GUCY1B1 - guanylate cyclase 1 soluble subunit beta 1 Gene

Homo sapiens

Also known as GUCB3; GC-SB3; GUC1B3; GUCSB3; GUCY1B3; GC-S-beta-1

Gene ID: 2983 | Gene type: protein coding

About GUCY1B1

Cytogenetic location: 4q32.1 Genomic coordinates (GRCh38): 4:155,759,021-155,807,811 (from NCBI)

This gene has 8 transcripts (splice variants), 211 orthologues and 17 paralogues. Broad expression in brain (RPKM 21.9), placenta (RPKM 13.8) and 21 other tissues.

Summary

This gene encodes the beta subunit of the soluble Guanylate Cyclase (sGC), which catalyzes the conversion of GTP (guanosine triphosphate) to cGMP (cyclic guanosine monophosphate). The encoded protein contains an HNOX domain, which serves as a receptor for ligands such as nitric oxide, oxygen and nitrovasodilator drugs. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]

GUCY1B1 Products(6)

mRNA	Protein	Name
NM_000857.5	NP_000848.1	guanylate cyclase soluble subunit beta-1 isoform 2
NM_001291951.3	NP_001278880.1	guanylate cyclase soluble subunit beta-1 isoform 1
NM_001291952.3	NP_001278881.1	guanylate cyclase soluble subunit beta-1 isoform 3
NM_001291953.3	NP_001278882.1	guanylate cyclase soluble subunit beta-1 isoform 4
NM_001291954.3	NP_001278883.1	guanylate cyclase soluble subunit beta-1 isoform 5
NM_001291955.3	NP_001278884.1	guanylate cyclase soluble subunit beta-1 isoform 6

GUCY1B1 Protein Structure

HNOB

HNOBA

Guanylate_cyc

0
100
200
300
400
500
619 a.a.

Protein Preferred Names

Protein Names

guanylate cyclase soluble subunit beta-1

GCS-beta-1

Related Diseases

Diseases

Alias

Nemaline Myopathy 7

NEM7	Nemaline Myopathy 7, Autosomal Recessive
Cfl2-Related Nemaline Myopathy	Myopathy, Nemaline, Type 7

Bartter Syndrome, Type 2, Antenatal

Bartter Disease Type 2	BARTS2
Hyperprostaglandin E Syndrome 2	Bartter Syndrome, Type 2
Bartter Syndrome Type 2	Hypokalemic Alkalosis With Hypercalciuria Antenatal 2
Hypokalemic Alkalosis With Hypercalciuria 2, Antenatal	Bartter Syndrome Type 2 Antenatal
Hypokalemic Alkalosis With Hypercalciuria 2 Antenatal	Bartter Syndrome Antenatal Type 2
Bartter Syndrome Type Ii	Bartter Syndrome 2, Antenatal
Abs2	Antenatal Bartter Syndrome 2
Bartter Syndrome 2	Bs2
Hyperprostanglandin E Syndrome 2	Bartter Syndrome, Antenatal , Type 2
Antley-Bixler Syndrome, Autosomal Dominant

Moyamoya Disease 1

Moyamoya Disease	Spontaneous Occlusion Of The Circle Of Willis
Mymy	Progressive Intracranial Arterial Occlusion
Moyamoya Syndrome	MYMY1
Cerebrovascular Moyamoya Disease	Moya-Moya Disease
Progressive Intracranial Occlusive Arteropathy	Idiopathic Moyamoya Disease

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-RS05920	GUCY1B1 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	GUCY1B1	VGNC	VGNC:29721
Macaca mulatta	GUCY1B1	VGNC	VGNC:73328
Rattus norvegicus	GUCY1B1	RGD	RGD:2769
Mus musculus	GUCY1B1	MGD	MGI:1860604
Canis familiaris	GUCY1B1	VGNC	VGNC:41568
Felis catus	GUCY1B1	VGNC	VGNC:67515

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