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Gene: AF067845.2 (novel transcript) Homo sapiens
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Symbol: AF067845.2
Name: novel transcript
Description: ASSOCIATED WITH schizophrenia
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC286083; uncharacterized LOC286083
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl81,296,034 - 1,302,607 (-)EnsemblGRCh38hg38GRCh38
GRCh3881,296,034 - 1,302,607 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh3781,244,294 - 1,250,827 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p23.3NCBI
HuRef81,072,867 - 1,079,365 (-)NCBIHuRef
CHM1_181,242,381 - 1,248,867 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics


Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on AF067845.2
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 16567554
Created: 2020-01-08
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.