2. Gene
  3. GML - glycosylphosphatidylinositol anchored molecule like Gene

GML - glycosylphosphatidylinositol anchored molecule like Gene

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

中文名称：糖基磷脂酰肌醇锚定分子

种属: Homo sapiens

同用名: LY6DL

基因 ID: 2765 | 基因类型: protein coding

关于 GML

Cytogenetic location: 8q24.3 Genomic coordinates (GRCh38): 8:142,834,801-142,846,851 (from NCBI)

This gene has 2 transcripts (splice variants), 55 orthologues and 1 paralogue. Low expression observed in reference dataset.

功能概要

预计参与 DNA 损伤反应，p53 类介质的信号转导导致细胞周期停滞；凋亡过程；和细胞群增殖的负调节。预测为膜的外在成分。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to be involved in DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest; apoptotic process; and negative regulation of cell population proliferation. Predicted to be extrinsic component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

GML 基因产物(1)

mRNA Protein Name
NM_002066.3 NP_002057.1 glycosyl-phosphatidylinositol-anchored molecule-like protein precursor
蛋白主名 其他名称

glycosyl-phosphatidylinositol-anchored molecule-like protein

GPI anchored molecule like protein

关联疾病

疾病名称 别名
Large Congenital Melanocytic Nevus

Giant Pigmented Hairy Nevus

Giant Congenital Melanocytic Nevus

Gmn

Congenital Pigmented Nevus

Lcmn

Gphn

Giant Congenital Nevus

Bathing Trunk Nevus

Congenital Giant Pigmented Nevus

Congenital Hairy Nevus

Giant Hairy Nevus

Giant Pigmented Nevus

Congenital Giant Pigmented Nevus Of Skin

Congenital Melanocytic Nevus Syndrome

Giant Congenital Melanocytic Nevi

Giant Congenital Pigmented Nevus

Melanocytic Nevus Syndrome, Congenital
Peroneal Nerve Paralysis

Peroneal Nerve Palsy
Cantu Syndrome

Hypertrichotic Osteochondrodysplasia

Hypertrichotic Osteochondrodysplasia Cantu Type

Cantú Syndrome

Craniofaciocardioskeletal Syndrome

Hypertrichosis-Osteochondrodysplasia-Cardiomegaly Syndrome

Congenital Hypertrichosis-Acromegaloid Facial Features Spectrum

Congenital Hypertrichosis-Coarse Facial Features Spectrum

HTOCD

Osteochondrodysplasia, Hypertrichotic
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

Approval
生物活性分子 (3)
目录号 产品名 作用方式
纯度 是否罕见病
HY-P1956 Human serum albumin Inhibitor 99.9% 否
HY-B1831A Oritavancin diphosphate Inhibitor 99.93% 否
HY-B1831 Oritavancin Inhibitor / 否
Pre-clinical Phase
生物活性分子 (12)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-19805 STO-609 Inhibitor 98.13% 否
HY-P1956A Human serum albumin (Cell culture grade, Endotoxin<0.125 EU/mg) Inhibitor 99.60% 否
HY-19805A STO-609 acetate Inhibitor / 否
HY-123720 Sch 31828 Inhibitor / 否
HY-168371 1-Palmitoyl-2-13(S)-HODE-sn-glycero-3-PC / 否
HY-N8256 (–)-Mycousnine Inhibitor / 否
HY-N9179 3′,4′,5′,5,6,7-Hexamethoxyflavone Inhibitor / 否
HY-RS05521 GML Human Pre-designed siRNA Set A Pre-designed Set / 否
HY-N13938 Azinomycin A / 否
HY-N14558 3',8-Dihydroxy-4',6,7-trimethoxyisoflavone / 否
HY-N15046 Barminomycin I / 否
HY-N15047 Barminomycin II / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus GML RGD RGD:1307850
Macaca mulatta GML VGNC VGNC:73081
Bos taurus GML VGNC VGNC:29437
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