Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

GEMIN4

gem nuclear organelle associated protein 4

Chromosome
17
Cytoband
17p13.3
Variants (rsID)
19

GEMIN4 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p13.3). Its official name is “gem nuclear organelle associated protein 4”. The reference table lists 19 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

4 reference-table entries with clinical significance.

  • rs2740349Not classifiedmissense_variantDisease by Infectious Agent|Mycobacterium Tuberculosis 1|Colorectal Cancer|Lung Cancer Susceptibility 3
  • rs3744741Not classifiedmissense_variantDisease by Infectious Agent|Lymphoma|Mycobacterium Tuberculosis 1|Renal Cell Carcinoma, Nonpapillary
  • rs7813Not classifiedmissense_variantLung Cancer Susceptibility 3|Disease by Infectious Agent|Prostatic Hypertrophy|Prostatic Hyperplasia, Benign|Renal Cell Carcinoma, Nonpapillary|Mycobacterium Tuberculosis 1|Gastric Cancer|Prostatic Adenoma|Squamous Cell Carcinoma|Ovarian Cancer|Esophageal Cancer|Hepatitis B|Malignant Peripheral Nerve Sheath Tumor|Neurofibromatosis
  • rs910925Not classifiedmissense_variantRenal Cell Carcinoma, Nonpapillary

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.