ZMP
srpk1a
Ensembl ID:
ZFIN ID:
Description:
serine/arginine-rich protein specific kinase 1a [Source:RefSeq peptide;Acc:NP_955944]
Human Orthologue:
SRPK1
Human Description:
SRSF protein kinase 1 [Source:HGNC Symbol;Acc:11305]
Mouse Orthologue:
Srpk1
Mouse Description:
serine/arginine-rich protein specific kinase 1 Gene [Source:MGI Symbol;Acc:MGI:106908]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21285 | Essential Splice Site | Available for shipment | Available now |
| sa21286 | Essential Splice Site | Available for shipment | Available now |
| sa9382 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21287 | Essential Splice Site | Available for shipment | Available now |
| sa15574 | Nonsense | Available for shipment | Available now |
| sa21288 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21285
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 |
|---|---|---|---|---|---|
| ENSDART00000037109 | Essential Splice Site | 197 | 634 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 24720442)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23846260 |
| GRCz11 | 8 | 23867499 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAACTATCAAGGCTTACCTCTGCCCTGTGTGAAGAGCATCATTCGACAG[G/A]TAATTCAACACACCACCACACAACCAGATCAGTCTTCACCTAATTACCAT
Long Flanking Sequence:
TATTATATTATATTATATTATATTATATTATATTATATTATATTATATTTTATGTATGAATGTATGTGCAATTTTCTTTATTTTGTTTTCAGGTCAGAAATACAGACCCTGATGATCCAAACAGAGAGATGGTTGTGCAGCTACTGGATGATTTCAAGATCTCAGGGGTCAATGGCACTCGTATCCTTGAAAATGCACAATGTTGTTGTGAGTGTGAAAGAGAAAATGGGTCAGGAAGTCTTCTAAGCAGTCGTCTCGTGCTATTTTAGCATACCCTAAATTCTTTTACAGAAACGCTGACTTTAAAACGGTTGTTTTCGAGATCCTGTTTTGCAGATAGATTTTTGAACATGTAATTTTGCCAACAGCAGATTCCTTTACTTGAAGTTTTAGATGTCTGCATGGTGTTTGAAGTTCTAGGGCACCACTTGCTTAAATGGATTATCAAGTCCAACTATCAAGGCTTACCTCTGCCCTGTGTGAAGAGCATCATTCGACAG[G/A]TAATTCAACACACCACCACACAACCAGATCAGTCTTCACCTAATTACCATGTAGCTAATTAGCCTCTGTCCTGGATCCGGTGGATCTGTTACAGATTAATTATTGTTTGCACTTGTTTTGTGTTTATGCTTTTATGAATAAAAATTGCTAATGAAAACACTGAGGTGGAGGAAAAAACATGATAACAGGGCATGATGTACATTATTTAACATTTTTTAGTAAGTATTATTTTTTTTAAATAATATTTTTATTTGTGTGTATTAAAGTGAGTATTAAATTTATACAGAGACAACATTTTGAAACATTAATAATATTAAAAAGTTTAATTAATCTTAACTTTGTCATCAAAGTAATCAGTTTTCACAAGACATTAAACAGCATAACTGTAAACAGCAAACCAGTTTAAAACAATGATATTAATAATGAAAATCTTTTTAAAGTTGCAAATCTATATTACAGTAATTTCTGACACATTATGTGACTGTAATGGTTGCTGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21286
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 |
|---|---|---|---|---|---|
| ENSDART00000037109 | Essential Splice Site | 253 | 634 | 8 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 24721613)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23847431 |
| GRCz11 | 8 | 23868670 |
KASP Assay ID:
2260-0565.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCACTGAATGGCAGAAAGCAGGAGCTCCTCCTCCATCTGGATCAGCAGG[T/C]ATAGCAGTTCTGCTTTCTCACATATGACTGTGTGTCAACTTCTTCTTACT
Long Flanking Sequence:
TTATATATTGCTTTATCTTCTCCCTTCTTTGTCTCTGATACTTTTTTGCGCTTTATTTAGACACTTTGCGTATGCATTTTGTTTGTTAATATTTTATAGCATATTTTAATGTTGTTTTAAAGTTATGCTTATTCCTAGAATTGTTATAAAAACCAAAAAACTTTTAGTAACACATTTTTATTGTTCTGAAAGGCCATTAATGACCAACACAATCAATAAATAATGTTATTTAGCACTGAATAATAATTATTTTAAATTATGAGCCTTAATGTTATGTTCTCTTATGTTTAGAAAGATGCTAATGTTTGATATGTCTTTTACCTAATCTCTAAGGTTCTTCAGGGTCTGGATTACCTGCACACCAAGTGTCAAATCATCCACACAGACATTAAGCCAGAGAACATTCTGATGAGCGTGGAGGAGCTGTATGTCAGGCGACTGGCCGCAGAAGCCACTGAATGGCAGAAAGCAGGAGCTCCTCCTCCATCTGGATCAGCAGG[T/C]ATAGCAGTTCTGCTTTCTCACATATGACTGTGTGTCAACTTCTTCTTACTATATTTTTGGTTGATCACACACTCATGTTAACACAACTTGTTGGTTAAGTTTTCTTACCCTCAAGCATGCTGCTTATAAAGGGACAATTGATTTGTTTTTGTTAGCAGTCTCTGTGTCTCAGTTTCTTTTTTTTTATCTTCCAGTGAGCACTGCGCCTGCACCAAAACAGGTATGCTTTCCTCCTTTAACAAATACTTTTACACTATGTATTTTAGAAAATGAAATATACCCGAAGAAAACTTATTCAGAGAGTCAAGCTGATTCTTTAGTGCACTGAAGCTGGTTTGCAAAAGCTGATCTTTGTTGGAATAAAATATTATCTTAGGCTGTTGTTCTCAATGCCAGAAATGTTCTGGGTTTTGATGTTCTAAAAGGTTTTTGTTTTCACATTAATGTTGTACTTGAAAATGTTCTGTTCATCTAACCCTTTAAAAATGAGTTTTAAAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9382
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:
T > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000037109 | Nonsense | 394 | 634 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 24723011)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23848829 |
| GRCz11 | 8 | 23870068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACCACCATAACGCAAACGCAGGCCCAGAGGACACGGCTCAAAGCATGTA[T/G]GAGTACTGTAATGGGGCAGAATCCCCTGAACTTGATCAGGCCTGTTATAG
Long Flanking Sequence:
AAGAAGAAGCAGAAGCGTCAAGCGGAGCTCCTGGAGAAGTGCATCATGGACTTGGAAGAGATGGAGATTGGGCCTGAGGGCAGAGAGGAAGAAGAGGACGACCCAGAATCCCCCAAATCTCCCTCCTGCGCCCCACTTAGACAGGCGTCACTGCAGGAAATTGCTACTGAGGACATAATAAGTTAGTTTCTATTTGTACCTTGTATAAATTATGGTTATTTAGAAGGTGATTTGTTACTCAAGTGTACAGTTAGTGGCAATGATGTAATATAAATGGAGCCATTATAACTTCGCTATTTTTTTGCATCCCTTGTAATAGTGGACACCAGAGAGAGACTAACATCAGATGCTTCAGTCGAGCTTAACTGTAACGGCTGCCTGCACTCCAGTAAAACACAGCCTGAGGAGGACGAGCAAGGAGACCTGCAGTATGGCCAGTTACTACAAGAGGACCACCATAACGCAAACGCAGGCCCAGAGGACACGGCTCAAAGCATGTA[T/G]GAGTACTGTAATGGGGCAGAATCCCCTGAACTTGATCAGGCCTGTTATAGTAACGGCACCTCAGGCCAAGAGCAGCTGGAGGATGGAGAACTGGCAACCGAAGAGCAACATCAGCAAAAGACTAGAACCAGAGCCAGGGAACAGAACAAAGATAAGATAAAGGACGGTCAGTTCGAATTATATTCGTAATCATTTCCAGAAAACGTATGACATCTCTTTTAGATGTCCCTCCTGGCTTACTGCCAACTGTTTGTTTTAAATGGGTTGTTTTTATTTACTATCCCTTATAGTTTTAGATTCATGTAAACACAGTGAGAATTCTTGATGAGTCCGACTGCAGTAGTAGTTTGTAGTGAGGATGCATGGCTGTTTTTAATTGGCTCTTTTTCTGCTTGTAGACAAGTTGTCAGCTGGAAGCCTATTGGTCAACCCACTGGATCCGCTCAATGCTGACAAGATCAAGGTTAAGATTGCAGACCTTGGAAATGCCTGCTGGGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21287
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000037109 | Essential Splice Site | 450 | 634 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 24723409)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23849227 |
| GRCz11 | 8 | 23870466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTAGTGAGGATGCATGGCTGTTTTTAATTGGCTCTTTTTCTGCTTGTA[G/T]ACAAGTTGTCAGCTGGAAGCCTATTGGTCAACCCACTGGATCCGCTCAAT
Long Flanking Sequence:
GCCTGAGGAGGACGAGCAAGGAGACCTGCAGTATGGCCAGTTACTACAAGAGGACCACCATAACGCAAACGCAGGCCCAGAGGACACGGCTCAAAGCATGTATGAGTACTGTAATGGGGCAGAATCCCCTGAACTTGATCAGGCCTGTTATAGTAACGGCACCTCAGGCCAAGAGCAGCTGGAGGATGGAGAACTGGCAACCGAAGAGCAACATCAGCAAAAGACTAGAACCAGAGCCAGGGAACAGAACAAAGATAAGATAAAGGACGGTCAGTTCGAATTATATTCGTAATCATTTCCAGAAAACGTATGACATCTCTTTTAGATGTCCCTCCTGGCTTACTGCCAACTGTTTGTTTTAAATGGGTTGTTTTTATTTACTATCCCTTATAGTTTTAGATTCATGTAAACACAGTGAGAATTCTTGATGAGTCCGACTGCAGTAGTAGTTTGTAGTGAGGATGCATGGCTGTTTTTAATTGGCTCTTTTTCTGCTTGTA[G/T]ACAAGTTGTCAGCTGGAAGCCTATTGGTCAACCCACTGGATCCGCTCAATGCTGACAAGATCAAGGTTAAGATTGCAGACCTTGGAAATGCCTGCTGGGTGGTAAGAGTCAGTCGAAATCCAAATTGTTGTAATTTCTTGAAGAAGTGCAGCTATACATAATGTAGTGTATTTTTTCTTAGCTATGATAATATTGATTTAAATTATGGAAAGAACACTATAATTTGGGGTAATTAAATTTTTAAAATTATTTTAAATTAATCAAAATGCCTGTAAAGACACTTTTTTTAATGAAAGGTTCAAGTGACACTAGTATTGCTGAAAATCCAGCTTTGCCCATCACAAGAATACATAGAATTTACATTATATACATTTTACATAATATATATTTCACAATAAATTATTTTTATCGTATGTTTAATCAAATTATTGGTTTTACAAAATGTAATAAAGATGTTACTAGTACCACATTTTTAAATGGAAGTTTATTTGGCTCCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15574
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 |
|---|---|---|---|---|---|
| ENSDART00000037109 | Nonsense | 585 | 634 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 24731519)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23857337 |
| GRCz11 | 8 | 23878576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATGTGTTCTCTATAGGTGACCTGAAGCACATCACCAAACTGAAGCCATG[G/A]GGTYTGCTGGACGTCCTGATGGATAAGTACGAGTGGCCTCAGGAGGAAGC
Long Flanking Sequence:
GATATTTGTTTGTGGCTTGACATTCATTCCAAACACAAGATTAAACAAAACCATAAAGATTTCATTAGTTACCTTAAGTAAACACATCAACTAGCAGTATCTAACAATAAGCAGTATGTTTATTACAGTATTTAGGGATCTATTTATCTTTGTTGGTTTATTTAAAAGTAATTGTTGTTTCAGGTTTATTAAATATTTGCTTTTGAAATCATTGATTAATCAATTTAGTTGTTTAATGATGTCAAATGATACTGTAATATTACTTGTAGCCAAAAACTAGGGATGCTCTGGTCATTCTTTATTTGTCATAGAATGTATTATCAGCTAATACTGATCCAAAATTATTCAGAGCATCTCTTAAATAATAATAATAATAATAAAAATAATATATATATATATATATATAGGCAATAGCATGAACTGAATAGAACCAGTAGCCTGGTCTCTGATAATGTGTTCTCTATAGGTGACCTGAAGCACATCACCAAACTGAAGCCATG[G/A]GGTTTGCTGGACGTCCTGATGGATAAGTACGAGTGGCCTCAGGAGGAAGCCCAAACCTTCAGTGATTTCCTGCTTCCTATGCTGGAGCTCCTGCCTGAGAAAAGAGCCACGGCTTCTGACTGTCTGCGACACCCATGGCTTGCCCTCTAGTGGCTTCTCCACGCCACTGCACACTTCAGGCCACCTAAAGAGACTGCAACAGATCACTTTCAGTTTATAGAGCATATCGGCATACTACTTTTTCTTCCGTTCATCCGAGTCATTCGTTTTGCTTGGGAGGAATAGCAAACCTGTCTTTTTGTTCTCAACTGTTATTATTATTATACATTTTTTTTTCCAGAGTTGAGAGGTTTATTGTGAGGGTCAAATCTGCCGAGATCCTTCCGCCATTCCTCTTATTTTGGTAAAGGATGACTTGTAGACCTAGGAAATTCCTGTTTGTTTTGATTTCCAGAAGTCGTGAAATGTTTTTTGCAGTTCTGAACGGAGACTGCAGCGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21288
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 |
|---|---|---|---|---|---|
| ENSDART00000037109 | Nonsense | 626 | 634 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 24731642)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 23857460 |
| GRCz11 | 8 | 23878699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCCTATGCTGGAGCTCCTGCCTGAGAAAAGAGCCACGGCTTCTGACTG[T/A]CTGCGACACCCATGGCTTGCCCTCTAGTGGCTTCTCCACGCCACTGCACA
Long Flanking Sequence:
TACAGTATTTAGGGATCTATTTATCTTTGTTGGTTTATTTAAAAGTAATTGTTGTTTCAGGTTTATTAAATATTTGCTTTTGAAATCATTGATTAATCAATTTAGTTGTTTAATGATGTCAAATGATACTGTAATATTACTTGTAGCCAAAAACTAGGGATGCTCTGGTCATTCTTTATTTGTCATAGAATGTATTATCAGCTAATACTGATCCAAAATTATTCAGAGCATCTCTTAAATAATAATAATAATAATAAAAATAATATATATATATATATATATAGGCAATAGCATGAACTGAATAGAACCAGTAGCCTGGTCTCTGATAATGTGTTCTCTATAGGTGACCTGAAGCACATCACCAAACTGAAGCCATGGGGTTTGCTGGACGTCCTGATGGATAAGTACGAGTGGCCTCAGGAGGAAGCCCAAACCTTCAGTGATTTCCTGCTTCCTATGCTGGAGCTCCTGCCTGAGAAAAGAGCCACGGCTTCTGACTG[T/A]CTGCGACACCCATGGCTTGCCCTCTAGTGGCTTCTCCACGCCACTGCACACTTCAGGCCACCTAAAGAGACTGCAACAGATCACTTTCAGTTTATAGAGCATATCGGCATACTACTTTTTCTTCCGTTCATCCGAGTCATTCGTTTTGCTTGGGAGGAATAGCAAACCTGTCTTTTTGTTCTCAACTGTTATTATTATTATACATTTTTTTTTCCAGAGTTGAGAGGTTTATTGTGAGGGTCAAATCTGCCGAGATCCTTCCGCCATTCCTCTTATTTTGGTAAAGGATGACTTGTAGACCTAGGAAATTCCTGTTTGTTTTGATTTCCAGAAGTCGTGAAATGTTTTTTGCAGTTCTGAACGGAGACTGCAGCGTGATGCACATGAGATTTTTTGTTACTAGTTTTCAGAGATGGAAAGCGATGAGGGTTTTTGGAAAGGGAATTGTTGGTTTACCTTTATGACTGTAGAGTATAAATTAAGATTATTTTTGTTCGCCG
Associated Phenotype:
Not determined