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Fthl17b Gene Detail
Summary
  • Symbol
    Fthl17b
  • Name
    ferritin, heavy polypeptide-like 17, member B
  • Synonyms
    Gm5634
Location &
Maps
more
  • Sequence Map
    ChrX:8828373-8829214 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 4.07 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    103 from dbSNP Build 142
  • Strain Annotations
    11
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3642940
protein coding gene ChrX:8828373-8829214 (-)
129S1/SvImJ no annotation
A/J ENSMUSG00195038257
protein coding gene ChrX:3546694-3547535 (-)
AKR/J ENSMUSG00220034124
protein coding gene ChrX:3191185-3192026 (-)
BALB/cJ ENSMUSG00180029744
protein coding gene ChrX:3544468-3545309 (-)
C3H/HeJ ENSMUSG00175031299
protein coding gene ChrX:3558373-3559214 (-)
C57BL/6NJ ENSMUSG00215040554
protein coding gene ChrX:4217442-4218283 (-)
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J ENSMUSG00210033409
protein coding gene ChrX:3608349-3609190 (-)
DBA/2J ENSMUSG00185035396
protein coding gene ChrX:10199439-10200280 (-)
FVB/NJ ENSMUSG00205031629
protein coding gene ChrX:3380856-3381697 (-)
JF1/MsJ no annotation
LP/J no annotation
NOD/ShiLtJ ENSMUSG00190028629
protein coding gene ChrX:3550339-3551180 (-)
NZO/HlLtJ ENSMUSG00225045525
protein coding gene ChrX:19985316-19986157 (-)
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    FTH1P19, ferritin heavy chain 1 pseudogene 19
  • Vertebrate Orthologs
    7
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    FTH1P19, ferritin heavy chain 1 pseudogene 19
  • Synonyms
    FTHL19
  • Links
    NCBI Gene ID: 389844
    UniProt: P0C7X4

  • Chr Location
    Xp21.1; chrX:37491957-37492720 (+)  GRCh38

  • Human Ortholog
    FTHL17, ferritin heavy chain like 17
  • Synonyms
    CT38
  • Links
    NCBI Gene ID: 53940
    UniProt: Q9BXU8

  • Chr Location
    Xp21.2; chrX:31071233-31072041 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
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
  • Literature Summary
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 434726 NCBI Gene Model | MGI Sequence Detail 842 C57BL/6J ±  kb
transcript NM_001085524 RefSeq | MGI Sequence Detail 842 C57BL/6  
polypeptide NP_001078993 RefSeq | MGI Sequence Detail 176 C57BL/6  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 1
    Primer pair 1
References
more
  • Summaries
    All 12
    Developmental Gene Expression 1
    Gene Ontology 3
    Phenotypes 1
  • Earliest
    J:173437 Kobayashi S, et al., The X-linked imprinted gene family Fthl17 shows predominantly female expression following the two-cell stage in mouse embryos. Nucleic Acids Res. 2010 Jun 1;38(11):3672-81

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