1. Gene
  2. RCN3 - reticulocalbin 3 Gene

RCN3 - reticulocalbin 3 Gene

Homo sapiens

Also known as RLP49

Gene ID: 57333 | Gene type: protein coding

About RCN3

Cytogenetic location: 19q13.33 Genomic coordinates (GRCh38): 19:49,528,003-49,543,633 (from NCBI)

This gene has 5 transcripts (splice variants), 105 orthologues and 4 paralogues. Ubiquitous expression in fat (RPKM 12.8), placenta (RPKM 11.9) and 24 other tissues.

Summary

Enables calcium ion binding activity. Involved in several processes, including collagen biosynthetic process; positive regulation of peptidase activity; and regulation of protein kinase B signaling. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Apr 2022]

RCN3 Products(1)

mRNA Protein Name
NM_020650.3 NP_065701.2 reticulocalbin-3 precursor

RCN3 Protein Structure

EF-hand_7

EF-hand_7: EF-hand domain pair (80 - 141)

EF-hand_5

EF-hand_5: EF hand (207 - 226)

EF-hand_8

EF-hand_8: EF-hand domain pair (281 - 302)

  • 0
  • 100
  • 200
  • 300
  • 328 a.a.
Protein Preferred Names Protein Names

reticulocalbin-3

EF-hand calcium-binding protein RLP49

Recombinant RCN3 Proteins

Cat. No. Product Name Accession Purity
HY-P71253 RCN3 Protein, Human (HEK293, His) Q96D15 (K21-L328) ≥95%

Related Diseases

Diseases Alias
Myopathy, Distal, 3

MPD3

Distal Muscular Dystrophy 3

Distal Myopathy Type 3

Myopathy, Distal 3

Distal Myopathy 3

Finnish Upper Limb-Onset Distal Myopathy

Neonatal Respiratory Failure

Respiratory Failure Of Newborn

Inadequate Pulmonary Ventilation Of Newborn

Newborn Lung Insufficiency

Newborn Pulmonary Function Inadequate

Newborn Pulmonary Insufficiency

Newborn Respiration Failure

Newborn Respiratory Insufficiency

Respiratory Insufficiency Syndrome Of Newborn

Enchondromatosis, Multiple, Ollier Type

Ollier Disease

Enchondromatosis

Dyschondroplasia

Osteochondromatosis

Multiple Cartilaginous Enchondroses

Multiple Enchondromatosis

Enchondromatosis With Haemangiomata

Enchondromatosis, Multiple

Kast'S Syndrome

Ollier'S Syndrome

Enchondromatosis Multiple

ENCHOM

Maffucci Disease

Olliers Disease

Hereditary Multiple Exostoses

Chondromatosis

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

Orthologs Information

Species Symbol Source ID
Bos taurus RCN3 VGNC VGNC:33833
Canis familiaris RCN3 VGNC VGNC:45445
Mus musculus RCN3 MGD MGI:1277122
Rattus norvegicus RCN3 RGD RGD:1359365
Others RCN3 NCBI