ZMP
si:dkey-67c22.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC792544 [Source:RefSeq peptide;Acc:NP_001123872]
Human Orthologue:
SRRM5
Human Description:
serine/arginine repetitive matrix 5 [Source:HGNC Symbol;Acc:37248]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9800 | Nonsense | Available for shipment | Available now |
| sa2494 | Nonsense | Available for shipment | Available now |
| sa13667 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9800
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 |
|---|---|---|---|---|---|
| ENSDART00000077740 | Nonsense | 481 | 1069 | 4 | 7 |
| ENSDART00000122057 | Nonsense | 481 | 1069 | 5 | 7 |
| ENSDART00000122169 | None | None | 229 | None | 5 |
| ENSDART00000130549 | Nonsense | 481 | 1069 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 36889819)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 36027708 |
| GRCz11 | 9 | 35836893 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTTCATAGAAGATCAATTTCAAGAAGCCCAAGACGTCGAAGTAAATCT[C/T]GATCCCCCTAWCGCTCCAGGCCCTCTAAGTCACGTTCTCCTGCAGTCCGT
Long Flanking Sequence:
CTGTATCTGTCTCTGGTGGAAAAGATCGAACAAAACGTAGATGCTCAAGATCTCCTACTAAAGCAACAAAGAAGACTGTACGCAGGTCAAGGTCACTATCTGGTAAAAGAGGGTATCGCTCTGACTCAAGGTCTCGCACAAGGACCAAAAGATCCAGGAGTAAGTCCCTCCGACGTGGTCATCGTTCAAGGTCTAGGTCAACTGGAAGATCAAGACGGTCACGCTCAAGATCAAAGCAATCTGTTTCAAGAAGAAAGAATCGACGCTCACGATCTAGATCTTTACGCCGTGGAAGACACTCAAGGTCACGTTCTCGAAAAAGGACACCTGTTTCTCGAGCAAGACGATCCAGGTCCAGATCTGTCAGAAGAGCAAGACGAACACGCTCAAGATCCCCTGTGCTCCGTAGAAGATCCAGATCTCGCCCAAAAAGAAACAGAAGATCAAGATCTGTTCATAGAAGATCAATTTCAAGAAGCCCAAGACGTCGAAGTAAATCT[C/T]GATCCCCCTATCGCTCCAGGCCCTCTAAGTCACGTTCTCCTGCAGTCCGTAAAAGGAAGTCGAAGTCTAGGAGCCCTCATAGCACAAAGTCAGAATCAGTATCTCCTGTGCGACGTAAAAGATCAAAGTCACGGTCATCCTCACTTGATTCAAAGTCTGCATCACCAAAATTAAGAAAGACCAAAAAGCAAAAAAGTAAACTGTCGAGGTCCATTTCTCCGAAACGCAAATCAAGGTCAATTTCCAGGGAACAACAATCATCCGATAGAAGCATATCCCCTTCCATGAAAGCACACTCCCCATCTCCTGCTAAAGAAGACAAGTCTTTAAAGGATAAGAATTCAAAAGAAACCTCAGAAACCACACAGAAACTTTTGGTAGCCATAGAGGAAAAGTTTGAAGTAAAGGGGACAGCAGGGTCTGGTGGATGGAGACCTGTGACTACTGAATGTACATCTGTTCAAAAACCAAAAAATGAAGATGTAACATCAGAATGTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2494
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 |
|---|---|---|---|---|---|
| ENSDART00000077740 | Nonsense | 673 | 1069 | 4 | 7 |
| ENSDART00000122057 | Nonsense | 673 | 1069 | 5 | 7 |
| ENSDART00000122169 | None | None | 229 | None | 5 |
| ENSDART00000130549 | Nonsense | 673 | 1069 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 36890396)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 36028285 |
| GRCz11 | 9 | 35837470 |
KASP Assay ID:
554-2809.1 (used for ordering genotyping assays)
KASP Sequence:
GCCAGAGGATCCMTCTAAATGTGAAGAAAGACCTATCCGGTCCAGATCTT[T/A]GTCCTTAGATCCAGTTCCTCAACACGGTACAGMAGGGTCAGAAGAAGATT
Long Flanking Sequence:
TCATAGCACAAAGTCAGAATCAGTATCTCCTGTGCGACGTAAAAGATCAAAGTCACGGTCATCCTCACTTGATTCAAAGTCTGCATCACCAAAATTAAGAAAGACCAAAAAGCAAAAAAGTAAACTGTCGAGGTCCATTTCTCCGAAACGCAAATCAAGGTCAATTTCCAGGGAACAACAATCATCCGATAGAAGCATATCCCCTTCCATGAAAGCACACTCCCCATCTCCTGCTAAAGAAGACAAGTCTTTAAAGGATAAGAATTCAAAAGAAACCTCAGAAACCACACAGAAACTTTTGGTAGCCATAGAGGAAAAGTTTGAAGTAAAGGGGACAGCAGGGTCTGGTGGATGGAGACCTGTGACTACTGAATGTACATCTGTTCAAAAACCAAAAAATGAAGATGTAACATCAGAATGTGGCCCTCTAAGTGCAAAAGTCAAGGAAGAGCCAGAGGATCCCTCTAAATGTGAAGAAAGACCTATCCGGTCCAGATCTT[T/A]GTCCTTAGATCCAGTTCCTCAACACGGTACAGCAGGGTCAGAAGAAGATTATCAATCAGGGAGCTCACGATCACCTTCACCTATTACAAAAGAAGATTCAAAGTCCTCCAACAAAACATCACCTGTAAGAAAAAAACGCTCTAGGTCAACTTCATCCACCAAGAAGAGAAGATCCAAGTCAAAATCTGTTAGCAACAAGAGGAGGTCAAGATCTCCTGCTAGAAAACGTAAGTCGAGGTCTCCATCGCATAGTCGTAAAAGAAGGACAAAGTCAAGGTCACCTGTTCGTAAAAGGAGATCTCGATCCAGATCAACAAATCGAAGGGCAAAATCAAGGTCAAAATCTCACACAAGAACAAAGCGCTCTAAGTCAAAATCCCCCAAGCGGAAACGGTCAAAGTCTAGATCACCAGTTCGAAAGAGGAGGTCAAAGTCACCTGCAAGAAAGAGAAGATCTCGTTCAAGATCAAGGGCTCGTAGGTCACGATCCAAAAGGTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13667
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 |
|---|---|---|---|---|---|
| ENSDART00000077740 | Nonsense | 858 | 1069 | 4 | 7 |
| ENSDART00000122057 | Nonsense | 858 | 1069 | 5 | 7 |
| ENSDART00000122169 | None | None | 229 | None | 5 |
| ENSDART00000130549 | Nonsense | 858 | 1069 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 36890950)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 36028839 |
| GRCz11 | 9 | 35838024 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTGTCACGCCGGAGAAGACCAGCATTTAGAGGGCGATCATTTGACAGA[C/T]GAGATCGGTGGAAACGTGAACCAAGTCATTCCCCAATTTTAATTCTCCGC
Long Flanking Sequence:
AATCAGGGAGCTCACGATCACCTTCACCTATTACAAAAGAAGATTCAAAGTCCTCCAACAAAACATCACCTGTAAGAAAAAAACGCTCTAGGTCAACTTCATCCACCAAGAAGAGAAGATCCAAGTCAAAATCTGTTAGCAACAAGAGGAGGTCAAGATCTCCTGCTAGAAAACGTAAGTCGAGGTCTCCATCGCATAGTCGTAAAAGAAGGACAAAGTCAAGGTCACCTGTTCGTAAAAGGAGATCTCGATCCAGATCAACAAATCGAAGGGCAAAATCAAGGTCAAAATCTCACACAAGAACAAAGCGCTCTAAGTCAAAATCCCCCAAGCGGAAACGGTCAAAGTCTAGATCACCAGTTCGAAAGAGGAGGTCAAAGTCACCTGCAAGAAAGAGAAGATCTCGTTCAAGATCAAGGGCTCGTAGGTCACGATCCAAAAGGTCACGTTCTGTGTCACGCCGGAGAAGACCAGCATTTAGAGGGCGATCATTTGACAGA[C/T]GAGATCGGTGGAAACGTGAACCAAGTCATTCCCCAATTTTAATTCTCCGCAAAAGGAGGTCCACCTCAAGATCTCGACGGAGTTCTAGCAAGACGCCACCACGCCTTACTGACCTAGGTAAATATACTTTTTGCATGGCTCCACTTCTTAATAGCATTTTTTTTTAAATAATGACTGTAATCTCTCTCTTCAGATAAAGAGCAACTATTGGAGATTGCAAAGGCTAATGCTGCTGCAATGTGTGCTAAAGCTGGAATGCCCATACCTGAAAGTCTCAAGCCAAAGGCAATTCTACAGTTACCCCTGCCAACCCCTGCTCCAGCCCCCTTGTCTTTGCCTCTGCCACTGCCCGTGCCCAATTTACCTATGAATCTGCCCATGGGTATACCAGGTATGCCTCCAATGCCAAACATGACAATGAACGCTGCTGTGGCAAGTATGACTGCAGCAACTATGACCGCTGCTCTTTCAAACATGGGTGCCCTGGCTGCTATGCCCCC
Associated Phenotype:
Not determined