ZNF692 zinc finger protein 692

Information
Symbol
ZNF692
Type
protein-coding
Description
zinc finger protein 692
Entrez Gene ID
55657
Genome
hg19
Position
chr1:249,144,265-249,153,059
Genome
hg38
Position
chr1:248,850,066-248,858,860
MIM
617758 OMIM
HGNC
HGNC:26049 HGNC
Ensembl
ENSG00000171163 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Uncertain significance 0 64
Ranking
ClinVar
0
0
0
66
2
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
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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 AREBP
SYNONYM Zfp692
MIM 617758 OMIM
HGNC HGNC:26049 HGNC
Ensembl ENSG00000171163 Ensembl
AllianceGenome HGNC:26049
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000306601.9 hg38 chr1 248,850,008 248,859,085 9,078
ENST00000366471.7 hg38 chr1 248,850,008 248,859,085 9,078
ENST00000451251.5 hg38 chr1 248,850,066 248,858,860 8,795
ENST00000306601.9 hg19 chr1 249,144,207 249,153,284 9,078
ENST00000366471.7 hg19 chr1 249,144,207 249,153,284 9,078
ENST00000451251.5 hg19 chr1 249,144,265 249,153,059 8,795
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