MAP6 microtubule associated protein 6

Information
Symbol
MAP6
Type
protein-coding
Description
microtubule associated protein 6
Entrez Gene ID
4135
Genome
hg19
Position
chr11:75,297,963-75,380,083
Genome
hg38
Position
chr11:75,586,918-75,669,038
MIM
601783 OMIM
HGNC
HGNC:6868 HGNC
Ensembl
ENSG00000171533 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 14
not provided 9 0
Uncertain significance 0 48
Ranking
ClinVar
0
0
2
68
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 MAP6-N
SYNONYM MTAP6
SYNONYM N-STOP
SYNONYM STOP
MIM 601783 OMIM
HGNC HGNC:6868 HGNC
Ensembl ENSG00000171533 Ensembl
AllianceGenome HGNC:6868
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000526740.3 hg38 chr11 75,586,919 75,668,607 81,689
ENST00000304771.8 hg38 chr11 75,586,918 75,669,038 82,121
ENST00000434603.2 hg38 chr11 75,602,860 75,668,434 65,575
ENST00000304771.8 hg19 chr11 75,297,963 75,380,083 82,121
ENST00000526740.3 hg19 chr11 75,297,964 75,379,652 81,689
ENST00000434603.2 hg19 chr11 75,313,905 75,379,479 65,575
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