CASR (calcium sensing receptor)

symbol:
CASR
locus group:
protein-coding gene
location:
3q13.33-q21.1
gene_family:
Calcium-sensing receptors
alias symbol:
FHH|NSHPT|GPRC2A
alias name:
severe neonatal hyperparathyroidism
entrez id:
846
ensembl gene id:
ENSG00000036828
ucsc gene id:
uc003eev.5
refseq accession:
NM_000388
hgnc_id:
HGNC:1514
approved reserved:
1992-12-04
3q13.33-q21.1
基因染色体位置图

CASR(钙敏感受体,Calcium-Sensing Receptor)是一种G蛋白偶联受体(GPCR),主要表达于甲状旁腺、肾脏、肠道和骨骼等组织中,负责感知细胞外钙离子浓度并调控钙磷代谢平衡。其生物学功能是通过激活下游信号通路(如PLC、MAPK等)调节甲状旁腺激素(PTH)的分泌、肾脏钙重吸收及骨代谢。当血钙升高时,CASR被激活并抑制PTH释放,促进尿钙排泄;反之,低钙血症会减弱CASR活性,刺激PTH分泌以提升血钙水平。CASR的突变可导致功能异常:激活突变(如常染色体显性低钙血症)会过度抑制PTH,引发低钙血症;失活突变(如家族性低尿钙高钙血症)则导致PTH持续分泌,引发高钙血症。该基因与慢性肾病、骨质疏松和甲状旁腺肿瘤等疾病密切相关。CASR过表达会增强对钙的敏感性,可能造成低钙血症并抑制骨吸收;表达降低则可能导致高钙血症和甲状旁腺增生。CASR属于C家族GPCR(Class C GPCR),该家族共性为具有大型胞外结构域,用于识别配体(如钙离子、氨基酸等),并通过跨膜区传递信号。其功能异常可能间接影响维生素D代谢、FGF23(成纤维细胞生长因子23)等钙磷相关基因的表达。

The protein encoded by this gene is a G protein-coupled receptor that is expressed in the parathyroid hormone (PTH)-producing chief cells of the parathyroid gland, and the cells lining the kidney tubule. It senses small changes in circulating calcium concentration and couples this information to intracellular signaling pathways that modify PTH secretion or renal cation handling, thus this protein plays an essential role in maintaining mineral ion homeostasis. Mutations in this gene cause familial hypocalciuric hypercalcemia, familial, isolated hypoparathyroidism, and neonatal severe primary hyperparathyroidism. [provided by RefSeq, Jul 2008]

由该基因编码的蛋白质是在甲状旁腺激素(PTH)-producing衬肾小管细胞甲状旁腺主细胞,和表达的G蛋白偶联受体。它感觉循环钙浓度和夫妇此信息来修改PTH分泌或肾阳离子处理细胞内信号通路,从而这种蛋白质对维持矿物质离子平衡中起重要作用的微小变化。突变这个基因家族事业高钙血症低钙,家庭,孤立的甲状旁腺功能减退症和新生儿严重的原发性甲状旁腺功能亢进。 [由RefSeq的,2008年7月提供]

CASR基因的碱基序列:[NCBI]
Loading Gene Browser...
CASR基因的碱基突变:           仅显示部分snp
rs9740       rs10190       rs884086       rs937625       rs937626       rs937627       rs1042636       rs1048213       rs1354158       rs1354159       rs1354160       rs1354162       rs1393198       rs1393199       rs1393200       rs1463890       rs1463891      

CASR基因在不同组织中的表达:    [UniProt]

基因在不同组织中的表达图
正向引物序列
正向Tm值
反向引物序列
反向Tm值
评分
ATCAAGATCTCAAATCAAGGCC
59
AACCCACGGAAATTATACCTG
58
GTGATGAGACAGATGCCAG
58
GATCTCCTTGGCAATGCAG
59
TGATGAGACAGATGCCAGTG
60
GATCTCCTTGGCAATGCAG
59
CAAGATCTCAAATCAAGGCCG
60
GAAACCCACGGAAATTATACCTG
60
GATCAAGATCTCAAATCAAGGC
58
ACCCACGGAAATTATACCTG
57
GATGAGACAGATGCCAGTG
58
GATCTCCTTGGCAATGCAG
59
转录因子
影响基因
影响类型
参考文献链接(PubMed)
BRCA1
CASR
Unknown
GCM2
CASR
Activation

CASR基因(以及对应的蛋白质)的细胞分布位置:

[UniProt]     [GenomeNet]

" d="M482.414,245.296c3.539,4.293,4.455,10.009,0.202,11 c-4.244,0.996-4.983-10.983-8.293-8.438c-5.271,4.08,9.834,12.271,5.144,17.287c-3.717,3.607-6.172-5.75-10.839-1.976 c-4.673,3.776,6.781,7.299,2.831,11.326c-4.354,4.045-6.979-1.449-9.837-5.517c-1.193-1.742-2.059-3.851-3.595-2.748 c-1.516,1.078-1.854,1.795-0.938,3.666c2.374,4.854,9.235,10.119,5.156,12.535c-5.636,3.346-5.044-8.871-9.426-7.574 c-4.388,1.291,2.557,10.66-1.245,11.141c-4.089,0.545-3.483-10.239-6.979-8.575c-2.522,1.206-0.929,3.071-0.938,4.899 c0.004,1.32-0.964,3.6-2.372,4.062c-3.593,1.171-8.544-1.065-10.251-3.59c-6.04-8.93,0.396-15.997,4.639-7.015 c3.023,4.642,5.182,0.834,2.839-2.219c-1.032-1.354-4.309-5.901-0.781-7.252c2.904-1.113,4.271,1.941,5.985,4.592 c2.61,4.016,5.485,0.117,3.031-3.414c-1.828-2.633-2.74-3.803,3.156-7.42c6.405-4.369,6.52,3.869,10.077,0.646 c2.309-1.832-4.783-5.149,0.06-8.995c2.896-2.293,5.18,6.207,7.961,3.516c3.523-2.737-7.717-7.369,0.117-11.736 C473.413,240.77,480.519,242.891,482.414,245.296z"/> Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
  • 质膜
  • 细胞质
  • 细胞外
  • 高尔基体
  • 囊泡
  • 细胞骨架
  • 内质网
  • 细胞核
  • 内体
  • 溶酶体
  • 线粒体

CASR基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0000287
E7ENE0 (UniProtKB)
IEA
GO:0001503
E7ENE0 (UniProtKB)
IEA
GO:0002931
E7ENE0 (UniProtKB)
IEA
GO:0004930
E7ENE0 (UniProtKB)
IEA
GO:0005178
E7ENE0 (UniProtKB)
IEA
GO:0005509
E7ENE0 (UniProtKB)
IEA
GO:0005634
E7ENE0 (UniProtKB)
IEA
GO:0005737
E7ENE0 (UniProtKB)
IEA
GO:0006816
E7ENE0 (UniProtKB)
IEA
GO:0006874
E7ENE0 (UniProtKB)
IEA
GO:0006915
E7ENE0 (UniProtKB)
IEA
GO:0007193
E7ENE0 (UniProtKB)
IEA
GO:0007200
E7ENE0 (UniProtKB)
IEA
GO:0007254
E7ENE0 (UniProtKB)
IEA
GO:0008144
E7ENE0 (UniProtKB)
IEA
GO:0008284
E7ENE0 (UniProtKB)
IEA
GO:0009986
E7ENE0 (UniProtKB)
IEA
GO:0010628
E7ENE0 (UniProtKB)
IEA
GO:0016021
E7ENE0 (UniProtKB)
IEA
GO:0016323
E7ENE0 (UniProtKB)
IEA
GO:0016324
E7ENE0 (UniProtKB)
IEA
GO:0019808
E7ENE0 (UniProtKB)
IEA
GO:0019901
E7ENE0 (UniProtKB)
IEA
GO:0032024
E7ENE0 (UniProtKB)
IEA
GO:0032781
E7ENE0 (UniProtKB)
IEA
GO:0035729
E7ENE0 (UniProtKB)
IEA
GO:0042311
E7ENE0 (UniProtKB)
IEA
GO:0043025
E7ENE0 (UniProtKB)
IEA
GO:0043679
E7ENE0 (UniProtKB)
IEA
GO:0044325
E7ENE0 (UniProtKB)
IEA
GO:0045907
E7ENE0 (UniProtKB)
IEA
GO:0048754
E7ENE0 (UniProtKB)
IEA
GO:0050927
E7ENE0 (UniProtKB)
IEA
GO:0051592
E7ENE0 (UniProtKB)
IEA
GO:0060613
E7ENE0 (UniProtKB)
IEA
GO:0071305
E7ENE0 (UniProtKB)
IEA
GO:0071333
E7ENE0 (UniProtKB)
IEA
GO:0071404
E7ENE0 (UniProtKB)
IEA
GO:0071456
E7ENE0 (UniProtKB)
IEA
GO:0071774
E7ENE0 (UniProtKB)
IEA
GO:0090280
E7ENE0 (UniProtKB)
IEA
GO:1901653
E7ENE0 (UniProtKB)
IEA
GO:0001503
P41180 (UniProtKB)
TAS
GO:0004435
P41180 (UniProtKB)
TAS
GO:0004930
P41180 (UniProtKB)
IEA
GO:0005513
P41180 (UniProtKB)
TAS
GO:0005515
P41180 (UniProtKB)
IPI
GO:0005886
P41180 (UniProtKB)
TAS
GO:0005886
P41180 (UniProtKB)
TAS
GO:0005886
P41180 (UniProtKB)
TAS
GO:0005886
P41180 (UniProtKB)
TAS
GO:0005886
P41180 (UniProtKB)
TAS
GO:0005886
P41180 (UniProtKB)
TAS
GO:0005886
P41180 (UniProtKB)
TAS
GO:0005887
P41180 (UniProtKB)
TAS
GO:0006874
P41180 (UniProtKB)
TAS
GO:0007186
P41180 (UniProtKB)
IEA
GO:0007635
P41180 (UniProtKB)
TAS
GO:0009653
P41180 (UniProtKB)
TAS
GO:0070509
P41180 (UniProtKB)
IDA

可能调控 CASR基因的相关microRNA:     

Reactome

BioGrid

mentha

基因与其他基因之间的相互作用关系图
序号 作用方式 资源库来源/分值 基因名称 基因名称
疾病名称 关系值 NofPmids NofSnps 来源
疾病名称 关系值 NofPmids NofSnps 来源
Hypocalciuric hypercalcemia, familial, type 1 0.588425452 103 28 BeFree_CLINVAR_CTD_human_GAD_MGD_ORPHANET_UNIPROT
HYPERPARATHYROIDISM, NEONATAL SEVERE 0.56 5 9 CLINVAR_CTD_human_MGD_ORPHANET_UNIPROT
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1 0.320542884 17 0 BeFree_MGD_ORPHANET_UNIPROT
Familial benign hypercalcemia 0.240814326 3 17 BeFree_CLINVAR_ORPHANET
Hypoparathyroidism familial isolated 0.240542884 2 1 BeFree_CLINVAR_CTD_human
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 8 0.24 1 1 CLINVAR_UNIPROT
Hypercalcemia 0.177628636 57 3 BeFree_CTD_human_GAD_LHGDN
Hyperparathyroidism 0.140603295 24 2 BeFree_CTD_human_GAD_LHGDN
Hypoparathyroidism 0.133787454 23 0 BeFree_CTD_human_GAD_LHGDN
Hypoparathyroidism - autosomal dominant 0.130857675 40 21 BeFree_CLINVAR

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