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Gene: Fuom MGI:1916314

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Not currently registered for phenotyping at IMPC

Phenotyping is currently not planned for a knockout strain of this gene.

Gene Summary

Name:
fucose mutarotase
Synonyms:
1810014F10Rik

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IMPC Data Collections

  • No Body Weight Data
  • No Embryo Imaging Data
  • No Viability Data

IMPC Phenotype Summary

Significant
Not Significant
Not tested

View all our phenotype data below

Phenotypes

The IMPC applies a panel of phenotyping screens to characterise single-gene knockout mice by comparison to wild types. Click on the different tabs to visualise significant phenotypes identified by the IMPC, as well as all data that was measured.

lacZ Expression

Expression data not available

Associated Images

Images submitted by IMPC centres for a selection of procedures. Each set of images is available to view in our image comparator.

Phenotype associated images not available

Human diseases caused by Fuom mutations

The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.

Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.

No human diseases associated to this gene by orthology or annotation.

The table below shows human diseases predicted to be associated to Fuom by phenotypic similarity.

Disease Similarity of
phenotypes		 Matching phenotypes Source
Autism, Susceptibility To, 20
Impaired social interactions OMIM:618830
Hereditary Geniospasm
Abnormal social behavior ORPHA:53372
Intellectual Disability-Expressive Aphasia-Facial Dysmorphism Syndrome
Abnormal social behavior ORPHA:436151
11Q22.2Q22.3 Microdeletion Syndrome
Abnormal social behavior, Obesity ORPHA:444002
Lamb-Shaffer Syndrome
Fused cervical vertebrae, Abnormal social behavior, Thoracic kyphosis, Scoliosis ORPHA:530983
Hsd10 Disease
Abnormal social behavior ORPHA:391417
Female Restricted Epilepsy With Intellectual Disability
Abnormal social behavior ORPHA:101039
48,Xxxy Syndrome
Abnormal social behavior, Obesity, Scoliosis ORPHA:96263
Childhood Absence Epilepsy
Abnormal social behavior ORPHA:64280
Early-Onset Autosomal Dominant Alzheimer Disease
Abnormal social behavior ORPHA:1020
Fg Syndrome Type 1
Abnormal social behavior, Slender build ORPHA:93932
Prader-Willi Syndrome Due To Translocation
Abnormal social behavior, Scoliosis, Obesity, Impaired social interactions ORPHA:177907
Mend Syndrome
Kyphosis, Failure to thrive, Abnormal social behavior ORPHA:401973
Metachromatic Leukodystrophy, Late Infantile Form
Abnormal social behavior ORPHA:309256
Metachromatic Leukodystrophy, Juvenile Form
Abnormal social behavior ORPHA:309263
Koolen-De Vries Syndrome Due To A Point Mutation
Small for gestational age, Hyperlordosis, Kyphosis, Inappropriate laughter, Scoliosis, Abnormal s... ORPHA:363965
17Q21.31 Microdeletion Syndrome
Small for gestational age, Hyperlordosis, Kyphosis, Inappropriate laughter, Scoliosis, Abnormal s... ORPHA:363958
Metachromatic Leukodystrophy, Adult Form
Abnormal social behavior ORPHA:309271
Dihydropyrimidine Dehydrogenase Deficiency
Abnormal social behavior ORPHA:1675
Williams Syndrome
Failure to thrive in infancy, Hyperlordosis, Kyphosis, Spina bifida occulta, Obesity, Abnormal fo... ORPHA:904
Non-Progressive Cerebellar Ataxia With Intellectual Disability
Abnormal social behavior ORPHA:314647
Tuberous Sclerosis Complex
Abnormal social behavior ORPHA:805
Niemann-Pick Disease Type C
Abnormal social behavior ORPHA:646

Histopathology

Summary table of phenotypes displayed during the Histopathology procedure which are considered significant. Full histopathology data table, including submitted images, can be accessed by clicking any row in this table.

There is no histopathology data for Fuom

IMPC related publications

The table below lists publications which used either products generated by the IMPC or data produced by the phenotyping efforts of the IMPC. These publications have also been associated to Fuom.

No publications found that use IMPC mice or data for Fuom.

Order Mouse and ES Cells

All available products are supplied via our member's centres or partnerships. When ordering a product from the IMPC you will be redirected to one of their websites or prompted to start an email.

MGI Allele Allele Type Produced
Fuomtm1(KOMP)Mbp Reporter-tagged deletion allele (with selection cassette) Targeting vectors, ES Cells
Fuomtm441783(Ifitm2_intron_L1L2_GT1_LF2A_LacZ_BetactP_neo) KO first allele (reporter-tagged insertion with conditional potential) Targeting vectors
Fuomtm1(KOMP)Wtsi Reporter-tagged deletion allele (with selection cassette) Targeting vectors, ES Cells
Fuomem1(IMPC)Hmgu Exon Deletion Mice

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