ZMP
spag6
Ensembl ID:
ZFIN ID:
Description:
sperm-associated antigen 6 [Source:RefSeq peptide;Acc:NP_001002210]
Human Orthologue:
SPAG6
Human Description:
sperm associated antigen 6 [Source:HGNC Symbol;Acc:11215]
Mouse Orthologues:
BC061194, Spag6
Mouse Descriptions:
cDNA sequence BC061194 Gene [Source:MGI Symbol;Acc:MGI:3040687]
sperm associated antigen 6 Gene [Source:MGI Symbol;Acc:MGI:1354388]
sperm associated antigen 6 Gene [Source:MGI Symbol;Acc:MGI:1354388]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6762 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13900 | Splice Site, Nonsense | Available for shipment | Available now |
sa44115 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31100 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6762
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 |
---|---|---|---|---|---|
ENSDART00000017605 | Splice Site, Nonsense | 97 | 507 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 17822532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17129008 |
GRCz11 | 24 | 17273427 |
KASP Assay ID:
554-5357.1 (used for ordering genotyping assays)
KASP Sequence:
TATGATTGCTTTGTCCATTCCCCTATGAATAYATGGGATATGAAAGACAG[C/T]GATTCTATAAGAARGCTGCTGCATTCGTTCTTCGGGCTRTTGCTAAGCAT
Long Flanking Sequence:
AATTTGGATCCTTATTTTGTATTTTCTATTGGATTCCAGTCAGGTGATTGGCTGGGCCATTCTACAACTTGATTTTCTTTTTTTGAAAGCATTTGTGAGTTACTTTGGCTGTGTTTTGGATAATTGTCTTGCTGTAATATCCACCCTGGCTTCATCATCTTGTTAATGTAGAGGTCAGCTTGAAGCAGCTGTAATAATTTACAATGATAAAGGTTAGATGGTTGCTGAATAACTACTAAGAGATTTCAGCTGCTGTCTGGGCATTCACTAATTTGGTGAATTGAATTGAATTAATTTCTACATCTTCTTTTCTTCATGTGTTCAATACTTTTTCCCAGTGTCCTAAGTTTTTCTCAGAGGATGAAAAAAATAAAACCTTGATAAATTCTATAAATATCTAAAGCTGCATTTCAGGACTGCTTGTCATTCCTTTCTTAAGTGTAATTAATATATGATTGCTTTGTCCATTCCCCTATGAATATATGGGATATGAAAGACAG[C/T]GATTCTATAAGAAAGCTGCTGCATTCGTTCTTCGGGCTGTTGCTAAGCATTCCCCCGAGCTGGCCCAGGCTGTGGTGGACTGTGGAGCAGTGGACGCTCTTGTCATCTCCCTGGAGGAGTTCGATCCTGGGGTCAAAGAGGCTGCTGCATGGGCTATAGGCAACATCGCCAGACATAATGGCCGTAAGTGTAAAGCTAAAAGGGTTTTTTAATGTTTACGGTAATGTTGCCCTAGCTGTTCATCTTTTCTCTCCTGGTGTGCAGAGCTGTCTCAGGCAGTGGTTGATGCTGGAGTTGTGCCTCTGCTCGTGTTATGCATCCAGGAACCTGAAATAGCCCTGAAGAGAGTTGCTGCTTCTGCTCTGAGCGATATAGCCAAACATTCTCCAGAGCTGGCTCAAACTGTGGTGGACACAGGGGCAATCGCACACCTTGCACAGATGATCCTAAACCCAGATGCCAAATTGAAGGTCACAAAGCCTACAGATATTATAATCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13900
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:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017605 | Splice Site, Nonsense | 226 | 507 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 17823000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17129476 |
GRCz11 | 24 | 17273895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGCAATCGCACACCTTGCACAGATGATCCTAAACCCAGATGCCAAATTG[A/T]AGGTCACAAAGCCTACAGATATTATAATCAATGACTCGCAAAGGGATAGT
Long Flanking Sequence:
TCCCCTATGAATATATGGGATATGAAAGACAGCGATTCTATAAGAAAGCTGCTGCATTCGTTCTTCGGGCTGTTGCTAAGCATTCCCCCGAGCTGGCCCAGGCTGTGGTGGACTGTGGAGCAGTGGACGCTCTTGTCATCTCCCTGGAGGAGTTCGATCCTGGGGTCAAAGAGGCTGCTGCATGGGCTATAGGCAACATCGCCAGACATAATGGCCGTAAGTGTAAAGCTAAAAGGGTTTTTTAATGTTTACGGTAATGTTGCCCTAGCTGTTCATCTTTTCTCTCCTGGTGTGCAGAGCTGTCTCAGGCAGTGGTTGATGCTGGAGTTGTGCCTCTGCTCGTGTTATGCATCCAGGAACCTGAAATAGCCCTGAAGAGAGTTGCTGCTTCTGCTCTGAGCGATATAGCCAAACATTCTCCAGAGCTGGCTCAAACTGTGGTGGACACAGGGGCAATCGCACACCTTGCACAGATGATCCTAAACCCAGATGCCAAATTG[A/T]AGGTCACAAAGCCTACAGATATTATAATCAATGACTCGCAAAGGGATAGTTCAGCCAAAAATGAAAATCTGTCATTGTTTACTCATCCTTTACTTGATTCAAACCTTAATGAGTTTCTTTCTTATGTTCAACACAAATAGTGAGTTTAATTTCATTTTTGGGTGAACTATATTGTTAATGGTTTTTTTCATACTTGACATAATAAATCTTTGTCATTCTAACCCCCCTGGAAAATGCAATCTTAGGTCAGTCTTTCGCGTTTCACATCACTCAGAGGTTAAGAATTAATCCTGGGCATTTGTAAACTGACATTTCACACTGTACATTTCCAAACCCCGAGTTAACATTCTTAATGCTCTTGGGGTGAATGACATTTTAGAACCGTATTTGGACTTACGTACAAACTTAGTCCTGGAGGGTCACTGTCCTGCAGGGTCTAACTACAGCTTGACTTAACACAACTGAATGTGTGTGCTAGGACATTATATATTAAGGAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44115
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017605 | Nonsense | 481 | 507 | 10 | 11 |
ENSDART00000017605 | Nonsense | 481 | 507 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 17825573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17132049 |
GRCz11 | 24 | 17276468 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCTGGTTCTGCAATTCAGGAATATATTAATGCAATCAACAACTGTTA[C/A]CCTGAAGAGATTGTCAGGTACATGCACATTTATATGCATAATAAAAAGCA
Long Flanking Sequence:
CCTCTATTTGGACACAGAGAGTTCTGAAGATCTGCAGGTCAAGGTGAACAAAGACATATTTGTGACTGATAGGGGTGTGTATTCATTTGGATGTTTTTTCACTGATTTTTAGACCCTAATGGTGTCTTCTATTGGCTTTGTGTTTGTACTCAAAAAGGCCAAAAAGGGACTGAAGAGCATCCTTCAGAAGTGTACTTATCTACCAGCACTGGAGCCTCTTCTCTATGAAGCTCCCAGCAACATTCTTAAACATGTCATCTGCCAGTTCAGTAAGGTAGCAGGAACATATTGCTTTTATTATCAAACATTTGAACAATGTGTTCTTACTGAGAACTGCTTAAAATACTTTACTGTTTCTTTTCAATCTCAAAGGTTCTTCCTCATGACAGCAAGGCACGGCGTTTGTTTGTTACCAGTGGTGGCTTGAAGAAGGTACAAGAGATCAAAGCAGAACCTGGTTCTGCAATTCAGGAATATATTAATGCAATCAACAACTGTTA[C/A]CCTGAAGAGATTGTCAGGTACATGCACATTTATATGCATAATAAAAAGCACCATATCAAAATATTTTAAACCAAACAATGTGGTTCTGTATTGATTTGATATGTTGTATGATTTTTTTTTCAATTAAATGTTTTCTGCTTTTACAGATATTATTCCCCTGGTTACTCCGAGACCTTGCTGGAAAGGATTGAAAAATATCAGCCAACATGACTTTATGAAACACTAAAACCACTCCATTTTAAACACTTGTGAAAAACAAAGAAGTAAATAAAATGTAATAAAGAAATTAGCAATAGCAATGAATTTAATTTAGTTTGTTTGTCTTGTTTCATGTACAATAGGCCTGTTAAACAAAAGTATATTTTATAGTGGTGTGGATTATTGTGTTTGTAATTAATCAGAGACAACAAAGCTTAGTTTAACCTATTTTTTAAAACTCTGTCTTTGAGAAATCTTGGTCTACAACACGAAAAGGTATTTTATCACATACACTCAGTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31100
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017605 | Nonsense | 481 | 507 | 10 | 11 |
ENSDART00000017605 | Nonsense | 481 | 507 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 17825573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 17132049 |
GRCz11 | 24 | 17276468 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCTGGTTCTGCAATTCAGGAATATATTAATGCAATCAACAACTGTTA[C/A]CCTGAAGAGATTGTCAGGTACATGCACATTTATATGCATAATAAAAAGCA
Long Flanking Sequence:
CCTCTATTTGGACACAGAGAGTTCTGAAGATCTGCAGGTCAAGGTGAACAAAGACATATTTGTGACTGATAGGGGTGTGTATTCATTTGGATGTTTTTTCACTGATTTTTAGACCCTAATGGTGTCTTCTATTGGCTTTGTGTTTGTACTCAAAAAGGCCAAAAAGGGACTGAAGAGCATCCTTCAGAAGTGTACTTATCTACCAGCACTGGAGCCTCTTCTCTATGAAGCTCCCAGCAACATTCTTAAACATGTCATCTGCCAGTTCAGTAAGGTAGCAGGAACATATTGCTTTTATTATCAAACATTTGAACAATGTGTTCTTACTGAGAACTGCTTAAAATACTTTACTGTTTCTTTTCAATCTCAAAGGTTCTTCCTCATGACAGCAAGGCACGGCGTTTGTTTGTTACCAGTGGTGGCTTGAAGAAGGTACAAGAGATCAAAGCAGAACCTGGTTCTGCAATTCAGGAATATATTAATGCAATCAACAACTGTTA[C/A]CCTGAAGAGATTGTCAGGTACATGCACATTTATATGCATAATAAAAAGCACCATATCAAAATATTTTAAACCAAACAATGTGGTTCTGTATTGATTTGATATGTTGTATGATTTTTTTTTCAATTAAATGTTTTCTGCTTTTACAGATATTATTCCCCTGGTTACTCCGAGACCTTGCTGGAAAGGATTGAAAAATATCAGCCAACATGACTTTATGAAACACTAAAACCACTCCATTTTAAACACTTGTGAAAAACAAAGAAGTAAATAAAATGTAATAAAGAAATTAGCAATAGCAATGAATTTAATTTAGTTTGTTTGTCTTGTTTCATGTACAATAGGCCTGTTAAACAAAAGTATATTTTATAGTGGTGTGGATTATTGTGTTTGTAATTAATCAGAGACAACAAAGCTTAGTTTAACCTATTTTTTAAAACTCTGTCTTTGAGAAATCTTGGTCTACAACACGAAAAGGTATTTTATCACATACACTCAGTTAT
Associated Phenotype:
Not determined