About   Help   FAQ
Fthl17b Gene Detail
Summary
  • Symbol
    Fthl17b
  • Name
    ferritin, heavy polypeptide-like 17, member B
  • Synonyms
    Gm5634
  • Feature Type
    protein coding gene
  • IDs
    MGI:3642940
    NCBI Gene: 434726
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    ChrX:8828373-8829214 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome X, 4.07 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    103 from dbSNP Build 142
  • Strain Annotations
    5
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 no annotation
AKR/J MGP_AKRJ_G0035459
 protein coding gene ChrX:3804352-3806631 (+)
BALB/cJ no annotation
C3H/HeJ no annotation
C57BL/6NJ MGP_C57BL6NJ_G0036050
 protein coding gene ChrX:3833104-3833936 (+)
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J no annotation
DBA/2J MGP_DBA2J_G0035360
 protein coding gene ChrX:3678639-3679372 (-)
FVB/NJ no annotation
LP/J no annotation
NOD/ShiLtJ no annotation
NZO/HlLtJ no annotation
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ MGP_WSBEiJ_G0034666
 protein coding gene ChrX:3742683-3743080 (+)



Homology
more
  • Human Ortholog
    FTH1P19, ferritin heavy chain 1 pseudogene 19
  • Vertebrate Orthologs
    5
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
    neXtProt AC: NX_Q9BXU8
    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
    3
  • GO References
    1
Molecular Function

Biological Process

Cellular Component

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
    714
  • Tissues
    4
  • Literature Summary
    1
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 9
    Developmental Gene Expression 1
    Gene Ontology 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
11/12/2024
MGI 6.24 		The Jackson Laboratory