ZMP
sipa1l1
Ensembl ID:
ZFIN ID:
Description:
signal-induced proliferation-associated 1-like protein 1 [Source:RefSeq peptide;Acc:NP_001025340]
Human Orthologue:
SIPA1L1
Human Description:
signal-induced proliferation-associated 1 like 1 [Source:HGNC Symbol;Acc:20284]
Mouse Orthologue:
Sipa1l1
Mouse Description:
signal-induced proliferation-associated 1 like 1 Gene [Source:MGI Symbol;Acc:MGI:2443679]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43461 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa3071 | Nonsense | F2 line generated | Not yet available |
| sa5675 | Nonsense | F2 line generated | Not yet available |
| sa45702 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43461
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011018 | Nonsense | 293 | 1794 | 1 | 20 |
| ENSDART00000114611 | Nonsense | 240 | 1715 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 28723311)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 28794524 |
| GRCz11 | 20 | 28697403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAAGAAAGGGAAAAACAAATGAAAAGGCGCTCAAAGTCAGAAACTGGT[G/T]GAGAGTCCATATTTCGAAAGCTGCGGAGTGTCAAAGCTGAAGGCGATTCG
Long Flanking Sequence:
GCCACCTGATCAGCCCTCAGGACTCCTCCATGTTGCGTAACATTCACAACACGCTAAAGAACAAGATGCAGAGCAAAGGCAAAGACAATCGCTTTCTGTCACCTGACGGCTATCTTGGATCGCCCCGCAAAGGCATGCGGCGAATTAGACAACGCAGCAACAGTGATATTACCATTAGTGAACTAGATGGCGATGGAAGCGAAGGCTGGTCTTTTTCAGGATGGACCCCCATGCATCGAGAGTATGGCAGTACCTCGTCTATCGACAAGCATGGTGTGTCAGGTGAAAGCTTCTTCGACATGCTCAAAGGCTACACGACAGATGCTCCAGACCAGCGCAGTCCTGCCCCTGAAAAGCTAAGTGAGTTACTGACAGTCGCCCATAAACAGACAGCCCTCGACTTGCCCGATGGACCTCTTGGTCCTCCTCGGGGAAGTCCTGCCAGTCGCCTGAAAGAAAGGGAAAAACAAATGAAAAGGCGCTCAAAGTCAGAAACTGGT[G/T]GAGAGTCCATATTTCGAAAGCTGCGGAGTGTCAAAGCTGAAGGCGATTCGTCACGTGCAGGTTCAGATGCAGAGGATGGAAAGTCTGATGACTTGGGTCCTCCTCCAAAACCATGGGTCTGCCAGAAAGGGTTTGCACACTTTGATGTCCAGAGTATACTGTTTGACCTGAATGAGGTTGTGCAGAGTCGGCAAAGTGCCGCTAAGCGAAAGAACACCACCACTGGTGCCTCTGCTGCTGCTGCAGCCTCGGCCTCCAACACGTCATCTCTCTCGTCCACCCAAAGTGGGGCTTATGGTTCTCCTTGTGGGAGTCAGGAAGAGCTCAGCGTCAAGGATGGGCCTTCTCTTGACTCGGGTGATGACAAGAGCAATGATTTAGTTCTCAGCTGTCCTTGTTTCCGGAATGAAATTGGCGGTGAGGGAGAGAGAAACATCAGCCCTTCAAAACAGGGCAGTATCGGCAGTGGTGCCTCCAGCTCTTCTAGAGATGAAGAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3071
Status:
F2 line generated
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011018 | Nonsense | 1025 | 1794 | 8 | 20 |
| ENSDART00000114611 | Nonsense | 972 | 1715 | 8 | 20 |
| ENSDART00000011018 | Nonsense | 1025 | 1794 | 8 | 20 |
| ENSDART00000114611 | Nonsense | 972 | 1715 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 28706591)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 28777804 |
| GRCz11 | 20 | 28680683 |
KASP Assay ID:
554-2905.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGATTAGTGGAAATTTGCAAGGTGGCTGTGGCAACACTTTCGCACGAG[C/T]AGATGATAGACCTGCTCCGCACATCAGTTACTGTAAAAGTTGTCATCATT
Long Flanking Sequence:
TGTCACTCTTGAAGTGGAGGAGCTGTTGCCATGGTAACTAGTACTCGGCAAACTGAATGCTCATGATCTCCATCACAGTCATAAAACATATTAGCAAAGCCTTCTTTTCATTTTAAGAAAGAAGTCTTGTTCGTGATTTGCAGTCACTGACAATAGTTTGTGATAGACATATCTAGTCCATTCTGTCCATTTTAACAATGCCTCGCATCCTTAATAGAGGAAATTGGACTGTGAATTGTAATAAACTGCTGCAGAATCCAGTTAGACACTGTCTTATCAGTCTGTTTTTCCCCTCTTCCCCTCAGCACCTTACTAAAGGCTGTGAAACATCTGAGATGACCTTAAGGAGGAACGGACTGGGCCAGCTTGGCTTTCACGTTAACTATGAAGGCATTGTGGCAGAGGTGGAGCCCTATGGCTACGCCTGGCAAGCAGGGCTGAGGCAAGGCAGCAGATTAGTGGAAATTTGCAAGGTGGCTGTGGCAACACTTTCGCACGAG[C/T]AGATGATAGACCTGCTCCGCACATCAGTTACTGTAAAAGTTGTCATCATTCCACCTCACGAAGATGCCACACCTCGCAGGTAAGTCTTTCAACATCGCTTAATGGTTTGGTTCATTATTTCTTGAGTGAATCTTGTTGAAGTAAAGTGAAGCAAGCAGCAATTATTTTTGGCAGGTAGAAAAGTAAACAAGTCATTTCAAGTTTTGCAGTAAGACAACAATACAAAACATTGCACCTTTATGCCCACACATGCAAACCAAAATAGATGAGATCCGCCTTCCCAGTCTTGGCTCGCCTGCAGGCACTGTGCCAACTTGAAGGTTATAATGATCAGGGTCTAAGCTACAATTCATCAGACCCACCAGATTTTGATTTGAGTTGAGTGTGCTTTTTTCTGCTTTGGTTGTGCGTTATTATTATCCTTCGAATACCTGCTGTTTCCATTTTTGACAGTTTATGTTTTTGTCTAAACTGGAAACTGGCTCTACAGTATATGTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5675
Status:
F2 line generated
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011018 | Nonsense | 1025 | 1794 | 8 | 20 |
| ENSDART00000114611 | Nonsense | 972 | 1715 | 8 | 20 |
| ENSDART00000011018 | Nonsense | 1025 | 1794 | 8 | 20 |
| ENSDART00000114611 | Nonsense | 972 | 1715 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 28706591)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 28777804 |
| GRCz11 | 20 | 28680683 |
KASP Assay ID:
554-2905.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGATTAGTGGAAATTTGCAAGGTGGCTGTGGCAACACTTTCGCACGAG[C/T]AGATGATAGACCTGCTCCGCACATCAGTTACTGTAAAAGTTGTCATCATT
Long Flanking Sequence:
TGTCACTCTTGAAGTGGAGGAGCTGTTGCCATGGTAACTAGTACTCGGCAAACTGAATGCTCATGATCTCCATCACAGTCATAAAACATATTAGCAAAGCCTTCTTTTCATTTTAAGAAAGAAGTCTTGTTCGTGATTTGCAGTCACTGACAATAGTTTGTGATAGACATATCTAGTCCATTCTGTCCATTTTAACAATGCCTCGCATCCTTAATAGAGGAAATTGGACTGTGAATTGTAATAAACTGCTGCAGAATCCAGTTAGACACTGTCTTATCAGTCTGTTTTTCCCCTCTTCCCCTCAGCACCTTACTAAAGGCTGTGAAACATCTGAGATGACCTTAAGGAGGAACGGACTGGGCCAGCTTGGCTTTCACGTTAACTATGAAGGCATTGTGGCAGAGGTGGAGCCCTATGGCTACGCCTGGCAAGCAGGGCTGAGGCAAGGCAGCAGATTAGTGGAAATTTGCAAGGTGGCTGTGGCAACACTTTCGCACGAG[C/T]AGATGATAGACCTGCTCCGCACATCAGTTACTGTAAAAGTTGTCATCATTCCACCTCACGAAGATGCCACACCTCGCAGGTAAGTCTTTCAACATCGCTTAATGGTTTGGTTCATTATTTCTTGAGTGAATCTTGTTGAAGTAAAGTGAAGCAAGCAGCAATTATTTTTGGCAGGTAGAAAAGTAAACAAGTCATTTCAAGTTTTGCAGTAAGACAACAATACAAAACATTGCACCTTTATGCCCACACATGCAAACCAAAATAGATGAGATCCGCCTTCCCAGTCTTGGCTCGCCTGCAGGCACTGTGCCAACTTGAAGGTTATAATGATCAGGGTCTAAGCTACAATTCATCAGACCCACCAGATTTTGATTTGAGTTGAGTGTGCTTTTTTCTGCTTTGGTTGTGCGTTATTATTATCCTTCGAATACCTGCTGTTTCCATTTTTGACAGTTTATGTTTTTGTCTAAACTGGAAACTGGCTCTACAGTATATGTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45702
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000011018 | Essential Splice Site | 1721 | 1794 | 19 | 20 |
| ENSDART00000114611 | Essential Splice Site | 1642 | 1715 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 28680267)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 28751480 |
| GRCz11 | 20 | 28654359 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATATTGTCTAAGTGTCTTGCATTTTGACCTTTCTCTTGTTCTCCTTTT[A/C]GTGAGGGGCCTTCAAGCTACGGTGGGAAGGTTTCTCAGCTGGAGGCTTTG
Long Flanking Sequence:
GGTTACAGATTTTTCATTCATTTTGTGCAATATCATAGAGTGATATTGTTTGTTGAAATGTAATGTTTTGGAATAATTTGTTAATTTTATATTAAGACCATGTCCTCTGAGGGCCTGCACTGATGGACAGATGGGAAATTGTGTGTTGGAATGTGCATCTGTGTTGAGCTTGAGGTGCTGCTTCATCATACATGCCCAACACTGCCTTTAACTTTTATTCATTACATCATCATCATCATCATCTCTCTCTCTCTCTCTCTCCCTCCCATCTCTTCATTTCCTCCTCAGTGCAGCGAGGGTTCATGTTTAGCTCTCAGGACGTTAGTCATAGAGGAGAGACTTCACTCAGTCTTCAGCATCTAGATCTGCAGCCGGTGCCGCACACCAGACTCTCCCCCAGGTATATCCAGGATCCATATCCTAATAGATCAACAAATAGTATTTTTTGATTCATATTGTCTAAGTGTCTTGCATTTTGACCTTTCTCTTGTTCTCCTTTT[A/C]GTGAGGGGCCTTCAAGCTACGGTGGGAAGGTTTCTCAGCTGGAGGCTTTGGTGAAGATGTTGCAGGAGGATTTGAAGAAAGTAAGCAGAACATACACAATATTCACACACATGTATTGAACTCTTTATGGTAAAATAGATTCAGAATATTTGACAGTCGTACAATTACTGAAATGTTATTCACATCTGCGGCCAAGGATTTCAGAGGGGCTTTTAGTGTTTATTGCTTCAGCCTCCCCTCAGTTAAAAATGATTATCCAACTGGAATTTTAAAAAACTTTTCTTAAAGGGAGTAGTTCTCCCAGAAATAAAAATTCTGCTATTATTTACTCAAACCTGTTTGAGTTTCATTCTTCTGTTCGGCACAAAAGAAGATGTCCTGAAGAAAGTTGGAAAACTGTTACCATTGATTCCCGTTGTTTTTCCTACTATGGAAGTCAATGATTAGAGGTTTTCAGCTTTATTGAAAATATTCAATTAATTAATATTTGGTGTTTGATA
Associated Phenotype:
Not determined