Details of FUS gene in Homo sapiens

IDs
Link outs	Gene Name	Alias	Uniprot ID	SwissProt ID	NCBI gene ID	ENSEMBL ID	Description	Source
	FUS	TLS	P35637	FUS_HUMAN	2521	ENSG00000089280	RNA-binding protein FUS	trunk

Disease
Disease	OMIM id
Note=A chromosomal aberration involving FUS is found in a patient with malignant myxoid liposarcoma. Translocation t(1216)(q13p11) with DDIT3.	---
Note=A chromosomal aberration involving FUS is a cause of acute myeloid leukemia (AML). Translocation t(1621)(p11q22) with ERG.	---
Angiomatoid fibrous histiocytoma (AFH) [MIM:612160]: A distinct variant of malignant fibrous histiocytoma that typically occurs in children and adolescents and is manifest by nodular subcutaneous growth. Characteristic microscopic features include lobulated sheets of histiocyte-like cells intimately associated with areas of hemorrhage and cystic pseudovascular spaces	mimicking a lymph node metastasis. Note=The disease may be caused by mutations affecting the gene represented in this entry. A chromosomal aberration
Amyotrophic lateral sclerosis 6 (ALS6) [MIM:608030]: A neurodegenerative disorder affecting upper motor neurons in the brain and lower motor neurons in the brain stem and spinal cord	presence of ubiquitin-positive inclusions within surviving motor neurons
Tremor	legs

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Orthologs in other species
M. musculus	D. melonogaster	C. elegans	S. purpuratus