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  2. PLSCR3 - phospholipid scramblase 3 Gene

PLSCR3 - phospholipid scramblase 3 Gene

中文名称:磷脂加扰酶 3

种属: Homo sapiens

基因 ID: 57048 | 基因类型: protein coding

关于 PLSCR3

Cytogenetic location: 17p13.1 Genomic coordinates (GRCh38): 17:7,389,727-7,394,525 (from NCBI)

This gene has 13 transcripts (splice variants), 1 gene allele, 407 orthologues and 4 paralogues. Ubiquitous expression in spleen (RPKM 12.9), fat (RPKM 12.1) and 25 other tissues.

功能概要

启用多种功能,包括钙依赖性蛋白质结合活性;金属离子结合活性;和磷脂加扰酶活性。参与多个过程,包括心磷脂生物合成过程;细胞凋亡过程的调节;和调节线粒体中细胞色素 c 的释放。位于胞质溶胶中;线粒体;和质膜。 [由基因组资源联盟提供,2022 年 4 月]

Enables several functions, including calcium-dependent protein binding activity; metal ion binding activity; and phospholipid scramblase activity. Involved in several processes, including cardiolipin biosynthetic process; regulation of apoptotic process; and regulation of release of cytochrome c from mitochondria. Located in cytosol; mitochondrion; and plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

PLSCR3 基因产物(6)

mRNA Protein Name
NM_001201576.2 NP_001188505.1 phospholipid scramblase 3 isoform 1
NM_001369407.1 NP_001356336.1 phospholipid scramblase 3 isoform 1
NM_001369420.1 NP_001356349.1 phospholipid scramblase 3 isoform 2
NM_001369421.1 NP_001356350.1 phospholipid scramblase 3 isoform 3
NM_001369422.1 NP_001356351.1 phospholipid scramblase 3 isoform 3
NM_020360.4 NP_065093.2 phospholipid scramblase 3 isoform 1
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables calcium ion binding IMP
IMP: 通过突变表型推断
18358005 GOA
enables calcium-dependent protein binding IPI
IPI: 通过物理相互作用推断
18256029 GOA
enables lead ion binding IMP
IMP: 通过突变表型推断
31769662 GOA
enables magnesium ion binding IMP
IMP: 通过突变表型推断
29337693 GOA
enables mercury ion binding IMP
IMP: 通过突变表型推断
31769662 GOA
enables phospholipid scramblase activity IMP
IMP: 通过突变表型推断
14573790 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
12649167 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in apoptotic process IMP
IMP: 通过突变表型推断
12649167 GOA
involved in cardiolipin biosynthetic process IMP
IMP: 通过突变表型推断
16939411 GOA
involved in regulation of apoptotic process IMP
IMP: 通过突变表型推断
14573790 GOA
involved in regulation of release of cytochrome c from mitochondria IMP
IMP: 通过突变表型推断
14573790 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytosol IDA
IDA: 通过直接分析推断
12649167 GOA
located in mitochondrion IDA
IDA: 通过直接分析推断
12649167 GOA
located in plasma membrane IDA
IDA: 通过直接分析推断
19333378 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

PLSCR3 蛋白结构

Scramblase

Scramblase: Scramblase (64 - 284)

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

phospholipid scramblase 3

PL scramblase 3

PLSCR3 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
PLSCR3 Q9NRY6 KRTAP19-7 Homo sapiens Q3SYF9 32296183
种属内
PLSCR3 Q9NRY6 KRTAP19-7 Homo sapiens Q3SYF9 32296183
种属内
PLSCR3 Q9NRY6 LCE4A Homo sapiens Q5TA78 32296183
种属内
PLSCR3 Q9NRY6 LCE4A Homo sapiens Q5TA78 32296183
种属内
PLSCR3 Q9NRY6 KRTAP11-1 Homo sapiens Q8IUC1 32296183
种属内
PLSCR3 Q9NRY6 KRTAP11-1 Homo sapiens Q8IUC1 32296183
种属内
PLSCR3 Q9NRY6 LCE2B Homo sapiens O14633 32296183
种属内
PLSCR3 Q9NRY6 LCE2B Homo sapiens O14633 32296183
种属内
PLSCR3 Q9NRY6 LCE5A Homo sapiens Q5TCM9 32296183
种属内
PLSCR3 Q9NRY6 LCE5A Homo sapiens Q5TCM9 32296183
种属内
PLSCR3 Q9NRY6 ACTMAP Homo sapiens Q5BKX5-3 32296183
种属内
PLSCR3 Q9NRY6 ACTMAP Homo sapiens Q5BKX5-3 32296183
种属内
PLSCR3 Q9NRY6 KRTAP15-1 Homo sapiens Q3LI76 32296183
种属内
PLSCR3 Q9NRY6 KRTAP15-1 Homo sapiens Q3LI76 32296183
种属内
PLSCR3 Q9NRY6 S100A7L2 Homo sapiens Q5SY68 32296183
种属内
PLSCR3 Q9NRY6 S100A7L2 Homo sapiens Q5SY68 32296183
种属内
PLSCR3 Q9NRY6 WWOX Homo sapiens Q9NZC7-5 32296183
种属内
PLSCR3 Q9NRY6 WWOX Homo sapiens Q9NZC7-5 32296183
种属内
PLSCR3 Q9NRY6 WWOX Homo sapiens Q9NZC7-5 32296183
种属内
PLSCR3 Q9NRY6 KRTAP6-1 Homo sapiens Q3LI64 32296183
种属内
PLSCR3 Q9NRY6 KRTAP6-1 Homo sapiens Q3LI64 32296183
种属内
PLSCR3 Q9NRY6 LCE1C Homo sapiens Q5T751 32296183
种属内
PLSCR3 Q9NRY6 LCE1C Homo sapiens Q5T751 32296183
种属内
PLSCR3 Q9NRY6 KRTAP19-6 Homo sapiens Q3LI70 32296183
种属内
PLSCR3 Q9NRY6 KRTAP19-6 Homo sapiens Q3LI70 32296183
种属内
PLSCR3 Q9NRY6 C10orf55 Homo sapiens Q5SWW7 32296183
种属内
PLSCR3 Q9NRY6 C10orf55 Homo sapiens Q5SWW7 32296183
种属内
PLSCR3 Q9NRY6 TRIP13 Homo sapiens Q15645 25416956
种属内
PLSCR3 Q9NRY6 TRIP13 Homo sapiens Q15645 32296183
种属内
PLSCR3 Q9NRY6 TRIP13 Homo sapiens Q15645 32296183
种属内
PLSCR3 Q9NRY6 KRTAP3-3 Homo sapiens Q9BYR6 32296183
种属内
PLSCR3 Q9NRY6 KRTAP3-3 Homo sapiens Q9BYR6 32296183
种属内
PLSCR3 Q9NRY6 INCA1 Homo sapiens Q0VD86 32296183
种属内
PLSCR3 Q9NRY6 INCA1 Homo sapiens Q0VD86 32296183
种属内
PLSCR3 Q9NRY6 AIPL1 Homo sapiens Q9NZN9 32296183
种属内
PLSCR3 Q9NRY6 C22orf39 Homo sapiens Q6P5X5 32296183
种属内
PLSCR3 Q9NRY6 C22orf39 Homo sapiens Q6P5X5 32296183
种属内
PLSCR3 Q9NRY6 HOXA1 Homo sapiens P49639 32296183
种属内
PLSCR3 Q9NRY6 HOXA1 Homo sapiens P49639 32296183
种属内
PLSCR3 Q9NRY6 CATSPER1 Homo sapiens Q8NEC5 25416956
种属内
PLSCR3 Q9NRY6 CATSPER1 Homo sapiens Q8NEC5 25416956
种属内
PLSCR3 Q9NRY6 CATSPER1 Homo sapiens Q8NEC5 25416956
种属内
PLSCR3 Q9NRY6 STK16 Homo sapiens O75716 25416956
种属内
PLSCR3 Q9NRY6 SMCP Homo sapiens P49901 32296183
种属内
PLSCR3 Q9NRY6 SMCP Homo sapiens P49901 32296183
种属内
PLSCR3 Q9NRY6 KRTAP3-2 Homo sapiens Q9BYR7 32296183
种属内
PLSCR3 Q9NRY6 KRTAP3-2 Homo sapiens Q9BYR7 32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

PLSCR3 抗体

目录号 产品名 应用 反应物种
HY-P81927 PLSCR3 Antibody (YA1672) WB Human, Mouse, Rat

关联疾病

疾病名称 别名
Barth Syndrome

3-Methylglutaconic Aciduria Type 2

BTHS

Cardioskeletal Myopathy With Neutropenia And Abnormal Mitochondria

Mga Type Ii

Mga2

Mgca2

Mga Type 2

3-Methylglutaconic Aciduria Type Ii

3-Methylglutaconic Aciduria, Type Ii

Mga, Type Ii

3-Methylglutaconicaciduria Type 2

3-Methylglutaconicaciduria Type Ii

Taz Defect

3 Methylglutaconic Aciduria, Type Ii

Dnajc19 Defect

Cardioskeletal Myopathy-Neutropenia Syndrome

X-Linked Cardioskeletal Myopathy And Neutropenia

3-Alpha-Methylglutaconic Aciduria Type 2

Agm2

Cardioskeletal Myopathy-Neutropenia

Invm

Left Ventricular Non-Compaction Isolated X-Linked

Non-Compaction Of Left Ventricular Myocardium Isolated X-Linked

Agammaglobulinemia 2, Autosomal Recessive

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

直系同源

种属 基因名 来源 基因 ID
Mus musculus PLSCR3 MGD MGI:1917560
Felis catus PLSCR3 VGNC VGNC:64247
Bos taurus PLSCR3 VGNC VGNC:55863
Rattus norvegicus PLSCR3 RGD RGD:1307016
Macaca mulatta PLSCR3 VGNC VGNC:76035
Canis familiaris PLSCR3 VGNC VGNC:56014