LOC124901322 (uncharacterized LOC124901322) - Rat Genome Database

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Gene: LOC124901322 (uncharacterized LOC124901322) Homo sapiens
Analyze
Symbol: LOC124901322
Name: uncharacterized LOC124901322
RGD ID: 151669730
Description:
Type: ncrna
RefSeq Status: MODEL
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38644,306,984 - 44,314,547 (+)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map6p21.1NCBI
T2T-CHM13v2.0644,141,152 - 44,148,671 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


References

Genomics

Variants

.
Variants in LOC124901322
177 total Variants

Expression


Sequence


Reference Sequences
RefSeq Acc Id: XR_007059594
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38644,306,984 - 44,314,547 (+)NCBI
RefSeq Acc Id: XR_007076804
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0644,141,152 - 44,148,671 (+)NCBI

Additional Information

Database Acc Id Source(s)
COSMIC LOC124901322 COSMIC
GTEx LOC124901322 GTEx
Human Proteome Map LOC124901322 Human Proteome Map
NCBI Gene LOC124901322 ENTREZGENE