2. Gene
  3. KCP - kielin cysteine rich BMP regulator Gene

KCP - kielin cysteine rich BMP regulator Gene

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

中文名称：kielin 富半胱氨酸的 BMP 调节因子

种属: Homo sapiens

同用名: KCP1; CRIM2; NET67

基因 ID: 375616 | 基因类型: protein coding

关于 KCP

Cytogenetic location: 7q32.1 Genomic coordinates (GRCh38): 7:128,876,865-128,910,709 (from NCBI)

This gene has 12 transcripts (splice variants), 150 orthologues and 19 paralogues. Biased expression in kidney (RPKM 3.0), fat (RPKM 0.8) and 8 other tissues.

功能概要

预测作用于造血祖细胞分化的上游或内部，并正向调节 BMP 信号通路。预计位于细胞外空间。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to act upstream of or within hematopoietic progenitor cell differentiation and positive regulation of BMP signaling pathway. Predicted to be located in extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

KCP 基因产物(2)

mRNA Protein Name
NM_001366122.1 NP_001353051.1 kielin/chordin-like protein isoform 3 precursor
NM_199349.3 NP_955381.2 kielin/chordin-like protein isoform 2 precursor
蛋白主名 其他名称

kielin/chordin-like protein

cysteine rich BMP regulator 2 (chordin-like)

关联疾病

疾病名称 别名
Hereditary Hemorrhagic Telangiectasia

Rendu-Osler-Weber Disease

Hht

Osler-Weber-Rendu Disease

Telangiectasia, Hereditary Hemorrhagic

Osler Hemorrhagic Telangiectasia Syndrome

Orw Disease

Osler Weber Rendu Syndrome

Osler-Rendu-Weber Disease

Osler-Weber-Rendu Syndrome

Rendu-Osler Disease

Telangiectasia Hereditary Hemorrhagic

Telangiectasia Hemorrhagic, Hereditary

Hht - [Hereditary Haemorrhagic Telangiectasia]

Osler Haemorrhagic Telangiectasia Syndrome
Renal Fibrosis
Myasthenic Syndrome, Congenital, 5

Endplate Acetylcholinesterase Deficiency

Congenital Myasthenic Syndrome 5

CMS5

Ead

Engel Congenital Myasthenic Syndrome

Myasthenic Syndrome, Congenital, Engel Type

Cms Ic

Congenital Myasthenic Syndrome Type Ic

Congenital Myasthenic Syndrome Type Ic, Formerly

Cms1c, Formerly

Cms Ic, Formerly

Congenital Myasthenic Syndrome Engel Type

End Plate Acetylcholinesterase Deficiency

Synaptic Congenital Myasthenic Syndromes

Cms1c

Cmse

Congenital Myasthenic Syndrome Type 1c

End-Plate Acetylcholinesterase Deficiency

Myasthenic Syndrome, Congenital, Type 5
Cone-Rod Dystrophy 2

Cone-Rod Dystrophy

CORD2

Cone-Rod Retinal Dystrophy

Rcrd2

Cone-Rod Retinal Dystrophy 2

Crd2

Cord

Crd

Retinal Cone-Rod Dystrophy

Cone-Rod Retinal Dystrophy-2

Retinal Cone-Rod Dystrophy 2

Tapetoretinal Degeneration

Cone-Rod Degeneration

Cone Rod Dystrophy

Dystrophy, Cone-Rod

Dystrophy, Cone-Rod, Type 2

Retinitis Pigmentosa

Retinitis Pigmentosa 2

Progressive Cone-Rod Dystrophy
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-RS07185 KCP Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus KCP RGD RGD:1561119
Mus musculus KCP MGD MGI:2141640
Felis catus KCP VGNC VGNC:82338
Canis familiaris KCP VGNC VGNC:42299
Macaca mulatta KCP VGNC VGNC:81627
Bos taurus KCP VGNC VGNC:53650
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