PDZD11 - PDZ domain containing 11 Gene

Homo sapiens

Also known as PISP; AIPP1; PDZK11

Gene ID: 51248 | Gene type: protein coding

About PDZD11

Cytogenetic location: Xq13.1 Genomic coordinates (GRCh38): X:70,286,595-70,289,927 (from NCBI)

This gene has 6 transcripts (splice variants), 215 orthologues and 3 paralogues. Ubiquitous expression in brain (RPKM 12.6), thyroid (RPKM 10.9) and 25 other tissues.

Summary

Enables protein C-terminus binding activity. Involved in pore complex assembly. Located in basolateral plasma membrane and cytosol. Part of pore complex. [provided by Alliance of Genome Resources, Apr 2022]

PDZD11 Products(6)

mRNA	Protein	Name
NM_001370174.1	NP_001357103.1	PDZ domain-containing protein 11 isoform 1
NM_001370175.1	NP_001357104.1	PDZ domain-containing protein 11 isoform 1
NM_001370176.1	NP_001357105.1	PDZ domain-containing protein 11 isoform 1
NM_001370177.1	NP_001357106.1	PDZ domain-containing protein 11 isoform 1
NM_001370178.1	NP_001357107.1	PDZ domain-containing protein 11 isoform 2
NM_016484.5	NP_057568.1	PDZ domain-containing protein 11 isoform 1

PDZD11 Protein Structure

PDZ

0
100
140 a.a.

Protein Preferred Names

Protein Names

PDZ domain-containing protein 11

ATPase-interacting PDZ protein

Recombinant PDZD11 Proteins

Cat. No.	Product Name	Accession	Purity
HY-P77130	PDZD11 Protein, Human (His)	Q5EBL8 (D2-H140)	≥95%

Related Diseases

Diseases

Alias

Purulent Acute Otitis Media

Acute Suppurative Otitis Media	Acute Or Subacute Suppurative Otitis Media
Acute Or Subacute Purulent Otitis Media

Epiphyseal Dysplasia, Multiple, 2

EDM2	Multiple Epiphyseal Dysplasia 2
Dysplasia, Epiphyseal, Multiple, Type 2

Multiple Epiphyseal Dysplasia Due To Collagen 9 Anomaly

Epiphyseal Dysplasia, Multiple, 3

EDM3	Multiple Epiphyseal Dysplasia 3
Epiphyseal Dysplasia, Multiple, 3, With Or Without Myopathy	Multiple Epiphyseal Dysplasia 3 With Or Without Myopathy
Epiphyseal Dysplasia Multiple 3	Dysplasia, Epiphyseal, Multiple, Type 3

Multiple Epiphyseal Dysplasia

Med	Polyepiphyseal Dysplasia
Edm	Epiphyseal Dysplasia, Multiple, 1
Epiphyseal Dysplasia, Multiple, 2	Epiphyseal Dysplasia, Multiple, 3
Epiphyseal Dysplasia, Multiple, 4	Epiphyseal Dysplasia, Multiple, 5
Epiphyseal Dysplasia, Multiple	Edm1
Edm2	Edm3
Edm4	Edm5
Epiphyseal Dysplasia, Fairbank Type	Epiphyseal Dysplasia, Ribbing Type
Multiple Epiphyseal Dysplasia, Autosomal Dominant	Multiple Epiphyseal Dysplasia, Autosomal Recessive
Rmed	Dysplasia, Epiphyseal, Multiple
Osteochondrodysplasias

Suppurative Otitis Media

Otitis Media With Effusion - Purulent	Purulent Otitis Media
Otitis Media, Suppurative

Osteochondrodysplasia

Skeletal Dysplasia	Chondrodystrophy
Congenital Anomaly Of Cartilage	Osteochondrodysplasias
Cartilage Development Disorder	Osteochondrodysplasia Syndrome
Dysplasia, Skeletal	Mucopolysaccharidosis Iv

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-RS10300	PDZD11 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	PDZD11	VGNC	VGNC:32724
Mus musculus	PDZD11	MGD	MGI:1919871
Rattus norvegicus	PDZD11	RGD	RGD:1560007
Canis familiaris	PDZD11	VGNC	VGNC:44399
Others	PDZD11	NCBI

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