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Gene: C13orf42 (chromosome 13 open reading frame 42) Homo sapiens
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Symbol: C13orf42
Name: chromosome 13 open reading frame 42
Description: ASSOCIATED WITH Chromosome 13q Deletion Syndrome; chromosome 13q14 deletion syndrome; INTERACTS WITH aflatoxin B1; benzo[e]pyrene; methapyrilene
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: LINC00371; LINC00372; long intergenic non-protein coding RNA 371; long intergenic non-protein coding RNA 372; RP11-547C18.3; uncharacterized protein C13orf42
Orthologs:
Mus musculus (house mouse) : Gm4131 (predicted gene 4131)  MGI  Alliance
Pan paniscus (bonobo/pygmy chimpanzee) : C13H13orf42 (chromosome 13 C13orf42 homolog)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381351,082,119 - 51,172,388 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371351,658,151 - 51,687,364 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361350,556,288 - 50,621,130 (-)NCBINCBI36hg18NCBI36
Celera1332,707,440 - 32,735,212 (-)NCBI
Cytogenetic Map13q14.3NCBI
HuRef1332,447,155 - 32,476,357 (-)NCBIHuRef
CHM1_11351,624,514 - 51,714,055 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on C13orf42
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 7242868
Created: 2013-04-23
Species: Homo sapiens
Last Modified: 2019-11-26
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.