CRYGN crystallin gamma N

Information
Symbol
CRYGN
Type
protein-coding
Description
crystallin gamma N
Entrez Gene ID
155051
Genome
hg19
Position
chr7:151,125,918-151,137,227
Genome
hg38
Position
chr7:151,428,832-151,440,141
MIM
609603 OMIM
HGNC
HGNC:20458 HGNC
Ensembl
ENSG00000127377 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Uncertain significance 0 24
Ranking
ClinVar
0
0
0
28
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 :
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
MIM 609603 OMIM
HGNC HGNC:20458 HGNC
Ensembl ENSG00000127377 Ensembl
AllianceGenome HGNC:20458
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000644350.1 hg38 chr7 151,429,970 151,440,044 10,075
ENST00000491928.1 hg38 chr7 151,430,001 151,440,008 10,008
ENST00000337323.3 hg38 chr7 151,428,832 151,440,141 11,310
ENST00000337323.3 hg19 chr7 151,125,918 151,137,227 11,310
ENST00000644350.1 hg19 chr7 151,127,056 151,137,130 10,075
ENST00000491928.1 hg19 chr7 151,127,087 151,137,094 10,008
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