1. Gene
  2. PRKACB - protein kinase cAMP-activated catalytic subunit beta Gene

PRKACB - protein kinase cAMP-activated catalytic subunit beta Gene

中文名称:蛋白激酶 cAMP 激活的催化亚基 β

种属: Homo sapiens

同用名: CAFD2; PKACB; PKA C-beta

基因 ID: 5567 | 基因类型: protein coding

关于 PRKACB

Cytogenetic location: 1p31.1 Genomic coordinates (GRCh38): 1:84,078,079-84,238,498 (from NCBI)

This gene has 18 transcripts (splice variants), 302 orthologues, 5 paralogues and is associated with 2 phenotypes. Broad expression in brain (RPKM 61.5), colon (RPKM 21.8) and 22 other tissues.

功能概要

该基因编码的蛋白质是丝氨酸/苏氨酸蛋白激酶家族的成员。编码的蛋白质是 cAMP (环 AMP) 依赖性蛋白激酶的催化亚基,它通过 cAMP 介导信号传导。 cAMP 信号对许多过程都很重要,包括细胞增殖和分化。已经观察到编码不同同种型的多个选择性剪接的转录物变体。[RefSeq 提供,2014 年 7 月]

The protein encoded by this gene is a member of the serine/threonine protein kinase family. The encoded protein is a catalytic subunit of cAMP (cyclic AMP)-dependent protein kinase, which mediates signalling though cAMP. cAMP signaling is important to a number of processes, including cell proliferaton and differentiation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2014]

PRKACB 基因产物(30)

mRNA Protein Name
NM_001242857.3 NP_001229786.1 cAMP-dependent protein kinase catalytic subunit beta isoform 4
NM_001242858.3 NP_001229787.1 cAMP-dependent protein kinase catalytic subunit beta isoform 5
NM_001242859.3 NP_001229788.1 cAMP-dependent protein kinase catalytic subunit beta isoform 6
NM_001242860.3 NP_001229789.1 cAMP-dependent protein kinase catalytic subunit beta isoform 7
NM_001242861.3 NP_001229790.1 cAMP-dependent protein kinase catalytic subunit beta isoform 8
NM_001242862.3 NP_001229791.1 cAMP-dependent protein kinase catalytic subunit beta isoform 9
NM_001300915.2 NP_001287844.1 cAMP-dependent protein kinase catalytic subunit beta isoform 10
NM_001300916.2 NP_001287845.1 cAMP-dependent protein kinase catalytic subunit beta isoform 11
NM_001300917.2 NP_001287846.1 cAMP-dependent protein kinase catalytic subunit beta isoform 12
NM_001375560.1 NP_001362489.1 cAMP-dependent protein kinase catalytic subunit beta isoform 13
NM_001375561.1 NP_001362490.1 cAMP-dependent protein kinase catalytic subunit beta isoform 14
NM_001375562.1 NP_001362491.1 cAMP-dependent protein kinase catalytic subunit beta isoform 15
NM_001375563.1 NP_001362492.1 cAMP-dependent protein kinase catalytic subunit beta isoform 16
NM_001375564.1 NP_001362493.1 cAMP-dependent protein kinase catalytic subunit beta isoform 17
NM_001375565.1 NP_001362494.1 cAMP-dependent protein kinase catalytic subunit beta isoform 18
NM_001375569.1 NP_001362498.1 cAMP-dependent protein kinase catalytic subunit beta isoform 20
NM_001375571.1 NP_001362500.1 cAMP-dependent protein kinase catalytic subunit beta isoform 21
NM_001375572.1 NP_001362501.1 cAMP-dependent protein kinase catalytic subunit beta isoform 22
NM_001375573.1 NP_001362502.1 cAMP-dependent protein kinase catalytic subunit beta isoform 23
NM_001375574.1 NP_001362503.1 cAMP-dependent protein kinase catalytic subunit beta isoform 26
NM_001375575.1 NP_001362504.1 cAMP-dependent protein kinase catalytic subunit beta isoform 24
NM_001375576.1 NP_001362505.1 cAMP-dependent protein kinase catalytic subunit beta isoform 25
NM_001375577.1 NP_001362506.1 cAMP-dependent protein kinase catalytic subunit beta isoform 27
NM_001375578.1 NP_001362507.1 cAMP-dependent protein kinase catalytic subunit beta isoform 28
NM_001375579.1 NP_001362508.1 cAMP-dependent protein kinase catalytic subunit beta isforom 29
NM_001375580.1 NP_001362509.1 cAMP-dependent protein kinase catalytic subunit beta isoform 30
NM_001375581.1 NP_001362510.1 cAMP-dependent protein kinase catalytic subunit beta isoform 19
NM_002731.4 NP_002722.1 cAMP-dependent protein kinase catalytic subunit beta isoform 2
NM_182948.4 NP_891993.1 cAMP-dependent protein kinase catalytic subunit beta isoform 1
NM_207578.3 NP_997461.1 cAMP-dependent protein kinase catalytic subunit beta isoform 3
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 ATP binding IDA
IDA: 通过直接分析推断
12420224 GOA
enables cAMP-dependent protein kinase activity IDA
IDA: 通过直接分析推断
12420224 GOA
enables magnesium ion binding IDA
IDA: 通过直接分析推断
12420224 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
21880142 GOA
enables ubiquitin protein ligase binding IDA
IDA: 通过直接分析推断
21423175 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of TORC1 signaling IDA
IDA: 通过直接分析推断
31112131 GOA
involved in protein phosphorylation IDA
IDA: 通过直接分析推断
12420224 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in centrosome IDA
IDA: 通过直接分析推断
21399614 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

PRKACB 蛋白结构

Pkinase

Pkinase: Protein kinase domain (45 - 298)

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

cAMP-dependent protein kinase catalytic subunit beta

protein kinase A catalytic subunit beta

PRKACB 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
PRKACB P22694 PKIA Homo sapiens P61925 32296183
种属内
PRKACB P22694 HSP90AB1 Homo sapiens P08238 22939624
种属内
PRKACB P22694 HSP90AB1 Homo sapiens P08238
TAP
23455922
种属内
PRKACB P22694 APPBP2 Homo sapiens Q92624 25416956
种属内
PRKACB P22694 AVPI1 Homo sapiens Q5T686 32296183
种属内
PRKACB P22694 AVPI1 Homo sapiens Q5T686 32296183
种属内
PRKACB P22694 AVPI1 Homo sapiens Q5T686 32296183
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
Cardioacrofacial Dysplasia 2

CAFD2

Breast Ductal Adenoma
Breast Adenoma

Ademoma - Breast

Atrioventricular Septal Defect

AVSD

Atrioventricular Canal Defect

Avcd

Endocardial Cushion Defect

Ecd

Avc Defect

Atrioventricular Septal Defect, Susceptibility To, 1

Atrioventricular Septal Defect 1

Endocardial Cushion Defects

Septal Defect, Atrioventricular

Atrioventricular Defect With Atrial Shunting Only

Incomplete Atrioventricular Septal Defect With Isolated Atrial Component

Incomplete Atrioventricular Canal Defect With Isolated Atrial Component

Primum Atrial Septal Defect

Partial Atrioventricular Canal Defect With Isolated Atrial Component

Partial Atrioventricular Septal Defect, Ostium Primum Type

Ostium Primum Atrial Septal Defect

Partial Atrioventricular Canal Defect

Partial Atrioventricular Septal Defect

Atrial Septum Primum Defect

Atrioventricular Canal Defect With Isolated Ventricular Component

Atrioventricular Canal Defect With Isolated Ventricular Communication

Atrioventricular Septal Defect With Isolated Ventricular Component

Atrioventricular Septal Defect With Atrial Shunting And Restrictive Ventricular Shunting

Intermediate Atrioventricular Canal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valve

Transitional Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valves

Atrioventricular Canal Defect Associated With A Restrictive Ventricular Septal Defect

Intermediate Atrioventricular Canal Defect

Intermediate Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valvar Orifices

Intermediate Atrioventricular Septal Defect

Transitional Atrioventricular Canal Defect

Transitional Atrioventricular Septal Defect

Complete Atrioventricular Canal With Atrial And Ventricular Components

Complete Atrioventricular Canal Defect

Complete Atrioventricular Septal Defect

Melanotic Neurilemmoma

Melanotic Schwannoma

Pigmented Neurilemmoma

Pigmented Schwannoma

Cervical Non-Keratinizing Squamous Cell Carcinoma
Primary Pigmented Nodular Adrenocortical Disease

Ppnad

Primary Pigmented Nodular Adrenal Dysplasia

Pigmented Nodular Adrenocortical Disease, Primary, 2

Pigmented Nodular Adrenocortical Disease, Primary, 1

Fibrolamellar Carcinoma

Fibrolamellar Hepatocellular Carcinoma

Fhcc

Fibrolamellar Hepatocarcinoma

Hepatocellular Carcinoma, Fibrolamellar

Oncocytic Hepatocellular Tumor

Eosinophilic Glassy Cell Hepatoma

Eosinophilic Hepatocellular Carcinoma With Lamellar Fibrosis

Fl-Hcc

Fibrolamellar Oncocytic Hepatoma

Hepatocellular Carcinoma With Increased Stromal Fibrosis

Polygonal Cell Hepatocellular Carcinoma With Fibrous Stroma

Cervical Keratinizing Squamous Cell Carcinoma
Carney Complex Variant

Carney Complex

Carney Syndrome

Carney Complex, Type 1

Lamb Syndrome

Name Syndrome

Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome

Carney Complex - Trismus - Pseudocamptodactyly Syndrome

Carney Complex, Type 2

Car

Cnc1

Carney Myxoma-Endocrine Complex

Myxoma - Spotty Pigmentation - Endocrine Overactivity

Myxoma, Spotty Pigmentation, And Endocrine Overactivity

Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome

Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome

Carney Complex-Trismus-Pseudocamptodactyly Syndrome

CACOV

Thrombophilia Due To Hrg Deficiency

Hereditary Thrombophilia Due To Congenital Histidine-Rich Glycoprotein Deficiency

Hereditary Thrombophilia Due To Congenital Hrg Deficiency

Thph11

Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

Mccune-Albright Syndrome

Mass Syndrome

Polyostotic Fibrous Dysplasia

MAS

Fibrous Dysplasia Of Bone

Albright Syndrome

Mass Phenotype

Overlap Connective Tissue Disease

Mccune Albright Syndrome

Osteitis Fibrosa Disseminata

OCTD

Albright'S Disease

Pfd

Pofd

Albright'S Syndrome

Mccune-Albright Syndrome, Somatic, Mosaic

Albright'S Disease Of Bone

Albright'S Syndrome With Precocious Puberty

Albright-Mccune-Sternberg Syndrome

Albright-Sternberg Syndrome

Fibrous Dysplasia With Pigmentary Skin Changes And Precocious Puberty

Gonadotropin-Independent Female-Limited Sexual Precocity

Fibrous Dysplasia Polyostotic

Fibrous Dysplasia, Polyostotic

Osteogenesis Imperfecta, Type Iv

Osteogenesis Imperfecta Type 4

Osteogenesis Imperfecta Type Iv

OI4

Oi, Type Iv

Osteogenesis Imperfecta With Normal Sclerae

Oi Type Iv

Oi Type 4

Osteogenesis Imperfecta With Normal Sclera

Common Variable Oi With Normal Sclerae

Osteogenesis Imperfecta 4

Oi-Iv

Brachydactyly
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 PRKACB VGNC VGNC:33321
Canis familiaris PRKACB VGNC VGNC:44971
Rattus norvegicus PRKACB RGD RGD:1310574
Mus musculus PRKACB MGD MGI:97594
Felis catus PRKACB VGNC VGNC:80322
Macaca mulatta PRKACB VGNC VGNC:97808
Others PRKACB NCBI