ZMP
mphosph10
Ensembl ID:
ZFIN ID:
Human Orthologues:
AC007342.1, MPHOSPH10
Human Description:
M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) [Source:HGNC Symbol;Acc:7213]
Mouse Orthologue:
Mphosph10
Mouse Description:
M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) Gene [Source:MGI Symbol;Acc:MGI:191
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa371 | Nonsense | Available for shipment | Available now |
| sa13196 | Essential Splice Site | Available for shipment | Available now |
| sa15514 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa371
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 |
|---|---|---|---|---|---|
| ENSDART00000004782 | Nonsense | 184 | 695 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 32115092)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30507434 |
| GRCz11 | 7 | 30778584 |
KASP Assay ID:
554-0243.1 (used for ordering genotyping assays)
KASP Sequence:
CCGATTTGGACTTTGATGTAGATAAATTTGAGAAACAAACCAAACAGAGA[C/T]AGTCTGCTGCTGGCAAGTTAACAAAATCTAAACCGAACTGGACTCAGTCT
Long Flanking Sequence:
ATGATATATTTTATCATCTTATCTATTATTGCAGTGTCCAGGATGTTTTGGCAACAGACTTCAGATCACTTACAAAGATTCTTTATGACCTGCAAAAAGCCCACGAGCCTGCAGACTGTAAAGGAAGCCCACTGGAGCAGCTGGTGGTTGAAAACTTCGACGAGGAGCAAATTTGGCAGGAGCTGGAGCTTCAAAACAGCGCATTACTGACACACTTTGAGCAGGCAGTCGAGCAGGCGGTCACTGATGATGCTATAACATTTCTGAATGATGAAGATGATGATGTTGAAGAAGACGAAGAGGAGTTGGAGGAAGTTGATGATGAGGAAATTGCTGATAACTTGGAGCAAGGGAGTGCAGAGGAGGAGGACGATGAAGATGGAGAGGAGGAAACTACACAGAGGCTGAAACCTACAAGCAATGGGGAAGATGACTTCTCTGGCGAAGACTCCGATTTGGACTTTGATGTAGATAAATTTGAGAAACAAACCAAACAGAGA[C/T]AGTCTGCTGCTGGCAAGTTAACAAAATCTAAACCGAACTGGACTCAGTCTGAAGTGGATGACACGTTTTTTAAACTGTCAGAAATGGAGGCTTTTCTGGATGACATGGATAAAAGAGAGGGAAAAGGGAATGAAGGGGAGGAAATTGATTACTTTCAGGATCTGCCGTCTGATGAAGACGATGAACTGAGCTTTGATAAACCAGTCGTGAAGAAGAAACTTAAGGTAATGGTGTTTATTTTAAGCAGCAACATACTTCTTTGTGTTATTTTGATACTTTTTATGTTTTAATTTTACAGTATTACATCAGTCTACAGGGCTCTGGTTGTTTAATATTAGGTTGTATAGATATGTTGTGTAATGCAGTGCTCAACATAATTGAGTACAACCCGTTTTGAAAATGAATATCTTTATCCATATTTATTTATCCAATAAAACAGATTTAGTAAACAGATGTATTAATTAAAATAATATTTTAGTCACCAAACATATTCAGAAATT
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
pericardium ZFA:0000054 |
edematous PATO:0001450 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
necrotic PATO:0000647 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa13196
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 |
|---|---|---|---|---|---|
| ENSDART00000004782 | Essential Splice Site | 258 | 695 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 32114866)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30507208 |
| GRCz11 | 7 | 30778358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACGATGAACTGAGCTTTGATAAACCAGTCGTGAAGAAGAAACTYAAGG[T/A]AATGGTGTTTATTTTAAGCAGYAACATASTTCTTTGTGTTATTTTGATAC
Long Flanking Sequence:
AGTCGAGCAGGCGGTCACTGATGATGCTATAACATTTCTGAATGATGAAGATGATGATGTTGAAGAAGACGAAGAGGAGTTGGAGGAAGTTGATGATGAGGAAATTGCTGATAACTTGGAGCAAGGGAGTGCAGAGGAGGAGGACGATGAAGATGGAGAGGAGGAAACTACACAGAGGCTGAAACCTACAAGCAATGGGGAAGATGACTTCTCTGGCGAAGACTCCGATTTGGACTTTGATGTAGATAAATTTGAGAAACAAACCAAACAGAGACAGTCTGCTGCTGGCAAGTTAACAAAATCTAAACCGAACTGGACTCAGTCTGAAGTGGATGACACGTTTTTTAAACTGTCAGAAATGGAGGCTTTTCTGGATGACATGGATAAAAGAGAGGGAAAAGGGAATGAAGGGGAGGAAATTGATTACTTTCAGGATCTGCCGTCTGATGAAGACGATGAACTGAGCTTTGATAAACCAGTCGTGAAGAAGAAACTTAAGG[T/A]AATGGTGTTTATTTTAAGCAGCAACATACTTCTTTGTGTTATTTTGATACTTTTTATGTTTTAATTTTACAGTATTACATCAGTCTACAGGGCTCTGGTTGTTTAATATTAGGTTGTATAGATATGTTGTGTAATGCAGTGCTCAACATAATTGAGTACAACCCGTTTTGAAAATGAATATCTTTATCCATATTTATTTATCCAATAAAACAGATTTAGTAAACAGATGTATTAATTAAAATAATATTTTAGTCACCAAACATATTCAGAAATTGAAAGATAATACAATTAAGTTCAAGCATAATATAAAAAAAAATGACAAACTGCAAAATTTCAACAATTTTTTTTCCATTTTTCTGTTTCTCTTGGATTTTATTTTTTTCTCTTTTAAATTTGTATTTAATATTTTTATATAACATATAAATTTGGGTGTACTAGTAACGGAAGTTATTTTGTTAGATAAGCTCCAGATTTGGCTTCAGTACTGACTAATCTAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15514
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 |
|---|---|---|---|---|---|
| ENSDART00000004782 | Nonsense | 464 | 695 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 7 (position 32111892)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30504234 |
| GRCz11 | 7 | 30775384 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGATGATGTGGTCAGGAAAGAGAAGCCTAAAGAAGAGGTGTTTGAGTA[T/A]AARAAGAGACTSACTCTGGATCAKGAGAAGAGCAAACTGAGTCTGGCTGA
Long Flanking Sequence:
CAGATTGAAGAGCTGGAAAATGCTGCGTTGTCAGAGAAGCCGTGGCAGCTGTCAGGAGAGGTGACTGCTCAGACTCGACCAGAGAACAGCATGCTGGAAGAGGACATAGCCTTTGATCAGGCCTCTCGAATGGGTGAGAGCTTTACTCGGGCGTTCACAGCAGAAAGCAAACAAATCTAAGCATACTATCAGTGCATGACTTGCTTTCTCTCCTCCACAGCTCCTGCAATCACTGAGGAAACTACCTTACAACTTGAGGATATCATCAAACAGAGAATCAAAGATCAGGTTTGTATACAACTTTAGAAAATAGTGGAAAATAATTAGTACATTTAATGCAGATTGTCCTTTTTAAATAAATACAACCTCAAATGATTTTCTTCTTCATGAATAAGATCATGTCTCTCACCGTATCTGATCAGTTTTTGTTGTGTTTGTTTGTCTCAGGTGTGGGATGATGTGGTCAGGAAAGAGAAGCCTAAAGAAGAGGTGTTTGAGTA[T/A]AAGAAGAGACTCACTCTGGATCATGAGAAGAGCAAACTGAGTCTGGCTGAGGTTTATGAGCAGGAGTATATCAAGCAGACACAGGTGAGCTCAGTGGATCATATCATTTCCTGTCTGTAAGGAATATTTCTGAAGGTAAAATGAAATTTCTACCATTTTTTTATTTGTTCCAAAATTAAAACAGAGTTTTGTTGTTCTGTTGAAAACAAAAGTAGATATTTTAAAGAAAGCTAGATACCTGTTGCCATTAGCTTCCATAGTATTTGTTGTTCTTACTATGGAAGTTAATGTTTTCATGTTAAAGGTTTCAGCTTTTTTCATAACCAAATCAAAGAAAGAACTAAAAGGTTTGGAACTGCTTTAGTGTGAGTAAATTTTCATTTTTTGTGGAACAATCTCGGTGAATATGATTATAGGGAAGGGAAAAGGGCTTTTCATGCATTAAAATGATAAGTGTAATACTGCTTCATTAGATTTTGTCTTTGCAAAAAACATGTCTA
Associated Phenotype:
Not determined