ZMP
si:dkey-149j18.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate signal-induced proliferation-associated 1 like family [Source:Un
Human Orthologue:
SIPA1L3
Human Description:
signal-induced proliferation-associated 1 like 3 [Source:HGNC Symbol;Acc:23801]
Mouse Orthologue:
Sipa1l3
Mouse Description:
signal-induced proliferation-associated 1 like 3 Gene [Source:MGI Symbol;Acc:MGI:1921456]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23346 | Essential Splice Site | Available for shipment | Available now |
| sa15094 | Nonsense | Available for shipment | Available now |
| sa23347 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23346
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000088293 | Essential Splice Site | 455 | 1718 | None | 20 |
| ENSDART00000147385 | Essential Splice Site | 415 | 1678 | None | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 35461174)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 37140330 |
| GRCz11 | 18 | 37121338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGTTGACCTGGGGGCCAGAAACTACCATGAGCACTTCTATGGGAAAGG[T/A]AAGAAATCTATTGCTTCCATCTAGATAATACATTACACTACGAGATGTAA
Long Flanking Sequence:
GCAGCTCGTCGCAGCTATGCTGCCCAGCGGCGGAACACAGCCACTGGAGCTTCAGCCGCTTCTTCAGCTGGTGTTTCATTGGCAGTTTCCAGAGCTATTGCTCTGGGAGGTGTAGAGCCTAGCTTTTCCAGCACTGATGACCTCAGTGTCAAGGACCTTTTAGAAGGATCAACCCCAGGGCTAGAACTTTTAGAGCAAGGTAGTTCAGCTAGCCTCAACCCCAACTCTCAGCACCAGCTTTTGCTGAGCTGCCCACACTTCCTAAATGAGACCGGAAGCTACGGAGAACGTAACGTCAGCTTTTTGAGCTCATGGGCAGAAAGAGGAGAGGCTTGTGCAGTGGAAGCCCGGCTGCGTCCACGCTGCAGTAATGCCAGTGTATCCATACTGGATGTGTCTCCGGAAGATCAAAACAGCAGGTTAGAGAGACTGCAGCAGCACTGCATCGAGCACGTTGACCTGGGGGCCAGAAACTACCATGAGCACTTCTATGGGAAAGG[T/A]AAGAAATCTATTGCTTCCATCTAGATAATACATTACACTACGAGATGTAATCAGTTTTGGGTTTGGTCAACTAGAATCACATATCACAATGTTATGTCACTGTGCATCAGAATATCACTGCATTTGAAACCTACAGTGTTTGTGGTATCAAAGAGGTGGCTCTAAAATCTTTGCACAGCTCTATCCTCAGTTATTCTCTTTTATGATTTCCCTTTATTTACTTTTATTACAGAATTTTGTATTGAGTATTTACTAGTACTAAGCAAAAGTTTTGTATGTTTTGTTACTATTTATGTGTTTGTATCACATGCAGGTTATTGTATAGGTTATTATACGGACGGGCCCCCTGTTGTATTTGAGTTTGAGGATGGGTAGATGGTAGTTATAGATGATAGTGTTCATGTGTTCTCTGAATACATGTTTCAAAAAATGTATGACTGAGTTTTTATTATACAATATTTATCCTGTTGATTTTGAATCTTGCACCTAACAAATATCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15094
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 |
|---|---|---|---|---|---|
| ENSDART00000088293 | Nonsense | 1027 | 1718 | 9 | 20 |
| ENSDART00000147385 | Nonsense | 987 | 1678 | 9 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 35518137)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 37197293 |
| GRCz11 | 18 | 37178301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCGGAGCCAGTGGCCGCAGGCTATCGAGCAGKGCAGCGAACCCCAGTAT[G/A]GCGCTGGGACAGTCCTCCTGCTACTCACAGCTCTGCCCAGCGCTGGACCC
Long Flanking Sequence:
AATGTTTCAGTTTAAAAGCTGTAGTTTAGTTTAAATTGTACATACTTTCACCCAACGAATAGAGGACAATGCAGACACTTTGGTGAGCAAATCAAGGCAGATTCTGCTTGACTAGTGTATTCAGCATTGAACTCCAGTGTCTTATAAATGTGATTGTTTTTATTGCAATAAGATTCAAAGTGATGTTTTCTATTTATTTTGAAATATTATTAAATAAATTATCAAATGACTCATGGCAACTTTAATGTTAAATAGTTTGGTATGTTTATCTTTGGCCTACGGCACTTAATGATATTTGGTTTGTGGCCCTTCACATGAAAGAGTTTGGGCACCCCTGGTTTAGAGCATCAAGGGTGTTTACATCTGCAAATCTGAATAGTTTGTGATGATTGTTTGTTGCAGGGGCTGTACGGAGGAGTACGAGATGAAGATGATGGAGCAGAAGGGAGAAGCGGAGCCAGTGGCCGCAGGCTATCGAGCAGGGCAGCGAACCCCAGTAT[G/A]GCGCTGGGACAGTCCTCCTGCTACTCACAGCTCTGCCCAGCGCTGGACCCCCAGCGGACCCCCACCAGTCCCCAGCCGCACACACAAAGCTCTGGTTCCCGTTCCATACAGAGAGCCGCAACACATCTCTGCTAAACGGTGACACATTTCAGCATATGCTCGAAATAAAAAAATTAAAAAATCAGCTATTTGCCACTCTTAGTTTTTGGGATTTGTTTTTCTTCTCACTAGCTATTTCTGTCTCCTCCCACAGGCCTGTCAGTTATCCAGAAAACCATTACAGCGTGTCTCCTCTTGCTGGGGACAGAGGGCCGTACAGAAACCCTTCGGCTAGTTTCTCCAGTTCAGGCTCTGGCTTCAGCTCCACTGCGTTGGTGGTGCCAGGACTCAGTGGACCCTTCGTCCGCTATAAACCCTCTCGAGACGGGTCTGTTCTAATTCATTGTTGTTAAGATAGACTTGGGGAAAATATTGTCTGTTGGTATCTTAGAATAGAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23347
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 |
|---|---|---|---|---|---|
| ENSDART00000088293 | Nonsense | 1588 | 1718 | 17 | 20 |
| ENSDART00000147385 | Nonsense | 1548 | 1678 | 17 | 20 |
Genomic Location (Zv9):
Chromosome 18 (position 35537319)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 37216475 |
| GRCz11 | 18 | 37197483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGCTGGATCCTGGACTCATGCCTCTTCCTGACACTGCCTGTGGTCTC[G/T]AGTGGTCCAGCCTCGTCAATGCAGCCAAAGCTTATGAAGGTACGAGTGAG
Long Flanking Sequence:
TAAACTAATTCTTTTATGGATGAACAGATGTGTTTGCATACACTTTGGCCATTAAAGCTCATTCAGATTCTGCTATCGTACTGATTTGTTGTTGTTGTGTGTGTGTGTGCTTGTCTCCAGTCTCCTCATCGGACACTGCAGCGCACTTTCTCAGATGAGAGTCTGTGCAGTGGCCGCAGAGACTCCAGTTATGCAAGCACAGCTCTGTTTGAAGGACAAGTGCCACCCTGTGACCTTCTCTTCACATGCACACTGCCTACCCGACGCCATGGGCACAACACCAACCACGGGGCGCTTATGCCCAGTAAGAAAGGTTGGTGGGGTTTTATTGGTCATTGCTGTGTTTTGTGATGTGTGTTTGAATAAAGGGTGCATTTCTCATTGCTCCAGTGCCATTATCTGCATCAGAGTTATCTTTGACTGAGGTGAGGGATAAAGTTCCCCCTCTAAGAAGGCTGGATCCTGGACTCATGCCTCTTCCTGACACTGCCTGTGGTCTC[G/T]AGTGGTCCAGCCTCGTCAATGCAGCCAAAGCTTATGAAGGTACGAGTGAGTGTTTGGATAATTCTAAGCCACTGTTTTAAGTCTAAATTAGTTTCAATATTTTATTATTAGAAATTTTTGCAGACATTTACTTGAAAATACACTTTTTTTTAAACATAAACATAAAACTTGCATTCAAACAATGAGACATTTGAAAAAAAAATTATAATAATAATAAGAAAACAGTCATAAAAATAATAATTAAACAGAAAAATAAATGTGCATTCCCCCAACCTACCACCCACCAGTGCTATCAAACAATAAACGTAGGTACTAAAGGCATGGCAAACATATTAATCACAAGTATGTAAAAAGGAATTAAAAGGGGACCAAAATTTTTTTCAAATAACAAAACTTTGTCTATTAGGGTATATCTGATTTTTTCCAGATGTAATGTACAGGTTAACTCTGTCAGCCGTAATTTAAGAGTTGGAACTTCTTTTTTCTTCCAAAACAAAAGG
Associated Phenotype:
Not determined