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Gene: AC124242.1 (novel transcript) Homo sapiens
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Symbol: AC124242.1
Name: novel transcript
Description: ASSOCIATED WITH spinal muscular atrophy with progressive myoclonic epilepsy
Type: ncrna
RefSeq Status: VALIDATED
Also known as: LOC101929066; uncharacterized LOC101929066
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38.p13 Ensembl - Human Genome Assembly GRCh38 Ensembl
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl818,084,386 - 18,097,644 (+)EnsemblGRCh38hg38GRCh38
GRCh38818,084,868 - 18,097,651 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37817,942,536 - 17,953,416 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map8p22NCBI
HuRef816,486,857 - 16,497,734 (+)NCBIHuRef
CHM1_1818,143,830 - 18,156,613 (+)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 AC124242.1
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 16557951
Created: 2020-01-08
Species: Homo sapiens
Last Modified: 2020-09-08
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.