TMIGD2 transmembrane and immunoglobulin domain containing 2
Information
- Symbol
- TMIGD2
- Type
- protein-coding
- Description
- transmembrane and immunoglobulin domain containing 2
- Entrez Gene ID
- 126259
- Genome
- hg19
- Position
- chr19:4,292,229-4,302,428
- Genome
- hg38
- Position
- chr19:4,292,232-4,302,431
- MIM
- 614715 OMIM
- HGNC
- HGNC:28324 HGNC
- Ensembl
- ENSG00000167664 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 12 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 24 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
46 |
 |
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
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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
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CD28H |
| SYNONYM | IGPR-1 |
| SYNONYM | IGPR1 |
| MIM | 614715 OMIM |
| HGNC | HGNC:28324 HGNC |
| Ensembl | ENSG00000167664 Ensembl |
| AllianceGenome | HGNC:28324 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000301272.6 | hg38 | chr19 | 4,292,232 | 4,302,431 | 10,200 |
| ENST00000595645.6 | hg38 | chr19 | 4,292,227 | 4,302,389 | 10,163 |
| ENST00000600114.5 | hg38 | chr19 | 4,292,599 | 4,302,385 | 9,787 |
| ENST00000600349.1 | hg38 | chr19 | 4,292,599 | 4,302,385 | 9,787 |
| ENST00000595645.6 | hg19 | chr19 | 4,292,224 | 4,302,386 | 10,163 |
| ENST00000301272.6 | hg19 | chr19 | 4,292,229 | 4,302,428 | 10,200 |
| ENST00000600114.5 | hg19 | chr19 | 4,292,596 | 4,302,382 | 9,787 |
| ENST00000600349.1 | hg19 | chr19 | 4,292,596 | 4,302,382 | 9,787 |
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