GPAA1 - glycosylphosphatidylinositol anchor attachment 1 Gene

Also Known as GAA1; hGAA1; GPIBD15

生物種: Homo sapiens

遺伝子タイプ: protein coding

遺伝子ID: 8733

About GPAA1

Cytogenetic location: 8q24.3 Genomic coordinates (GRCh38): 8:144,082,634-144,086,216 (from NCBI)

This gene has 72 transcripts (splice variants), 195 orthologues and is associated with 3 phenotypes. Ubiquitous expression in kidney (RPKM 27.5), thyroid (RPKM 25.6) and 25 other tissues.

Summary

Posttranslational glycosylphosphatidylinositol (GPI) anchor attachment serves as a general mechanism for linking proteins to the cell surface membrane. The protein encoded by this gene presumably functions in GPI anchoring at the GPI transfer step. The mRNA transcript is ubiquitously expressed in both fetal and adult tissues. The anchor attachment protein 1 contains an N-terminal signal sequence, 1 cAMP- and cGMP-dependent protein kinase phosphorylation site, 1 leucine zipper pattern, 2 potential N-glycosylation sites, and 8 putative transmembrane domains. [provided by RefSeq, Jul 2008]

GPAA1 Products (1)

mRNA	Protein	Name
NM_003801.4	NP_003792.1	glycosylphosphatidylinositol anchor attachment 1 protein

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	参考文献	由来
contributes to GPI anchor binding	IMP IMP: Inferred from mutant phenotype	14660601	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	10793132	GOA

Biological Process GO Annotation	Evidence	参考文献	由来
involved in protein-containing complex assembly	IMP IMP: Inferred from mutant phenotype	14660601	GOA

Cellular Component GO Annotation	Evidence	参考文献	由来
part of GPI-anchor transamidase complex	IDA IDA: Inferred from direct assay	11483512	GOA
part of GPI-anchor transamidase complex	IPI IPI: Inferred from physical interaction	12802054	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

GPAA1 Protein Structure

Gaa1

0
100
200
300
400
500
621 a.a.

Protein Preferred Names	Protein Names
glycosylphosphatidylinositol anchor attachment 1 protein	GAA1 protein homolog

GPAA1 Protein-protein interaction Information

Type	タンパク質名	Protein ID	Interactor	Interactor Species	Interactor ID	Detection Method	参考文献
Intra	GPAA1	O43292	PIGT	Homo sapiens	Q969N2	TAP	11483512
Intra	GPAA1	O43292	PIGT	Homo sapiens	Q969N2	Anti Tag CoIP	11483512
Intra	GPAA1	O43292	PIGT	Homo sapiens	Q969N2	Anti Tag CoIP	33961781
Intra	GPAA1	O43292	PIGT	Homo sapiens	Q969N2	Anti Tag CoIP	28514442
Intra	GPAA1	O43292	PIGK	Homo sapiens	Q92643	TAP	11483512
Intra	GPAA1	O43292	PIGK	Homo sapiens	Q92643	Anti Tag CoIP	11483512

Cross: Cross-species interaction Intra: Intraspecies interaction

関連疾患

Diseases	Alias
Glycosylphosphatidylinositol Biosynthesis Defect 15	GPIBD15 Developmental Delay, Epilepsy, Cerebellar Atrophy, And Osteopenia Neurodevelopmental Delay-Seizures-Ophthalmic Anomalies-Osteopenia-Cerebellar Atrophy Syndrome Gpaa1-Related Biosynthesis Defect Glycosylphosphatidylinositol Biosynthesis Defect, Type 15
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3	MCAHS3 Glycosylphosphatidylinositol Biosynthesis Defect 7 Gpibd7 Intellectual Disability-Seizures-Hypophosphatasia-Ophthalmic-Skeletal Anomalies Syndrome Congenital Disorder Of Glycosylation Due To Pigt Deficiency Mcahs Type 3 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Type 3 Pigt-Cdg Multiple Congenital Anomalies, Hypotonia, Seizures Syndrome, Type 3
Autosomal Recessive Cerebellar Ataxia	Arca
Hereditary Ataxia	Sca Spinocerebellar Ataxia Ataxias Hereditary Ataxias, Hereditary
Cerebellar Disease	Cerebellar Diseases Cerebellar Dysfunction Cerebellar Abnormality Cerebellar Disorders
Early Infantile Epileptic Encephalopathy	Early Infantile Epileptic Encephalopathy With Burst-Suppression Early Infantile Epileptic Encephalopathy With Suppression Bursts Eiee Early Infantile Epileptic Encephalopathy With Suppression-Bursts Ohtahara Syndrome Encephalopathy, Epileptic, Early Infantile

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

Pre-clinical Phase

Bioactive Molecules (1)

製品番号	製品名	製品効果	純度	Rare Diseases
HY-RS05614	GPAA1 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

生物種	Symbol	由来	ID
Rattus norvegicus	GPAA1	RGD	RGD:1303197
Bos taurus	GPAA1	VGNC	VGNC:29508
Felis catus	GPAA1	VGNC	VGNC:67401
Macaca mulatta	GPAA1	VGNC	VGNC:73116
Canis familiaris	GPAA1	VGNC	VGNC:41358
Mus musculus	GPAA1	MGD	MGI:1202392
Others	GPAA1	NCBI