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Gene: AXDND1 (axonemal dynein light chain domain containing 1) Homo sapiens
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Symbol: AXDND1
Name: axonemal dynein light chain domain containing 1
Description: ASSOCIATED WITH 1q24 Deletion Syndrome; nephrotic syndrome type 1; nephrotic syndrome type 2; INTERACTS WITH aflatoxin B2; benzo[a]pyrene; calcitriol
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: axonemal dynein light chain domain-containing protein 1; C1orf125; DKFZp686H1423; FLJ25438; FLJ32940; hypothetical protein LOC126859; RP11-215I23.2
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1179,365,720 - 179,554,735 (+)Ensembl
GRCh381179,365,704 - 179,554,735 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371179,334,855 - 179,523,870 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361177,601,738 - 177,790,493 (+)NCBINCBI36hg18NCBI36
Celera1152,443,132 - 152,631,501 (+)NCBI
Cytogenetic Map1q25.2NCBI
HuRef1150,562,063 - 150,750,488 (+)NCBIHuRef
CHM1_11180,758,360 - 180,947,690 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction 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
Nomenclature History
 
More on AXDND1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1605000
Created: 2007-04-28
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.