tcf20 Phenotypes

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Phenotypes

Gene Literature (2)

Nucleotides (237)

Interactants (97)

XB-GENEPAGE-484161

Gene Symbol: tcf20 Gene Name: transcription factor 20 (AR1)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (63 sources): Abnormal cerebral white matter morphology, Abnormal facial shape, Abnormal foot morphology, Aggressive behavior, Anxiety, Ataxia, Autistic behavior, Brachycephaly, Broad hallux, Broad nasal tip, Bulbous nose, Clinodactyly, Clinodactyly of the 5th finger, Compulsive behaviors, Constipation, Deeply set eye, Delayed ability to walk, Delayed speech and language development, Depressed nasal bridge, Downturned corners of mouth, Epicanthus, Feeding difficulties, Frontal bossing, Generalized hypotonia, Global developmental delay, High forehead, Hyperactivity, Hypertelorism, Intellectual disability, Inverted nipples, Long face, Low-set ears, Macrocephaly, Microcephaly, Micrognathia, Midface retrusion, Motor delay, Myopia, Narrow mouth, Obesity, Open mouth, Overlapping toe, Pes planus, Plagiocephaly, Poor coordination, Posteriorly rotated ears, Prominent nose, Sandal gap, Scoliosis, Seizure, Short nose, Short palpebral fissure, Short stature, Sleep disturbance, Slender finger, Small hand, Spasticity, Strabismus, Tall stature, Tapered finger, Tented upper lip vermilion, Thin upper lip vermilion, Upslanted palpebral fissure [+]
Mouse (10 sources): abnormal adipose tissue amount, abnormal body length, abnormal bone mineralization, abnormal lean body mass, decreased body length, decreased bone mineral content, decreased lean body mass, increased circulating alkaline phosphatase level, increased circulating iron level, increased total body fat amount
View all ortholog results at Monarch