HIGD1C HIG1 hypoxia inducible domain family member 1C

Information
Symbol
HIGD1C
Type
protein-coding
Description
HIG1 hypoxia inducible domain family member 1C
Entrez Gene ID
613227
Genome
hg19
Position
chr12:51,346,327-51,364,390
Genome
hg38
Position
chr12:50,952,544-50,970,607
MIM
620803 OMIM
HGNC
HGNC:28044 HGNC
Ensembl
ENSG00000214511 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 12
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 :
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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 GM921
MIM 620803 OMIM
HGNC HGNC:28044 HGNC
Ensembl ENSG00000214511 Ensembl
AllianceGenome HGNC:28044
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000398455.3 hg38 chr12 50,953,922 50,970,506 16,585
ENST00000695930.1 hg38 chr12 50,952,538 50,970,594 18,057
ENST00000695931.1 hg38 chr12 50,952,544 50,970,607 18,064
ENST00000695930.1 hg19 chr12 51,346,321 51,364,377 18,057
ENST00000695931.1 hg19 chr12 51,346,327 51,364,390 18,064
ENST00000398455.3 hg19 chr12 51,347,705 51,364,289 16,585
KeyValue
strand+
start51,347,781
Gene SymbolHIGD1C
Entrez GeneId613,227
Chr Band12q13.12
end51,364,288
chrchr12
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