ZMP
si:ch211-195m20.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to SPEG complex locus (Speg) [Source:UniProtKB/TrEMBL;Acc:B0S5V2]
Human Orthologue:
SPEG
Human Description:
SPEG complex locus [Source:HGNC Symbol;Acc:16901]
Mouse Orthologue:
Speg
Mouse Description:
SPEG complex locus Gene [Source:MGI Symbol;Acc:MGI:109282]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15486 | Nonsense | Available for shipment | Available now |
| sa10121 | Nonsense | Available for shipment | Available now |
| sa31739 | Nonsense | Available for shipment | Available now |
| sa34720 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15274 | Essential Splice Site | Available for shipment | Available now |
| sa17142 | Nonsense | Available for shipment | Available now |
| sa732 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15486
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059586 | Nonsense | 505 | 2702 | 3 | 31 |
| ENSDART00000138473 | None | None | 366 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 42688497)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41813667 |
| GRCz11 | 9 | 41615454 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TASWGGAGGGATACAACAGCAAATTAAWGTATTTTRTATACAGTTATATG[G/A]AAGAAAGACAACACTGAGGTCAAGAACAGTCCCACTCATGTTGTAAAGAT
Long Flanking Sequence:
AACTTGCACATTGTCAGCTGTACAAACCTTTCTAAATTATACCTGCAGATGGTAAAACCTTTCTTGCATTGCAAGTCTTTGGGTCTTAAGCAGGTCGCACACCAGAAGCGCCGCTCGGCGCCGCGACACGGCGCGTACATGACAGTTTAAAGTATCACACACCAGACGCGCACATTCGAATGATATTTAACATGAAACTAATCAGATGGCGCTCTGTGGCGCGGCTGAAAAATGAACTGCGTCCTGAGCCGTCGCCGGGCGCCGCCGACAGCCGCCGACTTGCGGCGCCGGGGTGTGTATCCTGATAGAAACCTATCTTTAGAATTCTAAAATACATGGCGCTGCGTGGCGCTGCGCGGCGCGCCGCCGAGCGGCGCTTCTGGTGTGCGACCTGCTTTAGAGGTTACATTTCAAGAATAGGATGACATTTTCTAATTTAAACGGTTCTGCTACTGGAGGGATACAACAGCAAATTAATGTATTTTGTATACAGTTATATG[G/A]AAGAAAGACAACACTGAGGTCAAGAACAGTCCCACTCATGTTGTAAAGATAGAGGGGGAACGCCACTCCTTGCTCATCAAATGGACAAAGCCAAGTGATGCAGGAACCTACACAGTTACCGCTGTCAATGAGGTCGGTGAGGTGTCCAGCAGTGCTACACTTTTCATCAAACCAGGTGAGTGTTTATTGGTGAACATTGTACTCCATCTTACAGCAAGATGCTCTGTTGTTGCTTGTAAATAGGCATCCATATTTAACTGTTCCAGATGATGGATCACCATCTAGATTCCCATTGTTATTCATCACATCACTTATTTGCATATTGCTGAGCTCGGCAACTGCCAGTGGATGTCACTCAAGTCACTTAGAATCACCGTTAAATAAAATGAATCAGAAGTATCCTCACGGGCTGTATGTGAGATCCAACTAATTGATGATTTTAGAAGAGAGCTATTTTATTTACTTACCTTGAAAGTTAATTTTAAACATAATACTTTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10121
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059586 | Nonsense | 995 | 2702 | 11 | 31 |
| ENSDART00000138473 | None | None | 366 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 42710308)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41835478 |
| GRCz11 | 9 | 41637265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCACAGCCTGGTGGTCCGCTGTGTTTGTCATGCTCACGGAGGGGTTTA[C/A]AAGTGTGTCAKWTCCAATAAAGTGGGCAAGGCCACCTGCTATTCTCATCT
Long Flanking Sequence:
TGAGATGATTAATTTCATTTTTTACAACATGGTCATGTTCTTTAATTCGTGAGGATGTTGTTGTTTTACCAGAGCGAAGCTGGAAAAAATGCCTTCCATTCCCGAAGAACCCGAAGTTCCTGAAAATGAGATTGAGCGTTTCACCATGCCTGACTTCGTAAAGCCGCTTTATGATATGGATGTAGTGGAGGGCAGAGAGGCTGTGCTCAGGTGCAAAGTGGCCGGCTTGCCGTACCCCACCATAACATGGTTTCACAATGGCAAGAGAATTGACAGCACGGAGGACAGAAAGATGACACAGTGTAAGTTAGCTAAAACCATAATTCAATTCTCCTACAGTACTGAGCCGTTCCAGAAAGCAGCCCCTATGGAAATGAATAGCCTGGGTAAGGAGAATAACAGGAATATAAAACCTTTGTTATTTTTATTGTCTCTTCTGCAGTCAGAGATGTTCACAGCCTGGTGGTCCGCTGTGTTTGTCATGCTCACGGAGGGGTTTA[C/A]AAGTGTGTCATATCCAATAAAGTGGGCAAGGCCACCTGCTATTCTCATCTTTACGTGACAGGTGAGTTTAATATCTTCATAAGTTTTGGTTATGTCAGCTTATATGTGTTTAAAAAGAGCAACTTAAAGTAAAAAAAGAAAAGATTTATATGTAATCATCACTGGGAAATGTAAAAAATTAATGGCCATAATATTCACACAAGAAATTTTATAACATGTGGCATATTAGTAAGAGTACTATATTATTTCCCATAATAAATCTCACAATAAACAATAAAACAAATAAAATAAATATAATAAAAAAAAGAGTTTCTACAGGAGAAAAAATATTACCAGACATACTGTGAAAAATCTTTGAAAAACGAAATACAGTTATGAATATATTATTTTCCTTTTTAATAATTTTTCAAAGTATGATTTTTTTTCTATGGGCTAATCATTTTGACTTCAAAATTTGGAATATAATGGATATTACATTCATCAGTTATAAACTGTAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31739
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 |
|---|---|---|---|---|---|
| ENSDART00000059586 | Nonsense | 1057 | 2702 | 13 | 31 |
| ENSDART00000138473 | None | None | 366 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 42714263)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41839433 |
| GRCz11 | 9 | 41641220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACTCCAAAAAATCGTATTTATGTTTCCAGACCCCAGCTCCCTGATGTA[T/A]GCCATTCAGCAACAGGCCCTGGGGTCGATCCAGTGGACCATCATCGCTTC
Long Flanking Sequence:
CCACACAGAAATGCCAACTGAGCCGGCCGAGGTTCGACCCAGCGACCTTCTTGCTGTGAGGCAAACGTGCTACCCACTACGCCACTGCGTCGCCCCATTTTATTTATGTGAAATCCAAATATGAACATGAATACGTCATACATTTATACTTAATTTGTATTTATTGCCAAATATCAGATTTCTATATGGGATAAATCATTTGGAATTTCTCTAATTATTAAAATGATGTTCAATAAGGTCATCAAAAATCCACAGCAAAATATAAAAGTGATTAGATGTCCTTTTTGTTTGTGTGTGTTTAGGTTTCCCAGTACAGGGTTGCAGCAGGGAGGGCATCCGCTGCGTAAAACATATGCTGGAATAGTTGGCGGTTCATTCCGCTGTGGCGACCCCTGATAAATAAGCCTAAAGAAAATGCATAGATGAATGTGTGTGTTTAGCATTAAAACTTAACTCCAAAAAATCGTATTTATGTTTCCAGACCCCAGCTCCCTGATGTA[T/A]GCCATTCAGCAACAGGCCCTGGGGTCGATCCAGTGGACCATCATCGCTTCTTGCCTGAAACAGACCACCTATACCATCAGCAATCTGTCTAAAGGTGTCCGCTACGCCTTCAGGGTGCTATCAATCACCAGCAAGGCCTTTAGCAAGCCGTCGCCTGCCACCGAGCCAATGCAGCTGCTAGATAGAGGTACGGCTGAGCAGACAAGGACAGCCACAGTCAGACGGGTCAATGAGATGTATGAGTTACTTCAGGACACTGGCTTTTATCTCTCTGTCTGCAGGTCCGTACGTCCAGGAGGCTCCGGTAATCATTGACAAGCCAGATATCGTGTATATGGTGGAGAAGCAGCCCTTGAGCATCACAGTCACTCTCAACCACGTCAACGCATCGGTCACATGGAAGAGGTATTTTGCAGTTTAATTACATTGACTAATTTTTAAACTGATGATTATTGATGAAGGTGTTGAATAAATATATTTTAAAGTGACAAAAATATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34720
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:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059586 | Splice Site, Nonsense | 1314 | 2702 | 18 | 31 |
| ENSDART00000138473 | None | None | 366 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 42721597)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41846767 |
| GRCz11 | 9 | 41648554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGTCTGATCAAGCAAATCTTACCCATTTTTGAATTTCTCCACATAGCC[A/T]AACAGTACAAAGACGACCCGATGGAGGATGAGGCGTCCATCCTCAGAAAG
Long Flanking Sequence:
TAACTTACATCCAGTTGAAGTCAAAATGATTAGCCCTCTTGTGAAACGAGGTTTAACAGAGCAAGGAAATTTCAGTAGTATGTCTGATAATAATTTTTCTTCTGGAGAAAGTCCTATTTGCTTTATTTCGGCTAGAATAAAAGCAGTTTTTAATTTTTTAAAAAACATTTTAAGGTCAAAATTATTAGCCCTCTTAAGCTATTGTTTTTCTCGATAGTCTACAGAACAAACCATAGTTATACAATGACTTGCCTTATTGCTCTAACTTGCCTAGATAATCTGATTTAACCTAGTCAAGCCTTTCAATGTCACTTTGAGCTGAATACTGGTGTCTTGATCAATATATGGTAAAATATTGTGTACTGTCATCATGGCAAAGGTAAAAGAAATCTGTTATTAGAAATTAGTTAATTACTGTACCCGCAGTTAGAAAGGCTAAATACTGTATGTGCAGTCTGATCAAGCAAATCTTACCCATTTTTGAATTTCTCCACATAGCC[A/T]AACAGTACAAAGACGACCCGATGGAGGATGAGGCGTCCATCCTCAGAAAGATGCGGAGGCTCACTGATTACTATGATGTGCACAAGGAAATTGGGAGGTGAGTCATCCGCCCGGAGCCACATTTGGACACGCACCATTTATCTCTAATGATTTCCTCTGACGGCCTAGAAAACTCAAAGCAAACTCCATCAGCTCTCACTGATGACAGATCTCAGGTCTTCTGACTCATCACACACACACACACTTCTCAAGTTTAATAAAGCATCAGACGGAAAAAGGGTTGGGACATTATTGAAAACACACTTTTGGTCGGGAAGTATGCAATTTCATGGTGCGCAATCAAAGGATGATTCAGCCACCTCAGAAGAGGCCGCGACACCCTTGAAGTTTTTTTGGCACTAAAAATATTTCTGGAGACTTTTTATTACATTTGCACAAGTTCTGTATATTGAGTAACGACCCAGAACCCCTTAATATAAATATTAAAGAAATAAATCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15274
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059586 | Essential Splice Site | 1413 | 2702 | 20 | 31 |
| ENSDART00000138473 | None | None | 366 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 42725179)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41850349 |
| GRCz11 | 9 | 41652136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATGAGTTGATTTTCTCCATCACTGTGATTGTCTTTGACAACATGCAAA[G/A]ATGCCATGAGGAGCTTCTCGATAGGCTTACAAAGAAATCAACCATCTTGG
Long Flanking Sequence:
GAATAGAGTCCTTCTGCATTGAGAACAGCTGTTTTTGTAATCTGGACACCACAGACTTTTAATGTGTTCACAGACTTTTAATGTGTTCACTCCTGACTTACTCATCTGCCTAAAATGCAGCCGCTTTATATGACTTTGGTCTATCTGTCCATTGACTGTCACATACTGTTTAGGTTATGGATCCATCAGAGTCTTTAGAGGAAGCAGAGAGAGGACTTCTTACATTAAAAATGCACTTCAATAGATGCCATAACATATAAAAATCTGTAATTTAAACAGTTTAGAACAAGCAAACAAACAAACACTAAGACGGTAATTTTTCAGTTCAACACTGAGCTGATTGTTATGTAAATGGTATGTAAAACAGATACATTTTCACTAGTGGGCTGTTTAAACTATCACACTTTCAAGCTCGCTCCATCACACTCTCTCTTTCACGCATTGTAGTGATAATGAGTTGATTTTCTCCATCACTGTGATTGTCTTTGACAACATGCAAA[G/A]ATGCCATGAGGAGCTTCTCGATAGGCTTACAAAGAAATCAACCATCTTGGAGTCCGAGGTCAGTAAACCAGTTTAATCTTTCAAAAGCCTTGTTTACACCTGGAATTATGATGTGTCTTGTTTGATTTAGATTAGACAAGGTAAACATTTCTGTTTTGCATTTTATTGTGTTAATTTTGTCCACTTTGTTCTATTGGTAAAGGCCTACGTTTAAGCTGAACATTTAATAGGTTATACTTTGAAATAGGGTCACATATTTTAACATTGTATACACTTAAAAATGATCAACACAGACTTTGTGTCTTTTCGTGCTCACCAGCTGACTGCTTACCTCCGTATGAACAACTTTCTCACTGTTACCAGTTTGTCCAGGTGCTTGCCATGTATGTCAGCAGACTTGATACATCGAGAGTAGTTGACCACGAAGATGGGGTTTGAGTTCGCGAATTATGTAGCCAGAAGTATGTCTGGTTGCATTTTGTCTTTAAAACGAACACTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17142
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059586 | Nonsense | 2270 | 2702 | 26 | 31 |
| ENSDART00000138473 | None | None | 366 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 42732044)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41857214 |
| GRCz11 | 9 | 41659001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACGTTTCKCATTTCAGAAGACTGAAGACAAGYCYTCCACTGTTTCTCCT[G/T]AAACTGCWGAAGAAMTGTATCRCCCTGGACCAACTGGTGCTCCTTTAGAG
Long Flanking Sequence:
GTGTATCAACCTATGTTACCCCATCTCCCCCTGCACGCACAGTGCTCCCAGATGGTAGGATGTCCGCATATGCCAGTATTATGCAGACTATCATGGTACCATCTGTCCCAGCAAATACCCAATCTGACACTGTTCCTATTCCTACACCAACTTCCACTCCACCATCAGTTCCAGTCTATGCACCCATTTCCAGACACATCTCAGAACCAACCCTTTCATCAACTTCTTCATCCAAATCAGATCTTCACCAAACAACTGAGCATCCTGCAGTCTTTTCTCGGGTTGCCTCCACTGAACACCCTCCCAAAGAGCCAAGTCCTCCTAAGACACCCACTCGCGCCTCCCCTAAGCGAGAGCCATCTCCTGGAAGCAACATCCAGGACCTTGCATCCGAGGAGGTTTTTGAAGCTCGCTTCAAGAAACGTGAGTCTTCTCTAACTCGTAGTCTCAAACGTTTCTCATTTCAGAAGACTGAAGACAAGCCCTCCACTGTTTCTCCT[G/T]AAACTGCTGAAGAAATGTATCGCCCTGGACCAACTGGTGCTCCTTTAGAGTTTGTGCCAAGGAGGTTGGAGGAGAAGTCCAAATCAGTACAAGATCTTCGAGAGGCAGAGAAGGACCCTGGGTTCATGAGGCGACTCTCCATGCGCTTGAAAAGGACCCCATCAGTGGAAAAGCAGGAGGAGAAGCTCAAAGAGGAGGAGGCTTCAGCACCCAGGCGTCGTCTTTCTTGGGCACTGGGACGGAGGGGATCCCAAGAGAAGAAGGAGATTGAGATGATGAGGTTGGATGGGGGTCCTGAGCCTCCCCCAGAGCCTGAGTCTAAAGCACCTTCTGAGTCACCTATTCTTGCCATGCGCAAGAAGATTGGCAGCACCATGGCAAGCTTATCTACAAGAATTAGGAGCCATTCTGAGGACAGGAAAGATGACAGTGAAGGCAAGATGGAGACCAAGAGGACTCCTATATTCAACAAACTAAGGCGTTCCACTTCTGAGGGGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa732
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000059586 | Essential Splice Site | 2512 | 2702 | 27 | 31 |
| ENSDART00000138473 | None | None | 366 | None | 6 |
Genomic Location (Zv9):
Chromosome 9 (position 42732849)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41858019 |
| GRCz11 | 9 | 41659806 |
KASP Assay ID:
554-0639.1 (used for ordering genotyping assays)
KASP Sequence:
AAGACAGTTTCCCAACCAGACATCCCAGCTTCCATTGCTAGAGAGAATGG[T/C]TCTCTACGRTCTCGCCAATATACACGTCTAACATCTGGTACTGCACATTT
Long Flanking Sequence:
CCCAGAGCCTGAGTCTAAAGCACCTTCTGAGTCACCTATTCTTGCCATGCGCAAGAAGATTGGCAGCACCATGGCAAGCTTATCTACAAGAATTAGGAGCCATTCTGAGGACAGGAAAGATGACAGTGAAGGCAAGATGGAGACCAAGAGGACTCCTATATTCAACAAACTAAGGCGTTCCACTTCTGAGGGGGGCAGTCTGAAGAGAATGGGTATCCCACAAAACCAACTGGCTGCTCAGTCAGGGCAAGGGACCTCATCAGAATCTCTTGATTCTATGTCAAGCATCCAGTCAGAATCAGCTATTAAAAGTATGCAATTTTTCATTCATTGCTTTATTTTGTTGTCAGTTCTTCTAATTTTAAAGGGCATTAAATGTCTTTTCCAGATGCAGAACTTGACCGCAGATCACGGTGGGACCGATGGGGCTTGACTCGAGGGAAAAAGGACAAGACAGTTTCCCAACCAGACATCCCAGCTTCCATTGCTAGAGAGAATGG[T/C]TCTCTACGGTCTCGCCAATATACACGTCTAACATCTGGTACTGCACATTTTACTTGTATATTTCACTGTAACTTTGCAGAAATAGAGAAATCTGTTTGAATACTTGCTGCTTTGTCATAAACCTAAAATAATCATTGAGTCAATTATGAATATGTACTTGCTTTGGCACAGCAGTGAAAGATACATGATGCTTGTCTCACGGTTTTTTTAATCATTCAATCAAAAAATAGACTTCCCTCCGGTGTTCCATATCAAACTGAGGGACCATGTACTCTTGGAGGGAGATCCTGTCACTCTCAGCTGCCTCCCTGCTGGCAGTCCTCACCCACACATCTCATGGATGAAAGGTCTGATTGAATTTTTAATATTAGCTTCTGTTGTACTAAAGATAATATAATCTGGCCTAAATTGAAAGCAATGTCCATAGAGACTGATCTAATAAAATTGCAAGTGTGCCGTCTCTTTTATATAGATTTGTTTCACTATATTGGCTTTGTGTT
Associated Phenotype:
Not determined