TMEM9B TMEM9 domain family member B

Information
Symbol
TMEM9B
Type
protein-coding
Description
TMEM9 domain family member B
Entrez Gene ID
56674
Genome
hg19
Position
chr11:8,968,749-8,985,989
Genome
hg38
Position
chr11:8,947,202-8,964,442
MIM
620293 OMIM
HGNC
HGNC:1168 HGNC
Ensembl
ENSG00000175348 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Uncertain significance 0 14
Ranking
ClinVar
0
0
0
14
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
SYNONYM C11orf15
MIM 620293 OMIM
HGNC HGNC:1168 HGNC
Ensembl ENSG00000175348 Ensembl
AllianceGenome HGNC:1168
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000534025.6 hg38 chr11 8,947,202 8,964,442 17,241
ENST00000525069.5 hg38 chr11 8,947,501 8,965,011 17,511
ENST00000309134.9 hg38 chr11 8,947,294 8,964,441 17,148
ENST00000528117.5 hg38 chr11 8,952,692 8,964,402 11,711
ENST00000534025.6 hg19 chr11 8,968,749 8,985,989 17,241
ENST00000309134.9 hg19 chr11 8,968,841 8,985,988 17,148
ENST00000525069.5 hg19 chr11 8,969,048 8,986,558 17,511
ENST00000528117.5 hg19 chr11 8,974,239 8,985,949 11,711
Genome browser