LMNTD1 lamin tail domain containing 1

Information
Symbol
LMNTD1
Type
protein-coding
Description
lamin tail domain containing 1
Entrez Gene ID
160492
Genome
hg19
Position
chr12:25,629,016-25,706,217
Genome
hg38
Position
chr12:25,476,082-25,553,283
MIM
617254 OMIM
HGNC
HGNC:26683 HGNC
Ensembl
ENSG00000152936 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
not provided 1 0
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
44
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
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 IFLTD1
SYNONYM LMNARS1
SYNONYM PAS1C1
MIM 617254 OMIM
HGNC HGNC:26683 HGNC
Ensembl ENSG00000152936 Ensembl
AllianceGenome HGNC:26683
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000539744.5 hg38 chr12 25,476,110 25,553,252 77,143
ENST00000458174.7 hg38 chr12 25,476,082 25,553,283 77,202
ENST00000445693.5 hg38 chr12 25,497,513 25,648,554 151,042
ENST00000282881.10 hg38 chr12 25,476,082 25,553,244 77,163
ENST00000413632.6 hg38 chr12 25,499,852 25,553,281 53,430
ENST00000282881.10 hg19 chr12 25,629,016 25,706,178 77,163
ENST00000458174.7 hg19 chr12 25,629,016 25,706,217 77,202
ENST00000539744.5 hg19 chr12 25,629,044 25,706,186 77,143
ENST00000445693.5 hg19 chr12 25,650,447 25,801,488 151,042
ENST00000413632.6 hg19 chr12 25,652,786 25,706,215 53,430
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