ING4 inhibitor of growth family member 4
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 12 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
 |
0 |
 |
12 |
 |
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
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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 | |||||||||||
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MGeND data only
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| 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
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | my036 |
| SYNONYM | p29ING4 |
| MIM | 608524 OMIM |
| HGNC | HGNC:19423 HGNC |
| Ensembl | ENSG00000111653 Ensembl |
| AllianceGenome | HGNC:19423 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000396807.8 | hg38 | chr12 | 6,650,591 | 6,663,140 | 12,550 |
| ENST00000446105.6 | hg38 | chr12 | 6,650,626 | 6,663,142 | 12,517 |
| ENST00000423703.6 | hg38 | chr12 | 6,651,195 | 6,663,101 | 11,907 |
| ENST00000341550.9 | hg38 | chr12 | 6,650,301 | 6,663,119 | 12,819 |
| ENST00000619641.4 | hg38 | chr12 | 6,650,539 | 6,663,142 | 12,604 |
| ENST00000412586.6 | hg38 | chr12 | 6,651,195 | 6,663,101 | 11,907 |
| ENST00000444704.5 | hg38 | chr12 | 6,651,195 | 6,663,101 | 11,907 |
| ENST00000341550.9 | hg19 | chr12 | 6,759,467 | 6,772,285 | 12,819 |
| ENST00000396807.8 | hg19 | chr12 | 6,759,757 | 6,772,306 | 12,550 |
| ENST00000446105.6 | hg19 | chr12 | 6,759,792 | 6,772,308 | 12,517 |
| ENST00000412586.6 | hg19 | chr12 | 6,760,361 | 6,772,267 | 11,907 |
| ENST00000423703.6 | hg19 | chr12 | 6,760,361 | 6,772,267 | 11,907 |
| ENST00000444704.5 | hg19 | chr12 | 6,760,361 | 6,772,267 | 11,907 |
| ENST00000619641.4 | hg19 | chr12 | 6,759,705 | 6,772,308 | 12,604 |
| Key | Value |
|---|---|
| strand | - |
| UniProt | TSG |
| start | 6,759,703 |
| Gene Symbol | ING4 |
| Entrez GeneId | 51,147 |
| Chr Band | 12p13.31 |
| end | 6,772,307 |
| chr | chr12 |
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