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Gene: MIR200CHG (MIR200C and MIR141 host gene) Homo sapiens
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Symbol: MIR200CHG
Name: MIR200C and MIR141 host gene
Description: ASSOCIATED WITH hyperphosphatemic familial tumoral calcinosis; Hyperphosphatemic Familial Tumoral Calcinosis 1
Type: ncrna
RefSeq Status: VALIDATED
Also known as: U47924.27
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl126,963,246 - 6,964,447 (+)Ensembl
GRCh38126,963,245 - 6,964,447 (+)NCBIGRCh38GRCh38hg38GRCh38
Cytogenetic Map12p13.31NCBI
CHM1_1127,071,361 - 7,072,563 (+)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
Promoters
Clinical Variants

Additional Information

External Database Links
 
More on MIR200CHG
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 12792116
Created: 2017-03-07
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.