PIM2 Proto-Oncogene, Serine/Threonine Kinase

A key regulator of cell survival, proliferation, and hematological malignancies

Gene Information Card

Symbol PIM2
Full Name Pim-2 proto-oncogene, serine/threonine kinase
Gene Type protein-coding
Chromosomal Location Xp11.23
NCBI Gene ID 11040 ncbi.nlm.nih.gov/gene/11040
Ensembl ID ENSG00000102096
UniProt ID Q9P1W9
OMIM ID 300295
HGNC ID 8987
Aliases PIM2H, PIM2L

Description

PIM2 encodes a serine/threonine kinase that belongs to the PIM family of proto-oncogenes. The protein is involved in cell cycle progression, apoptosis inhibition, and regulation of transcription and translation. It is frequently overexpressed in hematological malignancies and is considered a therapeutic target.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Multiple myeloma Overexpression of PIM2 promotes cell survival and resistance to apoptosis via phosphorylation of BAD and 4E-BP1 PMID: 16912224; COSMIC
Diffuse large B-cell lymphoma PIM2 is upregulated and contributes to proliferation and survival through STAT3/5 signaling PMID: 23341540; COSMIC
Acute myeloid leukemia PIM2 expression is elevated and associated with poor prognosis; kinase activity supports leukemic cell growth PMID: 25205116; COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Bone marrow 12.5 Medium
Lymph node 10.8 Medium
Spleen 9.2 Medium
Thymus 7.1 Low
Peripheral blood leukocytes 6.3 Low
Cell Line Expression
Cell Line nTPM Notes
K-562 (chronic myeloid leukemia) 15.2 High expression
Raji (Burkitt lymphoma) 12.8 High expression
MOLT-4 (T-cell leukemia) 10.5 Medium expression
HL-60 (acute promyelocytic leukemia) 9.1 Medium expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.331C>T (p.Arg111Trp) Missense <1% Unknown functional effect; reported in COSMIC
c.487G>A (p.Gly163Arg) Missense <1% Unknown functional effect; reported in COSMIC
c.614A>G (p.Asn205Ser) Missense <1% Unknown functional effect; reported in COSMIC
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in COSMIC or ClinVar.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported; overexpression is the primary oncogenic mechanism.

Dominant Negative (DN)

No dominant-negative mutations described.

Pathways

PI3K/Akt signaling (Reactome: R-HSA-1257604)
JAK/STAT signaling (Reactome: R-HSA-8950505)
mTOR signaling (Reactome: R-HSA-165159)
Apoptosis modulation (Reactome: R-HSA-109581)

Protein Summary

PIM2 is a 34 kDa serine/threonine kinase with a short half-life. It phosphorylates substrates such as BAD, 4E-BP1, and MYC to promote cell survival and protein translation. The kinase domain is highly conserved among PIM family members. PIM2 lacks a regulatory domain and is constitutively active when expressed. It is predominantly cytoplasmic but can shuttle to the nucleus.

Related Products

Product name Cat.No. Species Gene ID
PIM2 Knockout HEK293 Cell Line EDJ-KQ2068 Human 11040 Details Get a Quote
PIM2 Knockout A-549 Cell Line EDJ-KQ22136 Human 11040 Details Get a Quote
PIM2 Knockout HCT 116 Cell Line EDJ-KQ22137 Human 11040 Details Get a Quote
PIM2 Knockout HeLa Cell Line EDJ-KQ22138 Human 11040 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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