2. Gene
  3. ASRGL1 - asparaginase and isoaspartyl peptidase 1 Gene

ASRGL1 - asparaginase and isoaspartyl peptidase 1 Gene

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

中文名称：天冬酰胺酶和异天冬氨酰肽酶 1

种属: Homo sapiens

同用名: ALP; ALP1; CRASH

基因 ID: 80150 | 基因类型: protein coding

关于 ASRGL1

Cytogenetic location: 11q12.3 Genomic coordinates (GRCh38): 11:62,337,448-62,401,431 (from NCBI)

This gene has 11 transcripts (splice variants), 211 orthologues, 2 paralogues and is associated with 1 phenotype. Biased expression in testis (RPKM 38.7), kidney (RPKM 13.5) and 10 other tissues.

功能概要

启用天冬酰胺酶活性和 β-天冬氨酰肽酶活性。通过 L-天冬氨酸参与天冬酰胺分解代谢过程。位于细胞质中。 [由基因组资源联盟提供，2022 年 4 月]

Enables asparaginase activity and beta-aspartyl-peptidase activity. Involved in asparagine catabolic process via L-aspartate. Located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

ASRGL1 基因产物(2)

mRNA Protein Name
NM_001083926.2 NP_001077395.1 isoaspartyl peptidase/L-asparaginase
NM_025080.4 NP_079356.3 isoaspartyl peptidase/L-asparaginase

ASRGL1 蛋白结构

Asparaginase_2

Asparaginase_2: Asparaginase (4 - 292)

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

isoaspartyl peptidase/L-asparaginase

L-asparaginase

关联疾病

疾病名称 别名
Immunodeficiency 48

Combined Immunodeficiency Due To Zap70 Deficiency

IMD48

Selective T-Cell Defect

Stcd

Zeta-Associated-Protein 70 Deficiency

Severe Combined Immunodeficiency, Atypical

Immunodeficiency, Type 48

Zap70 Deficiency
Aspartylglucosaminuria

Aspartylglycosaminuria

Glycosylasparaginase Deficiency

Aspartylglucosaminidase Deficiency

Aga Deficiency

AGU

Aspartylglucosamidase Deficiency

Glycoasparaginase

Aspartylglucosamidase Deficiency

Hyperammonemia, Type Iii
Corneal Dystrophy, Meesmann, 1

Meesmann Corneal Dystrophy

Mecd

Corneal Dystrophy, Meesmann Epithelial

Juvenile Hereditary Epithelial Dystrophy

Corneal Dystrophy, Juvenile Epithelial Of Meesmann

MECD1

Meesmann Corneal Dystrophy 1

Meesmann Corneal Epithelial Dystrophy

Meesmann Epithelial Corneal Dystrophy

Corneal Dystrophy, Juvenile Epithelial, Of Meesmann

Stocker-Holt Dystrophy

Meesman Dystrophy

Meesman'S Corneal Dystrophy

Juvenile Hereditary Epithelial Dystrophy Of Meesmann

Corneal Dystrophy, Meesmann 1

Juvenile Epithelial Corneal Dystrophy Of Meesmann

Mcd

Dystrophy, Corneal, Meesmann
Normal Pressure Hydrocephalus

Low Pressure Hydrocephalus

Hydrocephalus Normal Pressure

Hydrocephalus, Normal Pressure

Normal Pressure Hydrocephalus Nos

Nph - [Normal Pressure Hydrocephalus]

Normal Pressure Hydrocephaly
Retinal Degeneration

Degeneration Of Retina
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 (3)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS01108 ASRGL1 Human Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS21095 Asrgl1 Mouse Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS27613 Asrgl1 Rat Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta ASRGL1 VGNC VGNC:70081
Bos taurus ASRGL1 VGNC VGNC:26223
Mus musculus ASRGL1 MGD MGI:1913764
Canis familiaris ASRGL1 VGNC VGNC:38192
Felis catus ASRGL1 VGNC VGNC:59980
Rattus norvegicus ASRGL1 RGD RGD:708526
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