RBM27 - RNA binding motif protein 27 Gene

Homo sapiens

Also known as Psc1; ARRS1; ZC3H18; ZC3H20

Gene ID: 54439 | Gene type: protein coding

About RBM27

Cytogenetic location: 5q32 Genomic coordinates (GRCh38): 5:146,203,605-146,289,223 (from NCBI)

This gene has 2 transcripts (splice variants), 206 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 10.3), bone marrow (RPKM 8.5) and 25 other tissues.

Summary

Enables RNA binding activity. Predicted to be involved in mRNA processing. Predicted to be located in cytoplasm and nuclear speck. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

RBM27 Products(1)

mRNA	Protein	Name
NM_018989.2	NP_061862.1	RNA-binding protein 27

RBM27 Protein Structure

PWI

zf-CCCH

RRM_5

0
200
400
600
800
1000
1060 a.a.

Protein Preferred Names

Protein Names

RNA-binding protein 27

acidic rich RS domain containing 1

Related Diseases

Diseases

Alias

Osteogenesis Imperfecta, Type Xv

Osteogenesis Imperfecta Type 15	OI15
Osteogenesis Imperfecta Type Xv	Oi, Type Xv
Osteogenesis Imperfecta 15	Oi Type Xv
Oi-Xv

Brachydactyly, Type B1

Brachydactyly Type B1	Brachydactyly Type B
BDB1	Brachydactyly, Type B
Bdb	Brachydactyly B1

Osteopetrosis, Autosomal Dominant 1

OPTA1	Autosomal Dominant Osteopetrosis 1
Autosomal Dominant Osteopetrosis Type 1	Osteopetrosis Autosomal Dominant Type 1
Osteopetrosis, Autosomal Dominant, Type I	Osteopetrosis, Autosomal Dominant, Type 1

Robinow Syndrome, Autosomal Recessive 1

Robinow Syndrome, Autosomal Recessive	Autosomal Recessive Robinow Syndrome
Covesdem Syndrome	RRS1
Costovertebral Segmentation Defect-Mesomelia Syndrome	Rrs
Costovertebral Segmentation Defect With Mesomelia, Formerly	Covesdem Syndrome, Formerly
Costovertebral Segmentation Defect With Mesomelia	Robinow Syndrome Autosomal Recessive With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals
Robinow Syndrome Autosomal Recessive With Brachy-Syn-Polydactyly	Robinow Syndrome, Autosomal Recessive, With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals
Robinow Syndrome, Autosomal Recessive, With Brachy-Syn-Polydactyly	Robinow, Autosomal Recessive Syndrome, Type 1

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-RS11745	RBM27 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	RBM27	RGD	RGD:1311966
Mus musculus	RBM27	MGD	MGI:2147194

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