormality of the musculature of the neck, Abnormality of the myocardium, Abnormality of the neck, Abnormality of the nervous system, Abnormality of the oral cavity, Abnormality of the palate, Abnormality of the respiratory system, Abnormality of the seventh cranial nerve, Abnormality of the skeletal system, Abnormality of the sternum, Abnormality of the thorax, Abnormality of the upper respiratory tract, Abnormality of the vertebral column, Abnormality of the voice, Abnormal joint morphology, Abnormal muscle tone, Age of onset, All, Amyotrophy, Autosomal dominant inheritance, Autosomal recessive inheritance, Bulbar palsy, Cardiomyopathy, Centrally nucleated skeletal muscle fibers, Cognitive impairment, Congenital hip dislocation, Congenital onset, Cranial nerve paralysis, Decreased body weight, Decreased fetal movement, Dilated cardiomyopathy, Distal lower limb muscle weakness, Distal muscle weakness, Dysphagia, EMG abnormality, EMG: myopathic abnormalities, Facial diplegia, Facial palsy, Failure to thrive, Flexion contracture, Functional respiratory abnormality, Generalized muscle weakness, Global developmental delay, Growth abnormality, Heterogeneous, High palate, Hip dislocation, Hyperlordosis, Joint dislocation, Juvenile onset, Limb-girdle muscle atrophy, Limb joint contracture, Lumbar hyperlordosis, Malformation of the heart and great vessels, Mode of inheritance, Morphological abnormality of the central nervous system, Motor delay, Muscle fiber cytoplasmatic inclusion bodies, Muscle fiber inclusion bodies, Muscle weakness, Muscular hypotonia, Myopathy, Narrow face, Narrow palate, Neck muscle weakness, Nemaline bodies, Neonatal hypotonia, Onset, Onset and clinical course, Ophthalmoparesis, Ophthalmoplegia, Pectus excavatum, Pes cavus, Phenotypic abnormality, Phenotypic variability, Prenatal movement abnormality, Proximal muscle weakness, Ptosis, Respiratory insufficiency, Respiratory insufficiency due to muscle weakness, Scoliosis, Shoulder girdle muscle atrophy, Type 1 fibers relatively smaller than type 2 fibers, Variable expressivity, Weak cry, Weakness of muscles of respiration.
Orthologs in other species | |||||||||
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M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
Tpm3 | Tm2 | lev-11 | Sp-Tropmy1 |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
---|---|---|---|---|---|---|---|---|---|
TPM3 | ACTN2 | 0.960705313 | TPM3 | ACTN2 | cpx750 | no | yes | no | Known |
TPM3 | CKB | 0.98213195 | TPM3 | CKB | cpx245 | no | yes | no | Known |
TPM3 | CKMT1B | 0.993354649 | TPM3 | CKMT1B | cpx245 | no | yes | no | Known |
ACTN4 | TPM3 | 0.937284926 | ACTN4 | TPM3 | cpx766 | no | yes | no | Known |
ACTN1 | TPM3 | 0.901887872 | ACTN1 | TPM3 | cpx750 | no | yes | no | Known |
MYH7B | TPM3 | 0.999989487 | MYH7B | TPM3 | cpx245 | no | no | no | Novel |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
---|---|---|---|---|
TPM1 | TPM3 | 0.533507612 | TPM1 | TPM3 |
ATP5F1 | TPM3 | 0.142055469 | ATP5F1 | TPM3 |
NDUFB10 | TPM3 | 0.173017075 | NDUFB10 | TPM3 |
MTCH1 | TPM3 | 0.108006879 | MTCH1 | TPM3 |
PSMA6 | TPM3 | 0.152769774 | PSMA6 | TPM3 |
TBCD | TPM3 | 0.089933549 | TBCD | TPM3 |
COX4I1 | TPM3 | 0.323246473 | COX4I1 | TPM3 |
PSMA2 | TPM3 | 0.082353903 | PSMA2 | TPM3 |
TPM3 | CYC1 | 0.214904264 | TPM3 | CYC1 |
TPM3 | AHCYL1 | 0.082036141 | TPM3 | AHCYL1 |
UQCRC2 | TPM3 | 0.115689167 | UQCRC2 | TPM3 |
STMN1 | TPM3 | 0.195341233 | STMN1 | TPM3 |
TPM3 | COX5A | 0.134722245 | TPM3 | COX5A |
TPM3 | OSTF1 | 0.169048503 | TPM3 | OSTF1 |
TPM3 | ATP1A1 | 0.074691207 | TPM3 | ATP1A1 |