PCDH11X

GENERAL INFORMATION

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Gene name

PCDH11X

Gene description

Protocadherin 11 X-linked

Protein class

Predicted membrane proteins

Predicted localization

Membrane

Number of transcripts

7
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Tissue enhanced (cerebral cortex, ovary)
GTEx:Tissue enhanced (cerebral cortex, ovary)

Protein evidence

Evidence at transcript level

Protein localization

Membranous and cytoplasmic expression in several tissues, granular pattern in subsets of cells in brain and testis.

ANTIBODY RELIABILITY

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Data reliability
description

Caution, targets protein from more than one gene. Secreted protein, tissue location of RNA and protein might differ and correlation is complex. Pending external verification.

Data reliability

Uncertain based on 1 antibody.
HPA000432
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Tissue enhanced (cerebral cortex, ovary)

Organ

Expression

GTEx dataset
RNA tissue category:  Tissue enhanced (cerebral cortex, ovary)

Organ

Expression



GENE INFORMATION

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Gene name

PCDH11X (HGNC Symbol)

Synonyms

PCDH-X, PCDH11, PCDHX, PPP1R119

Description

Protocadherin 11 X-linked (HGNC Symbol)

Entrez gene summary

This gene belongs to the protocadherin gene family, a subfamily of the cadherin superfamily. The encoded protein consists of an extracellular domain containing 7 cadherin repeats, a transmembrane domain and a cytoplasmic tail that differs from those of the classical cadherins. The gene is located in a major X/Y block of homology and its Y homolog, despite divergence leading to coding region changes, is the most closely related cadherin family member. The protein is thought to play a fundamental role in cell-cell recognition essential for the segmental development and function of the central nervous system. Disruption of this gene may be associated with developmental dyslexia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]

Chromosome

X

Cytoband

q21.31

Chromosome location (bp)

91779261 - 92623230

Protein evidence

Evidence at transcript level (all genes)

Ensembl

ENSG00000102290 (version 78.38)

Entrez gene

27328

UniProt

Q9BZA7 (UniProt - Evidence at transcript level)

neXtProt

NX_Q9BZA7

Antibodypedia

PCDH11X antibodies


PROTEIN BROWSER

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ENST00000361655
 
ENST00000373088
 
ENST00000373094
 
ENST00000373097
 
ENST00000395337
 
ENST00000406881
 
ENST00000504220
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

PCDH11X-001 ENSP00000362186
ENST00000373094
Q9BZA7
Show all »
Show » Show » 1347 147.6 Yes 1
PCDH11X-002 ENSP00000362189
ENST00000373097
Q9BZA7
Show all »
Show » Show » 1337 146.5 Yes 1
PCDH11X-003 ENSP00000362180
ENST00000373088
Q9BZA7
Show all »
Show » Show » 1310 143.3 Yes 1
PCDH11X-006 ENSP00000423762
ENST00000504220
Q9BZA7
Show all »
Show » Show » 1065 117.6 Yes 1
PCDH11X-007 ENSP00000355105
ENST00000361655
Q9BZA7
Show all »
Show » Show » 1329 145.7 Yes 1
PCDH11X-008 ENSP00000384758
ENST00000406881
Q9BZA7
Show all »
Show » Show » 1339 146.7 Yes 1
PCDH11X-201 ENSP00000378746
ENST00000395337
Show » Show » 1016 112.3 Yes 1