MISP (Mitotic Spindle Positioning) Gene

Comprehensive gene card for MISP, a regulator of mitotic spindle orientation and cell polarity.

Gene Information Card

Symbol MISP
Full Name Mitotic Spindle Positioning
Gene Type Protein coding
Chromosomal Location 19p13.3
NCBI Gene ID 126353 ncbi.nlm.nih.gov/gene/126353
Ensembl ID ENSG00000167552
UniProt ID Q8TAC9
OMIM ID 611488
HGNC ID 27000
Aliases C19orf21, MISP1, FLJ11273

Description

MISP (Mitotic Spindle Positioning) is a protein-coding gene located on chromosome 19p13.3. It encodes a protein involved in the regulation of mitotic spindle orientation, cell polarity, and asymmetric cell division. MISP interacts with the actin cytoskeleton and the microtubule network to ensure proper spindle positioning during mitosis. Dysregulation of MISP has been implicated in cancer progression and metastasis.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer MISP overexpression promotes cell migration and invasion through altered spindle orientation and polarity defects. PMID: 23431171
Colorectal cancer MISP upregulation correlates with poor prognosis and increased metastatic potential. PMID: 25944712
Lung cancer MISP expression is elevated in non-small cell lung cancer and associated with tumor aggressiveness. PMID: 27323850

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 12.5 Medium
Bone marrow 8.2 Low
Lymph node 6.7 Low
Brain 4.1 Low
Breast 3.9 Low
Cell Line Expression
Cell Line nTPM Notes
HeLa 15.3 Cervical cancer cell line
MCF7 11.8 Breast cancer cell line
A549 9.4 Lung cancer cell line
HCT116 8.7 Colorectal cancer cell line
HEK293 6.2 Embryonic kidney cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1015C>T (p.Arg339Trp) Missense <0.01% Unknown functional effect
c.1246G>A (p.Glu416Lys) Missense <0.01% Unknown functional effect
c.1489_1491del (p.Glu497del) In-frame deletion <0.01% Unknown functional effect
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in MISP.

Gain of Function (GOF)

Overexpression of wild-type MISP is associated with gain-of-function effects in cancer, but specific gain-of-function mutations are not characterized.

Dominant Negative (DN)

No dominant-negative mutations have been described for MISP.

Pathways

REACT:14797 (Mitotic Spindle Positioning)
REACT:172623 (Cell Cycle
Mitotic)

Protein Summary

The MISP protein (UniProt Q8TAC9) is a 647-amino acid protein that localizes to the centrosome and the cell cortex. It contains an N-terminal calponin homology (CH) domain that binds actin, and a C-terminal region that interacts with microtubules. MISP regulates the positioning of the mitotic spindle by linking the astral microtubules to the cortical actin cytoskeleton. It is essential for asymmetric cell division and proper orientation of the mitotic spindle, which are critical for tissue morphogenesis and stem cell maintenance.

Related Products

Product name Cat.No. Species Gene ID
MISP Knockout HEK293 Cell Line EDJ-KQ3156 Human 126353 Details Get a Quote
MISP3 Knockout HEK293 Cell Line EDJ-KQ7414 Human 113230 Details Get a Quote
MISP Knockout A-549 Cell Line EDJ-KQ24559 Human 126353 Details Get a Quote
MISP Knockout HCT 116 Cell Line EDJ-KQ24560 Human 126353 Details Get a Quote
MISP Knockout HeLa Cell Line EDJ-KQ24561 Human 126353 Details Get a Quote
MISP3 Knockout A-549 Cell Line EDJ-KQ32591 Human 113230 Details Get a Quote
MISP3 Knockout HCT 116 Cell Line EDJ-KQ32592 Human 113230 Details Get a Quote
MISP3 Knockout HeLa Cell Line EDJ-KQ32593 Human 113230 Details Get a Quote
Displaying Records 1 To 8 Of 8 Records
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