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STOML3 - stomatin like 3 Gene

Also Known as SRO; Epb7.2l

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 161003

About STOML3

Cytogenetic location: 13q13.3 Genomic coordinates (GRCh38): 13:38,965,925-38,990,831 (from NCBI)

This gene has 2 transcripts (splice variants), 276 orthologues and 4 paralogues. Biased expression in lung (RPKM 1.0), endometrium (RPKM 0.3) and 2 other tissues.

Summary

Predicted to act upstream of or within signal transduction. Predicted to be located in cilium and membrane raft. Predicted to be integral component of membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

STOML3 Products (2)

mRNA	Protein	Name
NM_001144033.2	NP_001137505.1	stomatin-like protein 3 isoform 2
NM_145286.3	NP_660329.1	stomatin-like protein 3 isoform 1

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	References	Source
enables protein binding	IPI IPI: Inferred from physical interaction	32296183	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

STOML3 Protein Structure

Band_7

0
100
200
291 a.a.

Protein Preferred Names	Protein Names
stomatin-like protein 3	EPB72-like 3

STOML3 Protein-protein interaction Information

Type	Protein Name	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	References
Intra	STOML3	Q8TAV4	SEC22A	Homo sapiens	Q96IW7	Validated Y2H	32296183

Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases	Alias
Overhydrated Hereditary Stomatocytosis	Ohs Potassium Sodium Disorder Of Erythrocyte OHST Stomatocytosis I Potassium-Sodium Disorder Of Erythrocyte Stomatocytosisiohst Hereditary, Overhydrated, Cation-Leak Stomatocytosis Overhydrated Cation Leak Stomatocytosis Stomatocytosis, Overhydrated Hereditary
Oculomotor Nerve Paralysis	Iii Nerve Palsy Iiird Nerve Paralysis Third Cranial Nerve Paralysis
Herpes Zoster Oticus	Nervus Intermedius Neuralgia Ramsay Hunt Syndrome Type 2 Geniculate Herpes Zoster Geniculate Neuralgia Herpes Zoster Auricularis Herpetic Geniculate Ganglionitis Ramsay Hunt Syndrome Type Ii Ramsey Hunt Syndrome Facial Nerve Palsy Due To Vzv Facial Nerve Palsy Due To Herpes Zoster Infection Facial Nerve Paralysis Due To Vzv Hunt Syndrome Hunt'S Syndrome Ramsay Hunt Syndrome Myoclonus And Ataxia
Gliosarcoma	Glioblastoma With Sarcomatous Component Sarcomatous Glioblastoma
Abducens Palsy	Sixth Nerve Palsy Abducens Nerve Palsy Abducens Nerve Disease Abducens Nerve Weakness Lateral Rectus Muscle Denervation Paresis Lateral Rectus Muscle Innervation Disorder Sixth Cranial Nerve Disorder 6th Nerve Palsy Abducens Nerve Diseases Vith Nerve Disorder Vith Nerve Paralysis Cranial Mononeuropathy Vi Cranial Nerve Vi Palsy Sixth Cranial Nerve Palsy Vi Nerve Palsy Abducens Nerve Disorder Abducens Sixth Nerve Palsy Abducens Nerve Paralysis Disease Or Disorder Of Abducent Nerve Sixth Cranial Nerve Disease Sixth Cranial Nerve Weakness Disorder Of Sixth Cranial Nerve Isolated Abducent Nerve Palsy Atrophy Of Sixth Cranial Nerve Paralysis Of Sixth Cranial Nerve
Facial Neuralgia
Dehydrated Hereditary Stomatocytosis 1 With Or Without Pseudohyperkalemia And/Or Perinatal Edema	Dehydrated Hereditary Stomatocytosis Hereditary Xerocytosis Xerocytosis, Hereditary Pshk1 Pseudohyperkalemia Edinburgh Dehydrated Hereditary Stomatocytosis With Or Without Pseudohyperkalemia And/Or Perinatal Edema DHS1 Dhs Hereditary Desiccytosis Dehydrated Hereditary Stomatocytosis 1 Desiccytosis, Hereditary Pseudohyperkalemia, Familial, 1, Due To Red Cell Leak Pseudohyperkalemia Familial 1, Due To Red Cell Leak Desiccytosis Hereditary Xerocytosis Hereditary Familial Pseudohyperkalemia 1 Due To Red Cell Leak Stomatocytosis, Dehydrated, Hereditary, With/Without Pseudohyperkalemia And/Or Perinatal Edema Xerocytosis
Third Cranial Nerve Disease	Disorder Of Oculomotor Nerve Oculomotor Nerve Disorder Oculomotor Nerve Paralysis Third Cranial Nerve Disorder
Intracranial Hypotension
Brooke-Spiegler Syndrome	Cyld Cutaneous Syndrome Spiegler-Brooke Syndrome Familial Cylindromatosis BRSS Bss Sbs Multiple Familial Trichoepithelioma Ancell-Spiegler Cylindromas Familial Multiple Trichoepithelioma Trichoepithelioma Fc Mft Multiple Familial Trichoepitheliomas Ccs Turban Tumor Syndrome Schilbach-Rott Syndrome Eccrine Dermal Cylindroma Familial Multiple Trichoepitheliomata

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

Pre-clinical Phase

Bioactive Molecules (6)

Cat. No.	상품명	효과	Purity	Rare Diseases
HY-122671	OB-1	Inhibitor	99.40%	Unkown
HY-119519	OB-2	Inhibitor	/	Unkown
HY-122671S	OB-1-d3	Control	/	Unkown
HY-RS13951	STOML3 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS21948	Stoml3 Mouse Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-RS28465	Stoml3 Rat Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	STOML3	MGD	MGI:2388072
Rattus norvegicus	STOML3	RGD	RGD:1311090
Bos taurus	STOML3	VGNC	VGNC:35412
Macaca mulatta	STOML3	VGNC	VGNC:78170
Canis familiaris	STOML3	VGNC	VGNC:46932
Felis catus	STOML3	VGNC	VGNC:65795
Others	STOML3	NCBI