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Slc26a8 Gene Detail
Summary
  • Symbol
    Slc26a8
  • Name
    solute carrier family 26, member 8
  • Synonyms
    MGC:38861
  • Feature Type
    protein coding gene
  • IDs
    MGI:2385046
    NCBI Gene: 224661
  • Alliance
    gene page
  • Transcription Start Sites
    5 TSS
Location &
Maps
more
  • Sequence Map
    Chr17:28856757-28909207 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 17, 14.82 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    176 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2385046
 protein coding gene Chr17:28856757-28910242 (-)
129S1/SvImJ MGP_129S1SvImJ_G0023447
 protein coding gene Chr17:28075584-28135457 (-)
A/J MGP_AJ_G0023405
 protein coding gene Chr17:27130035-27191697 (-)
AKR/J MGP_AKRJ_G0023370
 protein coding gene Chr17:27340188-27400324 (-)
BALB/cJ MGP_BALBcJ_G0023410
 protein coding gene Chr17:27408815-27461339 (-)
C3H/HeJ MGP_C3HHeJ_G0023171
 protein coding gene Chr17:27741841-27798279 (-)
C57BL/6NJ MGP_C57BL6NJ_G0023852
 protein coding gene Chr17:29200414-29266332 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0021327
 protein coding gene Chr17:24496885-24548506 (-)
CAST/EiJ MGP_CASTEiJ_G0022672
 protein coding gene Chr17:27704425-27768718 (-)
CBA/J MGP_CBAJ_G0023145
 protein coding gene Chr17:30274218-30342204 (-)
DBA/2J MGP_DBA2J_G0023276
 protein coding gene Chr17:26686205-26739792 (-)
FVB/NJ MGP_FVBNJ_G0023246
 protein coding gene Chr17:26509993-26568947 (-)
LP/J MGP_LPJ_G0023354
 protein coding gene Chr17:28325006-28385658 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0023264
 protein coding gene Chr17:29666309-29736960 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0023894
 protein coding gene Chr17:27787795-27843580 (-)
PWK/PhJ MGP_PWKPhJ_G0022422
 protein coding gene Chr17:25504336-25564581 (-)
SPRET/EiJ MGP_SPRETEiJ_G0022240
 protein coding gene Chr17:25769277-25831613 (-)
WSB/EiJ MGP_WSBEiJ_G0022734
 protein coding gene Chr17:27769098-27827232 (-)



Homology
more
  • Human Ortholog
    SLC26A8, solute carrier family 26 member 8
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    SLC26A8, solute carrier family 26 member 8
  • Synonyms
    AZON, SPGF3, TAT1
  • Links
    NCBI Gene ID: 116369
    neXtProt AC: NX_Q96RN1
    UniProt: Q96RN1

  • Chr Location
    6p21.31; chr6:35943516-36024868 (-)  GRCh38
Human Diseases
more
  • Diseases
    1 with human SLC26A8 associations

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

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    12 phenotypes from 1 allele in 1 genetic background
    9 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.
Mice homozygous for a targeted allele exhibit male sterility associated with sperm immotility, abnormal flagella and reduced acrosomal reaction.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    30
  • GO References
    6
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

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
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
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
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
    707
  • Tissues
    1
  • cDNA Data
    6
  • Literature Summary
    1
  • Comparison Matrix
    Gene Expression + Phenotype
    • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000036196 Ensembl Gene Model | MGI Sequence Detail 52451 C57BL/6J ±  kb
    transcript ENSMUST00000114764 Ensembl | MGI Sequence Detail 3670 Not Applicable  
    polypeptide ENSMUSP00000110412 Ensembl | MGI Sequence Detail 999 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 6
      cDNA 6

      Microarray probesets 2
    References
    more
    • Summaries
      All 31
      Developmental Gene Expression 1
      Gene Ontology 6
      Phenotypes 9
    • 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:181151 Rode B, et al., The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation. Hum Mol Genet. 2012 Mar 15;21(6):1287-98
    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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    Send questions and comments to User Support.     		last database update
    11/05/2024
    MGI 6.24     		The Jackson Laboratory