NLE1 notchless homolog 1

Information
Symbol
NLE1
Type
protein-coding
Description
notchless homolog 1
Entrez Gene ID
54475
Genome
hg19
Position
chr17:33,455,749-33,469,322
Genome
hg38
Position
chr17:35,128,730-35,142,303
HGNC
HGNC:19889 HGNC
Ensembl
ENSG00000073536 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 10
Uncertain significance 0 66
Ranking
ClinVar
0
0
0
78
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
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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 NLE
SYNONYM Rsa4
HGNC HGNC:19889 HGNC
Ensembl ENSG00000073536 Ensembl
AllianceGenome HGNC:19889
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000586869.5 hg38 chr17 35,128,753 35,142,284 13,532
ENST00000442241.9 hg38 chr17 35,128,730 35,142,303 13,574
ENST00000360831.9 hg38 chr17 35,132,071 35,142,303 10,233
ENST00000442241.9 hg19 chr17 33,455,749 33,469,322 13,574
ENST00000586869.5 hg19 chr17 33,455,772 33,469,303 13,532
ENST00000360831.9 hg19 chr17 33,459,090 33,469,322 10,233
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