1. Gene
  2. PROC - protein C, inactivator of coagulation factors Va and VIIIa Gene

PROC - protein C, inactivator of coagulation factors Va and VIIIa Gene

中文名称:蛋白 C,凝血因子 Va 和 VIIIa 的灭活因子

种属: Homo sapiens

同用名: PC; APC; PROC1; THPH3; THPH4

基因 ID: 5624 | 基因类型: protein coding

关于 PROC

Cytogenetic location: 2q14.3 Genomic coordinates (GRCh38): 2:127,418,427-127,429,242 (from NCBI)

This gene has 10 transcripts (splice variants), 102 orthologues, 1 paralogue and is associated with 4 phenotypes. Biased expression in liver (RPKM 55.9) and kidney (RPKM 6.8).

功能概要

该基因编码维生素 K 依赖性血浆糖蛋白。编码的蛋白质被凝血酶-凝血调节蛋白复合物切割成其活化形式。这种活化形式包含丝氨酸蛋白酶结构域,并在凝血因子 V 和 VIII 的活化形式的降解中发挥作用。该基因的突变与蛋白 C 缺乏引起的血栓形成倾向、新生儿暴发性紫癜和复发性静脉血栓形成有关。[RefSeq 提供,2009 年 12 月]

This gene encodes a vitamin K-dependent plasma glycoprotein. The encoded protein is cleaved to its activated form by the thrombin-thrombomodulin complex. This activated form contains a serine protease domain and functions in degradation of the activated forms of coagulation factors V and VIII. Mutations in this gene have been associated with thrombophilia due to protein C deficiency, neonatal purpura fulminans, and recurrent venous thrombosis.[provided by RefSeq, Dec 2009]

PROC 基因产物(12)

mRNA Protein Name
NM_000312.4 NP_000303.1 vitamin K-dependent protein C isoform 10 preproprotein
NM_001375602.1 NP_001362531.1 vitamin K-dependent protein C isoform 2
NM_001375603.1 NP_001362532.1 vitamin K-dependent protein C isoform 4 precursor
NM_001375604.1 NP_001362533.1 vitamin K-dependent protein C isoform 6 precursor
NM_001375605.1 NP_001362534.1 vitamin K-dependent protein C isoform 5 preproprotein
NM_001375606.1 NP_001362535.1 vitamin K-dependent protein C isoform 3 precursor
NM_001375607.1 NP_001362536.1 vitamin K-dependent protein C isoform 1
NM_001375608.1 NP_001362537.1 vitamin K-dependent protein C isoform 9 precursor
NM_001375609.1 NP_001362538.1 vitamin K-dependent protein C isoform 8
NM_001375610.1 NP_001362539.1 vitamin K-dependent protein C isoform 7 preproprotein
NM_001375611.1 NP_001362540.1 vitamin K-dependent protein C isoform 10 preproprotein
NM_001375613.1 NP_001362542.1 vitamin K-dependent protein C isoform 10 preproprotein
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 protein binding IPI
IPI: 通过物理相互作用推断
15248212 GOA
enables serine-type endopeptidase activity IMP
IMP: 通过突变表型推断
25748729 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of apoptotic process IMP
IMP: 通过突变表型推断
12563316 GOA
involved in negative regulation of coagulation IMP
IMP: 通过突变表型推断
25651845 GOA
involved in negative regulation of inflammatory response IMP
IMP: 通过突变表型推断
25651845 GOA
involved in positive regulation of establishment of endothelial barrier IMP
IMP: 通过突变表型推断
25651845 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in Golgi apparatus IDA
IDA: 通过直接分析推断
25748729 GOA
located in endoplasmic reticulum IDA
IDA: 通过直接分析推断
25748729 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

PROC 蛋白结构

Gla

Gla: Vitamin K-dependent carboxylation/gamma-carboxyglutamic (GLA) domain (47 - 87)

FXa_inhibition

FXa_inhibition: Coagulation Factor Xa inhibitory site (140 - 175)

Trypsin

Trypsin: Trypsin (213 - 445)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 461 a.a.
蛋白主名 其他名称

vitamin K-dependent protein C

Protein C-Nagoya

PROC 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
PROC P04070 MMP15 Homo sapiens P51511
Anti Bait CoIP
15248212
种属内
PROC P04070 CYSRT1 Homo sapiens A8MQ03
Y2H Array
32296183
种属内
PROC P04070 CYSRT1 Homo sapiens A8MQ03
Y2H Prey Pooling
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 PROC 蛋白

目录号 产品名 蛋白编号 纯度
HY-P74237 Coagulation Factor XIV/PROC Protein, Human (HEK293, His) P04070 (T19-P461) ≥95%

PROC 抗体

目录号 产品名 应用 反应物种
HY-P82716 Protein C Antibody (YA2461) WB Human

关联疾病

疾病名称 别名
Thrombophilia Due To Protein C Deficiency, Autosomal Recessive

THPH4

Autosomal Recessive Thrombophilia Due To Protein C Deficiency

Autosomal Recessive Protein C Deficiency

Autosomal Recessive Thrombophilia Due To Pc Deficiency

Autosomal Recessive Thrombophilia Due To Congenital Protein C Deficiency

Hereditary Thrombophilia Due To Congenital Protein C Deficiency

Severe Hereditary Thrombophilia Due To Congenital Protein C Deficiency

Protein C Deficiency, Autosomal Recessive

Proc Deficiency, Autosomal Recessive

Thrombophilia 3 Due To Protein C Deficiency, Autosomal Recessive

Autosomal Recessive Proc Deficiency

Autosomal Recessive Hereditary Thrombophilia Due To Protein C Deficiency

Hereditary Thrombophilia Due To Pc Deficiency

Proc Deficiency Autosomal Recessive

Protein C Deficiency Autosomal Recessive

Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Recessive

Thrombophilia Due To Protein C Deficiency, Autosomal Dominant

THPH3

Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant

Protein C Deficiency, Autosomal Dominant

Proc Deficiency, Autosomal Dominant

Thrombophilia 3 Due To Protein C Deficiency, Autosomal Dominant

Autosomal Dominant Thrombophilia Due To Protein C Deficiency

Autosomal Dominant Proc Deficiency

Autosomal Dominant Protein C Deficiency

Proc Deficiency Autosomal Dominant

Protein C Deficiency Autosomal Dominant

Protein C Deficiency

Hereditary Thrombophilia Due To Protein C Deficiency

Proc Deficiency

Congenital Thrombotic Disease, Due To Protein C Deficiency

Purpura Fulminans

Purpura Gangrenosa

Purpura

Purpuric Disorder

Thrombophilia

Hypercoagulability State

Thrombosis

Thrombosis Of Blood Vessel

Thrombophilia Due To Thrombin Defect

Venous Thromboembolism

Venous Thrombosis

Thrombophilia Due To Factor 2 Defect

Thromboembolism

THPH1

Thromboembolism, Susceptibility To

Venous Thromboembolism, Susceptibility To

Venous Thrombosis, Protection Against

Prothrombin-Related Thrombophilia

Hyperprothrombinemia

Venous Thrombosis, Susceptibility To

Thrombophilia 1 Due To Thrombin Defect

F2-Related Thrombophilia

Factor Ii-Related Thrombophilia

Prothrombin 20210g>A Thrombophilia

Prothrombin G20210a Thrombophilia

Prothrombin Thrombophilia

Cerebral Palsy

Infantile Cerebral Palsy

Mixed Cerebral Palsy

Palsy Cerebral

Palsy, Cerebral

Cerebral Palsy, Mixed

Inner Ear Cancer
Internal Auditory Canal Meningioma

Meningioma Of The Internal Auditory Canal

Protein S Deficiency

Protein S Deficiency Disease

Hereditary Thrombophilia Due To Protein S Deficiency

Thrombophlebitis

Phlebitis And Thrombophlebitis Of Superficial Vessels Of Lower Extremities

Superficial Thrombophlebitis Of Leg

Thrombophlebitis Of A Superficial Leg Vein

Thrombophlebitis Of Superficial Veins Of Lower Extremity

Pulmonary Embolism

Pulmonary Artery Embolism

Pulmonary Embolus

Pulmonary Emboli

Neuronal Ceroid Lipofuscinosis

Hereditary Ceroid Lipofuscinosis

Batten Disease

Ncl

Neuronal Ceroid-Lipofuscinoses

Lipofuscinosis, Ceroid, Neuronal

Juvenile Neuronal Ceroid Lipofuscinosis

Cerebromacular Dystrophy

Cerebromacular Degeneration

Ceroid-Lipofuscinosis

Ncl - [Neuronal Ceroid Lipofuscinosis]

Amaurotic Familial Idiocy

Amaurotic Idiocy

Amaurotic Idiot

Neuronal Lipofuscinosis

Pigmentary Retinal Lipoid Neuronal Heredodegeneration

Thrombocytopenia

Low Platelet Count

Low Platelets

Decreased Platelets

Platelet Dysfunction Nos

Inflammatory Bowel Disease

Inflammatory Bowel Diseases

Bowel Disease, Inflammatory

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
Bos taurus PROC VGNC VGNC:56139
Mus musculus PROC MGD MGI:97771
Canis familiaris PROC VGNC VGNC:45006
Rattus norvegicus PROC RGD RGD:3411
Macaca fascicularis PROC NCBI NCBI:102136210
Others PROC NCBI