Gene Expression: SLC16A2

Gene Data

  • Gene Symbol: SLC16A2
  • Gene ID: 6567
  • Synonyms: AHDS, DXS128, DXS128E, MCT 7, MCT 8, MCT7, MCT8, MRX22, XPCT
  • Description: solute carrier family 16, member 2 (thyroid hormone transporter)
  • Database Refs: HGNC:10923, MIM:300095, Ensembl:ENSG00000147100, HPRD:02106, Vega:OTTHUMG00000021857
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 6 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters:

Disease Associations

This gene is associated with the following diseases. Clicking on the disease will take you to the disease association entry for that disease.

This gene is associated with 21 diseases, scroll to view all:
  1. Allan-Herndon-Dudley syndrome
  2. Coffin-Lowry syndrome
  3. Congenital hypothyroidism
  4. Developmental disease of mental health
  5. Disease
  6. Disease of anatomical entity
  7. Disease of mental health
  8. Endocrine system disease
  9. Genetic disease
  10. Hypothyroidism
  11. Intellectual disability
  12. Menkes disease
  13. Monogenic disease
  14. Paraplegia
  15. Pelizaeus-Merzbacher disease
  16. Spastic cerebral palsy
  17. Spastic paraplegia
  18. Spastic quadriplegia
  19. Specific developmental disease
  20. Thyroid gland disease
  21. Thyroid hormone resistance syndrome

Stage Associations

This gene is associated with the following stages: