rlim Phenotypes

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Phenotypes

Gene Literature (5)

Nucleotides (236)

Interactants (171)

XB-GENEPAGE-492019

Gene Symbol: rlim Gene Name: ring finger protein, LIM domain interacting

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (57 sources): Abnormal cerebral white matter morphology, Abnormal heart morphology, Aggressive behavior, Anxiety, Behavioral abnormality, Brachydactyly, Broad forehead, Broad hallux, Broad nasal tip, Broad thumb, Broad-based gait, Clinodactyly, Congenital diaphragmatic hernia, Cryptorchidism, Decreased testicular size, Delayed speech and language development, Downslanted palpebral fissures, Downturned corners of mouth, Dysphagia, Epicanthus, Feeding difficulties, Fine hair, Generalized hypotonia, Global developmental delay, Growth delay, Hyperreflexia, Hypertelorism, Hypospadias, Hypotelorism, Intellectual disability, Malar flattening, Microcephaly, Micrognathia, Micropenis, Narrow face, Narrow mouth, Overlapping toe, Pes planus, Poor speech, Prominent nasal bridge, Prominent nose, Pulmonary hypoplasia, Sandal gap, Self-injurious behavior, Short palpebral fissure, Short stature, Shyness, Slender finger, Small hand, Small nail, Spasticity, Strabismus, Thin upper lip vermilion, Tremor, Upslanted palpebral fissure, Velopharyngeal insufficiency, Wide nasal bridge [+]
Mouse (14 sources): abnormal dosage compensation, by inactivation of X chromosome, abnormal embryo development, abnormal extraembryonic tissue morphology, abnormal large unstained cell number, abnormal mean corpuscular hemoglobin, abnormal mean corpuscular volume, abnormal thymus morphology, decreased startle reflex, embryonic lethality during organogenesis, incomplete penetrance, enlarged lymph nodes, enlarged thymus, fusion of vertebral arches, no abnormal phenotype detected, transmission ratio distortion [+]
View all ortholog results at Monarch