TEX14 testis expressed 14, intercellular bridge forming factor
Information
- Symbol
- TEX14
- Type
- protein-coding
- Description
- testis expressed 14, intercellular bridge forming factor
- Entrez Gene ID
- 56155
- Genome
- hg19
- Position
- chr17:56,634,041-56,769,384
- Genome
- hg38
- Position
- chr17:58,556,680-58,692,023
- MIM
- 605792 OMIM
- HGNC
- HGNC:11737 HGNC
- Ensembl
- ENSG00000121101 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 14 |
| Likely pathogenic | 0 | 4 |
| Benign | 0 | 26 |
| Likely benign | 0 | 52 |
| Conflicting classifications of pathogenicity | 0 | 8 |
| Uncertain significance | 0 | 166 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
4 |
 |
252 |
 |
6 |
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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| 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 | CT113 |
| SYNONYM | SPGF23 |
| SYNONYM | SgK307 |
| MIM | 605792 OMIM |
| HGNC | HGNC:11737 HGNC |
| Ensembl | ENSG00000121101 Ensembl |
| AllianceGenome | HGNC:11737 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000240361.12 | hg38 | chr17 | 58,556,680 | 58,692,023 | 135,344 |
| ENST00000349033.10 | hg38 | chr17 | 58,556,678 | 58,692,045 | 135,368 |
| ENST00000389934.7 | hg38 | chr17 | 58,556,678 | 58,692,055 | 135,378 |
| ENST00000349033.10 | hg19 | chr17 | 56,634,039 | 56,769,406 | 135,368 |
| ENST00000389934.7 | hg19 | chr17 | 56,634,039 | 56,769,416 | 135,378 |
| ENST00000240361.12 | hg19 | chr17 | 56,634,041 | 56,769,384 | 135,344 |
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