TEX28 testis expressed 28
Clinical Significance
MGeND | ClinVar | |
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not provided | 8 | 0 |
Ranking
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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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CXorf2 |
SYNONYM | MRX99 |
SYNONYM | TEX28P1 |
SYNONYM | TEX28P2 |
SYNONYM | fTEX |
MIM | 300092 OMIM |
HGNC | HGNC:2563 HGNC |
Ensembl | ENSG00000278057 Ensembl |
AllianceGenome | HGNC:2563 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000617225.5 | hg38 | chrX | 154,271,265 | 154,295,124 | 23,860 |
ENST00000619903.4 | hg38 | chrX | 154,271,265 | 154,295,211 | 23,947 |
ENST00000610938.1 | hg38 | chrX | 154,271,415 | 154,292,117 | 20,703 |
ENST00000610938.1 | hg19 | chrX | 153,499,080 | 153,500,191 | 1,112 |
ENST00000617225.5 | hg19 | chrX | 153,520,459 | 153,523,477 | 3,019 |
ENST00000619903.4 | hg19 | chrX | 153,520,459 | 153,523,564 | 3,106 |
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