ZMP
msna
Ensembl ID:
ZFIN ID:
Description:
moesin [Source:RefSeq peptide;Acc:NP_001004296]
Human Orthologue:
MSN
Human Description:
moesin [Source:HGNC Symbol;Acc:7373]
Mouse Orthologue:
Msn
Mouse Description:
moesin Gene [Source:MGI Symbol;Acc:MGI:97167]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1265 | Nonsense | Available for shipment | Available now |
| sa20388 | Essential Splice Site | Available for shipment | Available now |
| sa18450 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1265
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 |
|---|---|---|---|---|---|
| ENSDART00000016214 | Nonsense | 21 | 579 | 2 | 14 |
| ENSDART00000112536 | Nonsense | 20 | 578 | 2 | 14 |
| ENSDART00000124048 | Nonsense | 21 | 579 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 23934905)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21647777 |
| GRCz11 | 5 | 22151577 |
KASP Assay ID:
554-1180.1 (used for ordering genotyping assays)
KASP Sequence:
AGATCAGTGTTCGTGTGACTACAATGGATGCCGAGCYGGAGTTTGCCATC[C/T]AACCCAGCACCACAGGGAAACAGTTATTTGACCAGGTTTGTGTGTGGCCT
Long Flanking Sequence:
GTTTGCATTGGCCAAAACTGATTAACTGAAGTGGATTCCACTTCGTCTTAAAGCCTTTTTCGATGGGTCATTTTTGCCATTTATGATGGCATATCAGTCAAAATAGGACAAATTAGCATATGAATGGGACAAATTCTGGACCTTTGTCAGTGAAGGGTGGGTCTTCCGAACCTCTCCTGGCTACAGGCCTGATCTGTGTACACTGAAAAAAATATGATTCCCTGGATTTGCTAAATTTAAGTTAAGTGGTTGTAAACAGTTTATTTGGGCTGAGTTTAAACAAACAAATGAAGTTGAATATTACTAAATTTAATTAGTTTAAATTCAACCAATAAAATTTGTTTGCAGACAGCATTTTTTTTCAGTGTACTGCATCTTTGTTGGTGTTTTCTCTCTTTTACTTCCTTCATTCATTCATTGACATTTAATATTATTTATTTGTTGATTTTCAGATCAGTGTTCGTGTGACTACAATGGATGCCGAGCTGGAGTTTGCCATC[C/T]AACCCAGCACCACAGGGAAACAGTTATTTGACCAGGTTTGTGTGTGGCCTCTTTTTTTCTTCTTCTTCTTTGTAGCCGTGCCCTTGTTCAATAACCTCCTAAATACAGCTATATATTAAATGTGTTCTGCTGTTTAATTTTTGCTGCGAACAGACAAACAGTTTGGCAGTGAAGGCCATGTCAGAGAAGCTGTGTGTGCATGTTTAGTTTAAGAACTGGAAATCCTTCTTGTGGAGGATTTCACTCTCCCTCCACCCTTCCTCTTTCTGACTCTGCTTCTACCTCGGCCTGTAATTCTGTACAGTCCCATCTTCCTCACTCTTAGTCACTGTGACCGTCACGTTCATGAAGTCGCTCTTTCTGAGACTCGATAATAGGCGGCTTTGTTCTTGAGCAACCTTTAATTTCTCATACAAACACACACGCTCATGCAGACCTACACACAGCCTTCATTCTTCAGGCAGTTGTGTAGGTTTTAGAGTCACGTTTGTTTCCGACAG
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa20388
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000016214 | Essential Splice Site | 156 | 579 | 5 | 14 |
| ENSDART00000112536 | Essential Splice Site | 155 | 578 | 5 | 14 |
| ENSDART00000124048 | Essential Splice Site | 156 | 579 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 23943408)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21656280 |
| GRCz11 | 5 | 22160080 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCCCACACTCCTGGATACTTGTCCAATGAGAAGCTGCTCCCACAGAGG[T/C]GTGCATATGCAGATATTGTTGTAGCAGTGAAAACACATTGAGGAAGCATG
Long Flanking Sequence:
AAAAGATGGATGCTGACAGACAGGAGGAATAAATGAACGCCAGACTGAAAGTGATTCTCGTTGGTTCCTCATTTAGGTTACGGCTCAAGACGTCCGCAAGGAGAGTCCTTTGCTGTTTAAATTCAGAGCAAAGTTTTACCCAGAAGACGTTTCTGAGGAACTGATTCAGGAGGCCACTCAAAGACTCTTCTTCCTTCAGGTGTGTTTGCATACGCTGTCTCAGATATATTATCAAAGAACGCAGGTCAAATGGAAGCAGATGGAAATGAATGCAGGGTCTTGAATAGTGATGCATCTGGTGGACAGTGAAGGAATTGTACAGTATTTGCATTATTGGTTCGTTTCAGGTTAAAGAGGGCATCCTGAATGACGATATCTACTGCCCTCCTGAGACTGCGGTTTTGCTGGCCTCTTATGCTGTACAGGCCAAATATGCAGACTACAACAAAGATGCCCACACTCCTGGATACTTGTCCAATGAGAAGCTGCTCCCACAGAGG[T/C]GTGCATATGCAGATATTGTTGTAGCAGTGAAAACACATTGAGGAAGCATGGATAACTGTTTTCTAATATGAAGCGTTTCTTCTAAATTAGATTTTTTTAAAGTATCATTAAATGTGAAAGGAAATGATTGAAAATTGTGATATTTATAAATCATAATAGACAGTGTTGTGGTTGCTGAAATAAAACAACACATTTTTGTGTAGAATTAAATGCAAAGTTTTAATTGTGTTAATATGAACATGAAAAACAAAAAATAAATGAAATATATACAGTGCTCAGCATATATAAGTACACCCCTCACAAATCTCTCTTTTAAATTCACATTTTCTATATTAAGCTATACAATTTTATGATTGTGCATGTACATTAGATTAGTCAGTACTGAAGCCAAATCTGGAGTTTATCTAACAAAATAACTTAAGATAATGCTCCAAAAACAAGTACACCCTAATTTATGTTATAGAAAAATATTAAATACAAATTCAAAAAATATAGAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18450
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 |
|---|---|---|---|---|---|
| ENSDART00000016214 | Nonsense | 291 | 579 | 9 | 14 |
| ENSDART00000112536 | Nonsense | 290 | 578 | 9 | 14 |
| ENSDART00000124048 | Nonsense | 291 | 579 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 5 (position 23947300)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 21660172 |
| GRCz11 | 5 | 22163972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCATTAAWAAGAGGATTCTGGCTCTGTGCATGGGGAAYCATGAGCTTTA[T/A]ATGAGACGCCGTAAACCAGACACCATCGAGGTCCAGCAGATGAAGGCAYA
Long Flanking Sequence:
ATAAGAAATTTGTCATCAAACCCATTGATAAAAAAGCCCCGGTATGTCAAGCTCGATTTTCCAGCTGTCTGACTTATCACAGTTTCAATCCAATTTCTCTGTAAACAGACTTTAAAGAAGGGAAAGGCTGTAATTGTGAAGCCCTGGAGTGGTGTAATGTTTGATGATGTCATCTGAGGATGTTGAAATCAAAGTATACACCAGACTTTCCATTGAAGAAGCACGTTTCTCTTTGTGACATTTTATCAAAGACAAATACGAGTCTGGATGTGGACATGTCTGCTTATTTCTTTCTATTTTATCCCTCACTCCCTTAACTATATGTTTTGGCTTGGCTCCAAAACTCTGGGGTTTCATATGTAGGTAGTATTTTATGGCATCTTCAGAAGGATATTTTTTAATGTTCTCCCTCTTTCCCTTCAGGACTTTGTGTTCTATGCCCAGCGTTTACGCATTAATAAGAGGATTCTGGCTCTGTGCATGGGGAACCATGAGCTTTA[T/A]ATGAGACGCCGTAAACCAGACACCATCGAGGTCCAGCAGATGAAGGCACAGGCCAAGGAGGAAAAGAACCACAAGAAGATGGAAAGGTGAAGAAACTGTGTGCTATAGTAACACATTTTTTTAGGGGTGTAGCAAACGTGGGGAGATGTCCCCCTCACTTTTAGACACAGACCATTTAGGAACAGGTGATTAAAAATTATATAAACGTAAACTAACGGATCTCATTCAGCTGCCACCCCTCCCACACACAAACACACTTTTAAAATGTCCGCTACACCCCTGGATTTAATTGGTGGTGATTTGGATTCATTTAAGTGACTACGCTTTGATTTATGCTCTTCAAAGGTCTTCATTCAGATGTGGTTTTTCTTGTGTGTTATATTTATTACACCAATAGATGGCGACCCGATAATGTCATCCAAAATCAAATCATTCTTCCCCATTTATCACCTAATAGAAAAAGACTTTTTAAATGAAATGAGCAAAGATTTAATGTTTGC
Associated Phenotype:
Not determined