TMED4 transmembrane p24 trafficking protein 4
Information
- Symbol
- TMED4
- Type
- protein-coding
- Description
- transmembrane p24 trafficking protein 4
- Entrez Gene ID
- 222068
- Genome
- hg19
- Position
- chr7:44,617,493-44,621,830
- Genome
- hg38
- Position
- chr7:44,577,894-44,582,231
- MIM
- 612038 OMIM
- HGNC
- HGNC:22301 HGNC
- Ensembl
- ENSG00000158604 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 20 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
22 |
 |
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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| 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 | ERS25 |
| SYNONYM | GMP25iso |
| SYNONYM | HNLF |
| SYNONYM | p24a3 |
| SYNONYM | p24alpha3 |
| MIM | 612038 OMIM |
| HGNC | HGNC:22301 HGNC |
| Ensembl | ENSG00000158604 Ensembl |
| AllianceGenome | HGNC:22301 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000481238.1 | hg38 | chr7 | 44,579,897 | 44,582,231 | 2,335 |
| ENST00000289577.9 | hg38 | chr7 | 44,577,894 | 44,582,287 | 4,394 |
| ENST00000457408.7 | hg38 | chr7 | 44,577,894 | 44,582,231 | 4,338 |
| ENST00000457408.7 | hg19 | chr7 | 44,617,493 | 44,621,830 | 4,338 |
| ENST00000289577.9 | hg19 | chr7 | 44,617,493 | 44,621,886 | 4,394 |
| ENST00000481238.1 | hg19 | chr7 | 44,619,496 | 44,621,830 | 2,335 |
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