ZMP
speg
Ensembl ID:
ZFIN ID:
Description:
Striated muscle preferentially expressed protein kinase [Source:UniProtKB/Swiss-Prot;Acc:Q696W0]
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 19 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14081 | Nonsense | Available for shipment | Available now |
sa13872 | Nonsense | Available for shipment | Available now |
sa12597 | Nonsense | Available for shipment | Available now |
sa14625 | Essential Splice Site | Available for shipment | Available now |
sa9635 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14081
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
ENSDART00000029697 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22804436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19059882 |
GRCz11 | 6 | 21120104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCAGATGCAAAGGAAAGRTGGACARCCCTGCCAAAGGAGCAATCTTCC[C/T]GATTACCAAAAATTAACCTGGCAGATAAAACAAAACWGCCTSAAAATGAA
Long Flanking Sequence:
AAGTGTCACAGGCAAGTTCCAAAATTTTAGACAGAGTGAGAGCATTTGAAGAACAAAGCCACAACAGTAACATGCCAAAGGTGTCTTCAAGATTGTCATGGGGTTTCAATAGAACATCATCTTGCAATTCTGAGGATGAGACATGTAAAGCAGGGAAATTCCAAGCCAACACAAAGAGTGATGTAGCACTCAAGAGGTCTTTTTTCAAGCAGAAAGCATCCTCTCTAGAGGAACAGTCGACTTGTGTGCAGAAAAATTTTCAGAGTAAACTCTCCGAAGAGCTTCACAGAATAAAGAAACTAGTTGGAAAATCCAACATCAAGAAAGCCTTTTCAATGGAGCAGCTCACCCAGACCGACAAGCAGTCCAGTGTCAGCACAGAGTCAGTTCTAACGCAAGTAATTCAGAAGACTGAAGAAACTGGAAAGCATTTCACTAATTTAAAAGCTGTACCAGATGCAAAGGAAAGATGGACAACCCTGCCAAAGGAGCAATCTTCC[C/T]GATTACCAAAAATTAACCTGGCAGATAAAACAAAACAGCCTGAAAATGAAACACCCCCTGAAATGAATGAAAACCAGGAGAACAATTCTAAGCCTATACAGTTGTTAGATGGGCAAGTCCTCAATGAAAAGGTCAGCTTCATACCAGGGCAATGTTCACCAATGTTGCCTAGGACAAATGTTTCCAGAAAATGGCCAAAATCACCTGCCCAACCTATGGTGAAAGATGGTTTGGTGAAAGCCCCACAAAAGCCTCCAAGATTATTAGAATCAATTTCCACACTACCAACACCATTTAAAATGACCATACCTACTATTGTGGTTGAAAATAAGCCCGTGGATGAAGAGTTGGACCAAAAGGAAGGACAAATAATGAGACAAAACAGAGGTAAAAGTTTTTCCTGAACTTCTACCAGCTTCTTTGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGGCCAGATAGGGTAAAATATGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13872
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
ENSDART00000029697 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000133507 | Nonsense | 436 | 2995 | 5 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22804436)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19059882 |
GRCz11 | 6 | 21120104 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACCAGATGCAAAGGAAAGRTGGACARCCCTGCCAAAGGAGCAATCTTCC[C/T]GATTACCAAAAATTAACCTGGCAGATAAAACAAAACWGCCTSAAAATGAA
Long Flanking Sequence:
AAGTGTCACAGGCAAGTTCCAAAATTTTAGACAGAGTGAGAGCATTTGAAGAACAAAGCCACAACAGTAACATGCCAAAGGTGTCTTCAAGATTGTCATGGGGTTTCAATAGAACATCATCTTGCAATTCTGAGGATGAGACATGTAAAGCAGGGAAATTCCAAGCCAACACAAAGAGTGATGTAGCACTCAAGAGGTCTTTTTTCAAGCAGAAAGCATCCTCTCTAGAGGAACAGTCGACTTGTGTGCAGAAAAATTTTCAGAGTAAACTCTCCGAAGAGCTTCACAGAATAAAGAAACTAGTTGGAAAATCCAACATCAAGAAAGCCTTTTCAATGGAGCAGCTCACCCAGACCGACAAGCAGTCCAGTGTCAGCACAGAGTCAGTTCTAACGCAAGTAATTCAGAAGACTGAAGAAACTGGAAAGCATTTCACTAATTTAAAAGCTGTACCAGATGCAAAGGAAAGATGGACAACCCTGCCAAAGGAGCAATCTTCC[C/T]GATTACCAAAAATTAACCTGGCAGATAAAACAAAACAGCCTGAAAATGAAACACCCCCTGAAATGAATGAAAACCAGGAGAACAATTCTAAGCCTATACAGTTGTTAGATGGGCAAGTCCTCAATGAAAAGGTCAGCTTCATACCAGGGCAATGTTCACCAATGTTGCCTAGGACAAATGTTTCCAGAAAATGGCCAAAATCACCTGCCCAACCTATGGTGAAAGATGGTTTGGTGAAAGCCCCACAAAAGCCTCCAAGATTATTAGAATCAATTTCCACACTACCAACACCATTTAAAATGACCATACCTACTATTGTGGTTGAAAATAAGCCCGTGGATGAAGAGTTGGACCAAAAGGAAGGACAAATAATGAGACAAAACAGAGGTAAAAGTTTTTCCTGAACTTCTACCAGCTTCTTTGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGGCCAGATAGGGTAAAATATGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12597
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Nonsense | 1003 | 2995 | 13 | 38 |
ENSDART00000133507 | Nonsense | 1003 | 2995 | 13 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22822536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19077982 |
GRCz11 | 6 | 21138204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATTGCCTCCAGCCTCACAGACACCTCTTATACAGTCACCTCACTGTCT[A/T]AAGGAGTGTGCTATTCCTTCAGAGTCCTTAGTACAACTGGAAAAACACTA
Long Flanking Sequence:
GGTTGCTGCTTCTCCTGGTTTTCAGGTGGATTTTCTCTGGGTGCTCTCGTTTTTCCCCAGTCCAAAGACATGTGGAGGTTAATTGGGTAAACAAAATTGGCTGAAGTATGTGTGAATAAGGGAGTGTATGGGCTGATTTTTCAGTGCTGGGTTGCAACTGGATGGGCATACGTCACATAAAACTAATGAAAAAAACTTATGATAGAATAATTGGTGGTGTGTTCTGCTGTTGCAAACCTCATAAACTGGGTGTACTAAGGCAAAGAATAGACAGTGTGTGGTATTATTATACATGTTTGGCCATATTAATTTTTTTTAAATTTAAGCTTTTTTAAAAGGTTCTACTGTTTAGACTGTTTCACTCTTTAGCATCTTCTTTGTTAATTTCAGATCCCGCTTCACTGATGTATGTTGTTCAACAGCAAGTTCTGGGCTCCACCCAGTGGACAACCATTGCCTCCAGCCTCACAGACACCTCTTATACAGTCACCTCACTGTCT[A/T]AAGGAGTGTGCTATTCCTTCAGAGTCCTTAGTACAACTGGAAAAACACTAAGCAAACCATCACAACCAACTGATCTGGTCCAGCTCGTTGACAGAGGTATAGATTTGTGGGTAAAAAAATAGATATGTTACATTTTGATGAAACATCTTCTAATATATTGCAGAATTATTAATTAATGAATGCAGTTTTAATTAATGCAGTTCTCTTAGATATAGCTTTACTTAATTTTGGATTATTTTAGTGAAAATGTAACTTGCTTGTGAAATGCTGTATTTGTCATTGCCTGATAAATATATATTTTTTCCTTTATCACAGGAGAGTATTTTCGCAAAGCTCCAGTCATCATTGATAAGCCTGATATCGTGTACGCAGTTGAGAACCAGCCTGTAACCATTACAATTACAATTAATCATGTTCAAGCAACATGTACATGGAAAAGGTTAGTGGTAAAACAAGCCAGACATTGAAAGTACAATATGAATTATAAATATTAAGGATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14625
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000029697 | Essential Splice Site | 1134 | 2995 | 16 | 38 |
ENSDART00000133507 | Essential Splice Site | 1134 | 2995 | 16 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22824843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19080289 |
GRCz11 | 6 | 21140511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAAAGAGAGCATTATTTTTGGTAGTAAAGNTTTTTCTGTTGGCCATTTC[A/C]GTGCCCCCTATATTTGAAACCATCATGGAGGACTTGGATGTGTGTGTTGG
Long Flanking Sequence:
GCCCAGATATTAGCACTCTTGCCTCACAGCAAGAATGTCACTGGTTCTAGTCCTTACCAAGTCAGCAGACATTTCTGTGCAGAGTTTATACGCTCTCCCCATGCTCACGTGGGTTATCCCCACATAAGTTAATTGACTAATCCAAATCGACACCATAGACATGCTCCTAGTAAGTAGTTATCTCTTAAAAGCAATCTCTATATGTTCATTAGCTACTACAGCAGGAGAGTTCTCGAGATCTACCTGAGCTCAAACTCCCCTCTCGCCTTTCAAACGGGAGCGAGCCCGTGCTCGAGGATCTTAAAGCCAAACAAGCTTTATAATGAATCATCAGCTAAGTGTGAACTCTTGAAATATATTGTAAATAACTATATAACCATTGATTTCTGGAGGCAGCTGTTCCTTACTTTCCATTCTTTATATTGAGTTTTTCTTTTTCATTAAATGTGCTTAAAGAGAGCATTATTTTTGGTAGTAAAGTTTTTTCTGTTGGCCATTTC[A/C]GTGCCCCCTATATTTGAAACCATCATGGAGGACTTGGATGTGTGTGTTGGGGAAACATGTCATTTTGCTGTGGTTGTGGATGGAAAACCCGACCCTGATATCCTCTGGTACAAGGTCAGTATTCACTGACACACAGATTTTTTAAAGAACTGATTTAAAGATTATCATGCTACTGTAATTGACCTCATCCATGTGGGGCCCAGATGAGTTACCCTTGGACTGATATCTGGGGCTCTCCTGGGCTAGCCAACTGGGACAAATTTTGTTCTCGGTTTCATGATGGCCCCACGTGTCAGCCTAAGTGAATAATCATGGGTCTTTAATAGGCTCCATATGAGATGCCCACCTTAATTTACCCATGTGGGTTCTAACGGGGCTACCAAGGTGGGCCCCACATTGTCAGGGTTCTGCCACTCGGGCCTTGTGAATTCTTGTTTTGGTGGCAGAGTCCGAAGACTAGCTATGTCTTGTCCTTTTTCTGTCATTGTGTGTGTCTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9635
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 |
---|---|---|---|---|---|
ENSDART00000029697 | Essential Splice Site | 2844 | 2995 | 35 | 38 |
ENSDART00000133507 | Essential Splice Site | 2843 | 2995 | 35 | 38 |
ENSDART00000137461 | None | None | 164 | None | 4 |
Genomic Location (Zv9):
Chromosome 6 (position 22836190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 19091636 |
GRCz11 | 6 | 21151858 |
KASP Assay ID:
2259-7493.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGTCCCTCCAACAATGCAGCAGATATCTGGGAACTCTGGAATACATGG[G/A]TATGCACATACAATTTCTATGTTTTTCTASTAAAATTATTTAAAACATAT
Long Flanking Sequence:
AAGATAATACCCTATGATCAGAAAACCAAGCAAACCATTATAAAGGAATATGAGATTTTGAAGTCCCTTCGATGTGAAAGAATCATGGCCCTACATGAAGCTTATATCACACCACGCTACCTTGTACTCATAACAGAATATTGCTCAGGCAAGGAAATCCTGCAAAATCTAATTGACAGGTGTGTATGAGCCTTTCTTTGTGTGTGTGTGTTCAAGGACTTTGATAGCTGAACTGTGAAATTTAAGTCTTGACATCAATGGTATTTTCTCTTACAGATTCTGTTATTCTGAAGATGATGTAGTGGGTTTTATAGTCCAGATCCTTCAAGGTTTGGAATATCTCCACAACTGCAAAATTCTTCATCTGGACATTAAACCAGACAACATCATGGTCACCAACCTCAATGTAATTAAGATAATAGATTTTGGCAGTGCTCAAAGGTTTAACCCTCTGTCCCTCCAACAATGCAGCAGATATCTGGGAACTCTGGAATACATGG[G/A]TATGCACATACAATTTCTATGTTTTTCTACTAAAATTATTTAAAACATATTCATGCCATGCTGGTGTTAATGTTTTTTTCTGTCCTTTTTAAGCTCCTGAAATGCTGAAAGGAGATCTTGTTGGACCCCCAGCAGACATCTGGAGCTTGGGAGTTCTATCTTATATTATGTTAGTTTAGTCTATTTACAATTAAACACAACAGGACAGATTATGTTGATCCTAGAGCATAAGTCATGTTTAAAAATGTAATCCACATTCCAAATCCCCACCACTAAACCTAACTCTAACTGCCAATTATTCCCAAAATTACAAGGTGTTAATTGTTGGATAACAATGATGTAGAAGCACATAACCCTAAAGGCTGATTTATACTTCTGCATCAAACGGCGGCGTATGCTACGGCGTTGACGCATAGCTCTTCGCCGTGGCCGTCGGCGTCACTGACGTGCACCTCACAAAAAATGTAACTACACGTCGCAACAACGTGTAGCGCAAGCTT
Associated Phenotype:
Not determined