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Gene: LINC01957 (long intergenic non-protein coding RNA 1957) Homo sapiens
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Symbol: LINC01957
Name: long intergenic non-protein coding RNA 1957
Description: ASSOCIATED WITH autistic disorder
Type: ncrna
RefSeq Status: VALIDATED
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl5114,576,041 - 114,579,970 (+)Ensembl
GRCh385114,576,041 - 114,579,970 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh375113,911,738 - 113,915,667 (+)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic Map5q22.3NCBI
HuRef5109,093,969 - 109,097,898 (+)NCBIHuRef
CHM1_15113,344,446 - 113,348,375 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics

miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Clinical Variants

Additional Information

External Database Links
 
More on LINC01957
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 11570207
Created: 2016-12-13
Species: Homo sapiens
Last Modified: 2019-12-25
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.