PALM paralemmin

Information
Symbol
PALM
Type
protein-coding
Description
paralemmin
Entrez Gene ID
5064
Genome
hg19
Position
chr19:708,935-748,329
Genome
hg38
Position
chr19:708,935-748,329
MIM
608134 OMIM
HGNC
HGNC:8594 HGNC
Ensembl
ENSG00000099864 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 54
Likely benign 0 164
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 198
Ranking
ClinVar
0
0
30
386
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 :
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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 PALM1
MIM 608134 OMIM
HGNC HGNC:8594 HGNC
Ensembl ENSG00000099864 Ensembl
AllianceGenome HGNC:8594
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000592155.5 hg38 chr19 735,030 748,329 13,300
ENST00000338448.10 hg38 chr19 708,935 748,329 39,395
ENST00000264560.11 hg38 chr19 708,939 748,329 39,391
ENST00000590161.2 hg38 chr19 735,033 748,329 13,297
ENST00000338448.10 hg19 chr19 708,935 748,329 39,395
ENST00000264560.11 hg19 chr19 708,939 748,329 39,391
ENST00000592155.5 hg19 chr19 735,030 748,329 13,300
ENST00000590161.2 hg19 chr19 735,033 748,329 13,297
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