MICB MHC class I polypeptide-related sequence B

Information
Symbol
MICB
Type
protein-coding
Description
MHC class I polypeptide-related sequence B
Entrez Gene ID
4277
Genome
hg19
Position
chr6:31,465,922-31,478,901
Genome
hg38
Position
chr6:31,498,145-31,511,124
MIM
602436 OMIM
HGNC
HGNC:7091 HGNC
Ensembl
ENSG00000204516 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 8
not provided 88 0
Uncertain significance 0 40
Ranking
ClinVar
0
0
0
52
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 :
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 PERB11.2
MIM 602436 OMIM
HGNC HGNC:7091 HGNC
Ensembl ENSG00000204516 Ensembl
IMGT/GENE-DB MICB
AllianceGenome HGNC:7091
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000252229.7 hg38 chr6 31,498,145 31,511,124 12,980
ENST00000538442.5 hg38 chr6 31,494,881 31,511,123 16,243
ENST00000399150.7 hg38 chr6 31,498,086 31,511,124 13,039
ENST00000538442.5 hg19 chr6 31,462,658 31,478,900 16,243
ENST00000399150.7 hg19 chr6 31,465,863 31,478,901 13,039
ENST00000252229.7 hg19 chr6 31,465,922 31,478,901 12,980
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