CMTM1 CKLF like MARVEL transmembrane domain containing 1

Information
Symbol
CMTM1
Type
protein-coding
Description
CKLF like MARVEL transmembrane domain containing 1
Entrez Gene ID
113540
Genome
hg19
Position
chr16:66,600,342-66,613,038
Genome
hg38
Position
chr16:66,566,439-66,579,135
MIM
607884 OMIM
HGNC
HGNC:19172 HGNC
Ensembl
ENSG00000089505 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
26
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 :
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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 CKLFH
SYNONYM CKLFH1
SYNONYM CKLFSF1
MIM 607884 OMIM
HGNC HGNC:19172 HGNC
Ensembl ENSG00000089505 Ensembl
AllianceGenome HGNC:19172
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000336328.10 hg38 chr16 66,566,393 66,579,135 12,743
ENST00000528324.5 hg38 chr16 66,566,393 66,579,135 12,743
ENST00000529506.5 hg38 chr16 66,566,393 66,579,135 12,743
ENST00000533953.5 hg38 chr16 66,566,431 66,579,135 12,705
ENST00000328020.10 hg38 chr16 66,566,514 66,579,137 12,624
ENST00000379500.7 hg38 chr16 66,566,439 66,579,135 12,697
ENST00000533666.5 hg38 chr16 66,566,393 66,579,137 12,745
ENST00000531885.5 hg38 chr16 66,566,393 66,579,135 12,743
ENST00000332695.11 hg38 chr16 66,566,393 66,579,135 12,743
ENST00000457188.6 hg38 chr16 66,566,393 66,579,135 12,743
ENST00000328020.10 hg19 chr16 66,600,417 66,613,040 12,624
ENST00000531885.5 hg19 chr16 66,600,296 66,613,038 12,743
ENST00000529506.5 hg19 chr16 66,600,296 66,613,038 12,743
ENST00000528324.5 hg19 chr16 66,600,296 66,613,038 12,743
ENST00000457188.6 hg19 chr16 66,600,296 66,613,038 12,743
ENST00000336328.10 hg19 chr16 66,600,296 66,613,038 12,743
ENST00000332695.11 hg19 chr16 66,600,296 66,613,038 12,743
ENST00000533666.5 hg19 chr16 66,600,296 66,613,040 12,745
ENST00000533953.5 hg19 chr16 66,600,334 66,613,038 12,705
ENST00000379500.7 hg19 chr16 66,600,342 66,613,038 12,697
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