SPAG11B sperm associated antigen 11B
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 6 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
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
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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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | EDDM2B |
| SYNONYM | EP2 |
| SYNONYM | EP2C |
| SYNONYM | EP2D |
| SYNONYM | HE2 |
| SYNONYM | HE2C |
| SYNONYM | SPAG11 |
| SYNONYM | SPAG11A |
| MIM | 606560 OMIM |
| HGNC | HGNC:14534 HGNC |
| Ensembl | ENSG00000164871 Ensembl |
| AllianceGenome | HGNC:14534 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000361111.6 | hg38 | chr8 | 7,447,753 | 7,463,526 | 15,774 |
| ENST00000398462.7 | hg38 | chr8 | 7,450,603 | 7,463,542 | 12,940 |
| ENST00000297498.6 | hg38 | chr8 | 7,450,563 | 7,463,670 | 13,108 |
| ENST00000528168.3 | hg38 | chr8 | 7,450,603 | 7,452,365 | 1,763 |
| ENST00000458665.5 | hg38 | chr8 | 7,450,564 | 7,452,365 | 1,802 |
| ENST00000317900.7 | hg38 | chr8 | 7,461,114 | 7,463,674 | 2,561 |
| ENST00000359758.9 | hg38 | chr8 | 7,447,753 | 7,463,526 | 15,774 |
| ENST00000359758.9 | hg19 | chr8 | 7,305,275 | 7,321,048 | 15,774 |
| ENST00000361111.6 | hg19 | chr8 | 7,305,275 | 7,321,048 | 15,774 |
| ENST00000297498.6 | hg19 | chr8 | 7,308,085 | 7,321,192 | 13,108 |
| ENST00000458665.5 | hg19 | chr8 | 7,308,086 | 7,309,887 | 1,802 |
| ENST00000528168.3 | hg19 | chr8 | 7,308,125 | 7,309,887 | 1,763 |
| ENST00000398462.7 | hg19 | chr8 | 7,308,125 | 7,321,064 | 12,940 |
| ENST00000317900.7 | hg19 | chr8 | 7,318,636 | 7,321,196 | 2,561 |
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