ZMP
zgc:165467
Ensembl ID:
ZFIN ID:
Description:
zgc:165467 (zgc:165467), mRNA [Source:RefSeq DNA;Acc:NM_001103113]
Human Orthologue:
SPAG9
Human Description:
sperm associated antigen 9 [Source:HGNC Symbol;Acc:14524]
Mouse Orthologue:
Spag9
Mouse Description:
sperm associated antigen 9 Gene [Source:MGI Symbol;Acc:MGI:1918084]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19976 | Nonsense | Available for shipment | Available now |
sa40032 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19976
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113938 | Nonsense | 360 | 1289 | 9 | 30 |
ENSDART00000148132 | Nonsense | 360 | 1274 | 9 | 30 |
The following transcripts of ENSDARG00000074531 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 18078324)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 18199644 |
GRCz11 | 3 | 18349384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGAATGATGTGGTAAACTGTGTTGCGTTGTGTTGAAGTACGCCGACC[C/T]GAGGGATTGAGAACATGGCGTTTGACCGCAACACAGAATCCCTGTTTGAA
Long Flanking Sequence:
GGACCTTGGATATAAAGGCCCAAGGTAACTGATGTGCCATAAAATCAAACACGGCAAATAACATGCTGGAAAGTGTCTATAATGATGCCCAGAACTGCTGTTTAGGTAGTCAAAGTACCATGGTTTAAAATTGATATAAGCTTAGAGCAAAAATGATGCTTAAACAATATAAAGTGCCCAATACACTGTAAAAAAGGTGACAACTTAAAAATCATAAGGCAGCTTGCTGCACAGCTTATTTTTAACCCAAGTACTGCACTTGACTTGATTTGAGTCAACTAAAAAAACTCTGCAGAAAGTTGCCCTACAATTTGAAGTTGAGTCAACTAAAAAAGTAAAAGGTAAATGAGGGAAAAAAGGCTTTGGAGGTCAAATTTAATTTACAAATTCATGCTAAAGCTCATGACTAAAGTTAAAAAGTTCATGCTAAAGTGTGTTATATTGGGATATGTGTGAATGATGTGGTAAACTGTGTTGCGTTGTGTTGAAGTACGCCGACC[C/T]GAGGGATTGAGAACATGGCGTTTGACCGCAACACAGAATCCCTGTTTGAAGAAGTGTCATCGGCGGGCACGGGACTGATCGGAGATGTGGATGAAGGGGCCGATCTGTTGGGTAGGTTTGTTGCTGTTTGTGTTTAGAAATGTGGAAGGGAGTGCAAAGGGAGTATATATAGAGCAATAAAATAAGTCTGTCAAATTTCAGATGCAGGTTGTAAGGCTTGAAGCTTACGCAGCTATTCTGAACCAATAATCGGAAACAGAAAGCAGTTGAAGGAGGGCGTGTTTAAATCCATTATTTATCTGACTCCATTGTAATTAATCTGACTCCATTAAAGTTGTTATCATCATTGATAAAGAGAAAGAATCTCTACGTCTTAAAGCAGGCAACGTTTTTATTAAGTTACATGATCAAATATACAGACATTAGAATGACACAAACTAACATACTGTATAAAGAAATTAGCTGTAACATATGCACTGCTGAGCAACAAAGACAGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40032
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 |
---|---|---|---|---|---|
ENSDART00000113938 | Nonsense | 1045 | 1289 | 25 | 30 |
ENSDART00000148132 | Nonsense | 1030 | 1274 | 25 | 30 |
The following transcripts of ENSDARG00000074531 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 18051823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 18173143 |
GRCz11 | 3 | 18322883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACTGTGGTTCACGATAAAGTGTGGTGCGGCTACAGGAACAAGATCTA[C/A]ATCATTCAGCCCAAAGCTATGAAAATCGAGGTTCAGCATTATGTTTTAGT
Long Flanking Sequence:
AGCACTTATTCATTGTTGCTCTTATAGTTGTGTAAATTGCTTCCTTGTCCTCATTTGTAAGTCGCTTTGAATAAAAGCGTCTGCTAAATGACTAAATGTAAATGTAGTAGTTTGTTCATGTTAGTAAATACAATATTTTAAAGTGTTACCATCTTGGTCTTACAGGAGTAAATGTGAGTATACTTAAGAACTGGTAATATTTGATAGTATTTCTTTGCATAGACATGTGAAAGGCCGTGTTTTGGTGGCTCTAGCTGACGGGACACTGGCCATCTTCCATAGAGGTCTTGGTAAGGCACAAGTTTTATTTAACTGATAGTTCAGATACTCGTTCCAGCTTCAAATGATGAAATATAAAGCCACATTCCATGTACTTTTACAGACAGCCAGTGGGATTTAACCAACTACCATCTTCTGGACCTGGGCCGGCCGCATCACTCAATCCGCTGCATGACTGTGGTTCACGATAAAGTGTGGTGCGGCTACAGGAACAAGATCTA[C/A]ATCATTCAGCCCAAAGCTATGAAAATCGAGGTTCAGCATTATGTTTTAGTCTTCAGTAGTCTTAAAATTGTTTAATTACATTTAAATGTGGTTTCCTCAGCATGCCTAAAGTCTGTGTGAAGTTCCTGAGACCCTTATGTCAGTATGTTGATGTCCTTTCAAGTGAAACGGAGTATTGAGTAAGGGCCGGGACTTTGTTTATACGCATCATTCTCTCATAGCAAACCAATGGGAATGTACCTCCGTCATCTACTTGTTATCAACGCTTCTTAATAGCAGATGTAATCAGGGCCTTTGTGTTTGTATGTGAAAACAGAGGTCTTTTGATGCCCATCCGCGTAAGGAGAGTCAGGTGCGTCAGCTGGCCTGGGTGGGTGACGGGATCTGGGTGTCCATCCGGCTGGACTCAACGCTTCGCCTATTCCATGCTCACACCTTCCAGCATCTGCAGGACGTAGACATTGAGCCTTACGTCAGCAAAATGTTAGGTGAGGATGTGT
Associated Phenotype:
Not determined