MPZL3 - myelin protein zero like 3 Gene

Homo sapiens

Gene ID: 196264 | Gene type: protein coding

About MPZL3

Cytogenetic location: 11q23.3 Genomic coordinates (GRCh38): 11:118,226,690-118,252,365 (from NCBI)

This gene has 4 transcripts (splice variants), 197 orthologues and 6 paralogues. Broad expression in skin (RPKM 9.4), esophagus (RPKM 9.0) and 19 other tissues.

Summary

Predicted to be involved in cell adhesion. Predicted to act upstream of or within extracellular matrix organization and hair cycle. Predicted to be integral component of membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

MPZL3 Products(2)

mRNA	Protein	Name
NM_001286152.2	NP_001273081.1	myelin protein zero-like protein 3 isoform b precursor
NM_198275.3	NP_938016.1	myelin protein zero-like protein 3 isoform a precursor

MPZL3 Protein Structure

V-set

0
100
200
235 a.a.

Protein Preferred Names

Protein Names

myelin protein zero-like protein 3

Recombinant MPZL3 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P73804	MPZL3 Protein, Human (HEK293, His)	Q6UWV2-1 (L32-S158)	≥95%

Related Diseases

Diseases

Alias

Seborrheic Dermatitis

Seborrhoeic Dermatitis	Seborrhea
Seborrhoeic Eczema	Skin Seborrheic
Dermatitis, Seborrheic

Linear Skin Defects With Multiple Congenital Anomalies 2

LSDMCA2	Aplasia Cutis Congenita, Reticulolinear, With Microcephaly, Facial Dysmorphism, And Other Congenital Anomalies
Aplcc	Aplasia Cutis Congenita, Reticulolinear, With Microcephaly, Facial Dysmorphism And Other Congenital Anomalies

Seborrheic Infantile Dermatitis

Cradle Cap	Infantile Seborrhoeic Dermatitis
Seborrhoea Capitis	Seborrhoeic Dermatitis Of Scalp
Seborrhoeic Eczema Of Scalp	Complement 5 Dysfunction
Generalized Seborrheic Dermatitis Of Infants	Infantile Seborrheic Dermatitis
Pityriasis Capitis	Seborrhea Capitis
Seborrhea Sicca	Dandruff
Complement Component 5 Deficiency	Seborrheic Dermatitis
Seborrheic Dermatitis Of Scalp	Scurfiness Of Scalp
Seborrheic Dermatitis Of Infancy	Infantile Seborrhoeic Eczema
Neonatal Seborrhoeic Dermatitis	Infantile Seborrhoeic Dermatitis Of The Scalp

Axenfeld-Rieger Syndrome, Type 1

Axenfeld-Rieger Syndrome Type 1	RIEG1
Rieg	Rgs
Rieger Syndrome Type 1	Rieger Syndrome, Type 1
Axenfeld-Rieger Syndrome 1	Iridogoniodysgenesis With Somatic Anomalies

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-RS08636	MPZL3 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Macaca mulatta	MPZL3	VGNC	VGNC:74841
Canis familiaris	MPZL3	VGNC	VGNC:43356
Bos taurus	MPZL3	VGNC	VGNC:31594
Mus musculus	MPZL3	MGD	MGI:2442647
Felis catus	MPZL3	VGNC	VGNC:82016
Rattus norvegicus	MPZL3	RGD	RGD:1310980
Others	MPZL3	NCBI

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