Location [1]
Protein [2]
Schlafen family member 12
Synonyms [1]

SLFN12 is altered in 0.01% of all cancers with prostate adenocarcinoma having the greatest prevalence of alterations [3].

SLFN12 GENIE Cases - Top Diseases

The most common alteration in SLFN12 is SLFN12-NCOR1 Fusion (0.01%) [3].

SLFN12 GENIE Cases - Top Alterations

Significance of SLFN12 in Diseases

Anaplastic Astrocytoma +

Fallopian Tube Carcinoma +

Glioblastoma +

Melanoma +

Ovarian Carcinoma +

Primary Peritoneal Carcinoma +

Sarcoma +


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.