SPAG11A sperm associated antigen 11A
Information
- Symbol
- SPAG11A
- Type
- protein-coding
- Description
- sperm associated antigen 11A
- Entrez Gene ID
- 653423
- Genome
- hg19
- Position
- chr8:7,705,530-7,718,465
- Genome
- hg38
- Position
- chr8:7,848,008-7,860,943
- HGNC
- HGNC:33342 HGNC
- Ensembl
- ENSG00000178287 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 12 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
14 |
 |
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 | : |
|
| 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 | EDDM2A |
| SYNONYM | HE2 |
| HGNC | HGNC:33342 HGNC |
| Ensembl | ENSG00000178287 Ensembl |
| AllianceGenome | HGNC:33342 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000400125.6 | hg38 | chr8 | 7,847,876 | 7,850,436 | 2,561 |
| ENST00000434307.6 | hg38 | chr8 | 7,847,880 | 7,860,965 | 13,086 |
| ENST00000351436.8 | hg38 | chr8 | 7,848,024 | 7,863,797 | 15,774 |
| ENST00000454911.6 | hg38 | chr8 | 7,859,178 | 7,860,982 | 1,805 |
| ENST00000326625.5 | hg38 | chr8 | 7,859,178 | 7,860,982 | 1,805 |
| ENST00000326558.9 | hg38 | chr8 | 7,848,024 | 7,863,797 | 15,774 |
| ENST00000642566.2 | hg38 | chr8 | 7,848,008 | 7,860,943 | 12,936 |
| ENST00000400125.6 | hg19 | chr8 | 7,705,398 | 7,707,958 | 2,561 |
| ENST00000434307.6 | hg19 | chr8 | 7,705,402 | 7,718,487 | 13,086 |
| ENST00000642566.2 | hg19 | chr8 | 7,705,530 | 7,718,465 | 12,936 |
| ENST00000326558.9 | hg19 | chr8 | 7,705,546 | 7,721,319 | 15,774 |
| ENST00000351436.8 | hg19 | chr8 | 7,705,546 | 7,721,319 | 15,774 |
| ENST00000326625.5 | hg19 | chr8 | 7,716,700 | 7,718,504 | 1,805 |
| ENST00000454911.6 | hg19 | chr8 | 7,716,700 | 7,718,504 | 1,805 |
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