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Zdhhc13 Gene Detail
Summary
  • Symbol
    Zdhhc13
  • Name
    zinc finger, DHHC domain containing 13
  • Synonyms
    2410004E01Rik, Hip14l, kojak, skc4
  • Feature Type
    protein coding gene
  • IDs
    MGI:1919227
    NCBI Gene: 243983
Location & Maps
more
  • Sequence Map
    Chr7:48789003-48827440 bp, + strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      38438 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 7, 31.11 cM, cytoband B3
  • Mapping Data
    2 experiments
Homology
more
  • Human Ortholog
    ZDHHC13, zinc finger DHHC-type containing 13
  • Vertebrate Orthologs
    9
  • Human Ortholog
    ZDHHC13, zinc finger DHHC-type containing 13
    Orthology source: HomoloGene, HGNC
  • Synonyms
    HIP14L, HIP3RP
  • Links
    NCBI Gene ID: 54503
    neXtProt AC: NX_Q8IUH4

  • Chr Location
    11p15.1; chr11:19117099-19176420 (+)  GRCh38.p2

Human Diseases
more
  • Diseases
    1 with Zdhhc13 mouse models

Human Disease Mouse Models
       Huntington Disease; HD   OMIM: 143100 View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    50 phenotypes from 2 alleles in 4 genetic backgrounds
    6 images
    11 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.
  • All Mutations and Alleles
    5
  • Chemically induced (ENU)
    1
  • Gene trapped
    2
  • Spontaneous
    1
  • Targeted
    1
  • Incidental Mutations
Mice homozygous for an ENU mutation display wasting, weight loss, hair loss (alopecia), reduced bone mineral density (osteoporosis), and generalized amyloid deposition, which resulted in early death.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

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

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
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
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
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
Interactions
less
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000030356 VEGA Gene Model | MGI Sequence Detail 38438 C57BL/6J ±  kb
transcript OTTMUST00000075207 VEGA | MGI Sequence Detail 2410 Not Applicable  
polypeptide OTTMUSP00000039367 VEGA | MGI Sequence Detail 622 Not Applicable  
For the selected sequence
Polymorphisms
less
  • SNPs within 2kb
    320 from dbSNP Build 142
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 37
    cDNA 36
    Primer pair 1

    Microarray probesets 3
Other
Accession IDs
less
MGI:2671602
References
more
  • Summaries
    All 43
    Developmental Gene Expression 6
    Diseases 1
    Gene Ontology 7
    Phenotypes 11
  • Earliest
    J:65060 Kawai J, et al., Functional annotation of a full-length mouse cDNA collection. Nature. 2001 Feb 8;409(6821):685-90
  • Latest
    J:233660 Lemonidis K, et al., Identification of a Novel Sequence Motif Recognized by the Ankyrin Repeat Domain of zDHHC17/13 S-Acyltransferases. J Biol Chem. 2015 Sep 4;290(36):21939-50

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
11/29/2016
MGI 6.06
The Jackson Laboratory