IQCN IQ motif containing N

Information
Symbol
IQCN
Type
protein-coding
Description
IQ motif containing N
Entrez Gene ID
80726
Genome
hg19
Position
chr19:18,367,908-18,385,262
Genome
hg38
Position
chr19:18,257,098-18,274,452
MIM
620160 OMIM
HGNC
HGNC:29350 HGNC
Ensembl
ENSG00000130518 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 2
Likely benign 0 60
Uncertain significance 0 202
Ranking
ClinVar
0
0
0
264
2
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
SYNONYM KIAA1683
SYNONYM SPGF78
MIM 620160 OMIM
HGNC HGNC:29350 HGNC
Ensembl ENSG00000130518 Ensembl
AllianceGenome HGNC:29350
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000392413.5 hg38 chr19 18,257,098 18,274,452 17,355
ENST00000600328.7 hg38 chr19 18,257,098 18,274,487 17,390
ENST00000600359.7 hg38 chr19 18,257,098 18,274,500 17,403
ENST00000392413.5 hg19 chr19 18,367,908 18,385,262 17,355
ENST00000600328.7 hg19 chr19 18,367,908 18,385,297 17,390
ENST00000600359.7 hg19 chr19 18,367,908 18,385,310 17,403
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