ZMP
si:dkey-194n13.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate AN1, ubiquitin-like, homolog (Xenopus laevis) (ANUBL1) [Source:U
Human Orthologue:
ANUBL1
Human Description:
AN1, ubiquitin-like, homolog (Xenopus laevis) [Source:HGNC Symbol;Acc:23504]
Mouse Orthologue:
Anubl1
Mouse Description:
AN1, ubiquitin-like, homolog (Xenopus laevis) Gene [Source:MGI Symbol;Acc:MGI:1914742]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa22262 | Essential Splice Site | Available for shipment | Available now |
| sa35450 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31916 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22262
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109123 | Essential Splice Site | 174 | 637 | 5 | 8 |
| ENSDART00000134477 | None | None | 182 | None | 5 |
| ENSDART00000146772 | Essential Splice Site | 173 | 673 | 6 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 18087642)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 17907677 |
| GRCz11 | 13 | 18038669 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCACTATTAAACACAAATAATGAGAGTTACTTATTTTGTGTGCTTTC[A/G]GTGGTGCTTCTGTACGAAATGTGCGCGCAGAGGAGGAGGAGGAACAAGAA
Long Flanking Sequence:
TCTCCGTTAAACAGAAATTGGAGAAATGATTCTGACTTCAACTGTATGTGTGAATGAGAGTGTATGGGTGTTTCCCAGTGTTGGAAGGGCATTCGCTGTGTAAAACATATGCTGAATAAATGGTGGTTCATTGGTGGCAACCCCTGATTAATAAAAAGATAAAGCGGAAAAGAAATTGAATGAGTTACCAGCACTGTTAATACAACATTTAGCAAATTCCAAATATATAAGTGTAAAAAAAAAGAAAATTAATAACTCTGTTAAATACAATTAAAACAAAGTGTGTGCTTGTTAATAGAATTCCAAACATTTCTTTTTTCTTTTTTTTACAACATAAAATAAATGTAAAATGTTTTGTAAAACACACTAGTACTTGATCATCACTATTAATTCAATATTTATCAAATATCAAAATGAATATATATGTAAAAAAACAAACAAGCGAAACCATCACCACTATTAAACACAAATAATGAGAGTTACTTATTTTGTGTGCTTTC[A/G]GTGGTGCTTCTGTACGAAATGTGCGCGCAGAGGAGGAGGAGGAACAAGAAAGTGCTTCTTCAGAGCTGCAGACGCTAGAAAACTCCATCACAATGGGCAAAATGAAGCTGCTCAAGGCCAAGATGGAGAACATGAACCTTAACAAAAAGGTAACAGCGCAGGCGGTTGAGAAATACTCTTAATCTGTCTTTGCTCCTCCTCCACTGTTTCCAGCACAGTCATCTTATCCTGAAGCGCATGAACCTTCTTACTGTCAAACGCATCTGATTAGATCTGTCAGCCGAGCAGTATGGAAGTGCTCAATTCTCCAGCTGGCCTGAGGGAGTGCAGTCCAGCCCACGCCGAGTCTGATTATCTGGCGCTGTAATAACTAACAGCTCAGCGCATTGGCATATGAAGTTAATTATTCGCACTCAACTATGCATTGTTGACAGAAGATGTGTCTTAGTTACAGATGCTGTCTAGCTTGTCTACTTTAGCTTGCGTGTTTATGTGGGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35450
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109123 | Nonsense | 252 | 637 | 6 | 8 |
| ENSDART00000134477 | None | None | 182 | None | 5 |
| ENSDART00000146772 | Nonsense | 251 | 673 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 18082733)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 17902768 |
| GRCz11 | 13 | 18033760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGGGTCCGCGACCTTGCAGCGGTTCCCACGGCTCTGCCCGACACCAT[C/T]GAATGTTCCGTGTCCTTCCTCAAATAGGACACGCCTCTTCAACACATCTA
Long Flanking Sequence:
CTTGCCGTTTGTCGCTTCCGCCTAAATGAATCAATTATCTTTTGTTTCCATGCCACCTCATACTTAAGTTTCTCATCAAGTCTTCAAGACCAATCAAATGCTCTCTAGTATCTGACAAGCCCCACCTCTTTCAAGGTACTGCTTATTTGATGCACTTGATCTCAACCACTCTCACTGACAGAGCTGTTATAAAAACAAAACTCTATTGGCTGTTTTTTTAAAAGGGGAGGAGCTACTCTGTCCCACCCTCGGGATTTTTAAGTTGAGATCATGCCAGACATCAAATAAAAAATTTAAAGCATTTCATGGGACCTATAGGCCAGATACTTTCAGTAATGTGCCCCTGATCACAAAGGAATGCTCATTATATTTTCTCTGTTTACTTTCCTTAATAGACAAACTTGTTTTTTTTTCAGCCCAAAAAGACTGCTAAATTAAAAATCCGACCTCCAGTGGGTCCGCGACCTTGCAGCGGTTCCCACGGCTCTGCCCGACACCAT[C/T]GAATGTTCCGTGTCCTTCCTCAAATAGGACACGCCTCTTCAACACATCTACCTCCTATCGGTGATCAGCAGCAACCTGTATTGTCCACCCCCACTGCTGGCTCCGCCCACCAACCCTACACATCTCTCTCCAGTCCTGCTTCCTCAAGCCGTGCTCATCCATCCTCTGCAGCCTCTGGCATATACATGCTGCAGGCTGAGGAACCATGGGATAATCCAGTGCCCAGGAAGATTAGACTCCCTCCCAAAGTATCCCGGCTGGATATGAGAGGGCCTAAAGTCATGCGAGACTGCGTCTACCCGCCTCTATCTCTTCTGTCCAGCCCTGGAGTTCAGGATGAAGTCGATATCAAGAACGAACACCTAACACTAACTGAGAAAACCACAGTTATTGAGTCGCCCAAAGCTGTGCCCTTCAATCTTCCTGAACCCCTGAGTTTGGATGTATCTGCTCAGCGAGAGCGAAGTCTGAACTCTTTAACGATGCCTGAGGCCAACGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31916
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 |
|---|---|---|---|---|---|
| ENSDART00000109123 | Nonsense | 394 | 637 | 6 | 8 |
| ENSDART00000134477 | None | None | 182 | None | 5 |
| ENSDART00000146772 | Nonsense | 393 | 673 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 13 (position 18082307)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 17902342 |
| GRCz11 | 13 | 18033334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAACCACAGTTATTGAGTCGCCCAAAGCTGTGCCCTTCAATCTTCCT[G/T]AACCCCTGAGTTTGGATGTATCTGCTCAGCGAGAGCGAAGTCTGAACTCT
Long Flanking Sequence:
CTGCTAAATTAAAAATCCGACCTCCAGTGGGTCCGCGACCTTGCAGCGGTTCCCACGGCTCTGCCCGACACCATCGAATGTTCCGTGTCCTTCCTCAAATAGGACACGCCTCTTCAACACATCTACCTCCTATCGGTGATCAGCAGCAACCTGTATTGTCCACCCCCACTGCTGGCTCCGCCCACCAACCCTACACATCTCTCTCCAGTCCTGCTTCCTCAAGCCGTGCTCATCCATCCTCTGCAGCCTCTGGCATATACATGCTGCAGGCTGAGGAACCATGGGATAATCCAGTGCCCAGGAAGATTAGACTCCCTCCCAAAGTATCCCGGCTGGATATGAGAGGGCCTAAAGTCATGCGAGACTGCGTCTACCCGCCTCTATCTCTTCTGTCCAGCCCTGGAGTTCAGGATGAAGTCGATATCAAGAACGAACACCTAACACTAACTGAGAAAACCACAGTTATTGAGTCGCCCAAAGCTGTGCCCTTCAATCTTCCT[G/T]AACCCCTGAGTTTGGATGTATCTGCTCAGCGAGAGCGAAGTCTGAACTCTTTAACGATGCCTGAGGCCAACGCCGCAGCTCCTCTTCTTTCCCAAGCCGTCAACTCTAATTGGAGACTACCATCCCAACATGACCTTACCCTCACCACTGAGCCCTTCACACCTCCACGTCATTTTGAGTTCACCGGTTCCTCAGTTCATCCCAGTCCGTCTCATGCTCTCCTCAGAACTAGCCCATCTCTCCCCATCAGTTCTCCTTCAAAAACTACATTCAAAGTTGATAAGCACTCAGAGGTGATTTCCAAAAGCGAAGCCCGAGACATTACAAACCTGGCCAATAAAGCCACTAAAGAGCCATTGGGATCGGTGAGCAACGCAGAACTTCTGGCCTCCTTGGCGGGCAGCGGTGGTCAGGAGACCTTGACCAGTCCTTACGCTTTGGGAAGGTTGTGTGCCACCGCCGCGCCCCTTCCAAACAACATCCATCTGTTGCAGGAGGAC
Associated Phenotype:
Not determined