hcfc1 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (244)

Interactants (157)

XB-GENEPAGE-6076922

Gene Symbol: hcfc1 Gene Name: host cell factor C1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (50 sources): 2-3 toe syndactyly, Athetosis, Attention deficit hyperactivity disorder, Autistic behavior, Babinski sign, Bilateral tonic-clonic seizure, Brachycephaly, Broad nasal tip, Chorea, Clinodactyly of the 2nd toe, Delayed eruption of teeth, Delayed speech and language development, Depressed nasal bridge, Downslanted palpebral fissures, Drooling, Facial palsy, Failure to thrive, Generalized hypotonia, Generalized non-motor (absence) seizure, Global developmental delay, Homocystinuria, Hypotonia, Hypsarrhythmia, Intellectual disability, Intellectual disability, moderate, Intellectual disability, profound, Intellectual disability, severe, Long palpebral fissure, Long philtrum, Macrocephaly, Meckel diverticulum, Methylmalonic acidemia, Methylmalonic aciduria, Microcephaly, Midface retrusion, Mild neurosensory hearing impairment, Moderate sensorineural hearing impairment, Obesity, Periorbital fullness, Pes planus, Poor speech, Pyloric stenosis, Seizure, Short stature, 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 (10 sources): abnormal embryo morphology, abnormal extraembryonic tissue morphology, decreased body length, decreased cell proliferation, decreased embryo size, decreased lean body mass, embryonic lethality prior to organogenesis, embryonic lethality, complete penetrance, impaired liver regeneration, increased apoptosis
View all ortholog results at Monarch