Gene Expression: SHFM1

Gene Data

  • Gene Symbol: SHFM1
  • Gene ID: 7979
  • Synonyms: DSS1, ECD, SEM1, SHFD1, SHSF1, Shfdg1
  • Description: split hand/foot malformation (ectrodactyly) type 1
  • Database Refs: HGNC:10845, MIM:183600, HPRD:03182
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 4 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 33 diseases, scroll to view all:
  1. Amenorrhea
  2. Bone development disease
  3. Cellular leiomyoma
  4. Disease
  5. Disease by infectious agent
  6. Disease of anatomical entity
  7. Dysostosis
  8. Endocrine system disease
  9. Female reproductive system disease
  10. Goiter
  11. Gonadal disease
  12. Hepatitis A
  13. Hepatitis B
  14. Hyperpituitarism
  15. Hyperprolactinemia
  16. Hyperthyroidism
  17. Hypogonadism
  18. Hypothyroidism
  19. Infertility
  20. Mucinous adenofibroma
  21. Multinodular goiter
  22. Ovarian mucinous adenofibroma
  23. Pituitary disease
  24. Placental site trophoblastic tumor
  25. Polycystic ovary syndrome
  26. Precocious puberty
  27. Radioulnar synostosis
  28. Reproductive system disease
  29. Syndactyly
  30. Synostosis
  31. Thyroid gland disease
  32. Thyrotoxicosis
  33. Viral infectious disease

Stage Associations

This gene is associated with the following stages: