U.S. flag

An official website of the United States government

GTR Home > Genes

TCF19 transcription factor 19

Gene ID: 6941, updated on 10-Oct-2024
Gene type: protein coding
Also known as: SC1; TCF-19

Summary

This gene encodes a protein that contains a PHD-type zinc finger domain and likely functions as a transcription factor. The encoded protein plays a role proliferation and apoptosis of pancreatic beta cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
GeneReviews: Not available
A whole-genome association study of major determinants for allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients.
GeneReviews: Not available
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
GeneReviews: Not available
Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
GeneReviews: Not available
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.
GeneReviews: Not available
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.
GeneReviews: Not available

Genomic context

Location:
6p21.33
Sequence:
Chromosome: 6; NC_000006.12 (31158589..31164215)
Total number of exons:
4

Links

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.