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Gene: LOC642648 (uncharacterized LOC642648) Homo sapiens
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Symbol: LOC642648
Name: uncharacterized LOC642648
RGD ID: 38608700
Description: ASSOCIATED WITH Phelan-McDermid syndrome
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382246,064,651 - 46,071,021 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh372246,463,524 - 46,466,474 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map22q13.31NCBI
HuRef2229,407,595 - 29,408,877 (-)NCBIHuRef
CHM1_12246,422,389 - 46,426,302 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics


Expression


Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LOC642648
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 38608700
Created: 2020-09-16
Species: Homo sapiens
Last Modified: 2020-09-16
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.