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Melanoma of soft part
3 associated genes
142 connected diseases
No signs/symptoms info
Disease Type of connection
Extraskeletal Ewing sarcoma
Extraskeletal myxoid chondrosarcoma
Ewing sarcoma
Desmoplastic small round cell tumor
Familial pancreatic carcinoma
Familial prostate cancer
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Hereditary breast and ovarian cancer syndrome
B-cell chronic lymphocytic leukemia
Precursor B-cell acute lymphoblastic leukemia
Amyotrophic lateral sclerosis
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Primary peritoneal carcinoma
Adrenocortical carcinoma
Essential thrombocythemia
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Precursor T-cell acute lymphoblastic leukemia
17q11 microdeletion syndrome
Papillary or follicular thyroid carcinoma
Estrogen resistance syndrome
17q12 microdeletion syndrome
Autosomal dominant primary hypomagnesemia with hypocalciuria
Classic Mayer-Rokitansky-Küster-Hauser syndrome
MURCS association
Renal cysts and diabetes syndrome
Cornelia de Lange syndrome
Machado-Joseph disease type 1
Machado-Joseph disease type 2
Machado-Joseph disease type 3
Glucocorticoid resistance
Ataxia-telangiectasia
Ataxia-telangiectasia variant
Combined cervical dystonia
Mantle cell lymphoma
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
Weaver syndrome
Frontotemporal dementia with motor neuron disease
Juvenile amyotrophic lateral sclerosis
Myxofibrosarcoma
Myxoid / round cell liposarcoma
Alobar holoprosencephaly
Combined pituitary hormone deficiencies, genetic forms
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial isolated dilated cardiomyopathy
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Burkitt lymphoma
Catecholaminergic polymorphic ventricular tachycardia
Chronic myeloid leukemia
Charcot-Marie-Tooth disease type 4D
Cholesterol-ester transfer protein deficiency
Disseminated superficial actinic porokeratosis
Generalized juvenile polyposis / juvenile polyposis coli
Hereditary hemorrhagic telangiectasia
Hyperimmunoglobulinemia D with periodic fever
Isolated NADH-CoQ reductase deficiency
Leigh syndrome with leukodystrophy
MULIBREY nanism
Mevalonic aciduria
Myhre syndrome
Pulmonary capillary hemangiomatosis
Pulmonary venoocclusive disease
Pyruvate dehydrogenase E3-binding protein deficiency
Renal tubular dysgenesis of genetic origin
Coffin-Siris syndrome
Familial rhabdoid tumor
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome
Seckel syndrome
Syndromic multisystem autoimmune disease due to Itch deficiency
Coffin-Lowry syndrome
X-linked non-syndromic intellectual deficit
X-linked dystonia-parkinsonism
Acute myeloid leukemia with CEBPA somatic mutations
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Autosomal dominant secondary polycythemia
Brugada syndrome
COFS syndrome
Cabezas syndrome
Common variable immunodeficiency
Dedifferentiated liposarcoma
Dentatorubral pallidoluysian atrophy
Familial melanoma
Fibronectin glomerulopathy
Glycogen storage disease due to liver phosphorylase kinase deficiency
Hermansky-Pudlak syndrome without pulmonary fibrosis
Herpetic encephalitis
Hypomyelination - hypogonadotropic hypogonadism - hypodontia
ICF syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Inherited acute myeloid leukemia
Multiple paragangliomas associated with polycythemia
Nager syndrome
Odontoleukodystrophy
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Pseudohypoaldosteronism type 2E
Pulverulent cataract
Spinocerebellar ataxia type 19 / 22
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Translocation renal cell carcinoma
Uveal coloboma - cleft lip and palate - intellectual deficit
Well-differentiated liposarcoma
Wilson-Turner syndrome
Wolf-Hirschhorn syndrome
Xeroderma pigmentosum complementation group G
Autosomal recessive limb-girdle muscular dystrophy type 2Q
Epidermolysis bullosa simplex with muscular dystrophy
Epidermolysis bullosa simplex with pyloric atresia
Epidermolysis bullosa simplex, Ogna type
Cowden syndrome
Peripheral resistance to thyroid hormones
Proteus syndrome
46,XX ovotesticular disorder of sex development
46,XX testicular disorder of sex development
Autosomal dominant nonsyndromic intellectual deficit
Campomelic dysplasia
Familial thoracic aortic aneurysm and aortic dissection
Isolated delta-storage pool disease
MODY syndrome
Paris-Trousseau thrombocytopenia
Partial pancreatic agenesis
Peripheral primitive neuroectodermal tumor
Permanent neonatal diabetes mellitus
Autosomal recessive malignant osteopetrosis
Autosomal recessive optic atrophy, OPA7 type
Huntington disease
Juvenile Huntington disease
Kostmann syndrome
Synonym(s):
- Clear cell sarcoma of soft tissue
- Clear cell sarcoma of the tendons and aponeuroses
Classification (Orphanet):
- Rare oncologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
ATF1 P18846123803
CREB1 P16220123810
EWSR1 Q01844133450
No signs/symptoms info available.