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Apol9b Gene Detail
Summary
  • Symbol
    Apol9b
  • Name
    apolipoprotein L 9b
  • Synonyms
    2310016F22Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:1919148
    NCBI Gene: 71898
  • Alliance
  • Transcription Start Sites
    3 TSS
Location &
Maps
more
  • Sequence Map
    Chr15:77613248-77620582 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 15, 36.75 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    27 from dbSNP Build 142
  • Strain Annotations
    16
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1919148
protein coding gene Chr15:77613239-77620582 (+)
129S1/SvImJ MGP_129S1SvImJ_G0022028
protein coding gene Chr15:77860122-77862038 (+)
A/J MGP_AJ_G0021983
protein coding gene Chr15:74694931-74708202 (-)
AKR/J MGP_AKRJ_G0021964
protein coding gene Chr15:76739680-76747346 (-)
BALB/cJ MGP_BALBcJ_G0021997
protein coding gene Chr15:75174058-75181543 (+)
C3H/HeJ MGP_C3HHeJ_G0021763
protein coding gene Chr15:76818257-76820173 (-)
C57BL/6NJ MGP_C57BL6NJ_G0022439
protein coding gene Chr15:80895387-80906695 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0019960
protein coding gene Chr15:71331824-71339088 (-)
CAST/EiJ MGP_CASTEiJ_G0021282
protein coding gene Chr15:77587051-77731344 (-)
CBA/J MGP_CBAJ_G0021733
protein coding gene Chr15:83419582-83427290 (+)
DBA/2J MGP_DBA2J_G0021861
protein coding gene Chr15:74644634-74654054 (+)
FVB/NJ MGP_FVBNJ_G0021837
protein coding gene Chr15:73297448-73304868 (-)
LP/J MGP_LPJ_G0021926
protein coding gene Chr15:77629705-77640311 (-)
NOD/ShiLtJ no annotation
NZO/HlLtJ MGP_NZOHlLtJ_G0022450
protein coding gene Chr15:76989307-76991224 (-)
PWK/PhJ MGP_PWKPhJ_G0021025
protein coding gene Chr15:74405796-74407788 (-)
SPRET/EiJ no annotation
WSB/EiJ MGP_WSBEiJ_G0021341
protein coding gene Chr15:77634311-77642949 (+)



Homology
more
  • Human Ortholog
    APOL1, apolipoprotein L1
  • Vertebrate Orthologs
    6
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    APOL1, apolipoprotein L1
  • Synonyms
    APOL, APO-L, APOL-I, FSGS4
  • Links
    NCBI Gene ID: 8542
    neXtProt AC: NX_O14791
    UniProt: O14791

  • Chr Location
    22q12.3; chr22:36253071-36267530 (+)  GRCh38

  • Human Ortholog
    APOL2, apolipoprotein L2
  • Synonyms
    APOL3, APOL-II
  • Links
    NCBI Gene ID: 23780
    neXtProt AC: NX_Q9BQE5
    UniProt: Q9BQE5

  • Chr Location
    22q12.3; chr22:36226209-36239954 (-)  GRCh38

Human Diseases
more
  • Diseases
    1 with human APOL2,APOL4 associations

Human Disease Mouse Models
      
IDs
Click on a disease name to see all genes associated with that disease.

  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    25 phenotype references
  • All Mutations and Alleles
    9
  • Chemically induced (other)
    2
  • Endonuclease-mediated
    2
  • Radiation induced
    2
  • Targeted
    3
  • Genomic Mutations
    4 involving Apol9b
  • Find Mice (IMSR)
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
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
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
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
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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
  • cDNA Data
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 71898 NCBI Gene Model | MGI Sequence Detail 7335 C57BL/6J ±  kb
transcript NM_001168660 RefSeq | MGI Sequence Detail 1558 C57BL/6  
polypeptide NP_001162131 RefSeq | MGI Sequence Detail 310 C57BL/6  
For the selected sequence
Protein
Information
less
  • UniProt
    3 Sequences
  • InterPro Domains
    IPR008405 Apolipoprotein L
Molecular
Reagents
less
  • All nucleic 6
    cDNA 6

    Microarray probesets 4
References
more
  • Summaries
    All 44
    Diseases 1
    Gene Ontology 2
    Phenotypes 25
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:274872 Ingham NJ, et al., Mouse screen reveals multiple new genes underlying mouse and human hearing loss. PLoS Biol. 2019 Apr;17(4):e3000194

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
04/09/2024
MGI 6.23
The Jackson Laboratory