ZMP
SPATA20
Ensembl ID:
Description:
spermatogenesis associated 20 [Source:HGNC Symbol;Acc:26125]
Human Orthologue:
SPATA20
Human Description:
spermatogenesis associated 20 [Source:HGNC Symbol;Acc:26125]
Mouse Orthologue:
Spata20
Mouse Description:
spermatogenesis associated 20 Gene [Source:MGI Symbol;Acc:MGI:2183449]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22115 | Nonsense | Available for shipment | Available now |
sa22116 | Nonsense | Available for shipment | Available now |
sa13025 | Nonsense | Available for shipment | Available now |
sa15455 | Nonsense | Available for shipment | Available now |
sa44766 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22115
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066288 | Nonsense | 104 | 818 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 12 (position 29162275)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27499884 |
GRCz11 | 12 | 27591244 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAAGACCCCAAAGTATACCAACCGCCTGAGTCAAGAGAAGTCCTCCTA[T/A]CTTTTACAACATGCACACAACCCTGTGGACTGGTGAGGGTCTCTGAAATA
Long Flanking Sequence:
GCTTAAAAAGACAAAAACAAAATAAACTCTTAATTTGGACTTATTTCTTCTGATGGTTAAAACTAAACAATACTTTGGCTTACTCTAAGAATATATTTGATATTTGGACTGGAAATTAGAAAAAAACATAAGAAAAGTATATTTTTTATTGTAATTAATCAATTTCTGTATCTGCATAGTGTTAGACTCCCCATTAAACTGTCAAATAGTGCTATTCAAACCATCTTGTGAAACTGTATTCACATTGCAATATTTATTACAGAAAAATAAATTATTGCACAATATCATATTTTTCTAATATCAAGCAGCCCTAATCTATAGGAGCTTAGTGACACAGTCATAAAGCTTCATTAATGATTTGATTTACCAAAACCATATTCTCTGATTGTTTTCAGGTTTTCTGGAGTGTTTTTCTTTAGCATGGCATCAGGAAGTGACAGTCCGGACAGACTAAAGACCCCAAAGTATACCAACCGCCTGAGTCAAGAGAAGTCCTCCTA[T/A]CTTTTACAACATGCACACAACCCTGTGGACTGGTGAGGGTCTCTGAAATATTACATTGCTCTATGATACAATATCAATACAAACTCTTTGAAAGTAAATGTATCGCTTCGATGTCCTGGCCAAAGTCCCTCAATCGGTCCTTAAGATCATGGCCTTCCAATCATCCCCATCCTCTGAATTGGCTGTGTCACTGTCTCTCCACTCCCCGAATAGCTGGTGTGTGGTGAGCGTACTGGCGTGAATGTTCTGTGGCTGCCGTTGCATTATCCAAGTGGATGTTGCATACTGGTGGTGGTGTGGAGAGACACTCCCTCATGACGCTTTGGGTGTATGGCCATTTACAATAAATGCGCTATATAAATACACATTACATTACATTTTGCTGCTACTCTTTGACACCCGTCTGAAACACCACAACATCCCAATAATGTGGCGTGAGTTTTGAACTCTCAGACCTAACCGATAATATACTTAACACAAAACCGAGGCCTTGTTTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22116
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066288 | Nonsense | 128 | 818 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 12 (position 29164482)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27502091 |
GRCz11 | 12 | 27593451 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTGAACAGGTATCCATGGGGCCAAGAAGCCTTTGATAAAGCAAAATG[T/A]GAAGACAAGCCTATTTTTCTTTCAGGTAACGTAATATTATACTTGAAAAT
Long Flanking Sequence:
GCAAAAACTTGCAAAATTAAACAAATAGGTGTATATTTCTACTTTTTTTAGTGCTGATTTTTTTTTTTCTCAGTGTATGGGTGCGTTTACCTATTGCCTCCTGTTTATTTTTCCTGCAAAAATGTATAGTGTTTTTGTGTTACAAGATGAAATAGATATAGAAATCAGTCTACAGGCTTTCACAGACAGAATGTTGAGGAACATTGTTTTTTTAAGGTTTCATTATGAGATTCACACATTGTAAAAAACAACACAAAAAAAACAATGAATATATAATTTGAAAGGGGGCGGTGTGGTGGCGCAGTGGATATCGCTGTTGCCTCACAGCAAGAAGGTGGCTGGTTCTAGCCTCGTCTAGGTCATTTAGCATTTCTGTGTGGAGTTTACACGTTCTCCCTGTGTTCGTGTGAGTTATATACATATTTTGCTTCATAATTTCCTTTGTATTTTCATTTGAACAGGTATCCATGGGGCCAAGAAGCCTTTGATAAAGCAAAATG[T/A]GAAGACAAGCCTATTTTTCTTTCAGGTAACGTAATATTATACTTGAAAATGTATCAAATGTACATTGACTGTTTTATCCCACAGTTTTATTACTGCTTATAGTGGGTTATTCCACCTGTCACTGGTGTCACGTAATGGAGAGGGAATCCTTTGAGGATGAAGAGATTGGAAAAATACTCAGCGACAACTTTGTATGTATAAAGGTGGACAGAGAAGAGAGACCTGATGTGGACAAAGTTTATATGACATTTGTGCAGGTACGAGCTAGTTGAATTCACTGTGGTCAGTGCTGTAGCTTAAAAAGTGGCAAGCATTATTTAAATGAAGTGAATAAATTCTGCCCAGGCAACCAGTGGTGGAGGAGGCTGGCCAATGAGTGTGTGGCTCACACCAGATCTTAAACCGTTCATAGGTGGAACATACTTCCCACCCAGAGACAGCGGAAGAAGACCTGGACTGAAAACTGTGCTTTTACGGATAATAGAGCAAGTAAGAGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13025
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066288 | Nonsense | 412 | 818 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 12 (position 29169758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27507367 |
GRCz11 | 12 | 27598727 |
KASP Assay ID:
2260-5469.1 (used for ordering genotyping assays)
KASP Sequence:
CAGATTTGAKTTTGAGCATTGTGCTGCCCTCTGCAGTCTGGCGGCTTCTA[T/G]AGCGCTGAGGATGCAGAYTCCTTTCCCAYAGTGGAGTCCACAGAGAAGAG
Long Flanking Sequence:
CAAACTTTCTAATATCCAGCAAAGCACCAGCCATCTTTGGTGATGAATGAATTGGCCCAATTAAAACATCTATAAACATAAGTATCTATGATTATAAGATTTATGGAGTGATTTATATATCAACATAGAATACCTAGGACCTTATTTTTCTACGCTTGTATTGGCTGTAATATTTTATAGGTCTGTGTTTCCTCTTTAAAACCCCATCTTACACCAAAAAAAATGTTGGTAGTAAAGTGGCTAAAAACGTAGCATTTTCTTTGGACTATATAAATCATACCTTATTATATTTTAAACATCAACTAGAAGTGTTATTTGCTGAGCTCATGTACAGGAACATGTTTGAAGTTTTGTAACTGGAGAACTTTTTTTGCCGAGAAATAATTACTCCATGAAGAAACCACAACATATCTTTGAAAACAGCCTACAAGTGGCAAAAAGTAAATAAAGCAGATTTGATTTTGAGCATTGTGCTGCCCTCTGCAGTCTGGCGGCTTCTA[T/G]AGCGCTGAGGATGCAGATTCCTTTCCCACAGTGGAGTCCACAGAGAAGAGAGAGGGAGCGTTTTGTGTGTGGACAGCAGGAGAGATCAGAGAGCTGCTTCCTGATATCGTGGAAGGCGCCACAGGAGGTGCAACACAGGCGGATATCTTCATGCATCATTATGGTGTGAAAGAGCAAGGCAACGTGGATCCCGCTCAGGTTTGGGGAGATGAAGTTTTTATGAGAGCCAAATTCTTTTGATCCAACTTTCACTAATTCTTGGCTACAACAGTGAAAGAGAAAGTTTATGCATGGAATAATTCTGTAGATCCATTTGACTAGCACGTTTAAAGGTATAAAGTTATGTTTATTGGAAATATCCTGTTAAAAAAATAAACTTATAATAATCAACTATTATTTAAAAAGAAAATTCTTTCAAATGTCACTATCATTAGGGCAAAAATAGACTGTGTTATTAAAAGTAGTTTAACAAGATGCATACTAGTACTTGAAGAATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15455
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066288 | Nonsense | 412 | 818 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 12 (position 29169758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27507367 |
GRCz11 | 12 | 27598727 |
KASP Assay ID:
2260-5469.1 (used for ordering genotyping assays)
KASP Sequence:
CAGATTTGAKTTTGAGCATTGTGCTGCCCTCTGCAGTCTGGCGGCTTCTA[T/G]AGCGCTGAGGATGCAGAYTCCTTTCCCAYAGTGGAGTCCACAGAGAAGAG
Long Flanking Sequence:
CAAACTTTCTAATATCCAGCAAAGCACCAGCCATCTTTGGTGATGAATGAATTGGCCCAATTAAAACATCTATAAACATAAGTATCTATGATTATAAGATTTATGGAGTGATTTATATATCAACATAGAATACCTAGGACCTTATTTTTCTACGCTTGTATTGGCTGTAATATTTTATAGGTCTGTGTTTCCTCTTTAAAACCCCATCTTACACCAAAAAAAATGTTGGTAGTAAAGTGGCTAAAAACGTAGCATTTTCTTTGGACTATATAAATCATACCTTATTATATTTTAAACATCAACTAGAAGTGTTATTTGCTGAGCTCATGTACAGGAACATGTTTGAAGTTTTGTAACTGGAGAACTTTTTTTGCCGAGAAATAATTACTCCATGAAGAAACCACAACATATCTTTGAAAACAGCCTACAAGTGGCAAAAAGTAAATAAAGCAGATTTGATTTTGAGCATTGTGCTGCCCTCTGCAGTCTGGCGGCTTCTA[T/G]AGCGCTGAGGATGCAGATTCCTTTCCCACAGTGGAGTCCACAGAGAAGAGAGAGGGAGCGTTTTGTGTGTGGACAGCAGGAGAGATCAGAGAGCTGCTTCCTGATATCGTGGAAGGCGCCACAGGAGGTGCAACACAGGCGGATATCTTCATGCATCATTATGGTGTGAAAGAGCAAGGCAACGTGGATCCCGCTCAGGTTTGGGGAGATGAAGTTTTTATGAGAGCCAAATTCTTTTGATCCAACTTTCACTAATTCTTGGCTACAACAGTGAAAGAGAAAGTTTATGCATGGAATAATTCTGTAGATCCATTTGACTAGCACGTTTAAAGGTATAAAGTTATGTTTATTGGAAATATCCTGTTAAAAAAATAAACTTATAATAATCAACTATTATTTAAAAAGAAAATTCTTTCAAATGTCACTATCATTAGGGCAAAAATAGACTGTGTTATTAAAAGTAGTTTAACAAGATGCATACTAGTACTTGAAGAATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44766
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066288 | Splice Site, Nonsense | 735 | 818 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 12 (position 29193443)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 27531052 |
GRCz11 | 12 | 27622412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTGCCAGACATGGTCCGCGGTGTCATGGCCCACCATTACACTCTTAAA[C/T]AGGTAACGGCAGACTGGAGTACAGGCTACTGAATATGCAGTTTAAAGGTC
Long Flanking Sequence:
CTGATTTATAAAAGAAAGTCATATTTTGATTTGAAACCCCATAATATTTTCCTGAGATGTTGATTTATGTAAATATTTGTCAGATTTGCATGATGATTCATTTTTATTTCCCTTTGGTTGATGAAGAATGCTTGTGTTTTGCACATCCTATAACAGCCATGAAAACGTGAGACGGAAGTAGACACGTATAACAGTATGCACAAATAATTAACTGTTATTTAAATGATAATCAATAACATATATATAACGTATATTGACAACTTTACTATAACATTTGTGTTTTATATGTATTATTTTTTTCAGATCAGGACGGTGCTGAGCCTAGTGCAAACTCAGTGTCAGCCATGAATTTGCTCCGGCTTTCACACTTCACAGGCCGGCAGGACTGGATCCAGCGCTCGGAGCAGTTGCTGACCGCCTTTTCCGATCGACTGCTTAAGGTGCCAATCGCCCTGCCAGACATGGTCCGCGGTGTCATGGCCCACCATTACACTCTTAAA[C/T]AGGTAACGGCAGACTGGAGTACAGGCTACTGAATATGCAGTTTAAAGGTCCAGTTTGTCACAGCTTGTCACATCATGACCAGATGATGCAACGCCTATGAAATGATGCTTCTCTTCAGCTGTGACATCTACAATGAGACAGAAATGTTCACAAGTCCCTAAGGTAGAGTCTGTCTTAAGTGTCAGATCTCTTTCAAAGCCAGGTCGCAAGTCTTTCGATCAAGATTTTTTTTTTATAAACCCTTTCTAAGAACTGTTCTATATTAATAAATTATGTTTGTTATTATTATTATTATTATTATTATTAAGAATGCATTGTTATTTTAGTAAAAATAAAACACCAAAATTATTTATTAAATAATTATTCATTATTTCTTTTTTACCATTTTAACATTATAATATTTAACCAAATATTGTGTTTTATAATCAATTAATATTTGTTTATATTACAGTTTATTTTATTTATATTTAATATTTGGACTTTCTGCTTCTTCTTATTAT
Associated Phenotype:
Not determined