MAFF MAF bZIP transcription factor F

Information
Symbol
MAFF
Type
protein-coding
Description
MAF bZIP transcription factor F
Entrez Gene ID
23764
Genome
hg19
Position
chr22:38,598,001-38,612,514
Genome
hg38
Position
chr22:38,201,994-38,216,507
MIM
604877 OMIM
HGNC
HGNC:6780 HGNC
Ensembl
ENSG00000185022 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 16
Ranking
ClinVar
0
0
0
18
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 U-MAF
SYNONYM hMafF
MIM 604877 OMIM
HGNC HGNC:6780 HGNC
Ensembl ENSG00000185022 Ensembl
AllianceGenome HGNC:6780
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000407965.1 hg38 chr22 38,213,535 38,216,505 2,971
ENST00000338483.7 hg38 chr22 38,201,994 38,216,507 14,514
ENST00000538999.1 hg38 chr22 38,201,932 38,216,503 14,572
ENST00000538320.5 hg38 chr22 38,201,932 38,216,503 14,572
ENST00000426621.6 hg38 chr22 38,203,020 38,216,503 13,484
ENST00000538320.5 hg19 chr22 38,597,939 38,612,510 14,572
ENST00000538999.1 hg19 chr22 38,597,939 38,612,510 14,572
ENST00000338483.7 hg19 chr22 38,598,001 38,612,514 14,514
ENST00000426621.6 hg19 chr22 38,599,027 38,612,510 13,484
ENST00000407965.1 hg19 chr22 38,609,542 38,612,512 2,971
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