Gene Expression: CACNA1F

Gene Data

  • Gene Symbol: CACNA1F
  • Gene ID: 778
  • Synonyms: AIED, COD3, COD4, CORDX, CORDX3, CSNB2, CSNB2A, CSNBX2, Cav1.4, Cav1.4alpha1, JM8, JMC8, OA2
  • Description: calcium channel, voltage-dependent, L type, alpha 1F subunit
  • Database Refs: HGNC:1393, MIM:300110, Ensembl:ENSG00000102001, HPRD:02119, Vega:OTTHUMG00000022703
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 49 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 25 diseases, scroll to view all:
  1. Achromatopsia
  2. Aland Island eye disease
  3. Anaplastic oligoastrocytoma
  4. Astigmatism
  5. Bone structure disease
  6. cone-rod dystrophy
  7. Congenital nystagmus
  8. Congenital stationary night blindness
  9. Disease
  10. Disease of anatomical entity
  11. Eye and adnexa disease
  12. Eye disease
  13. Fundus albipunctatus
  14. Globe disease
  15. Hereditary night blindness
  16. Hyperopia
  17. Myopia
  18. Nervous system disease
  19. Night blindness
  20. Ocular albinism
  21. Pathologic nystagmus
  22. Refractive error
  23. Retinal disease
  24. Sensory system disease
  25. Spondylosis

Stage Associations

This gene is associated with the following stages: