2. Gene
  3. PNCK - pregnancy up-regulated nonubiquitous CaM kinase Gene

PNCK - pregnancy up-regulated nonubiquitous CaM kinase Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：妊娠上调非普遍存在的 CaM 激酶

种属: Homo sapiens

同用名: BSTK3; CaMK1b

基因 ID: 139728 | 基因类型: protein coding

关于 PNCK

Cytogenetic location: Xq28 Genomic coordinates (GRCh38): X:153,669,733-153,687,771 (from NCBI)

This gene has 32 transcripts (splice variants), 102 orthologues and 22 paralogues. Biased expression in brain (RPKM 7.4), prostate (RPKM 4.6) and 11 other tissues.

功能概要

PNCK 是蛋白丝氨酸/苏氨酸激酶的钙/钙调蛋白依赖性蛋白激酶家族的成员 (参见 CAMK1；MIM 604998) (Gardner 等人，2000 [PubMed 10673339]) 。[OMIM 提供，2008 年 3 月]

PNCK is a member of the calcium/calmodulin-dependent protein kinase family of protein serine/threonine kinases (see CAMK1; MIM 604998) (Gardner et al., 2000 [PubMed 10673339]).[supplied by OMIM, Mar 2008]

PNCK 基因产物(8)

mRNA Protein Name
NM_001039582.3 NP_001034671.3 calcium/calmodulin-dependent protein kinase type 1B isoform a
NM_001135740.2 NP_001129212.1 calcium/calmodulin-dependent protein kinase type 1B isoform b
NM_001366975.1 NP_001353904.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366976.1 NP_001353905.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366977.1 NP_001353906.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366978.1 NP_001353907.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366979.1 NP_001353908.1 calcium/calmodulin-dependent protein kinase type 1B isoform c
NM_001366980.1 NP_001353909.1 calcium/calmodulin-dependent protein kinase type 1B isoform c

PNCK 蛋白结构

Pkinase

Pkinase: Protein kinase domain (15 - 270)

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

calcium/calmodulin-dependent protein kinase type 1B

caM kinase I beta

关联疾病

疾病名称 别名
Syndromic X-Linked Intellectual Disability Lubs Type

Lubs X-Linked Mental Retardation Syndrome

Mecp2 Duplication Syndrome

Mental Retardation, X-Linked, Syndromic, Lubs Type

Mental Retardation, X-Linked, With Recurrent Respiratory Infections

Mrxsl

X-Linked Intellectual Disability-Hypotonia-Recurrent Infections Syndrome

Mental Retardation, X-Linked Syndromic, Lubs Type
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS10775 PNCK Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Bos taurus PNCK VGNC VGNC:33079
Mus musculus PNCK MGD MGI:1347357
Macaca mulatta PNCK VGNC VGNC:76020
Canis familiaris PNCK VGNC VGNC:44740
Felis catus PNCK VGNC VGNC:64258
Rattus norvegicus PNCK RGD RGD:69249
Others PNCK NCBI
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