1. Gene
  2. PKDCC - protein kinase domain containing, cytoplasmic Gene

PKDCC - protein kinase domain containing, cytoplasmic Gene

中文名称:含蛋白激酶结构域,细胞质

种属: Homo sapiens

同用名: Vlk; RLSDF; SGK493

基因 ID: 91461 | 基因类型: protein coding

关于 PKDCC

Cytogenetic location: 2p21 Genomic coordinates (GRCh38): 2:42,048,021-42,058,517 (from NCBI)

This gene has 9 transcripts (splice variants), 156 orthologues, 2 paralogues and is associated with 1 phenotype. Broad expression in ovary (RPKM 28.2), endometrium (RPKM 26.6) and 22 other tissues.

功能概要

启用非跨膜蛋白酪氨酸激酶活性。参与肽酰酪氨酸磷酸化和骨骼系统发育。位于胞外区。 [由基因组资源联盟提供,2022 年 4 月]

Enables non-membrane spanning protein tyrosine kinase activity. Involved in peptidyl-tyrosine phosphorylation and skeletal system development. Located in extracellular region. [provided by Alliance of Genome Resources, Apr 2022]

PKDCC 基因产物(1)

mRNA Protein Name
NM_138370.3 NP_612379.2 extracellular tyrosine-protein kinase PKDCC precursor
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 non-membrane spanning protein tyrosine kinase activity IDA
IDA: 通过直接分析推断
25171405 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in peptidyl-tyrosine phosphorylation IDA
IDA: 通过直接分析推断
25171405 GOA
involved in skeletal system development IMP
IMP: 通过突变表型推断
30478137 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in extracellular region IDA
IDA: 通过直接分析推断
25171405 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

PKDCC 蛋白结构

PIP49_C

PIP49_C: Protein-kinase domain of FAM69 (238 - 368)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 493 a.a.
蛋白主名 其他名称

extracellular tyrosine-protein kinase PKDCC

protein kinase domain containing, cytoplasmic homolog

关联疾病

疾病名称 别名
Rhizomelic Limb Shortening With Dysmorphic Features

RLSDF

N Syndrome

NSX

Intellectual Disability, Malformations, Chromosome Breakage, And Development Of T-Cell Leukemia

Amelogenesis Imperfecta, Type Ic

Amelogenesis Imperfecta Type 1c

AI1C

Amelogenesis Imperfecta Type Ic

Amelogenesis Imperfecta, Local Hypoplastic Type, Autosomal Recessive

Amelogenesis Imperfecta, Hypoplastic, With Or Without Open-Bite Malocclusion, Autosomal Recessive

Autosomal Recessive Amelogenesis Imperfecta Hypoplastic With Or Without Openbite Malocclusion

Autosomal Recessive Amelogenesis Imperfecta Local Hypoplastic Type

Amelogenesis Imperfecta 1c

Amelogenesis Imperfecta Hypoplastic With Or Without Openbite Malocclusion Autosomal Recessive

Amelogenesis Imperfecta Local Hypoplastic Type Autosomal Recessive

Cleft Palate, Isolated

Cleft Palate

Isolated Cleft Palate

CPI

Cp

Palatoschisis

Cleft Palate Isolated

Uranostaphyloschisis

Congenital Fissure Of Palate

Cleft Of Secondary Palate

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
Felis catus PKDCC VGNC VGNC:81149
Macaca mulatta PKDCC VGNC VGNC:106196
Canis familiaris PKDCC VGNC VGNC:44603
Mus musculus PKDCC MGD MGI:2147077
Bos taurus PKDCC VGNC VGNC:32938
Rattus norvegicus PKDCC RGD RGD:1311939