1. Gene
  2. PRRG4 - proline rich and Gla domain 4 Gene

PRRG4 - proline rich and Gla domain 4 Gene

中文名称:富脯氨酸和 Gla 结构域 4

种属: Homo sapiens

同用名: TMG4; PRGP4

基因 ID: 79056 | 基因类型: protein coding

关于 PRRG4

Cytogenetic location: 11p13 Genomic coordinates (GRCh38): 11:32,829,789-32,858,120 (from NCBI)

This gene has 1 transcript (splice variant), 196 orthologues and 3 paralogues. Broad expression in esophagus (RPKM 11.6), skin (RPKM 9.5) and 18 other tissues.

功能概要

启用 WW 域绑定活动。位于质膜。 [由基因组资源联盟提供,2022 年 4 月]

Enables WW domain binding activity. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

PRRG4 基因产物(1)

mRNA Protein Name
NM_024081.6 NP_076986.1 transmembrane gamma-carboxyglutamic acid protein 4 precursor
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables WW domain binding IDA
IDA: 通过直接分析推断
23873930 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
23873930 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in plasma membrane IDA
IDA: 通过直接分析推断
23873930 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

PRRG4 蛋白结构

Gla

Gla: Vitamin K-dependent carboxylation/gamma-carboxyglutamic (GLA) domain (57 - 97)

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

transmembrane gamma-carboxyglutamic acid protein 4

proline rich Gla (G-carboxyglutamic acid) 4 (transmembrane)

PRRG4 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
PRRG4 Q9BZD6 YAP1 Homo sapiens P46937 23873930
种属内
PRRG4 Q9BZD6 YAP1 Homo sapiens P46937 33961781
种属内
PRRG4 Q9BZD6 YAP1 Homo sapiens P46937-1 23873930
种属内
PRRG4 Q9BZD6 MAGI3 Homo sapiens Q5TCQ9 23873930
种属内
PRRG4 Q9BZD6 MAGI3 Homo sapiens Q5TCQ9 23873930
种属内
PRRG4 Q9BZD6 YAP1 Homo sapiens P46937-3 23873930
种属内
PRRG4 Q9BZD6 YAP1 Homo sapiens P46937-3 23873930
种属内
PRRG4 Q9BZD6 NEDD4L Homo sapiens Q96PU5 23873930
种属内
PRRG4 Q9BZD6 NEDD4L Homo sapiens Q96PU5 33961781
种属内
PRRG4 Q9BZD6 NEDD4L Homo sapiens Q96PU5 23873930
种属内
PRRG4 Q9BZD6 NEDD4 Homo sapiens P46934 33961781
种属内
PRRG4 Q9BZD6 NEDD4 Homo sapiens P46934 23873930
种属内
PRRG4 Q9BZD6 NEDD4 Homo sapiens P46934 23873930
种属间
PRRG4 Q9BZD6 Magi1 Mus musculus Q6RHR9-1 23873930
种属间
PRRG4 Q9BZD6 Magi1 Mus musculus Q6RHR9-1 23873930
种属内
PRRG4 Q9BZD6 WWTR1 Homo sapiens Q9GZV5 23873930
种属内
PRRG4 Q9BZD6 WWTR1 Homo sapiens Q9GZV5 23873930
种属内
PRRG4 Q9BZD6 WWTR1 Homo sapiens Q9GZV5 23873930
种属内
PRRG4 Q9BZD6 MAGI1 Homo sapiens Q96QZ7 33961781
种属内
PRRG4 Q9BZD6 MAGI1 Homo sapiens Q96QZ7 23873930
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome

Wagr Syndrome

11p Partial Monosomy Syndrome

Chromosome 11p13 Deletion Syndrome

Wilms Tumor, Aniridia, Genitourinary Anomalies And Mental Retardation Syndrome

11p Deletion Syndrome

Chromosome 11p Deletion Syndrome

Wagr Complex

Wilms Tumor-Aniridia-Genitourinary Anomalies-Intellectual Disability Syndrome

Deletion 11p13

WAGR

Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome

Chromosome 11p Deletion

11p Deletion

11p Monosomy

Deletion 11p

Monosomy 11p

Partial Monosomy 11p

Agr Triad

Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome

Wagr Contiguous Gene Syndrome

Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome

Wilms Tumor-Aniridia-Genitourinary Anomalies-Mr Syndrome

Del(11)(P13)

Monosomy 11p13

Chromosome 11, Deletion 11p

Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1

VKCFD1

Combined Deficiency Of Vitamin K-Dependent Clotting Factors 1

Vitamin K-Dependent Coagulation Defect

Multiple Coagulation Factor Deficiency Iii

Mcfd3

Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, Type 1

Vkcfd

Familial Multiple Coagulation Factor Deficiency Iii

Fmfd Iii

Factors Ii, Vii, Ix, And X, Combined Deficiency Of

Glutamic Acid, Deficient Gamma-Carboxylation Of

Hereditary Combined Deficiency Of Vitamin K-Dependent Clotting Factors

Hereditary Combined Deficiency Of Factors Ii, Vii, Ix And X

Vkcfd

Meckel Syndrome, Type 7

Meckel Syndrome 7

Nphp3-Related Meckel-Like Syndrome

MKS7

Goldston Syndrome

Meckel Syndrome Type 7

Meckel-Like Syndrome Type 1

Renal-Hepatic-Pancreatic Dysplasia-Dandy-Walker Cysts Syndrome

Renal Hepatic Pancreatic Dysplasia Dandy Walker Cyst

Renal-Hepatic-Pancreatic Dysplasia With Dandy-Walker Cyst

Meckel-Gruber Syndrome, Type 7

Dandy-Walker Cyst With Renal-Hepatic-Pancreatic Dysplasia

Aniridia 1

Aniridia

Congenital Aniridia

AN1

An

Cataract With Late-Onset Corneal Dystrophy

Aplasia Of Iris

Absent Iris

Irideremia

Aniridia Ii, Formerly

An2, Formerly

An2

Aniridia Type Ii

Aniridia, Type 1

An-1

Absence Of Iris

Agenesis Of Iris

Congenital Absence Of Iris

Hereditary Aniridia

Sporadic Aniridia

Iris Disease

Iris Diseases

Gillespie Syndrome

GLSP

Aniridia, Cerebellar Ataxia And Mental Deficiency

Aniridia Cerebellar Ataxia Mental Deficiency

Aniridia, Cerebellar Ataxia, And Mental Retardation

Aniridia-Cerebellar Ataxia-Intellectual Disability Syndrome

Aniridia-Cerebellar Ataxia-Intellectual Disability

Aniridia-Cerebellar Ataxia-Mental Deficiency

Partial Aniridia-Cerebellar Ataxia-Oligophrenia

Aniridia, Cerebellar Ataxia, And Intellectual Disability

Coloboma Of Optic Nerve

Morning Glory Disc Anomaly

Coloboma Of Optic Disc

Morning Glory Syndrome

Ectasic Coloboma

Coloboma Of Optic Papilla

Congenital Coloboma Of The Optic Nerve

Optic Nerve Coloboma

Optic Nerve Head Pits, Bilateral Congenital

Volubilis Syndrome

COLON

Coloboma Of Optic Disc, Unspecified Eye

Congenital Coloboma Of Optic Disc

Optic Disk Coloboma

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
Macaca mulatta PRRG4 VGNC VGNC:107629
Bos taurus PRRG4 VGNC VGNC:33409
Rattus norvegicus PRRG4 RGD RGD:1560542
Canis familiaris PRRG4 VGNC VGNC:45058
Felis catus PRRG4 VGNC VGNC:64393
Mus musculus PRRG4 MGD MGI:2442211