1. Gene
  2. GPR89A - G protein-coupled receptor 89A Gene

GPR89A - G protein-coupled receptor 89A Gene

Homo sapiens

Also known as GPHR; GPR89; SH120; GPR89B; UNQ192

Gene ID: 653519 | Gene type: protein coding

About GPR89A

Cytogenetic location: 1q21.1 Genomic coordinates (GRCh38): 1:145,607,988-145,670,650 (from NCBI)

This gene has 13 transcripts (splice variants), 201 orthologues and 1 paralogue. Ubiquitous expression in kidney (RPKM 15.4), testis (RPKM 12.4) and 25 other tissues.

Summary

GPR89A is a nearly identical copy of the GPR89B gene (MIM 612806).[supplied by OMIM, Jun 2009]

GPR89A Products(2)

mRNA Protein Name
NM_001097612.2 NP_001091081.1 Golgi pH regulator A isoform 1
NM_001097613.3 NP_001091082.2 Golgi pH regulator A isoform 2

GPR89A Protein Structure

GPHR_N

GPHR_N: The Golgi pH Regulator (GPHR) Family N-terminal (138 - 207)

ABA_GPCR

ABA_GPCR: Abscisic acid G-protein coupled receptor (273 - 447)

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  • 455 a.a.
Protein Preferred Names Protein Names

Golgi pH regulator A

protein GPR89

Related Diseases

Diseases Alias
Hemochromatosis, Type 2a

Hemochromatosis Type 2a

HFE2A

Juvenile Hemochromatosis

Hemochromatosis 2a

Hefe2

Hemochromatosis Type 2

Jh

Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb

Chromosome 1q21.1 Deletion Syndrome

1q21.1 Microdeletion Syndrome

Monosomy 1q21.1

1q21.1 Microdeletion

Chromosome 1q21.1 Microdeletion Syndrome

1q21.1 Contiguous Gene Deletion

1q21.1 Deletion

Del(1)(Q21)

1q21.1 Deletion Syndrome

Thrombocytopenia-Absent Radius Syndrome

Tar Syndrome

Radial Aplasia-Thrombocytopenia Syndrome

Absent Radii And Thrombocytopenia

TAR

Chromosome 1q21.1 Deletion Syndrome, 200-Kb

Thrombocytopenia Absent Radius Syndrome

Thrombocytopenia Absent Radii

Chromosome 1q21.1 Deletion Syndrome

Thrombocytopenia With Absent Radii Syndrome

Radial Aplasia-Amegakaryocytic Thrombocytopenia

Duodenal Atresia

Duodenal Stenosis

Familial Duodenal Atresia

Chromosome 1p36 Deletion Syndrome

1p36 Deletion Syndrome

Deletion 1p36

Monosomy 1p36

Subtelomeric 1p36 Deletion

Monosomy 1p36 Syndrome

Distal Monosomy 1p36

Del(1)(P36)

Deletion 1pter

Monosomy 1pter

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
Mus musculus GPR89A MGD MGI:1914799