2. Gene
  3. SCRN3 - secernin 3 Gene

SCRN3 - secernin 3 Gene

  • Gene
  • Protein
  • Disease
  • Agent
  • Ortholog
Homo sapiens

Also known as SES3

Gene ID: 79634 | Gene type: protein coding

About 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.

Summary

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 Products(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 Protein Structure

Peptidase_C69

Peptidase_C69: Peptidase family C69 (81 - 251)

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  • 424 a.a.
Protein Preferred Names Protein Names

secernin-3

Related Diseases

Diseases Alias
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
Diseases Alias
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

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS12564 SCRN3 Human Pre-designed siRNA Set A Pre-designed Sets / Unkown

Orthologs Information

Species Symbol Source 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