ZMP
mdm1
Ensembl ID:
ZFIN ID:
Description:
Nuclear protein MDM1 [Source:UniProtKB/Swiss-Prot;Acc:Q5RHU7]
Human Orthologue:
MDM1
Human Description:
Mdm1 nuclear protein homolog (mouse) [Source:HGNC Symbol;Acc:29917]
Mouse Orthologue:
Mdm1
Mouse Description:
transformed mouse 3T3 cell double minute 1 Gene [Source:MGI Symbol;Acc:MGI:96951]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38429 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33423 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18778 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38429
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102006 | Nonsense | 185 | 495 | 5 | 11 |
ENSDART00000102010 | Nonsense | 185 | 656 | 5 | 13 |
ENSDART00000132971 | Nonsense | 185 | 667 | 5 | 14 |
The following transcripts of ENSDARG00000045675 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 12628315)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13564942 |
GRCz11 | 4 | 13563791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTCATTGCAGCTCCTTGAGTTTTGAATTATTTTACATCTGCTAGATGT[T/A]ATACAGTAACAACAGAGCCATCCCACCCTTCAAAACAAACCCAGTGATTA
Long Flanking Sequence:
AACTCCCCAAAGATGATTTATTGGATTAAGATGTAGTGACTGTGAGGGCCATTTGAGTACAGTGAACTCATTGTCATGTTCAAGATACCAGCCTGTCTGGCATTAACAACCATGCCACGTTCAAAGTCACTTAAATCACCTTTCTTCCCGATTCTGATGCTTGGTTTGAATTGCAGCAGATCGTCTTGACCATGTCTATATGCCTAAATGCATTGAGTTGCTGCCATGTGATTGGCTGATTAGACATTTGCGCTAAAAAGCAGTTGGACAGGTGTATCTAATAAAGTGGCCGGTGAGTGTATATTCTAACATTAATGGTTATTTTATAATGTTGTTTGTTTGCAAGATTTAATTCTTTAAAATGGTATAGCTTATCTTATTAAACTGATTATTAATATGTTATTACAATTAGATCTTTTTCAAGTAATTATCTGAATACCATAGCCATCAGGTTCATTGCAGCTCCTTGAGTTTTGAATTATTTTACATCTGCTAGATGT[T/A]ATACAGTAACAACAGAGCCATCCCACCCTTCAAAACAAACCCAGTGATTATGGAGAGCGAGTACAAGAGAAGTTTCAAAGGATCGCCTCTTCCCAGGCCACCACGCTTGAGGCGAGATGTTGAACAGTATGAGGTCCCAGAGTTTCTAACAGAGAGCAAAACCCCAGAGAAGGTACACAGAAATATACCCTCTCAGTTCATTCACATACATCAATCATGAATGCAAACTTTCCAGGTATTACAGCGTCAGTATGGGATCTGGAAAATCTAGTTTCAATAACATATGTTATTTCCTTATAGTTTTTTTTCACGTGCTCTGCAACGTATAGAGAGGAAGTATACATTTACTAAAATGTTTGCACCTTTGACATAGTATTTCTGGCTCTTTTGCCTAAATGCCCATCAAACCAGAGTAAGAGAAAGAAGAAGAAGAAGGAGCGACCACACAGCAGGAAGTCAAGCCCAGAACAAGAAGTTGCCTATCTACAGCAACAGGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33423
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102006 | Nonsense | 213 | 495 | 5 | 11 |
ENSDART00000102010 | Nonsense | 213 | 656 | 5 | 13 |
ENSDART00000132971 | Nonsense | 213 | 667 | 5 | 14 |
The following transcripts of ENSDARG00000045675 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 12628231)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13564858 |
GRCz11 | 4 | 13563707 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAAACCCAGTGATTATGGAGAGCGAGTACAAGAGAAGTTTCAAAGGAT[C/A]GCCTCTTCCCAGGCCACCACGCTTGAGGCGAGATGTTGAACAGTATGAGG
Long Flanking Sequence:
ATACCAGCCTGTCTGGCATTAACAACCATGCCACGTTCAAAGTCACTTAAATCACCTTTCTTCCCGATTCTGATGCTTGGTTTGAATTGCAGCAGATCGTCTTGACCATGTCTATATGCCTAAATGCATTGAGTTGCTGCCATGTGATTGGCTGATTAGACATTTGCGCTAAAAAGCAGTTGGACAGGTGTATCTAATAAAGTGGCCGGTGAGTGTATATTCTAACATTAATGGTTATTTTATAATGTTGTTTGTTTGCAAGATTTAATTCTTTAAAATGGTATAGCTTATCTTATTAAACTGATTATTAATATGTTATTACAATTAGATCTTTTTCAAGTAATTATCTGAATACCATAGCCATCAGGTTCATTGCAGCTCCTTGAGTTTTGAATTATTTTACATCTGCTAGATGTTATACAGTAACAACAGAGCCATCCCACCCTTCAAAACAAACCCAGTGATTATGGAGAGCGAGTACAAGAGAAGTTTCAAAGGAT[C/A]GCCTCTTCCCAGGCCACCACGCTTGAGGCGAGATGTTGAACAGTATGAGGTCCCAGAGTTTCTAACAGAGAGCAAAACCCCAGAGAAGGTACACAGAAATATACCCTCTCAGTTCATTCACATACATCAATCATGAATGCAAACTTTCCAGGTATTACAGCGTCAGTATGGGATCTGGAAAATCTAGTTTCAATAACATATGTTATTTCCTTATAGTTTTTTTTCACGTGCTCTGCAACGTATAGAGAGGAAGTATACATTTACTAAAATGTTTGCACCTTTGACATAGTATTTCTGGCTCTTTTGCCTAAATGCCCATCAAACCAGAGTAAGAGAAAGAAGAAGAAGAAGGAGCGACCACACAGCAGGAAGTCAAGCCCAGAACAAGAAGTTGCCTATCTACAGCAACAGGAAGTGAAATCACCCCACAACCTGAAAGACCCTTCACCAAAGGTTATGAGGTGACTGTTGTGTTTTTACAGGATGTGCAAAAATAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18778
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102006 | None | None | 495 | None | 11 |
ENSDART00000102010 | None | None | 656 | None | 13 |
ENSDART00000132971 | Nonsense | 327 | 667 | 8 | 14 |
The following transcripts of ENSDARG00000045675 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 12624929)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 13561556 |
GRCz11 | 4 | 13560405 |
KASP Assay ID:
2259-4674.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGGTCTGTATGGTTAATCTTGCAGGGGTGTGATGGTTTTCACGAGTG[G/A]TATCATGAGGTAACATTTCACCTGTTACTTGCATCCTCTCACTGCTTCAG
Long Flanking Sequence:
TTCACAAATGGTGACTTCCTTTGTGTGGTTTTAAGCCTTTCTGAGTTTATTTCTTCTGTTAGACACAAATTAAGATATTCTGAAGAATGCTGCTTGTTGAGACCGATTGACTTCTGCAGTAGGAAAAAAACCCAGCAACCAGCATTCTTCAAAATACCTTCTTTTGTTTTCCAACAGAAGAAAGAAACTCAAACAGGTTTGGAACAAGTGAAGGGGGAGAAAGTGATGACAGATTTAAAATAATTTGGGTGAACTATCTCTTTAAGTCCCCAAAATTCTGCAAGTGAAATCAAGGCAAGAACCCATATGAATGTCAAATTAGTAGTTTGTTTGAAGTTGCTGAAACAAACTCACTTTAGGTTACTTTAGATGGTATATCAGGGCATGCAAGCTGTAGAATGGAGTGAAAGTGTCAGAGTTGCTAGAGTATGGCAAGATACTCTCTCTAATCACTGGTCTGTATGGTTAATCTTGCAGGGGTGTGATGGTTTTCACGAGTG[G/A]TATCATGAGGTAACATTTCACCTGTTACTTGCATCCTCTCACTGCTTCAGATCTCTCAACAGACGCTTTAATTTGCTTATGTGTCTGTTCTGTGCTGCTTCAGAAAATGTATGACATCATTGAAAGTTCGATTGTATGGACCTAGATTTGATCATGAGTGTGTGTGTGTGTGTATGTGTGTGCACGCATGTGGTGTATCAAGATGTTATCTGTCAGCATGTACAGAAACTTTGAAGTTGTCTGTGGTTTTGTTGGTAAATTTTTTTCTGTTTCTTGCACTTTCAGGTGTCTGGTAATCTTGTATTGACTTAAGATTTACTCAGTGATTATATACAAGTATATACAAATTTATAGGTGCAGTTTAGATGCATTTATTCATTTAGGTAATTCATGAATTTATGATTTTTTTAATTAGATTAGAAAAGCCTACAATATTGTTACATTTTAAATAATGAATAATGAAACACAATTAGCTTAAAAGCAAAATTGGCAGGGGATAA
Associated Phenotype:
Not determined