2. Gene
  3. AGBL2 - AGBL carboxypeptidase 2 Gene

AGBL2 - AGBL carboxypeptidase 2 Gene

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

中文名称：AGBL 羧肽酶 2

种属: Homo sapiens

同用名: CCP2

基因 ID: 79841 | 基因类型: protein coding

关于 AGBL2

Cytogenetic location: 11p11.2 Genomic coordinates (GRCh38): 11:47,659,591-47,715,369 (from NCBI)

This gene has 13 transcripts (splice variants), 1 gene allele, 191 orthologues and 5 paralogues. Biased expression in testis (RPKM 8.5), lung (RPKM 1.3) and 7 other tissues.

功能概要

预测可启用金属羧肽酶活性。预测参与蛋白质侧链脱谷氨酰化。位于中心粒和睫状基体。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable metallocarboxypeptidase activity. Predicted to be involved in protein side chain deglutamylation. Located in centriole and ciliary basal body. [provided by Alliance of Genome Resources, Apr 2022]

AGBL2 基因产物(1)

mRNA Protein Name
NM_024783.4 NP_079059.2 cytosolic carboxypeptidase 2
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
21303978 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in centriole IDA
IDA: 通过直接分析推断
23085998 GOA
located in ciliary basal body IDA
IDA: 通过直接分析推断
23085998 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

AGBL2 蛋白结构

Peptidase_M14

Peptidase_M14: Zinc carboxypeptidase (417 - 636)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 902 a.a.
蛋白主名 其他名称

cytosolic carboxypeptidase 2

ATP/GTP binding protein like 2

关联疾病

疾病名称 别名
Palindromic Rheumatism

Hench'S Syndrome

Hench-Rosenberg Syndrome

Palindromic Rheumatism Syndrome

Palindromic Arthritis
Tenosynovitis

Inflammation Of Tendon Sheath

Synovitis Or Tenosynovitis
Periarthritis
3mc Syndrome

Craniofacial-Ulnar-Renal Syndrome

Malpuech Facial Clefting Syndrome

Oculopalatoskeletal Syndrome

Carnevale Syndrome

Michels Syndrome

Malpuech-Michels-Mingarelli-Carnevale Syndrome

Carnevale-Krajewska-Fischetto Syndrome

Craniosynostosis With Lid Anomalies

Malpuech Syndrome

Mingarelli Syndrome

Oculo-Skeletal-Abdominal Syndrome

Osa Syndrome

Ptosis Of Eyelids With Diastasis Recti And Hip Dysplasia

Ptosis-Strabismus-Rectus Abdominis Diastasis
Crest Syndrome
Hemolytic Uremic Syndrome, Atypical 1

Atypical Hemolytic-Uremic Syndrome

Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 1

Atypical Hemolytic Uremic Syndrome

Hemolytic Uremic Syndrome, Atypical, Susceptibility To

Ahus

AHUS1

Hemolytic-Uremic Syndrome

Ahus 1

Ahus, Susceptibility To, 1

Hemolytic Uremic Syndrome, Atypical

Non-Shiga-Like Toxin-Associated Hus

Non-Stx-Hus

Nonenteropathic Hus

Atypical Hus

Shiga Toxin-Associated Hemolytic Uremic Syndrome

D+ Hus

Ehec-Hus

Hemolytic Uremic Syndrome Associated With Shiga Toxin-Producing Escherichia Coli

Hemolytic Uremic Syndrome With Diarrhea

Stec-Hus

Shiga-Like Toxin-Associated Hus

Stx-Hus

Typical Hus

Typical Hemolytic Uremic Syndrome

Atypical Hemolytic Uremic Syndrome With Anti-Factor H Antibodies

Atypical Hus With Anti-Factor H Antibodies

Ahus With Anti-Factor H Antibodies

Ahus With Neutralizing Autoantibodies Against Factor H

Hemolytic Uremic Syndrome Atypical 1

Atypical Hemolytic Uremic Syndrome With H Factor Anomaly

D Hus

Hemolytic-Uremic Syndrome Without Diarrhea

Hemolytic-Uremic Syndrome, Atypical, Type 1

Hemolytic Uremic Syndrome, Typical
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-RS00441 AGBL2 Human 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 AGBL2 VGNC VGNC:99539
Mus musculus AGBL2 MGD MGI:2443254
Bos taurus AGBL2 VGNC VGNC:106635
Felis catus AGBL2 VGNC VGNC:59677
Canis familiaris AGBL2 VGNC VGNC:37696
Rattus norvegicus AGBL2 RGD RGD:1306827
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