ZNF664 zinc finger protein 664

Information
Symbol
ZNF664
Type
protein-coding
Description
zinc finger protein 664
Entrez Gene ID
144348
Genome
hg19
Position
chr12:124,457,670-124,499,969
Genome
hg38
Position
chr12:123,973,123-124,015,422
MIM
617890 OMIM
HGNC
HGNC:25406 HGNC
Ensembl
ENSG00000179195 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 8
Ranking
ClinVar
0
0
0
10
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 ZFOC1
SYNONYM ZNF176
MIM 617890 OMIM
HGNC HGNC:25406 HGNC
Ensembl ENSG00000179195 Ensembl
AllianceGenome HGNC:25406
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000392404.7 hg38 chr12 123,973,212 124,015,426 42,215
ENST00000337815.9 hg38 chr12 123,973,215 124,015,427 42,213
ENST00000539644.5 hg38 chr12 123,973,123 124,015,422 42,300
ENST00000538932.6 hg38 chr12 123,973,215 124,015,439 42,225
ENST00000539644.5 hg19 chr12 124,457,670 124,499,969 42,300
ENST00000392404.7 hg19 chr12 124,457,759 124,499,973 42,215
ENST00000337815.9 hg19 chr12 124,457,762 124,499,974 42,213
ENST00000538932.6 hg19 chr12 124,457,762 124,499,986 42,225
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