2. Gene
  3. SCRN3 - secernin 3 Gene

SCRN3 - secernin 3 Gene

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

中文名称：切尔宁 3

种属: Homo sapiens

同用名: SES3

基因 ID: 79634 | 基因类型: protein coding

关于 SCRN3

Cytogenetic location: 2q31.1 Genomic coordinates (GRCh38): 2:174,395,730-174,429,575 (from NCBI)

This gene has 14 transcripts (splice variants), 203 orthologues and 2 paralogues. Ubiquitous expression in brain (RPKM 6.9), thyroid (RPKM 5.5) and 25 other tissues.

功能概要

预测启用半胱氨酸型外肽酶活性和二肽酶活性。预计参与蛋白水解。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable cysteine-type exopeptidase activity and dipeptidase activity. Predicted to be involved in proteolysis. [provided by Alliance of Genome Resources, Apr 2022]

SCRN3 基因产物(12)

mRNA Protein Name
NM_001193528.2 NP_001180457.1 secernin-3 isoform 2
NM_001412202.1 NP_001399131.1 secernin-3 isoform 1
NM_001412203.1 NP_001399132.1 secernin-3 isoform 1
NM_001412204.1 NP_001399133.1 secernin-3 isoform 1
NM_001412205.1 NP_001399134.1 secernin-3 isoform 1
NM_001412206.1 NP_001399135.1 secernin-3 isoform 1
NM_001412207.1 NP_001399136.1 secernin-3 isoform 1
NM_001412208.1 NP_001399137.1 secernin-3 isoform 1
NM_001412209.1 NP_001399138.1 secernin-3 isoform 3
NM_001412210.1 NP_001399139.1 secernin-3 isoform 4
NM_001412212.1 NP_001399141.1 secernin-3 isoform 5
NM_024583.5 NP_078859.2 secernin-3 isoform 1

SCRN3 蛋白结构

Peptidase_C69

Peptidase_C69: Peptidase family C69 (81 - 251)

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

secernin-3

关联疾病

疾病名称 别名
Acrodysostosis

Acrodysplasia

Arkless-Graham Syndrome

Maroteaux-Malamut Syndrome

Nasal Hypoplasia-Peripheral Dysostosis-Intellectual Disability Syndrome

Peripheral Dysostosis-Nasal Hypoplasia-Intellectual Disability Syndrome
Ebstein Anomaly

Ebstein'S Anomaly

Ebstein'S Anomaly Of Common Atrioventricular Valve

Ebstein'S Anomaly Of Right Atrioventricular Valve

Ebstein'S Anomaly Of Tricuspid Valve

Ebstein'S Malformation

Ebstein Malformation Of The Tricuspid Valve

Ebstein Anomaly Of The Tricuspid Valve

Ebstein Disease

Accessory Tricuspid Valve Tissue

Congenital Ebstein Deformity Of Tricuspid Valve

Ebstein Syndrome

Ebstein Cardiopathy

Ebstein Anomaly Of Tricuspid Valve
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

Approval
生物活性分子 (1)
目录号 产品名 作用方式
纯度 是否罕见病
HY-B1018A Phenelzine sulfate Inhibitor 99.96% 否
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-RS12564 SCRN3 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 SCRN3 MGD MGI:1921866
Rattus norvegicus SCRN3 RGD RGD:1305064
Canis familiaris SCRN3 VGNC VGNC:45933
Bos taurus SCRN3 VGNC VGNC:34368
Macaca mulatta SCRN3 VGNC VGNC:77134
Felis catus SCRN3 VGNC VGNC:80352
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