1. Gene
  2. GUCY1A1 - guanylate cyclase 1 soluble subunit alpha 1 Gene

GUCY1A1 - guanylate cyclase 1 soluble subunit alpha 1 Gene

Homo sapiens

Also known as GUCA3; MYMY6; GC-SA3; GUC1A3; GUCSA3; GUCY1A3; GCS-alpha-3; GC-S-alpha-1

Gene ID: 2982 | Gene type: protein coding

About GUCY1A1

Cytogenetic location: 4q32.1 Genomic coordinates (GRCh38): 4:155,666,848-155,737,059 (from NCBI)

This gene has 13 transcripts (splice variants), 203 orthologues, 17 paralogues and is associated with 2 phenotypes. Ubiquitous expression in prostate (RPKM 11.3), heart (RPKM 8.5) and 24 other tissues.

Summary

Soluble guanylate cyclases are heterodimeric proteins that catalyze the conversion of GTP to 3',5'-cyclic GMP and pyrophosphate. The protein encoded by this gene is an alpha subunit of this complex and it interacts with a beta subunit to form the Guanylate Cyclase enzyme, which is activated by nitric oxide. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]

GUCY1A1 Products(18)

mRNA Protein Name
NM_000856.6 NP_000847.2 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001130682.3 NP_001124154.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001130683.4 NP_001124155.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001130684.3 NP_001124156.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001130685.3 NP_001124157.1 guanylate cyclase soluble subunit alpha-1 isoform B
NM_001130687.3 NP_001124159.1 guanylate cyclase soluble subunit alpha-1 isoform D
NM_001256449.2 NP_001243378.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379666.1 NP_001366595.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379667.1 NP_001366596.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379668.1 NP_001366597.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379669.1 NP_001366598.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379670.1 NP_001366599.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379671.1 NP_001366600.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379672.1 NP_001366601.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379673.1 NP_001366602.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379674.1 NP_001366603.1 guanylate cyclase soluble subunit alpha-1 isoform A
NM_001379675.1 NP_001366604.1 guanylate cyclase soluble subunit alpha-1 isoform E
NM_001379676.1 NP_001366605.1 guanylate cyclase soluble subunit alpha-1 isoform F

GUCY1A1 Protein Structure

HNOB

HNOB: Haem-NO-binding (90 - 234)

HNOBA

HNOBA: Heme NO binding associated (273 - 466)

Guanylate_cyc

Guanylate_cyc: Adenylate and Guanylate cyclase catalytic domain (472 - 643)

  • 0
  • 200
  • 400
  • 600
  • 690 a.a.
Protein Preferred Names Protein Names

guanylate cyclase soluble subunit alpha-1

guanylate cyclase 1, soluble, alpha 3

Related Diseases

Diseases Alias
Moyamoya Disease 6 With Or Without Achalasia

Moyamoya Disease With Early-Onset Achalasia

MYMY6

Moyamoya 6 With Achalasia

Moyamoya, With Achalasia, Type 6

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

Myocardial Infarction

Heart Attack

Myocardial Infarction, Susceptibility To

Myocardial Infarction 1

Myocardial Infarction, Protection Against

Myocardial Infarction, Decreased Susceptibility To

Myocardial Infarction, Decreased

Myocardial Infarct

MCI1

Premature Myocardial Infarction

Myocardial Infarction, Susceptibility To, Type 1

Achalasia

Cardiospasm

Achalasia Of Cardia

Esophageal Achalasia

Hypertensive Lower Esophageal Sphincter

Idiopathic Achalasia

Achalasia Cardia

Idiopathic Achalasia Of Esophagus

Primary Achalasia

Achalasia Of Esophagus

Lack Of Reflex Relaxation Of Lower Oesophageal Sphincter

Aperistalsis Of The Oesophagus

Achalasia Of Oesophagus

Oesophageal Achalasia

Achalasia Nos

Cardia Spasm

Cardia Achalasia

Oesophageal Cardiospasm

Oesophagus Achalasia

Reflex Cardiospasm

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

Hemiplegia

Infantile Hemiplegia

Postnatal Infantile Hemiplegia

Hemiplegia, Infantile

Cerebral Arterial Disease

Cerebral Arterial Diseases

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
Felis catus GUCY1A1 VGNC VGNC:67514
Rattus norvegicus GUCY1A1 RGD RGD:68436
Macaca mulatta GUCY1A1 VGNC VGNC:73327
Mus musculus GUCY1A1 MGD MGI:1926562
Bos taurus GUCY1A1 VGNC VGNC:29720
Canis familiaris GUCY1A1 VGNC VGNC:41567