xylt1 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.

ExpressionExpr.

PhenotypesPheno.

Gene Literature (0)Lit. (0)

GO Terms (11)GO (11)

Nucleotides (93)Nucl. (93)

Proteins (46)Prot. (46)

Interactants (11)Interact. (11)

XB-GENEPAGE-949398

Gene Symbol: xylt1 Gene Name: xylosyltransferase I

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: xylt1 assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (85 sources): Abnormal eyelash morphology, Abnormal femoral neck/head morphology, Abnormal metaphysis morphology, Accelerated skeletal maturation, Acne, Advanced ossification of carpal bones, Anteverted nares, Aplasia/Hypoplasia of the abdominal wall musculature, Bell-shaped thorax, Bifid uvula, Blue sclerae, Broad foot, Broad ribs, Broad thumb, Camptodactyly of finger, Cleft palate, Clinodactyly, Clinodactyly of the 5th finger, Coxa valga, Coxa vara, Cutaneous syndactyly, Delayed speech and language development, Dental crowding, Depressed nasal bridge, Disproportionate short-limb short stature, Elbow dislocation, Epicanthus, Epiphyseal dysplasia, Failure to thrive, Flared metaphysis, Flat acetabular roof, Flat face, Generalized hypotonia, Genu recurvatum, Genu varum, Glaucoma, Global developmental delay, Growth delay, Hepatomegaly, Hirsutism, Hypodontia, Hypotonia, Intellectual disability, Intrauterine growth retardation, Joint dislocation, Long philtrum, Lumbar hyperlordosis, Metaphyseal widening, Microcephaly, Moderate intellectual disability, Moon facies, Myopia, Narrow chest, obsolete Hypotrichosis, obsolete Joint hyperflexibility, obsolete Joint laxity, obsolete Low-set, posteriorly rotated ears, Patellar dislocation, Pectus carinatum, Pectus excavatum, Pes planus, Platyspondyly, Proptosis, Radial head subluxation, Radioulnar synostosis, Relative macrocephaly, Respiratory distress, Round face, Scoliosis, Severe short stature, Short clavicles, Short femoral neck, Short long bone, Short metacarpal, Short neck, Short phalanx of finger, Short stature, Single transverse palmar crease, Small hand, Soft, doughy skin, Synophrys, Thick vermilion border, Toe clinodactyly, Truncal obesity, Ventricular septal defect [+]
Mouse (26 sources): abnormal anxiety-related response, abnormal endochondral bone ossification, abnormal forebrain development, abnormal forelimb stylopod morphology, abnormal forelimb zeugopod morphology, abnormal hindlimb stylopod morphology, abnormal hindlimb zeugopod morphology, abnormal osteoclast differentiation, abnormal tail bud morphology, abnormal vocalization, decreased body size, decreased bone trabecula number, decreased chondrocyte number, decreased thigmotaxis, decreased width of hypertrophic chondrocyte zone, disproportionate dwarf, growth/size/body region phenotype, increased trabecular bone connectivity density, increased trabecular bone thickness, increased trabecular bone volume, premature bone ossification, preweaning lethality, complete penetrance, preweaning lethality, incomplete penetrance, short mandible, skeleton phenotype, small thoracic cage [+]
View all ortholog results at Monarch