STK11IP - serine/threonine kinase 11 interacting protein Gene

Homo sapiens

Also known as LIP1; LKB1IP; STK11IP1

Gene ID: 114790 | Gene type: protein coding

About STK11IP

Cytogenetic location: 2q35 Genomic coordinates (GRCh38): 2:219,597,857-219,616,451 (from NCBI)

This gene has 14 transcripts (splice variants), 203 orthologues and 1 paralogue. Broad expression in testis (RPKM 10.6), spleen (RPKM 4.9) and 24 other tissues.

Summary

Enables protein kinase binding activity. Involved in protein localization. Located in cytoplasm and intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Apr 2022]

STK11IP Products(1)

mRNA	Protein	Name
NM_052902.4	NP_443134.3	serine/threonine-protein kinase 11-interacting protein

Protein Preferred Names

Protein Names

serine/threonine-protein kinase 11-interacting protein

LKB1-interacting protein 1

Related Diseases

Diseases

Alias

Peutz-Jeghers Syndrome

PJS	Polyposis, Hamartomatous Intestinal
Polyps-And-Spots Syndrome	Lentiginosis, Perioral
Periorificial Lentiginosis Syndrome	Hamartomatous Intestinal Polyposis
Hamartomatous Polyp	Colonic Hamartomatous Polyp
Gastric Peutz-Jeghers Polyp	Peutz Jeghers Colon Polyp
Peutz Jeghers Polyp	Peutz-Jeghers Polyp Of Small Intestine
Peutz-Jeghers Small Bowel Hamartoma	Peutz Jeghers Polyposis
Intestinal Polyposis-Cutaneous Pigmentation Syndrome	Peutz-Jeghers Polyposis
Polyposis, Intestinal, Ii	Intestinal Hamartomatous Polyposis
Peutz-Jeghers Polyp	Peutz-Jeghers Polyp Of The Stomach
Peutz Jehgers Polyp	Peutz-Jeghers Polyps Of Small Bowel

Cowden Syndrome 1

Bannayan-Riley-Ruvalcaba Syndrome	Pten Hamartoma Tumor Syndrome
Lhermitte-Duclos Disease	Bannayan-Zonana Syndrome
Phts	Riley-Smith Syndrome
Bzs	Ruvalcaba-Myhre-Smith Syndrome
Multiple Hamartoma Syndrome	Rmss
Brrs	Dysplastic Gangliocytoma Of The Cerebellum
CWS1	Cs
Cd	Mham
Pten Hamartoma Tumor Syndrome With Granular Cell Tumor	Macrocephaly Multiple Lipomas And Hemangiomata
Bannayan-Ruvalcaba-Riley Syndrome	Myhre-Riley-Smith Syndrome
LDD	Cerebelloparenchymal Disorder Vi
Hamartoma Syndrome, Multiple	Bbrs
Macrocephaly, Pseudopapilledema, And Multiple Hemangiomata	Macrocephaly, Multiple Lipomas, And Hemangiomata
Macrocephaly Pseudopapilledema And Multiple Hemangiomas	Ruvalcaba -Myhre-Smith Syndrome
Ruvalcaba-Myhre Syndrome	Cowden Disease
Macrocephaly Pseudopapilledema And Multiple Hemangiomata	Cerebellar Granule Cell Hypertrophy And Megalencephaly
Cpd6	Pten Hamartoma Tumor Syndromes
Cowden Syndrome, Type 1

Cowden Syndrome

Cowden Disease	Multiple Hamartoma Syndrome
Cowden'S Disease	Lhermitte-Duclos Disease
Cd	Cs
Mham	Dysplastic Gangliocytoma Of Cerebellum
Cowden'S Syndrome	Hamartoma Syndrome, Multiple

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13922	STK11IP Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	STK11IP	VGNC	VGNC:46905
Macaca mulatta	STK11IP	VGNC	VGNC:77963
Felis catus	STK11IP	VGNC	VGNC:65775
Mus musculus	STK11IP	MGD	MGI:1918978
Rattus norvegicus	STK11IP	RGD	RGD:1305046
Bos taurus	STK11IP	VGNC	VGNC:35386

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