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Gene: DCAF8L2 (DDB1 and CUL4 associated factor 8 like 2) Homo sapiens
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Symbol: DCAF8L2
Name: DDB1 and CUL4 associated factor 8 like 2
Description: ASSOCIATED WITH autistic disorder; Neurodevelopmental Disorders; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH aflatoxin B1; arsane; arsenic atom
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: DDB1 and CUL4 associated factor 8-like 2; DDB1- and CUL4-associated factor 8-like protein 2; WD repeat domain 42C; WD repeat-containing protein 42C; WDR42C
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX27,590,382 - 27,748,821 (+)Ensembl
GRCh38X27,468,941 - 27,749,942 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X27,734,205 - 27,768,050 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X27,662,480 - 27,677,442 (+)NCBINCBI36hg18NCBI36
CeleraX31,893,400 - 31,895,412 (+)NCBI
Cytogenetic MapXp21.3NCBI
HuRefX25,504,432 - 25,506,739 (+)NCBIHuRef
CHM1_1X27,795,652 - 27,797,664 (+)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
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on DCAF8L2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1342776
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-12-25
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.