OPN1LW opsin 1, long wave sensitive

Information
Symbol
OPN1LW
Type
protein-coding
Description
opsin 1, long wave sensitive
Entrez Gene ID
5956
Genome
hg19
Position
chrX:153,409,717-153,424,507
Genome
hg38
Position
chrX:154,144,243-154,159,032
MIM
300822 OMIM
HGNC
HGNC:9936 HGNC
Ensembl
ENSG00000102076 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 2 12
Benign 0 9
Likely benign 0 13
not provided 8 0
Uncertain significance 0 18
Ranking
ClinVar
0
0
2
38
9
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 CBP
SYNONYM COD5
SYNONYM RCP
SYNONYM ROP
MIM 300822 OMIM
HGNC HGNC:9936 HGNC
Ensembl ENSG00000102076 Ensembl
AllianceGenome HGNC:9936
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000369951.9 hg38 chrX 154,144,243 154,159,032 14,790
ENST00000369951.9 hg19 chrX 153,409,717 153,424,507 14,791
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