TMEM41B transmembrane protein 41B

Information
Symbol
TMEM41B
Type
protein-coding
Description
transmembrane protein 41B
Entrez Gene ID
440026
Genome
hg19
Position
chr11:9,302,201-9,336,140
Genome
hg38
Position
chr11:9,280,654-9,314,593
MIM
620271 OMIM
HGNC
HGNC:28948 HGNC
Ensembl
ENSG00000166471 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 4
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
42
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 :
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
MIM 620271 OMIM
HGNC HGNC:28948 HGNC
Ensembl ENSG00000166471 Ensembl
AllianceGenome HGNC:28948
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000528080.6 hg38 chr11 9,280,654 9,314,593 33,940
ENST00000611268.4 hg38 chr11 9,280,657 9,314,567 33,911
ENST00000527813.5 hg38 chr11 9,283,547 9,314,630 31,084
ENST00000533723.1 hg38 chr11 9,295,096 9,314,633 19,538
ENST00000528080.6 hg19 chr11 9,302,201 9,336,140 33,940
ENST00000611268.4 hg19 chr11 9,302,204 9,336,114 33,911
ENST00000527813.5 hg19 chr11 9,305,094 9,336,177 31,084
ENST00000533723.1 hg19 chr11 9,316,643 9,336,180 19,538
Genome browser