ZMP
Q5RII8_DANRE
Ensembl ID:
Description:
Novel protein similar to human MDN1, midasin homolog (Yeast) (MDN1) [Source:UniProtKB/TrEMBL;Acc:Q5R
Human Orthologue:
MDN1
Human Description:
MDN1, midasin homolog (yeast) [Source:HGNC Symbol;Acc:18302]
Mouse Orthologue:
Mdn1
Mouse Description:
midasin homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:1926159]
Alleles
There are 13 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23694 | Nonsense | Available for shipment | Available now |
| sa1349 | Nonsense | Available for shipment | Available now |
| sa23693 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23694
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 |
|---|---|---|---|---|---|
| ENSDART00000143005 | Nonsense | 115 | 2198 | 1 | 38 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 23880795)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 23999596 |
| GRCz11 | 20 | 23898696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTTTATCCTGATGTGGTGGTGCCTCTGCGGGCAGCTATTTTGCAGGTG[C/T]AGCATGGGATGCGACTCCTGGCTTCTCAGGTGTCCTTTTCAACGACTGCC
Long Flanking Sequence:
TGTGGTGCTCTGATTAATGTAAATGTTTTATTAATGAATATGTGTTATTTAACATGTTTGGGTGTGCACAGGGGCGCAGCAGTGTTGAGGATCTATGGTTTATCGCTATTGAATTTTAACTACAATTTGAGATGTCTTTTGTTGTATGTGATGTTTGTAGGTACTTATGGATCCGCATGCAGCAGGTAAAGGAGCAGATTTGTGAACTGAGCCGTAAACAAGCTTACCGTCCTCCTGAACCTCAGTACGGGCGCCTGTATCAGGAACTCCAGCACTACCTGTGCAGCATCGGGCAACCAGCTGCAGTGGGTGACCTGCTCTCACACCTCCTGAAGGCCCTACAAGCCCCAGGACCAAAATCTAAGCTAGGCGTTCAGGGTTTGTTGAAAGAGGAGGCCGTCTGGCAGGCTTCACAGCACCGCTTCTCCCAGCGGCTGCTTGAGGAATTCCCGCTTTATCCTGATGTGGTGGTGCCTCTGCGGGCAGCTATTTTGCAGGTG[C/T]AGCATGGGATGCGACTCCTGGCTTCTCAGGTGTCCTTTTCAACGACTGCCCAACCAGGTCTGGTGCACCTTGTGTCCACTATGCTTACTTTTCCCTGTCCAGTAGCATCCTCTGATCTGGCCTGTGCAGATTACCTGTGTTCAAGGGAGTGCTTGCGTACACTGAAAACACTGGGAAAGCAGCTGCCAGCTACAGAGGTCAGCCGTGTGATCCCAGATCATGCAGTGCTGCTGCTGAACGCACTGCTGTACATACAGAGTCACACACTGAGTGCTGGACAGCTCAGTGCAGAGGCGCAAAAGCTTTTCAGACATGTTTGCCAGGTGAGATATGGAGTAAACATATGACAAAAATGATAAACAATTGCAAATTTCAATTATATTTAAAACCTATGTATTTATAATTGATAGATGAAATAGATAGATAAAATGCTGTTGTACAAAACATCATTACATCATTTGTATCAGTGTTGACGTATATATTCATATTGTTTAAATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1349
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 |
|---|---|---|---|---|---|
| ENSDART00000143005 | Nonsense | 1245 | 2198 | 20 | 38 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 23870485)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 23989286 |
| GRCz11 | 20 | 23888386 |
KASP Assay ID:
554-1263.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCGTTTGGAGCCCATGCTGTGTCTCTACTCTGAATTGGTGAGGTATTA[T/A]CTTGCTGTGCTGATGGGGGCTCACCGTACCACYGGAAAGCTTTTGTCCGT
Long Flanking Sequence:
TTCAGACAGTAGTTAAGAGGAAGGAGAAGGAAAAGCAGGAGGATCAGCTGTCAGAAAGCAAGAGAGGTGCAAAATCAGCCATGAATTTGCATACGGCATGTTTTAGGAGATATATTTGTGTATATATGAGAGCTCATTTATGTTTTTTTATAGAGAGTGACTCAGAGGTAGTGGAGGAGCTCTTAAAACCAGGACACTTGAGCAGGTTGCTGGAAGAGGAACTGAGTGGAGACTTGTCCAGTCTCTCATTACCCGAGATCAATGGAGTCGTAACAGAGCTGCTGGAGAGACTTCGTTCACACAGGGACGACTGTCAGCCTCACCATTTACAGGTCAGTCATGCATTAAATATACATTAAATATTATACCCAAATGGTTACTGTCTGAAAATATCAGTTAAAATGTGTGTTGTTTTATATAAAGGAATTGAGAGAGGCTTGCAGGAGTGTGGTGCGTTTGGAGCCCATGCTGTGTCTCTACTCTGAATTGGTGAGGTATTA[T/A]CTTGCTGTGCTGATGGGGGCTCACCGTACCACCGGAAAGCTTTTGTCCGTCCTCGCTAATGTCTTCACTGAACTTGCACAAAAGGTAGATGTTGCTCTGCCTGCTTGCACTGCTTACTACAGACAGAGTTGCTCAAATTTCGGTTGTTACTACCTGTTTCTTTCTCATTTTGGTCAATTGTAATCTACATCGCCTATATGTCATGCCAGAGATCACTGTCTGTGAATTAAAACGATTAAGAAAAAAAATGTTCAATCAATATTTTATTGCAGTGTTCAAAAGTAAAACAGTTTAAAGGTCATATTTTTTTGCAGATGTTCGTCTTTAAATGTGTTGGTATAGATATAGTTTTTTTAATTTTAAATTTGATTTACAATCCTTTTATTGCTTCAAATTTGTAGTATTGCTGTAACATCCTAAATGGAAAACAAGGGTGCGGATTACATGGGGGTTTGGGGGGATTGACCCCCCTACTACCGCTTGATTCCCCCCTGAAGGCA
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 |
eye ZFA:0000107 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
gut ZFA:0000112 |
quality PATO:0000001 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
head ZFA:0001114 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
inner ear ZFA:0000217 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
melanocyte ZFA:0009091 |
quality PATO:0000001 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
pericardium ZFA:0000054 |
edematous PATO:0001450 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
swim bladder ZFA:0000076 |
aplastic PATO:0001483 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
decreased size PATO:0000587 |
abnormal PATO:0000460 |
| Larval:Day 5 ZFS:0000037 |
yolk ZFA:0000084 |
increased size PATO:0000586 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa23693
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000143005 | Essential Splice Site | 1908 | 2198 | None | 38 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 23863658)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 23982459 |
| GRCz11 | 20 | 23881559 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGCTTAAATGTGTGTGTATTTATTTGTGTGTTTTGCTGTTGTCCCTC[A/C]GGAGAGTGCTGCTGCAGCGTTGTGGCATCAGTACCAGACCCTGACATCTC
Long Flanking Sequence:
CATTAAGTAACATTAACTAATGAACCTTATTGTAAAGTGTGACCTAAAAATGAATTTCATCTAGAACATTAGATCAAAATAACAAATTATTTGTAATTTTACAGAACTGCTTTTAATTACTTTTGAACTTCTATTAATCAAAGAATCCTTCAGATCGATAAAATATAAAAATAATAATATTTATATAATTGTTTAGCAAATCTTAGTGATTTCTGAAGGACTGTGTCTCACCAAAGACAAGTGAAATTCATCTTATTTCAGAAAATTATTATTTTTACTGCATCTAAACTGAGCAGCACTTCTGTTTGTTTTATCAGGCAACTCTGATGAACCCAGAGGAGCTGAGAAGAGAGATGGAGCTGCAGTTAGAGGCCTGGCAGAGACAGACTTTAGGATCACATGAAGAGGTGAAGCCACATGACTAAGCAGATTTTCCTCACCTAGCAAATCTGTTGCTTAAATGTGTGTGTATTTATTTGTGTGTTTTGCTGTTGTCCCTC[A/C]GGAGAGTGCTGCTGCAGCGTTGTGGCATCAGTACCAGACCCTGACATCTCCACTGTCCCAGCAGCTCTGTGAGCAGCTCCGACTTGTCCTGGAGCCAACACAGGCTGCCAAACTCAGGTTGGTCTTTCTACCTTTCCGTTACAAATTAAAGGATTTCCCTACAAGCCAAAGGAATTATTATTTAAAGGTATAGTTCACTCCAACATGTGAACATTTCATCATTCTAAAATTTACTCGGACTGCACTTGTTCCAAACTTGTTTCATTTTGTTTCTTTTTGAGCCTAAAGAAACATATTCAGAAGCATGTTGACAAATGATAGCCATTGACTTTTTTTTCCCTATTATAGATGTATTATAGAAAATGGCTAGCAATTTTCAACATTCTTCAGAATATCTCATTTTGGGCTCAACAGAAAAAAAGAAACTCATAAAGGTTTTGAACTAATAAAGAAATGTTCATTTTTGAGTGAGCTACCCCTGTAAAAATGCTATATGTTAT
Associated Phenotype:
Not determined