T-Box Transcription Factor 19

Alternative Names

  • TBX19
  • T-Box 19
  • T-Box Factor, Pituitary
  • TPIT

Associated Diseases

ACTH Deficiency, Isolated
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OMIM Number

604614

NCBI Gene ID

9095

Uniprot ID

O60806

Length

33,550 bases

No. of Exons

8

No. of isoforms

1

Protein Name

T-box transcription factor TBX19

Molecular Mass

48238 Da

Amino Acid Count

448

Genomic Location

chr1:168,280,877-168,314,426

Gene Map Locus
1q24.2

Description

This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene were found in patients with isolated deficiency of pituitary POMC-derived ACTH, suggesting an essential role for this gene in differentiation of the pituitary POMC lineage. ACTH deficiency is characterized by adrenal insufficiency symptoms such as weight loss, lack of appetite (anorexia), weakness, nausea, vomiting, and low blood pressure. [From RefSeq]

Epidemiology in the Arab World

View Map
Variant NameCountryGenomic LocationClinvar Clinical SignificanceCTGA Clinical Significance Condition(s)HGVS ExpressionsdbSNPClinvar
NM_005149.3:c.604-1G>CUnited Arab EmiratesNC_000001.11:g.168297723G>CLikely PathogenicACTH Deficiency, IsolatedNG_008244.1:g.21684G>C; NM_005149.3:c.604-1G>C; NP_005140.1:p.?
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