SCARA5 - scavenger receptor class A member 5 Gene

Also Known as Tesr; NET33

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 286133

About SCARA5

Cytogenetic location: 8p21.1 Genomic coordinates (GRCh38): 8:27,869,883-27,992,673 (from NCBI)

This gene has 4 transcripts (splice variants), 188 orthologues and 3 paralogues. Broad expression in fat (RPKM 25.7), colon (RPKM 18.6) and 19 other tissues.

Summary

Predicted to enable ferritin receptor activity. Predicted to be involved in several processes, including cellular iron ion homeostasis; iron ion transmembrane transport; and protein homotrimerization. Predicted to act upstream of or within cellular response to heat. Predicted to be located in cell surface. Predicted to be integral component of plasma membrane. Predicted to be active in external side of plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

SCARA5 Products (4)

mRNA Protein Name
NM_001413201.1 NP_001400130.1 scavenger receptor class A member 5 isoform 2
NM_001413202.1 NP_001400131.1 scavenger receptor class A member 5 isoform 3
NM_001413203.1 NP_001400132.1 scavenger receptor class A member 5 isoform 4
NM_173833.6 NP_776194.2 scavenger receptor class A member 5 isoform 1

SCARA5 Protein Structure

Collagen

Collagen: Collagen triple helix repeat (20 copies) (305 - 357)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (327 - 379)

SRCR

SRCR: Scavenger receptor cysteine-rich domain (396 - 493)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 495 a.a.
Protein Preferred Names Protein Names

scavenger receptor class A member 5

  • scavenger receptor class A, member 5 (putative)

SCARA5 Antibodies

Cat. No. Product Name Application Reactivity
HY-P811334 SCARA5 Antibody WB, IHC-P Human, Mouse

Related Diseases

Diseases Alias
Prostate Leiomyosarcoma

  • Leiomyosarcoma Of The Prostate
Prostate Stromal Sarcoma

  • Stromal Sarcoma Of The Prostate
Facial Hemiatrophy

  • Parry-Romberg Syndrome
Hemochromatosis, Type 1

  • Hemochromatosis

  • Hemochromatosis Type 1

  • Hereditary Hemochromatosis

  • Hh

  • HFE1

  • Hfe Hemochromatosis, Modifier Of

  • Symptomatic Form Of Classic Hemochromatosis

  • Symptomatic Form Of Hemochromatosis Type 1

  • Symptomatic Form Of Hfe-Related Hereditary Hemochromatosis

  • Haemochromatosis

  • Iron Storage Disorder

  • Bronze Diabetes

  • Hereditary Haemochromatosis

  • Hlah

  • Hfe

  • Hemochromatosis, Hereditary

  • Diabetes Bronze

  • Classic Hemochromatosis

  • Hfe-Associated Hereditary Hemochromatosis

  • Hemochromatosis Classic

  • Bronzed Cirrhosis

  • Familial Hemochromatosis

  • Genetic Hemochromatosis

  • Hc

  • Pigmentary Cirrhosis

  • Primary Hemochromatosis

  • Troisier-Hanot-Chauffard Syndrome

  • Von Recklenhausen-Applebaum Disease

  • Hemochromatosis 1

  • Primary Hereditary Hemochromatosis

  • Bronze Cirrhosis
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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS12487 SCARA5 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus SCARA5 MGD MGI:1918395
Macaca mulatta SCARA5 VGNC VGNC:77117
Bos taurus SCARA5 VGNC VGNC:34323
Canis familiaris SCARA5 VGNC VGNC:45897
Rattus norvegicus SCARA5 RGD RGD:1306539
Felis catus SCARA5 VGNC VGNC:64900
Others SCARA5 NCBI