TF transferrin

Information
Symbol
TF
Type
protein-coding
Description
transferrin
Entrez Gene ID
7018
Genome
hg19
Position
chr3:133,465,237-133,515,485
Genome
hg38
Position
chr3:133,746,393-133,796,641
MIM
190000 OMIM
HGNC
HGNC:11740 HGNC
Ensembl
ENSG00000091513 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 10
Likely pathogenic 0 4
Benign 0 54
Likely benign 0 612
Conflicting classifications of pathogenicity 0 26
Uncertain significance 0 100
Ranking
ClinVar
0
0
56
690
16
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 HEL-S-71p
SYNONYM PRO1557
SYNONYM PRO2086
SYNONYM TFQTL1
MIM 190000 OMIM
HGNC HGNC:11740 HGNC
Ensembl ENSG00000091513 Ensembl
AllianceGenome HGNC:11740
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000402696.9 hg38 chr3 133,746,393 133,796,641 50,249
ENST00000402696.9 hg19 chr3 133,465,237 133,515,485 50,249
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