2. Gene
  3. MPZL3 - myelin protein zero like 3 Gene

MPZL3 - myelin protein zero like 3 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：髓磷脂蛋白零样 3

种属: Homo sapiens

基因 ID: 196264 | 基因类型: protein coding

关于 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.

功能概要

预计参与细胞粘附。预测作用于细胞外基质组织和毛发周期的上游或内部。预计是膜的组成部分。预计在质膜上有活性。 [由基因组资源联盟提供，2022 年 4 月]

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 基因产物(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 蛋白结构

V-set

V-set: Immunoglobulin V-set domain (38 - 147)

  • 0
  • 100
  • 200
  • 235 a.a.
蛋白主名 其他名称

myelin protein zero-like protein 3

重组 MPZL3 蛋白

目录号 产品名 蛋白编号 纯度
HY-P73804 MPZL3 Protein, Human (HEK293, His) Q6UWV2-1 (L32-S158) ≥95%

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS08636 MPZL3 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 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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