Gene Expression: SPG7

Gene Data

  • Gene Symbol: SPG7
  • Gene ID: 6687
  • Synonyms: CAR, CMAR, PGN, SPG5C
  • Description: spastic paraplegia 7 (pure and complicated autosomal recessive)
  • Database Refs: HGNC:11237, MIM:602783, Ensembl:ENSG00000197912, HPRD:04149, Vega:OTTHUMG00000138046
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 3 out of 23 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 32 diseases, scroll to view all:
  1. Blau syndrome
  2. Central nervous system disease
  3. Cranial nerve disease
  4. Crohn's disease
  5. Disease
  6. Disease of anatomical entity
  7. Focal glomerulosclerosis
  8. Focal segmental glomerulosclerosis
  9. Glomerulonephritis
  10. IgA glomerulonephritis
  11. KBG syndrome
  12. Kidney disease
  13. Lateral sclerosis
  14. Lupus erythematosus
  15. Membranoproliferative glomerulonephritis
  16. Membranous glomerulonephritis
  17. Mesangial proliferative glomerulonephrit
  18. Nephritis
  19. Nephrosis
  20. Nephrotic syndrome
  21. Nervous system disease
  22. Optic atrophy
  23. Optic nerve disease
  24. Orthostatic proteinuria
  25. Paraplegia
  26. Proliferative glomerulonephritis
  27. Proteinuria
  28. Spastic paraplegia
  29. Spinocerebellar ataxia
  30. Spinocerebellar degeneration
  31. Urinary system disease
  32. Visual pathway disease

Stage Associations

This gene is associated with the following stages: