KANSL2 KAT8 regulatory NSL complex subunit 2

Information
Symbol
KANSL2
Type
protein-coding
Description
KAT8 regulatory NSL complex subunit 2
Entrez Gene ID
54934
Genome
hg19
Position
chr12:49,046,994-49,076,021
Genome
hg38
Position
chr12:48,653,211-48,682,238
MIM
615488 OMIM
HGNC
HGNC:26024 HGNC
Ensembl
ENSG00000139620 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 34
Ranking
ClinVar
0
0
0
34
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 C12orf41
SYNONYM NSL2
MIM 615488 OMIM
HGNC HGNC:26024 HGNC
Ensembl ENSG00000139620 Ensembl
AllianceGenome HGNC:26024
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000550347.5 hg38 chr12 48,653,402 48,682,225 28,824
ENST00000420613.7 hg38 chr12 48,653,211 48,682,238 29,028
ENST00000553086.5 hg38 chr12 48,653,889 48,682,158 28,270
ENST00000420613.7 hg19 chr12 49,046,994 49,076,021 29,028
ENST00000550347.5 hg19 chr12 49,047,185 49,076,008 28,824
ENST00000553086.5 hg19 chr12 49,047,672 49,075,941 28,270
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