TCTE1 t-complex-associated-testis-expressed 1
Information
- Symbol
- TCTE1
- Type
- protein-coding
- Description
- t-complex-associated-testis-expressed 1
- Entrez Gene ID
- 202500
- Genome
- hg19
- Position
- chr6:44,246,471-44,265,435
- Genome
- hg38
- Position
- chr6:44,278,734-44,297,698
- MIM
- 186975 OMIM
- HGNC
- HGNC:11693 HGNC
- Ensembl
- ENSG00000146221 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 4 | 0 |
| Uncertain significance | 0 | 72 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
76 |
 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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
|
| 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 | D6S46 |
| SYNONYM | DRC5 |
| SYNONYM | FAP155 |
| MIM | 186975 OMIM |
| HGNC | HGNC:11693 HGNC |
| Ensembl | ENSG00000146221 Ensembl |
| AllianceGenome | HGNC:11693 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000371504.1 | hg38 | chr6 | 44,280,165 | 44,286,353 | 6,189 |
| ENST00000371505.5 | hg38 | chr6 | 44,278,734 | 44,297,698 | 18,965 |
| ENST00000371505.5 | hg19 | chr6 | 44,246,471 | 44,265,435 | 18,965 |
| ENST00000371504.1 | hg19 | chr6 | 44,247,902 | 44,254,090 | 6,189 |
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