src Phenotypes

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Phenotypes

Gene Literature (64)

Nucleotides (251)

Interactants (535)

XB-GENEPAGE-489819

Gene Symbol: src Gene Name: SRC proto-oncogene, non-receptor tyrosine kinase

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (14 sources): Abnormal bleeding, Bone marrow hypercellularity, Deeply set eye, Hereditary nonpolyposis colorectal carcinoma, Hypotelorism, Large forehead, Myelofibrosis, Neoplasm of the stomach, Osteoporosis, Renal cell carcinoma, Spontaneous, recurrent epistaxis, Thrombocytopenia, Transitional cell carcinoma of the bladder, Uterine leiomyosarcoma [+]
Mouse (33 sources): abnormal bone marrow cavity morphology, abnormal bone marrow morphology, abnormal craniofacial bone morphology, abnormal decidualization, abnormal learning/memory/conditioning, abnormal limb morphology, abnormal long bone diaphysis morphology, abnormal motor capabilities/coordination/movement, abnormal motor learning, abnormal response to novel object, abnormal response to social novelty, abnormal social investigation, abnormal social recognition, abnormal spatial reference memory, abnormal vocalization, decreased body size, decreased grip strength, decreased molar number, delayed endochondral bone ossification, delayed eyelid opening, diluted coat color, hematopoietic system phenotype, impaired cued conditioning behavior, increased long bone epiphyseal plate size, increased startle reflex, increased thigmotaxis, increased trabecular bone mass, nervous system phenotype, periodontium inflammation, postnatal lethality, incomplete penetrance, premature death, reproductive system phenotype, short basicranium [+]
View all ortholog results at Monarch