SCARA5 - scavenger receptor class A member 5 Gene

Homo sapiens

Also known as Tesr; NET33

Gene ID: 286133 | Gene type: protein coding

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

SRCR

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)

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS12487	SCARA5 Human Pre-designed siRNA Set A		/	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

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