Assay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
SPATA2L PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| SPATA2L - spermatogenesis associated 2 like | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| VPS9D1 - VPS9 domain containing 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_004913.2 | 3364 | Missense Mutation | CCT,TCT | P,S 456 | NP_004904.2 | |
| XM_005256329.4 | 3364 | Missense Mutation | CCT,TCT | P,S 457 | XP_005256386.1 | |
| XM_005256330.4 | 3364 | Missense Mutation | CCT,TCT | P,S 387 | XP_005256387.1 | |
| XM_005256331.2 | 3364 | Missense Mutation | CCT,TCT | P,S 291 | XP_005256388.1 | |
| XM_006721350.2 | 3364 | Missense Mutation | CCT,TCT | P,S 457 | XP_006721413.1 | |
| XM_011523476.2 | 3364 | Missense Mutation | CCT,TCT | P,S 456 | XP_011521778.1 | |
| XM_011523477.2 | 3364 | Missense Mutation | CCT,TCT | P,S 423 | XP_011521779.1 | |
| XM_011523478.2 | 3364 | Missense Mutation | CCT,TCT | P,S 422 | XP_011521780.1 | |
| XM_011523479.2 | 3364 | Missense Mutation | CCT,TCT | P,S 457 | XP_011521781.1 | |
| XM_011523480.2 | 3364 | Missense Mutation | CCT,TCT | P,S 387 | XP_011521782.1 | |
| VPS9D1-AS1 - VPS9D1 antisense RNA 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||

SPATA2L
Genomic Map