2. Gene
  3. SCCPDH - saccharopine dehydrogenase (putative) Gene

SCCPDH - saccharopine dehydrogenase (putative) Gene

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

中文名称：糖精脱氢酶 (假定)

种属: Homo sapiens

同用名: NET11; CGI-49

基因 ID: 51097 | 基因类型: protein coding

关于 SCCPDH

This gene has 1 transcript (splice variant) and 216 orthologues. Broad expression in testis (RPKM 87.1), liver (RPKM 34.8) and 22 other tissues.

功能概要

预测启用氧化还原酶活性。预测参与糖脂生物合成过程。位于脂滴和中体。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable oxidoreductase activity. Predicted to be involved in glycolipid biosynthetic process. Located in lipid droplet and midbody. [provided by Alliance of Genome Resources, Apr 2022]

SCCPDH 基因产物(1)

mRNA Protein Name
NM_016002.3 NP_057086.2 saccharopine dehydrogenase-like oxidoreductase
基因本体论
  • 细胞组分
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in lipid droplet IDA
IDA: 通过直接分析推断
14741744 GOA
located in midbody IDA
IDA: 通过直接分析推断
15166316 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

SCCPDH 蛋白结构

Sacchrp_dh_NADP

Sacchrp_dh_NADP: Saccharopine dehydrogenase NADP binding domain (11 - 421)

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

saccharopine dehydrogenase-like oxidoreductase

epididymis secretory sperm binding protein

关联疾病

疾病名称 别名
Hyperlysinemia, Type I

Hyperlysinemia

Lysine Intolerance

Alpha-Aminoadipic Semialdehyde Synthase Deficiency

Lysine:Alpha-Ketoglutarate Reductase Deficiency

L-Lysine:Nad-Oxido-Reductase Deficiency

Lysine Alpha-Ketoglutarate Reductase Deficiency

Alpha-Aminoadipic Semialdehyde Deficiency Disease

Lysine Alpha-Ketoglutarate Reductase Deficiency Disease

Saccharopinuria

Hyperlysinemia Type I

Hyperlysinemias

L-Lysine Nad-Oxido-Reductase Deficiency

Familial Hyperlysinemia

Saccharopine Dehydrogenase Deficiency Disease

Hyperlysinemia, 1

HYPLYS1

Saccharopine Dehydrogenase Deficiency
L-2-Hydroxyglutaric Aciduria

L-2-Hydroxyglutaric Acidemia

L2HGA

L-2-Hga

Aciduria, L-2-Hydroxyglutaric

Combined D-2- And L-2-Hydroxyglutaric Aciduria
Epilepsy, Pyridoxine-Dependent

Pyridoxine-Dependent Epilepsy

PDE

Pyridoxine Dependency With Seizures

Vitamin B6-Dependent Seizures

EPD

Aasa Dehydrogenase Deficiency

Antiquitin Deficiency

Pyridoxine Dependency

Glutamate Decarboxylase Deficiency

Pyridoxine-Dependent Seizures

Deficiency Of Glutamate Decarboxylase
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 (2)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-174821 VU439 Modulator / 否
HY-RS12493 SCCPDH Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Mus musculus SCCPDH MGD MGI:1924486
Rattus norvegicus SCCPDH RGD RGD:1311440
Canis familiaris SCCPDH VGNC VGNC:55761
Macaca mulatta SCCPDH VGNC VGNC:100132
Felis catus SCCPDH VGNC VGNC:107935
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