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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)
Chlorocebus sabaeus (African green monkey) : C19H22orf39 (chromosome 19 open reading frame, human C22orf39)
Heterocephalus glaber (naked mole-rat) : CUNH22orf39 (chromosome unknown C22orf39 homolog)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl2219,351,368 - 19,448,232 (-)EnsemblGRCh38hg38GRCh38
GRCh382219,440,886 - 19,447,711 (-)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

RNA-SEQ 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

RGD Object Information
RGD ID: 1606462
Created: 2007-04-29
Species: Homo sapiens
Last Modified: 2020-06-18
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.