MORF4L2 mortality factor 4 like 2

Information
Symbol
MORF4L2
Type
protein-coding
Description
mortality factor 4 like 2
Entrez Gene ID
9643
Genome
hg19
Position
chrX:102,930,428-102,943,086
Genome
hg38
Position
chrX:103,675,500-103,688,158
MIM
300409 OMIM
HGNC
HGNC:16849 HGNC
Ensembl
ENSG00000123562 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 6 0
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
10
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 :
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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 MORFL2
SYNONYM MRGX
MIM 300409 OMIM
HGNC HGNC:16849 HGNC
Ensembl ENSG00000123562 Ensembl
AllianceGenome HGNC:16849
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000441076.7 hg38 chrX 103,675,498 103,686,699 11,202
ENST00000433176.6 hg38 chrX 103,675,500 103,688,158 12,659
ENST00000360458.5 hg38 chrX 103,675,496 103,688,064 12,569
ENST00000451301.5 hg38 chrX 103,675,500 103,686,818 11,319
ENST00000360458.5 hg19 chrX 102,930,424 102,942,992 12,569
ENST00000441076.7 hg19 chrX 102,930,426 102,941,627 11,202
ENST00000451301.5 hg19 chrX 102,930,428 102,941,746 11,319
ENST00000433176.6 hg19 chrX 102,930,428 102,943,086 12,659
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