Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: AC138649.1 (novel transcript, sense overlapping NIPA1) Homo sapiens
Analyze
Symbol: AC138649.1
Name: novel transcript, sense overlapping NIPA1
CRRD ID: 16567140
Description: ASSOCIATED WITH autistic disorder; schizophrenia
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC283683; uncharacterized LOC283683
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1522,757,841 - 22,778,741 (+)EnsemblGRCh38hg38GRCh38
GRCh381522,757,857 - 22,778,737 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371523,094,331 - 23,115,254 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map15q11.2NCBI
HuRef151,405,882 - 1,424,577 (-)NCBIHuRef
CHM1_11523,043,631 - 23,063,998 (-)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 AC138649.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16567140
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-09-16
Status: ACTIVE



NHLBI Logo

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