About   Help   FAQ
Fthl17d Gene Detail
Summary
  • Symbol
    Fthl17d
  • Name
    ferritin, heavy polypeptide-like 17, member D
  • Synonyms
    Gm14458
Location &
Maps
more
  • Sequence Map
    ChrX:8852179-8852911 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 4.08 cM
Strain
Comparison
more
  • SNPs within 2kb
    48 from dbSNP Build 142
  • Strain Annotations
    13
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3713070
protein coding gene ChrX:8852139-8852994 (-)
129S1/SvImJ ENSMUSG00200032173
protein coding gene ChrX:3585178-3586018 (+)
A/J ENSMUSG00195037849
protein coding gene ChrX:3570460-3571315 (-)
AKR/J ENSMUSG00220034168
protein coding gene ChrX:3214952-3215807 (-)
BALB/cJ ENSMUSG00180027182
protein coding gene ChrX:3568233-3569088 (-)
C3H/HeJ ENSMUSG00175028587
protein coding gene ChrX:3582137-3582992 (-)
C57BL/6NJ ENSMUSG00215040567
protein coding gene ChrX:4241208-4242063 (-)
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J ENSMUSG00210032525
protein coding gene ChrX:3632109-3632964 (-)
DBA/2J ENSMUSG00185035885
protein coding gene ChrX:10223205-10224060 (-)
FVB/NJ ENSMUSG00205031735
protein coding gene ChrX:3404620-3405475 (-)
JF1/MsJ no annotation
LP/J ENSMUSG00230028420
protein coding gene ChrX:14791596-14792436 (+)
NOD/ShiLtJ ENSMUSG00190028948
protein coding gene ChrX:3574105-3574960 (-)
NZO/HlLtJ ENSMUSG00225044482
protein coding gene ChrX:20009080-20009935 (-)
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
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 100042782 NCBI Gene Model | MGI Sequence Detail 733 C57BL/6J ±  kb
transcript NM_001099326 RefSeq | MGI Sequence Detail 733 C57BL/6  
polypeptide NP_001092796 RefSeq | MGI Sequence Detail 176 C57BL/6  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
Molecular
Reagents
less
  • All nucleic 1
    Primer pair 1
References
more
  • Summaries
    All 10
    Developmental Gene Expression 1
    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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
09/08/2026
MGI 6.24
The Jackson Laboratory