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AB124611 Gene Detail
Summary
  • Symbol
    AB124611
  • Name
    cDNA sequence AB124611
  • Synonyms
    HIDE1, LOC382062
  • Feature Type
    protein coding gene
  • IDs
    MGI:3043001
    NCBI Gene: 382062
  • Alliance
  • Transcription Start Sites
    3 TSS
Location &
Maps
more
  • Sequence Map
    Chr9:21437472-21456629 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 9, 7.82 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    22 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3043001
protein coding gene Chr9:21437410-21456629 (+)
129S1/SvImJ MGP_129S1SvImJ_G0034455
protein coding gene Chr9:18747583-18771474 (+)
A/J MGP_AJ_G0034433
protein coding gene Chr9:18419575-18441529 (+)
AKR/J MGP_AKRJ_G0034360
protein coding gene Chr9:18777752-18800268 (+)
BALB/cJ MGP_BALBcJ_G0034424
protein coding gene Chr9:18306798-18326478 (+)
C3H/HeJ MGP_C3HHeJ_G0034136
protein coding gene Chr9:19064207-19087639 (+)
C57BL/6NJ MGP_C57BL6NJ_G0034945
protein coding gene Chr9:19500921-19527865 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0031875
protein coding gene Chr9:17537408-17555667 (+)
CAST/EiJ MGP_CASTEiJ_G0033459
protein coding gene Chr9:18903613-18925091 (+)
CBA/J MGP_CBAJ_G0034109
protein coding gene Chr9:20250063-20282560 (+)
DBA/2J MGP_DBA2J_G0034268
protein coding gene Chr9:18390736-18411141 (+)
FVB/NJ MGP_FVBNJ_G0034211
protein coding gene Chr9:17924897-17944598 (+)
LP/J MGP_LPJ_G0034353
protein coding gene Chr9:18905614-18926852 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0034254
protein coding gene Chr9:21820882-21846952 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0034965
protein coding gene Chr9:18717630-18742594 (+)
PWK/PhJ MGP_PWKPhJ_G0033165
protein coding gene Chr9:18385825-18405586 (+)
SPRET/EiJ MGP_SPRETEiJ_G0032999
protein coding gene Chr9:18774079-18794757 (+)
WSB/EiJ MGP_WSBEiJ_G0033574
protein coding gene Chr9:18439980-18466237 (+)



Homology
more
  • Human Ortholog
    C19orf38, chromosome 19 open reading frame 38
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C19orf38, chromosome 19 open reading frame 38
  • Synonyms
    HIDE1
  • Links
    NCBI Gene ID: 255809
    neXtProt AC: NX_A8MVS5
    UniProt: A8MVS5

  • Chr Location
    19p13.2; chr19:10836575-10869790 (+)  GRCh38

Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    5 phenotypes from 1 allele in 1 genetic background
    10 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.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
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
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000057191 Ensembl Gene Model | MGI Sequence Detail 19158 C57BL/6J ±  kb
    transcript ENSMUST00000086361 Ensembl | MGI Sequence Detail 1310 Not Applicable  
    polypeptide ENSMUSP00000083547 Ensembl | MGI Sequence Detail 222 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 14
      cDNA 14

      Microarray probesets 3
    Other
    Accession IDs
    less
    MGI:2686552
    References
    more
    • Summaries
      All 30
      Developmental Gene Expression 1
      Gene Ontology 1
      Phenotypes 10
    • Earliest
      J:86696 Zambrowicz BP, et al., Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14109-14
    • Latest
      J:236599 Dickinson ME, et al., High-throughput discovery of novel developmental phenotypes. Nature. 2016 Sep 14;537(7621):508-514

    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
    04/16/2024
    MGI 6.23
    The Jackson Laboratory