SCRN3 - secernin 3 Gene

Also Known as SES3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79634

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)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 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

  • Approval
  • Pre-clinical Phase

Approval

Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-B1018A Phenelzine sulfate Inhibitor 99.96% Unkown

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 Set / 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
Others SCRN3 NCBI