IGFBP7 insulin like growth factor binding protein 7
Information
- Symbol
- IGFBP7
- Type
- protein-coding
- Description
- insulin like growth factor binding protein 7
- Entrez Gene ID
- 3490
- Genome
- hg19
- Position
- chr4:57,896,939-57,976,551
- Genome
- hg38
- Position
- chr4:57,030,773-57,110,385
- MIM
- 602867 OMIM
- HGNC
- HGNC:5476 HGNC
- Ensembl
- ENSG00000163453 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 4 |
| Benign | 0 | 8 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 28 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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44 |
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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
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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 | AGM |
| SYNONYM | FSTL2 |
| SYNONYM | IBP-7 |
| SYNONYM | IGFBP-7 |
| SYNONYM | IGFBP-7v |
| SYNONYM | IGFBPRP1 |
| SYNONYM | MAC25 |
| SYNONYM | PSF |
| SYNONYM | RAMSVPS |
| SYNONYM | TAF |
| MIM | 602867 OMIM |
| HGNC | HGNC:5476 HGNC |
| Ensembl | ENSG00000163453 Ensembl |
| AllianceGenome | HGNC:5476 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000514062.2 | hg38 | chr4 | 57,032,038 | 57,110,385 | 78,348 |
| ENST00000295666.6 | hg38 | chr4 | 57,030,773 | 57,110,385 | 79,613 |
| ENST00000295666.6 | hg19 | chr4 | 57,896,939 | 57,976,551 | 79,613 |
| ENST00000514062.2 | hg19 | chr4 | 57,898,204 | 57,976,551 | 78,348 |
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