Gene PTPN11 function profile ��Ʈw

Gene Symbol

Gene Name	Aliases	Previous_Symbol
PTPN11	protein tyrosine phosphatase, non-receptor type 11 (Noonan syndrome 1)	BPTP3, SH-PTP2, SHP-2, PTP2C, SHP2, HGNC:8012	protein tyrosine phosphatase, non-receptor type 11

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MeSH term

Frequency	Condition_Probility
Acute Disease	4	0.0
Adult	11	0.0
Base Sequence	4	0.0
DNA, Neoplasm/genetics	2	0.0
Female	17	0.0
Humans	32	0.0
Leukemia, Myeloid/*genetics	5	3.0
Male	15	0.0
Middle Aged	3	0.0
Molecular Sequence Data	4	0.0
*Mutation	7	0.0
Proto-Oncogene Proteins/*genetics	2	0.0
Receptor Protein-Tyrosine Kinases/*genetics	2	0.0
Research Support, Non-U.S. Gov't	26	0.0
Adolescent	6	0.0
Amino Acid Sequence	2	0.0
Child	11	0.0
Child, Preschool	7	0.0
Exons	6	0.0
Mutation, Missense	2	0.0
Protein Structure, Tertiary	2	0.0
Protein-Tyrosine-Phosphatase/chemistry/*genetics	3	37.0
Sequence Analysis, DNA	3	0.0
Infant	5	0.0
Leukemia, Myelomonocytic, Chronic/*genetics	2	20.0
*Point Mutation	2	0.0
Research Support, U.S. Gov't, P.H.S.	12	0.0
Cohort Studies	3	0.0
DNA Mutational Analysis	8	0.0
Exons/genetics	2	0.0
*Genetic Heterogeneity	2	1.0
Genotype	3	0.0
Models, Molecular	2	0.0
Pedigree	5	0.0
Phenotype	6	0.0
Protein Conformation	2	0.0
Mutation, Missense/*genetics	2	1.0
Protein-Tyrosine-Phosphatase/*genetics	18	13.0
Research Support, U.S. Gov't, Non-P.H.S.	3	0.0
src Homology Domains	3	0.0
Abnormalities, Multiple/*genetics	3	0.0
*Mutation, Missense	5	0.0
Noonan Syndrome/enzymology/*genetics	3	100.0
Myelodysplastic Syndromes/*genetics	2	2.0
Polymerase Chain Reaction	2	0.0
Heart Defects, Congenital/genetics	2	5.0
Syndrome	4	0.0
*Germ-Line Mutation	2	0.0
Haplotypes	2	0.0
Introns	3	0.0
Noonan Syndrome/*genetics	5	41.0
Mutation	4	0.0
Noonan Syndrome/genetics	3	60.0
Chromosomes, Human, Pair 12/genetics	3	3.0
Signal Transduction	2	0.0
ras Proteins/metabolism	2	1.0
DNA Primers	2	0.0