ZMP
si:ch211-59d15.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate YLP motif containing 1 (YLPM1) [Source:UniProtKB/TrEMBL;Acc:Q5RG
Human Orthologue:
YLPM1
Human Description:
YLP motif containing 1 [Source:HGNC Symbol;Acc:17798]
Mouse Orthologue:
Ylpm1
Mouse Description:
YLP motif containing 1 Gene [Source:MGI Symbol;Acc:MGI:1926195]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10998 | Nonsense | Available for shipment | Available now |
| sa3057 | Nonsense | F2 line generated | Not yet available |
| sa23640 | Nonsense | Available for shipment | Available now |
| sa43386 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14245 | Nonsense | Available for shipment | Available now |
| sa11546 | Essential Splice Site | Available for shipment | Available now |
| sa17220 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10998
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 |
|---|---|---|---|---|---|
| ENSDART00000064140 | Nonsense | 226 | 1424 | 3 | 18 |
| ENSDART00000133012 | Nonsense | 226 | 1424 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9370461)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9204730 |
| GRCz11 | 20 | 9192469 |
KASP Assay ID:
2261-3996.1 (used for ordering genotyping assays)
KASP Sequence:
CTAGACAGAATACCCCTACACGCTTTGAAAGACCTCCTGTAGCYTCTCAA[C/T]AAACTRGTTCTGGTCAACAATCCARTCCTGTAACTGGCAATCAAACAAAG
Long Flanking Sequence:
CGTTAGACCGCCTGGTCCTGGCGTTGGACCGCCTGGTCCTGGGGCTGGACCAGGGGTTGGACAACCAAGACCGGGGGTTAGACCACCTGGACCGGGGGTTGGACCACCTGGCCCACAAGGTGTTAGACCATATGGACCAGGAGGTAGACCACCGGGGCCAGGAGTTAGACCATCTGGACCAGGAAGTGGACCGCCTGGACCCCATGGAAGATTTGACGGCCCAAGGTAATTCAGAAGAAAAATTACTTGGAATAACACATTTGTCTCGAGCTAGAGAACTAATTTTTGTTTTCTTTTTCAGATTTGAAGGTCCTAGAGGCCCACAATTTGAACAGCCACCCCAGCAACGATTTAGTGGACCACCCAGATTTGATGCTGGTCAGCGATTTAGCCAACCTCCTAGAGGTAATCCTCCCTTTCCAGGGGCTCCAGCAAGGCTGGAGAACCCCCCTAGACAGAATACCCCTACACGCTTTGAAAGACCTCCTGTAGCTTCTCAA[C/T]AAACTGGTTCTGGTCAACAATCCAGTCCTGTAACTGGCAATCAAACAAAGCAACAATCAGCAAAACCTGAGGCAAAGCCAGTTCCTCCATCTTATACAGACCCAGACAAAGCTAAAAGTCCTTTAAGTCAAAGTACTCAAAAAGAAAACAATTCCTCTGCTCCATCCATGACAGACGACCTTGTGGACTCAGTGGATGGATTTTTTATTCAGAGTGGACCCATTCCTCAAACTAAGGATTCTGATAAAACTGATGCAGACAGTGCAAAGCAAGATAAAACAAAAGAAGTTACTACAAAACCATCTGCACCTACGGATGCCCCAGACACCACAAACAAAAACTCTAACTTGCAACCTCCTAAGACCAGTCATACTGCTAATGGGCCACCACAACAAGTAAAGCCTCCTCAAAACAAATTTAAACCTGATACACCCAAGGAGACTCCTAGGATGCTACCCATGATGAATCAGCAAGTTCCACCACAGATGGCACGGGGAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3057
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 |
|---|---|---|---|---|---|
| ENSDART00000064140 | Nonsense | 445 | 1424 | 3 | 18 |
| ENSDART00000133012 | Nonsense | 445 | 1424 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9369804)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9204073 |
| GRCz11 | 20 | 9191812 |
KASP Assay ID:
554-2645.1 (used for ordering genotyping assays)
KASP Sequence:
AGGATTCCTATGACCATCAGGAACCAGGCAACGCAAGTCATRGCGAGGAT[C/T]AGGATCGTATTTGGAGAGATCCTTCTTTAGATGGTCCTGAAGAAATTGAT
Long Flanking Sequence:
CTGCTCCATCCATGACAGACGACCTTGTGGACTCAGTGGATGGATTTTTTATTCAGAGTGGACCCATTCCTCAAACTAAGGATTCTGATAAAACTGATGCAGACAGTGCAAAGCAAGATAAAACAAAAGAAGTTACTACAAAACCATCTGCACCTACGGATGCCCCAGACACCACAAACAAAAACTCTAACTTGCAACCTCCTAAGACCAGTCATACTGCTAATGGGCCACCACAACAAGTAAAGCCTCCTCAAAACAAATTTAAACCTGATACACCCAAGGAGACTCCTAGGATGCTACCCATGATGAATCAGCAAGTTCCACCACAGATGGCACGGGGAAGAGGACGAGGCCAAATACCAATGCCTCTCCGAGGCAGGGGTCGTGCACGTGGTCGAGGGCAGTATGGCGGACCAATGGCTGATCCCAACTTCCAAAGAGAAATTGAGGAGGATTCCTATGACCATCAGGAACCAGGCAACGCAAGTCATGGCGAGGAT[C/T]AGGATCGTATTTGGAGAGATCCTTCTTTAGATGGTCCTGAAGAAATTGATCAGGAAGCACCTTTAGAGATTTGGCAACCAGAGGAGGAACACTTTCCAGAGGAGTACCCAGAGGACACTCACCAAGATGAAAACTGGGAAGAAGAACCACAGGATTATTGGGAGGAAGAAGATCCATATTGGGCAGAGCAACGACCTGCCATGCGTGCTAGACCTCCTTTTCCTCCAGGTGGCCCCAGAAGACCTCCTTTCCATCCACGATTTATGCTTCAAGGTCCAAGGCGCCCTCCTCCTCCTGGAAGTTTGCAACATAACCCACTTGGACCTCCTCCGTTTCGACCACGTGGGGGAGTTGTACCACGATTCAGACGTGGTTTAGGCCCTTGGGGACCATTACCCCGCCATGACATGATGGAGCGAGATTTAAGACGACCACCAGCACCTCATGAAATTATAGCTAGGGAACCAGCTGGTCCTCATGGATATGAAGAAGAAATTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23640
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 |
|---|---|---|---|---|---|
| ENSDART00000064140 | Nonsense | 565 | 1424 | 3 | 18 |
| ENSDART00000133012 | Nonsense | 565 | 1424 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9369444)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9203713 |
| GRCz11 | 20 | 9191452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAACCCACTTGGACCTCCTCCGTTTCGACCACGTGGGGGAGTTGTACCA[C/T]GATTCAGACGTGGTTTAGGCCCTTGGGGACCATTACCCCGCCATGACATG
Long Flanking Sequence:
CAATGCCTCTCCGAGGCAGGGGTCGTGCACGTGGTCGAGGGCAGTATGGCGGACCAATGGCTGATCCCAACTTCCAAAGAGAAATTGAGGAGGATTCCTATGACCATCAGGAACCAGGCAACGCAAGTCATGGCGAGGATCAGGATCGTATTTGGAGAGATCCTTCTTTAGATGGTCCTGAAGAAATTGATCAGGAAGCACCTTTAGAGATTTGGCAACCAGAGGAGGAACACTTTCCAGAGGAGTACCCAGAGGACACTCACCAAGATGAAAACTGGGAAGAAGAACCACAGGATTATTGGGAGGAAGAAGATCCATATTGGGCAGAGCAACGACCTGCCATGCGTGCTAGACCTCCTTTTCCTCCAGGTGGCCCCAGAAGACCTCCTTTCCATCCACGATTTATGCTTCAAGGTCCAAGGCGCCCTCCTCCTCCTGGAAGTTTGCAACATAACCCACTTGGACCTCCTCCGTTTCGACCACGTGGGGGAGTTGTACCA[C/T]GATTCAGACGTGGTTTAGGCCCTTGGGGACCATTACCCCGCCATGACATGATGGAGCGAGATTTAAGACGACCACCAGCACCTCATGAAATTATAGCTAGGGAACCAGCTGGTCCTCATGGATATGAAGAAGAAATTGACAGAGAGCCTGCATGGCCTCATCCTCGTGGTAGAGGGATTAGACGACCACCTTTGCCACCCCATGAAATGGGAAGAGGCATTAGAAGACCACCCATGAGGCCTGCAATGCCAAGAGAAAGGTGGCATGGCCCACCACCTCATGAAGAAGAGAATTATGAGGAGGAATACCCATATGGTGCAGAGGATGATGTGTACAGAAGGCCACCTCATGAATACAATGAAGATTATGAGCATGGAGATGAGTATTATGGCTCTCGTGAGGAATGGGACGGGGAGCAACCTGAACGAGACTATCCTCCACATCGTCCTCCAGAACGTGTTAGAGAGGATCCATGGTTAGAGGAAAGAGAAAGATCATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43386
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 |
|---|---|---|---|---|---|
| ENSDART00000064140 | Nonsense | 664 | 1424 | 3 | 18 |
| ENSDART00000133012 | Nonsense | 664 | 1424 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9369147)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9203416 |
| GRCz11 | 20 | 9191155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCAAGAGAAAGGTGGCATGGCCCACCACCTCATGAAGAAGAGAATTAT[G/T]AGGAGGAATACCCATATGGTGCAGAGGATGATGTGTACAGAAGGCCACCT
Long Flanking Sequence:
ATTGGGAGGAAGAAGATCCATATTGGGCAGAGCAACGACCTGCCATGCGTGCTAGACCTCCTTTTCCTCCAGGTGGCCCCAGAAGACCTCCTTTCCATCCACGATTTATGCTTCAAGGTCCAAGGCGCCCTCCTCCTCCTGGAAGTTTGCAACATAACCCACTTGGACCTCCTCCGTTTCGACCACGTGGGGGAGTTGTACCACGATTCAGACGTGGTTTAGGCCCTTGGGGACCATTACCCCGCCATGACATGATGGAGCGAGATTTAAGACGACCACCAGCACCTCATGAAATTATAGCTAGGGAACCAGCTGGTCCTCATGGATATGAAGAAGAAATTGACAGAGAGCCTGCATGGCCTCATCCTCGTGGTAGAGGGATTAGACGACCACCTTTGCCACCCCATGAAATGGGAAGAGGCATTAGAAGACCACCCATGAGGCCTGCAATGCCAAGAGAAAGGTGGCATGGCCCACCACCTCATGAAGAAGAGAATTAT[G/T]AGGAGGAATACCCATATGGTGCAGAGGATGATGTGTACAGAAGGCCACCTCATGAATACAATGAAGATTATGAGCATGGAGATGAGTATTATGGCTCTCGTGAGGAATGGGACGGGGAGCAACCTGAACGAGACTATCCTCCACATCGTCCTCCAGAACGTGTTAGAGAGGATCCATGGTTAGAGGAAAGAGAAAGATCATTCCCATATGAGGAAGACCGATATAGAGAAGAACGAAGGGGACCTTTTTACCCTGATGATCCACCTTATCAAGACCGAGATCGGGAGCCTCCATTTCATTCACGTTCTGATTGGGAAAGGCCCCCACCTCCACCCCCACCAGAAAGAGGATACTCCCGTTCACTTAGTGAAACGGATTATGAACATAAACTGGATCCACTAGCTAGCCTTCCCGCACCTCAAGCCACAGATTCCCCACTTGATGAGTCTTCACCTAGCGCAACTAAGGCTGTACTTGCTCTTTCTCAAAGGCAGCATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14245
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064140 | Nonsense | 753 | 1424 | 3 | 18 |
| ENSDART00000133012 | Nonsense | 753 | 1424 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9368878)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9203147 |
| GRCz11 | 20 | 9190886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGATATAGAGAAGAACGAAGGGGACCTTTTTACCCTGATGATCCACCTTA[T/G]CAAGACCGAGATCGGGAGCCTCCATTTCATTCACGTTCTGATTGGGAAAG
Long Flanking Sequence:
AGACGACCACCAGCACCTCATGAAATTATAGCTAGGGAACCAGCTGGTCCTCATGGATATGAAGAAGAAATTGACAGAGAGCCTGCATGGCCTCATCCTCGTGGTAGAGGGATTAGACGACCACCTTTGCCACCCCATGAAATGGGAAGAGGCATTAGAAGACCACCCATGAGGCCTGCAATGCCAAGAGAAAGGTGGCATGGCCCACCACCTCATGAAGAAGAGAATTATGAGGAGGAATACCCATATGGTGCAGAGGATGATGTGTACAGAAGGCCACCTCATGAATACAATGAAGATTATGAGCATGGAGATGAGTATTATGGCTCTCGTGAGGAATGGGACGGGGAGCAACCTGAACGAGACTATCCTCCACATCGTCCTCCAGAACGTGTTAGAGAGGATCCATGGTTAGAGGAAAGAGAAAGATCATTCCCATATGAGGAAGACCGATATAGAGAAGAACGAAGGGGACCTTTTTACCCTGATGATCCACCTTA[T/G]CAAGACCGAGATCGGGAGCCTCCATTTCATTCACGTTCTGATTGGGAAAGGCCCCCACCTCCACCCCCACCAGAAAGAGGATACTCCCGTTCACTTAGTGAAACGGATTATGAACATAAACTGGATCCACTAGCTAGCCTTCCCGCACCTCAAGCCACAGATTCCCCACTTGATGAGTCTTCACCTAGCGCAACTAAGGCTGTACTTGCTCTTTCTCAAAGGCAGCATGAGATCATTCTTAAAGCTGCCCAGGAGCTAAAAATGATCAGGTAAAATGGAATTTATCAAGAGCGTACAATTATTCAAATAACATGCAATTCATACACTCCAAACGGTTGAATTCACAACTTGATTAAACCTGTTTGTTCGTAGAGAGCTTCAGGAGACCAAAAAGGCTTTAGGAGAGGTTTCCACCACAGAGTCAGCTGGGTTGCCTTCAGAGCTTCCTGCTGGCATCCTTGGATTGGAAATTCCACCAGAGGTTAAAAGTGCCCTGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11546
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 |
|---|---|---|---|---|---|
| ENSDART00000064140 | Essential Splice Site | 1292 | 1424 | 14 | 18 |
| ENSDART00000133012 | Essential Splice Site | 1292 | 1424 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9361105)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9195374 |
| GRCz11 | 20 | 9183113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGYGMGACTAGATATCAGGTCTCTTCTGCAGGATGCAGCAATCGAGGATG[T/A]GAGTGTTTTSATGACTTATGCTGTTATGTTAATTNNNAAAGTCAATTTAAATH
Long Flanking Sequence:
TTGCTTCAACACACCTGCCTGGATGTTTCAAGTATACCTAGTAAGACCTTGATTAGCTTGTTCAGGTGTGTTTAATTAGGGTTGAAGCTAAGATCTGTATAGGACACCAGCCCTCCAGGAACAAGTTTGGTGACCCCTGACTTAGAATATGTATAACTCATTTTAAAACTCACTTATTAGTAATTAATGTTATCATTGATTAATTGTATAGCAACCCTTTCTTACTACTATATATTTTTAGGTGTATTTGGCTGAAATCACGACTGATCAGCAAACATGTGCCAAGAGAAACATCCATGGACGAACACTAAAGGATATTTCAAAGGTATATTCTTTAGCTTGGTTTGGATATCTGGCATTTTTATAAAGTATCCTAAATTCTGTAATATAGTCTTACTAATGCTATTGCTGACAGCTGTCCGGTGGCTGGGAGTCTGCACCGCCTCATATGGTGAGACTAGATATCAGGTCTCTTCTGCAGGATGCAGCAATCGAGGATG[T/A]GAGTGTTTTGATGACTTATGCTGTTATGTTAATTAAAGTCAATTTAAATAAATTTCCCTGATGCCCTTTTTCTCATAGTAACATAAACTGCTTGTGTGCTAGGTGGAGATGGAAGACTTCAACCCATCCGATGAACCAAAAGCTGAAGTGAAAAATGATGACGATGAGACTGATCTGGTAGGACCTCTCTTTTCATGCATGCCTTTTTTGTCCTATACTTGAAAGTGTGACTATAGTTAATTGTCCCAGTTTCTCACCCAAACAAGGTAAGTACTCCTCTGATCTTGCACTAGTGTAACTACTTTTTTTTCCTTTTTAGGAAACTACTTTTAGATTTAAAGACATTAAATCTCTTTTTAATCTAATCTTCAATCCATATTGTTAATATGGATGATTTAGTGCTTGTTTAAACATTTTGTCAACTGCAGTTGTATGTAATCTTATTAATGTAAGTTTTTGCTTTCAGTCAAGTAACTGAAAGCTCAAGTTGACTCATGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17220
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 |
|---|---|---|---|---|---|
| ENSDART00000064140 | Nonsense | 1392 | 1424 | 18 | 18 |
| ENSDART00000133012 | Nonsense | 1392 | 1424 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 20 (position 9351634)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 9185903 |
| GRCz11 | 20 | 9173642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGGTGCGCTGGGCTGATCTTGAAGAGCAGAAGGATGTCGACCGAAAG[C/T]GAGCGATTGGTTTTGTTGTCGGTCAGACAGACTGGGAAAAAATCACGGAT
Long Flanking Sequence:
CACAAATAAGTGTTTATTGAATGTAGAATTGGTGATGACTTTAGATGCTGCATTGTTCTTCCAGACAAACTGGATGGTCTGGTTGGCGGAGGCAAGAGAAAACGGGACGCTGGATTGTCCGGCATGGAAGACTTTCTTCAGCTGCCTGATGACTATGCCACTCGCATGTCTGAACCTGGCAAAAAGAGGGTAAAGCACTTCACTTCATTTCCAAGTCCTTTTCTTCTTCGGGGTCATGTGTTTAGTTTTGTTTTGTATGTTCTTGAGTTTTGCAGATTGATCCTCATCTTTTGAAAAGTATTGAATTGTTGGTCTGTATTTTTTATGTTACCGAACAAAACTTGATCTACTTTTCTTATGATCTATTTGATGAATAGTTAATTATTTTTTGTTAGCTTAGGGAGGATCATAATTTTTCAAAGTTTTAGCACTCATCAACCTTGCTGATCTTGCAGGTGCGCTGGGCTGATCTTGAAGAGCAGAAGGATGTCGACCGAAAG[C/T]GAGCGATTGGTTTTGTTGTCGGTCAGACAGACTGGGAAAAAATCACGGATGAGAGCGGCCAGATTGCTCAGAGAGCTCTCAACCGCACCAAGTATTTTTAGGAGATTTTGTAATGACGTATGTACAGAGTTAAGGGTGAGTATCTTGTCAATCTTTTTTTTTTTTTTTTTTAGAGAAGTCAAGACTTAGTTATTGCAATATGTGGATAGCAGTGTAGAGTCATTTTGTTTTCAACTTTTCGCTTTCTTATCAAAAGAGGGAGAGTTCGAGGGTGTTTTTACATCCTGTAGGTTACGTTTTTTTAATCAATGTAAAAAAAAAAAAAAAAACTGGTTCACTAGGCAACATTTCAAAGTTAGGCAACATTTCAAAAAATATATTTATATTGTAAAGCTGTTCTCATTTTTCAAAGCACATCTTTTCACATTATTTGTCATTTATCAAAATGAATAAATGCTTATTAGGGATGGCCTGCAATAAAAATGTTGGCCAATAACCAG
Associated Phenotype:
Not determined