NR2F1 nuclear receptor subfamily 2 group F member 1

Information
Symbol
NR2F1
Type
protein-coding
Description
nuclear receptor subfamily 2 group F member 1
Entrez Gene ID
7025
Genome
hg19
Position
chr5:92,918,928-92,930,317
Genome
hg38
Position
chr5:93,583,222-93,594,611
MIM
132890 OMIM
HGNC
HGNC:7975 HGNC
Ensembl
ENSG00000175745 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 86
Likely pathogenic 0 106
Benign 0 28
Likely benign 0 228
Conflicting classifications of pathogenicity 0 20
not provided 1 0
Uncertain significance 0 220
Ranking
ClinVar
0
0
96
524
24
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM BBOAS
SYNONYM BBSOAS
SYNONYM COUP-TFI
SYNONYM COUPTF1
SYNONYM EAR-3
SYNONYM EAR3
SYNONYM ERBAL3
SYNONYM SVP44
SYNONYM TCFCOUP1
SYNONYM TFCOUP1
MIM 132890 OMIM
HGNC HGNC:7975 HGNC
Ensembl ENSG00000175745 Ensembl
AllianceGenome HGNC:7975
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000327111.8 hg38 chr5 93,583,222 93,594,611 11,390
ENST00000647447.1 hg38 chr5 93,585,024 93,593,842 8,819
ENST00000615873.2 hg38 chr5 93,585,024 93,594,517 9,494
ENST00000700211.1 hg38 chr5 93,585,735 93,594,280 8,546
ENST00000502982.2 hg38 chr5 93,587,460 93,594,531 7,072
ENST00000512697.2 hg38 chr5 93,587,101 93,594,540 7,440
ENST00000327111.8 hg19 chr5 92,918,928 92,930,317 11,390
ENST00000647447.1 hg19 chr5 92,920,730 92,929,548 8,819
ENST00000615873.2 hg19 chr5 92,920,730 92,930,223 9,494
ENST00000700211.1 hg19 chr5 92,921,441 92,929,986 8,546
ENST00000512697.2 hg19 chr5 92,922,807 92,930,246 7,440
ENST00000502982.2 hg19 chr5 92,923,166 92,930,237 7,072
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