OCM - oncomodulin Gene

Homo sapiens

Also known as OM; OCM1; ONCM

Gene ID: 654231 | Gene type: protein coding

About OCM

Cytogenetic location: 7p22.1 Genomic coordinates (GRCh38): 7:5,859,718-5,886,363 (from NCBI)

This gene has 2 transcripts (splice variants), 148 orthologues and 2 paralogues. Low expression observed in reference dataset.

Summary

Oncomodulin is a high-affinity calcium ion-binding protein. It belongs to the superfamily of Calmodulin proteins, also known as the EF-hand proteins. Oncomodulin is an oncodevelopmental protein found in early embryonic cells in the placenta and also in tumors. [provided by RefSeq, Jul 2008]

OCM Products(3)

mRNA	Protein	Name
NM_001097622.2	NP_001091091.1	oncomodulin-1 isoform a
NM_001391990.1	NP_001378919.1	oncomodulin-1 isoform a
NM_001391991.1	NP_001378920.1	oncomodulin-1 isoform b

OCM Protein Structure

EF-hand_7

0
100
109 a.a.

Protein Preferred Names

Protein Names

oncomodulin-1

beta parvalbumin

Recombinant OCM Proteins

Cat. No.	Product Name	Accession	Purity
HY-P71100	Oncomodulin-1 Protein, Human (His)	P0CE72 (M1-S109)	≥95%

Related Diseases

Diseases

Alias

Fish Allergy

Allergy To Fish

Vulvar Leiomyoma

Vulvar Benign Neoplasm

Vegetable Allergy

Capillary Malformations, Congenital

Familial Multiple Nevi Flammei	Nevi Flammei, Familial Multiple
CMC	Port-Wine Stain
Capillary Malformations	Cmal
Familial Multiple Port-Wine Stains	Capillary Malformation
Capillary Malformations, Congenital, 1, Somatic, Mosaic	Congenital Capillary Malformations
Port-Wine Stain Familial Multiple	Hereditary Capillary Malformations
Capillary Malformations, Hereditary	Capillary Malformations, Congenital, Type 1, Somatic, Mosaic
Strawberry Nevus Of Skin	Naevus Flammeus

Bartholin'S Duct Cyst

Bartholin Duct Cyst	Bartholin'S Cyst
Cyst Of Bartholin'S Gland Duct	Cyst Of Bartholin'S Gland
Vulvovaginal Cyst	Cyst Of Bartholin Gland Duct

Deafness, Autosomal Dominant 27

DFNA27	Autosomal Dominant Nonsyndromic Deafness 27
Autosomal Dominant Deafness 27	Deafness, Autosomal Dominant, 27

Enterobiasis

Oxyuriasis	Pinworm Infection
Enterobius Vermicularis Infection	Threadworm Infection
Oxyuris Vermicularis Infection	Enterobiosis
Pinworm	Pinworm Disease
Seatworm Infection	Enterobiasis Threadworm
Pinworm Infestation	Seatworm

Vulvar Leiomyosarcoma

Deafness, Autosomal Dominant 50

DFNA50	Autosomal Dominant Nonsyndromic Deafness 50
Autosomal Dominant Deafness 50	Deafness, Autosomal Dominant, Type 50

Acute Hemorrhagic Leukoencephalitis

Ahl	Acute Haemorrhagic Leucoencephalitis Of Weston Hurst
Leukoencephalitis, Acute Hemorrhagic	Acute Hemorrhagic Encephalomyelitis
Acute Necrotizing Hemorrhagic Leukoencephalitis	Weston-Hurst Syndrome
Ahle	Acute Haemorrhagic Leucoencephalitis
Hurst Disease	Acute Haemorrhagic Leukoencephalitis, Postimmunization Or Postvaccinal
Postimmunization Or Postvaccinal Leukoencephalopathy

Vertigo, Benign Recurrent

Benign Paroxysmal Positional Vertigo	Bppv
Vestibulopathy, Familial	BRV
Vertigo, Benign Paroxysmal Positional	Benign Paroxysmal Positional Nystagmus
Benign Recurrent Vertigo	Familial Benign Recurrent Vertigo
Familial Vestibulopathy	Benign Paroxysmal Nystagmus
Bppv - [Benign Positional Paroxysmal Vertigo]

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 (2)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS09744	OCM Human Pre-designed siRNA Set A		/	Unkown
HY-RS09745	OCM2 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	OCM	MGD	MGI:97401
Rattus norvegicus	OCM	RGD	RGD:3222
Others	OCM	NCBI

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