ZMP
si:dkey-208b23.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JLM6]
Human Orthologue:
SPAG17
Human Description:
sperm associated antigen 17 [Source:HGNC Symbol;Acc:26620]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21219 | Nonsense | Available for shipment | Available now |
| sa969 | Splice Site, Nonsense | Available for shipment | Available now |
| sa31634 | Nonsense | Available for shipment | Available now |
| sa18106 | Nonsense | Available for shipment | Available now |
| sa21218 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21219
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081048 | Nonsense | 158 | 1612 | 5 | 42 |
| ENSDART00000126551 | Nonsense | 166 | 1743 | 5 | 45 |
| ENSDART00000129168 | Nonsense | 157 | 819 | 5 | 20 |
| ENSDART00000137784 | None | None | 413 | None | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 13577832)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 13023176 |
| GRCz11 | 8 | 13060881 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAACACAGAATATGAATATTTCAGGCCGTAGAGGAGAATGCTCATGTT[A/T]AAGTAGGACTGAATTCTGCCAATAAAGATCAGGGAGGTAAAGGAGCAGCA
Long Flanking Sequence:
TTATGAAGAAATTTACACTGGATTTCTGCTGTATAATACAAAACAACTTTCTACACAGTGATAACTGATAGTGTTTAAATTTTTGTGAATAATAGTGTATGCAACAAATATCAATAACAGGCATGTCCAAGCTCGGTCCTGGAGGGCCAGTGTCCTGCAAAGTTTAGTTCCAACCCCAATCAGACACACCTGGGCTAGCTAATCAAGTTCTTACCAGGCTTTCTAGAAACATCTTTGCAGGTGTGTTGAGGCAAGTTGAAGCTAAAATCTGCAGGACATCGGCCCTCCAGGACCGAGTTTGGACACCCCTGATCTATAACATGCCTGAGAAGTTATGTTTTTCTTTAATTGAGTTAAAGATTACATATTTATTTAGCAATAAATTAATTCTAATCTACAGTAGAAGAGTGTGCTTATGTTTTTTTTTTATTAACTATTTCTTAGATAAATAGTAACACAGAATATGAATATTTCAGGCCGTAGAGGAGAATGCTCATGTT[A/T]AAGTAGGACTGAATTCTGCCAATAAAGATCAGGGAGGTAAAGGAGCAGCAAAGGGGAAAAAAGTGGCTGACATTCCAGTTCCAACCAAAGACACCAAACTCAAACGCAGGGGGGAGGAGGAAAACACAATCAAATATATAGGTGAGGCATGACCACAGTTAACTAACCACCTTTATCAAAAAACAAGTCTGGTTTTGCACTGTTTATAGTGTTTTAATGTTCTCTTTAAACATGTCTGTCTAGATGATGAGCCTGATGATGGTCCACAGCAATACATTCTGATAGTGGGATTCTATGAACCCCTTCTGATTGCAGTGCTGGACTCAATGGGTATCCATGTGTCCAATGTTATTAAACTGGGTTTACAGAGAGATGAACATTCAGAGGCTCTAGAGGACACAGAGGCAGAGGAGGATCACCAGTCAAATGAAGACCAGGGCAAGATACTGTTTTTACATATATGTGTTCTGTTATAAATAACACAGTGCATGGAGAATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa969
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081048 | Nonsense | 722 | 1612 | 18 | 42 |
| ENSDART00000126551 | Nonsense | 737 | 1743 | 18 | 45 |
| ENSDART00000129168 | Splice Site | None | 819 | None | 20 |
| ENSDART00000137784 | None | None | 413 | None | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 13570678)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 13016022 |
| GRCz11 | 8 | 13053727 |
KASP Assay ID:
554-0874.1 (used for ordering genotyping assays)
KASP Sequence:
TGCACYATCATGAGMAATCAATTGATTTATAATATCCTATAAACTGATTA[T/G]AAAAAGGGTAAYGAAGTGACCCTGACAGACCTCCAGGAGACCCTAATTCG
Long Flanking Sequence:
TTTGGTTGCCTAGAAAATGTTTCTTGATTAAAGATTTTTTTAGATATTTGGACTAAAAAGAAGACAAAAAAATAAAAGAAAAGAATTTTTTTTTTGCAGTGTATGGTTTTGTTTCTTCATAGTCCTGCATTTTCCTCTTCTGTTATTTATCTAATGCACATGTAAATCTGTGGGCGGTGATAAACAGACTTTAACATGATCCTAAACATGATCCTCTGTGGAGGTGGAGTTTAGCCACATAATTACATAATAAATACGCACATTCCACAACCTGTTGTTTGTGACCCCTTTAAATACAAAACAAATATTTGACAAATCTTTAAAGCCTTTTGCCATTTTATATTTTATAGGATCAGCAAAACGCAGTGCTGAGAATGATGAACAAATGGTAGGATTAATGTTTTGAAACCAAAAGTTGACATTTCTATAAATACACTACACATTTATCTCTGCACCATCATGAGCAATCAATTGATTTATAATATCCTATAAACTGATTA[T/G]AAAAAGGGTAACGAAGTGACCCTGACAGACCTCCAGGAGACCCTAATTCGCCGACTGGAAGACTATAACTTTGTAGAGAAGCACAGTGCTGATGTTTTTCCCCAGGTAACAATCTTCAGAACACTATTTTCAATATTACTTTTAAAATCTATAAAACATTTAATTACAGATGAGTGTTTCTCTTTCAGGTCCTCCAATCTGCTTCCGAAATGTATAGATGTGTGGACACATTTCAGTGTAGAGACAATGCCGTGTATGTCATCTGCCACAATCCAATGAGCCAACAGAGGAGCTGCAAAGAATTCTGGGAAGGATCACTTCACACAGATGTGGGCTTCAGGTACTTTATCTCTTCTTTGAGATCACAAAATTATTTCAAAATTGATTTGCTATGTAATGACAATTTAGAATTAATTAGAATTTGAATAACTAATTTCTAATAACTAATTCATATTCTAAGAAATAATAATAGTACATACATTTTTAATATTTATTTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31634
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081048 | Nonsense | 794 | 1612 | 19 | 42 |
| ENSDART00000126551 | Nonsense | 809 | 1743 | 19 | 45 |
| ENSDART00000129168 | Nonsense | 724 | 819 | 17 | 20 |
| ENSDART00000137784 | None | None | 413 | None | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 13570381)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 13015725 |
| GRCz11 | 8 | 13053430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCCGTGTATGTCATCTGCCACAATCCAATGAGCCAACAGAGGAGCTGC[A/T]AAGAATTCTGGGAAGGATCACTTCACACAGATGTGGGCTTCAGGTACTTT
Long Flanking Sequence:
AAAACAAATATTTGACAAATCTTTAAAGCCTTTTGCCATTTTATATTTTATAGGATCAGCAAAACGCAGTGCTGAGAATGATGAACAAATGGTAGGATTAATGTTTTGAAACCAAAAGTTGACATTTCTATAAATACACTACACATTTATCTCTGCACCATCATGAGCAATCAATTGATTTATAATATCCTATAAACTGATTATAAAAAGGGTAACGAAGTGACCCTGACAGACCTCCAGGAGACCCTAATTCGCCGACTGGAAGACTATAACTTTGTAGAGAAGCACAGTGCTGATGTTTTTCCCCAGGTAACAATCTTCAGAACACTATTTTCAATATTACTTTTAAAATCTATAAAACATTTAATTACAGATGAGTGTTTCTCTTTCAGGTCCTCCAATCTGCTTCCGAAATGTATAGATGTGTGGACACATTTCAGTGTAGAGACAATGCCGTGTATGTCATCTGCCACAATCCAATGAGCCAACAGAGGAGCTGC[A/T]AAGAATTCTGGGAAGGATCACTTCACACAGATGTGGGCTTCAGGTACTTTATCTCTTCTTTGAGATCACAAAATTATTTCAAAATTGATTTGCTATGTAATGACAATTTAGAATTAATTAGAATTTGAATAACTAATTTCTAATAACTAATTCATATTCTAAGAAATAATAATAGTACATACATTTTTAATATTTATTTTGCAAGATACAAGTATTCCTGTTGAACAGCAATTTTTAAAGGCTTAAATAGGCAGGTTAGGTTTATTGGGAAGGTCAGTAGTTTGTTCAGCAGCCCCAAAAAAAAAAAATTCTTATGGAGCTAATTATCCATATCATATTGACATGGCAGTTAAAATAATATATTTATATATTTTTAATCCCAGCTAAACTAAAAGAAATAAGTCTTTCTCCAGAAGAAAAATATAATGCTATTTTTCTGTTCTGTTAAACATCACATTTGAGAAATCTTTGACAAAGAATAAAAATTTTAATCTAAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18106
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 |
|---|---|---|---|---|---|
| ENSDART00000081048 | None | None | 1612 | None | 42 |
| ENSDART00000126551 | Nonsense | 1150 | 1743 | 28 | 45 |
| ENSDART00000129168 | None | None | 819 | None | 20 |
| ENSDART00000137784 | None | None | 413 | None | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 13566246)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 13011590 |
| GRCz11 | 8 | 13049295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTTTGAAAATCATTTGGACAAGGAATATTTTGTCAACAAAATCACCTA[T/A]ACTGGCGTCACGGTGGCGCAATGGGTAGCAAGATCGCCTCATAGCAAGAA
Long Flanking Sequence:
ACTAAATATTTTTCTCTCTGCGCTGGACCAGCTTTTTCTTGGTCAAAGGCGCAGTCTATTTCAGTTTCTCAAAATAGCAACACTCCAACATTGCGCCTTAACACGCCTCCTTTATAAACCGGCACACCCATGAGTCCTCAAAGTAGCACAAATGGATTTGCTATTTAAACAATGTGGCGCAAAATGTGACAACTAGGGTTTGAAAATAGCAAAAAAAAATCGGGCAAAATACACCTTGCGCCGGGTGTATGATAGGGCCCTTTATGTGTTTTAAAATACAAAATTTTGCAAAGTACTTACAGTTTTTTTTTTTTAAATGATAATGCAAATCACTTGTTTTGGCTAATACTTAATGACTGAAACAACAATAGTGTACTACTACAGCCCTATGAGTTTGCAAAGTGGTATAGACAACTACTAGCCTTACATAAATAATAGTTTTTTTCTTGTCATTTTGAAAATCATTTGGACAAGGAATATTTTGTCAACAAAATCACCTA[T/A]ACTGGCGTCACGGTGGCGCAATGGGTAGCAAGATCGCCTCATAGCAAGAAACTGGTTCGAGCCCCGGCTGGGCCATTTGGCAATTGTGTGTGGAGTTTGCATGTTCTCCCCATGTTGGCGTGGGTTTCCTCCGGGTGCTCTGGTTTCTCCCACAGTTCAAAGACATGCGCTACAGGTGAATTAAATAAGTTAAATTGGCCAAAGTGTATCTGTGTGAAAGAGTGTGTATGGGTGCTTCCCAGTGTTGGGTTGTGGCTGGAAGGGCATCCACTACGTAAAACATATGCTGGATATGTTGGCGGTCCATTCCACTGTGGCGACCCCTGATTAATAAAGAGACTAAGCTGAAAAGATGAATGAATTTATTAATTAATCACCTATACTAAAAAACTGTTTTAGCACATTTAGTGCATTGTTTCATGTGAGTTTTAACATATCTTGTTTAAAAAAATAAATAACACTACAAAATTCCGCAAAACATGTAATTTCTACATGCAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21218
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 |
|---|---|---|---|---|---|
| ENSDART00000081048 | Nonsense | 1591 | 1612 | 42 | 42 |
| ENSDART00000126551 | Nonsense | 1722 | 1743 | 45 | 45 |
| ENSDART00000129168 | None | None | 819 | None | 20 |
| ENSDART00000137784 | Nonsense | 288 | 413 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 13554393)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 12999737 |
| GRCz11 | 8 | 13037442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCATATCTGGAGCAGTTGCTTCAGAGAGAGGCTCAGTGGGAGAAAATG[C/T]AGCTAAAGGATCCACGAACAGCACAGGAGAAGAGTCATCAGAATGAGCTG
Long Flanking Sequence:
TCTTGCCTAAATACCCTAACCTGCCCTAGCTAACCTAATTAAGCTAGTTAAGCCTTTCAATGTCACTTTAAGCTGTACAGAAGTGTCTTGAAAAATATCTAGGAAACTATTATCTACTGTTATCATGGCAAAGATAAAATAAATCAGTTATTAGGAATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAACACAGAAATTATGGAAAAAATAAACAGCTAATAATTCTGACTTTGACTGTATGTATGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATAATTTTTAGTGTTTACTTTATATTTCACTCATTTAAATATCCTTCTGTCTTCTTGTGTTGATGTATGTACTGTATATGTGCTCCTGAAAACCACAGAAAAACTTTAATAAAGCTCATTCTGATTCTGATATGGATTTAATCACGTAGGCATATCTGGAGCAGTTGCTTCAGAGAGAGGCTCAGTGGGAGAAAATG[C/T]AGCTAAAGGATCCACGAACAGCACAGGAGAAGAGTCATCAGAATGAGCTGCTGCGCCTTGTACTGGTCAGACAAGATCCTATGTTCTTAAACTATTCAGACGATTAAATAAATACAGATGGTGACTTATATAAATTGTTTTAGTCTCTGCCTGATGCTGTAGATCTTCCAGCTACCATAGATACAAGGCCTCAGTCAGGTGAGAAAATGTATTAACAAATTAAATAACAGTTCATTAAAATAAAAACTGTTTCTTAATATTGAATTTGATTTATTATTGAAGGTTATACATTGTTATATTTCCTAATGATAATAAATATAATAAATATATTATTGTTCATTAATTATAAGTTATTTAACCCTCTGATTCATCAATGTATTTGAGCATTAAATATGTTCAGTGTGATATTACATAGTGTCATAAACAATGGTTTTAAATAGGGAAAATGTTGTGGCAGCGCTGTAGCTAATGAATATTTTTAGCACTGTTAAGCTGTCATC
Associated Phenotype:
Not determined