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Gene: C22orf39 (chromosome 22 open reading frame 39) Homo sapiens
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Symbol: C22orf39
Name: chromosome 22 open reading frame 39
Description: ASSOCIATED WITH autism spectrum disorder; autistic disorder; DiGeorge syndrome; INTERACTS WITH (+)-catechin; 3-isobutyl-1-methyl-7H-xanthine; bisphenol A
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: DKFZp686I08210; hypothetical protein LOC128977; MGC74441; UPF0545 protein C22orf39
Orthologs:
Mus musculus (house mouse) : 2510002D24Rik (RIKEN cDNA 2510002D24 gene)  MGI  Alliance
Rattus norvegicus (Norway rat) : LOC498122 (similar to CG15908-PA)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : LOC102008776 (chromosome unknown open reading frame, human C22orf39)
Pan paniscus (bonobo/pygmy chimpanzee) : C22H22orf39 (chromosome 22 C22orf39 homolog)
Canis lupus familiaris (dog) : C26H22orf39 (chromosome 26 C22orf39 homolog)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : CUNH22orf39 (chromosome unknown C22orf39 homolog)
Sus scrofa (pig) : C14H22orf39 (chromosome 14 C22orf39 homolog)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382219,440,886 - 19,448,232 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372219,428,409 - 19,435,755 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362217,810,894 - 17,815,220 (-)NCBINCBI36hg18NCBI36
Celera223,280,666 - 3,288,012 (-)NCBI
Cytogenetic Map22q11.21NCBI
HuRef223,049,221 - 3,056,567 (-)NCBIHuRef
CHM1_12219,427,982 - 19,435,325 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
 
More on C22orf39
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1606462
Created: 2007-04-29
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.