Location [1]
Protein [2]
NUT family member 1
Synonyms [1]
FAM22H, C15orf55, NUT

NUTM1 is altered in 0.37% of all cancers with lung adenocarcinoma, melanoma, skin squamous cell carcinoma, conventional glioblastoma multiforme, and breast invasive ductal carcinoma having the greatest prevalence of alterations [3].

NUTM1 GENIE Cases - Top Diseases

The most common alterations in NUTM1 are NUTM1 Fusion (0.03%), NUTM1 P159L (0.06%), NUTM1 R203H (0.05%), NUTM1 S116L (0.05%), and NUTM1 R215H (0.04%) [3].

NUTM1 GENIE Cases - Top Alterations

Significance of NUTM1 in Diseases

NUT Midline Carcinoma Of The Head And Neck +

Malignant Solid Tumor +

Breast Carcinoma +

NUT Carcinoma +

Non-Small Cell Lung Carcinoma +

Prostate Carcinoma +


1. Hart R and Prlic A. Universal Transcript Archive Repository. Version uta_20180821. San Francisco CA: Github;2015. https://github.com/biocommons/uta

2. The UniProt Consortium. UniProt: a worldwide hub of protein knowledge. Nucleic Acids Research. 2019;47:D506-D515.

3. The AACR Project GENIE Consortium. AACR Project GENIE: powering precision medicine through an international consortium. Cancer Discovery. 2017;7(8):818-831. Dataset Version 8. This dataset does not represent the totality of the genetic landscape; see paper for more information.

4. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.