CLRN3 clarin 3

Information
Symbol
CLRN3
Type
protein-coding
Description
clarin 3
Entrez Gene ID
119467
Genome
hg19
Position
chr10:129,676,105-129,691,205
Genome
hg38
Position
chr10:127,877,841-127,892,941
MIM
620256 OMIM
HGNC
HGNC:20795 HGNC
Ensembl
ENSG00000180745 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 6
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
40
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 TMEM12
SYNONYM USH3AL1
MIM 620256 OMIM
HGNC HGNC:20795 HGNC
Ensembl ENSG00000180745 Ensembl
AllianceGenome HGNC:20795
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000368671.4 hg38 chr10 127,877,841 127,892,941 15,101
ENST00000368671.4 hg19 chr10 129,676,105 129,691,205 15,101
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