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Gene: CES1P1 (carboxylesterase 1 pseudogene 1) Homo sapiens
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Symbol: CES1P1
Name: carboxylesterase 1 pseudogene 1
Description: This gene is a member of the carboxylesterase (CES) gene family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. This gene does not encode a protein and the sequence is similar to the CES1 gene, so represents a pseudogene of the CES1 gene. [provided by RefSeq, Jun 2010]
Type: pseudo
RefSeq Status: REVIEWED
Also known as: CES1A2; CES1A3; CES4; CESR; PCE-3
Orthologs:
Rattus norvegicus (Norway rat) : Ces1c (carboxylesterase 1C)  Alliance
more info ...
Related Functional Gene: CES1  
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381655,760,599 - 55,774,926 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371655,794,511 - 55,808,838 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361654,352,012 - 54,364,924 (+)NCBINCBI36hg18NCBI36
Build 341654,352,011 - 54,366,325NCBI
Celera1640,308,919 - 40,322,909 (+)NCBI
Cytogenetic Map16q12.2NCBI
HuRef1641,682,025 - 41,696,055 (+)NCBIHuRef
CHM1_11657,201,909 - 57,216,238 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences

Additional Information

External Database Links
Nomenclature History
 
More on CES1P1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1344824
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.