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Foxh1 Gene Detail
Summary
  • Symbol
    Foxh1
  • Name
    forkhead box H1
  • Synonyms
    Fast2
  • Feature Type
    protein coding gene
  • IDs
    MGI:1347465
    NCBI Gene: 14106
  • Alliance
  • Transcription Start Sites
    5 TSS
Location &
Maps
more
  • Sequence Map
    Chr15:76552425-76554148 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 15, 36.24 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    69 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1347465
protein coding gene Chr15:76552029-76554286 (-)
129S1/SvImJ ENSMUSG00200050802
protein coding gene Chr15:73666618-73668341 (-)
A/J ENSMUSG00195050720
protein coding gene Chr15:73633946-73635669 (-)
AKR/J ENSMUSG00220048640
protein coding gene Chr15:73652126-73653849 (-)
BALB/cJ ENSMUSG00180050201
protein coding gene Chr15:73459078-73460801 (-)
C3H/HeJ ENSMUSG00175051409
protein coding gene Chr15:73822506-73824229 (-)
C57BL/6NJ ENSMUSG00215049397
protein coding gene Chr15:73558487-73560210 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0019941
protein coding gene Chr15:70612799-70614463 (-)
CAST/EiJ ENSTCUG00005039279
protein coding gene Chr15:73165499-73167222 (-)
CBA/J ENSMUSG00210048378
protein coding gene Chr15:73597706-73599429 (-)
DBA/2J ENSMUSG00185041628
protein coding gene Chr15:73582067-73583790 (-)
FVB/NJ ENSMUSG00205036706
protein coding gene Chr15:73327201-73328924 (-)
JF1/MsJ ENSUMUG00000051797
protein coding gene Chr15:73229171-73230891 (-)
LP/J ENSMUSG00230050215
protein coding gene Chr15:76940432-76942155 (-)
NOD/ShiLtJ ENSMUSG00190052724
protein coding gene Chr15:73581344-73583067 (-)
NZO/HlLtJ ENSMUSG00225051314
protein coding gene Chr15:77255443-77257166 (-)
PWK/PhJ ENSLUMG00010037625
protein coding gene Chr15:73521117-73522837 (-)
SPRET/EiJ ENSMSPG00010047224
protein coding gene Chr15:75131140-75132864 (-)
WSB/EiJ ENSIUOG00005047455
protein coding gene Chr15:73647395-73649118 (-)



Homology
more
  • Human Ortholog
    FOXH1, forkhead box H1
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    FOXH1, forkhead box H1
  • Synonyms
    FAST-1, FAST1
  • Links
    NCBI Gene ID: 8928
    UniProt: O75593

  • Chr Location
    8q24.3; chr8:144473412-144475873 (-)  GRCh38

Human Diseases
more
  • Diseases
    2 with Foxh1 mouse models

Human Disease Mouse Models
      
IDs
View 1 model
IDs
View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    75 phenotypes from 6 alleles in 4 genetic backgrounds
    24 images
    47 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Conditional knockout of this gene in the lateral plate mesoderm results in death within a few days after birth. Mutant animals exhibit right isomerism affecting the heart, lungs, and stomach.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
less
Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000033837 Ensembl Gene Model | MGI Sequence Detail 1724 C57BL/6J ±  kb
    transcript ENSMUST00000037824 Ensembl | MGI Sequence Detail 1365 Not Applicable  
    polypeptide ENSMUSP00000036591 Ensembl | MGI Sequence Detail 401 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 20
      Genomic 2
      cDNA 11
      Primer pair 3
      Other 4
      Antibodies 1

      Microarray probesets 4
    Other
    Accession IDs
    less
    MGI:1277981
    References
    more
    • Summaries
      All 104
      Developmental Gene Expression 28
      Diseases 2
      Gene Ontology 17
      Phenotypes 47
    • Earliest
      J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
    • Latest
      J:387680 Ahn B, et al., Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice. Genes (Basel). 2026 Jan 31;17(2)

    Contributing Projects:
    Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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    Funding Information
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    last database update
    09/01/2026
    MGI 6.24
    The Jackson Laboratory