ftsj1 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 (0)

Nucleotides (86)

Interactants (106)

XB-GENEPAGE-5798520

Gene Symbol: ftsj1 Gene Name: FtsJ RNA methyltransferase homolog 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (42 sources): 2-3 toe syndactyly, Abnormal distal phalanx morphology of finger, Attention deficit hyperactivity disorder, Autism, Autistic behavior, Babinski sign, Bilateral tonic-clonic seizure, Broad nasal tip, Clinodactyly of the 2nd toe, Delayed eruption of teeth, Delayed gross motor development, Delayed speech and language development, Depressed nasal bridge, Downslanted palpebral fissures, Drooling, Facial palsy, Generalized non-motor (absence) seizure, Global developmental delay, Intellectual disability, mild, Intellectual disability, moderate, Intellectual disability, profound, Intellectual disability, severe, Long palpebral fissure, Long philtrum, Macrocephaly, Macrotia, Meckel diverticulum, Midface retrusion, Mild neurosensory hearing impairment, Moderate sensorineural hearing impairment, Obesity, Periorbital fullness, Pes planus, Poor speech, Pyloric stenosis, Seizure, Shortening of all distal phalanges of the fingers, Small for gestational age, Thick lower lip vermilion, Thin upper lip vermilion, Urinary incontinence, Widened subarachnoid space [+]
Mouse (7 sources): abnormal retina inner nuclear layer morphology, abnormal retina vasculature morphology, decreased circulating alanine transaminase level, decreased circulating aspartate transaminase level, decreased total retina thickness, increased lean body mass, no abnormal phenotype detected
View all ortholog results at Monarch