Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: AC016065.1 (novel transcript) Homo sapiens
Analyze
Symbol: AC016065.1
Name: novel transcript
Description: ASSOCIATED WITH primary autosomal recessive microcephaly 1
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC100287015; uncharacterized LOC100287015
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl86,403,551 - 6,407,142 (-)EnsemblGRCh38hg38GRCh38
GRCh3886,403,556 - 6,406,548 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh3786,261,077 - 6,264,069 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p23.1NCBI
HuRef86,043,185 - 6,046,181 (-)NCBIHuRef
CHM1_186,349,877 - 6,352,867 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AC016065.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16557975
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-06-18
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.