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NM_015094.3 - NP_055909.2 (MANE)
DNA
Protein
Gene Info.
Genome Build
GRCh38
Chromosome
22
Location
Chr22:21,416,871-21,451,963
LOEUF
0.178
Variant filter
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ClinVar
Pathogenic/ Likely pa...
Risk factor
Drug response
Association
Affect
VUS
Benign/Likely benign
Others
GnomAD
Common [>1%]
Rare [<1%]
ToMMo
Common [>1%]
Rare [<1%]
By consequences
Missense
Loss-of-function
Synonymous
Others
Gene region:
CDS
SpliceSite
UTR
Intron
Flanking
External resources
NCBI Gene
23119
Ensembl
ENSG00000169635
GeneCards
HIC2
UniProt
Q96JB3
KEGG
hsa:23119
gnomAD
ENSG00000169635
ICGC
ENSG00000169635
RefDIC
23119
RefEx
23119
DTX
HIC2
AS-ALPS
HIC2
HIC2
HIC ZBTB transcriptional repressor 2
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Amino Acid Sequence
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