OPN1MW opsin 1, medium wave sensitive

Information
Symbol
OPN1MW
Type
protein-coding
Description
opsin 1, medium wave sensitive
Entrez Gene ID
2652
Genome
hg19
Position
chrX:153,448,085-153,462,352
Genome
hg38
Position
chrX:154,182,596-154,196,861
MIM
300821 OMIM
HGNC
HGNC:4206 HGNC
Ensembl
ENSG00000268221 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 4 10
Benign 0 4
Likely benign 0 20
not provided 8 0
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
24
20
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 CBBM
SYNONYM CBD
SYNONYM COD5
SYNONYM GCP
SYNONYM GOP
SYNONYM OPN1MW1
MIM 300821 OMIM
HGNC HGNC:4206 HGNC
Ensembl ENSG00000268221 Ensembl
AllianceGenome HGNC:4206
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000595290.6 hg38 chrX 154,182,596 154,196,861 14,266
ENST00000595290.6 hg19 chrX 153,448,085 153,462,352 14,268
Genome browser