ACP6 - acid phosphatase 6, lysophosphatidic Gene

Homo sapiens

Also known as LPAP; ACPL1; PACPL1

Gene ID: 51205 | Gene type: protein coding

About ACP6

Cytogenetic location: 1q21.2 Genomic coordinates (GRCh38): 1:147,629,658-147,670,524 (from NCBI)

This gene has 10 transcripts (splice variants), 220 orthologues and 5 paralogues. Ubiquitous expression in thyroid (RPKM 3.4), prostate (RPKM 3.3) and 25 other tissues.

Summary

This gene encodes a member of the histidine Acid Phosphatase protein family. The encoded protein hydrolyzes lysophosphatidic acid, which is involved in G protein-coupled receptor signaling, lipid raft modulation, and in balancing lipid composition within the cell. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2016]

ACP6 Products(2)

mRNA	Protein	Name
NM_001323625.2	NP_001310554.1	lysophosphatidic acid phosphatase type 6 isoform 2
NM_016361.5	NP_057445.4	lysophosphatidic acid phosphatase type 6 isoform 1

ACP6 Protein Structure

His_Phos_2

0
100
200
300
400
428 a.a.

Protein Preferred Names

Protein Names

lysophosphatidic acid phosphatase type 6

acid phosphatase-like protein 1

Recombinant ACP6 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P79288	ACP6 Protein, Human (CHO, His)	BAA91310 (E33-E428)	≥95%

Related Diseases

Diseases

Alias

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

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

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS00191	ACP6 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Felis catus	ACP6	VGNC	VGNC:59527
Mus musculus	ACP6	MGD	MGI:1931010
Bos taurus	ACP6	VGNC	VGNC:52602
Rattus norvegicus	ACP6	RGD	RGD:1306336
Macaca mulatta	ACP6	VGNC	VGNC:69548
Canis familiaris	ACP6	VGNC	VGNC:54914