ZMP
MIPOL1
Ensembl ID:
Description:
mirror-image polydactyly 1 [Source:HGNC Symbol;Acc:21460]
Human Orthologue:
MIPOL1
Human Description:
mirror-image polydactyly 1 [Source:HGNC Symbol;Acc:21460]
Mouse Orthologue:
Mipol1
Mouse Description:
mirror-image polydactyly gene 1 homolog (human) Gene [Source:MGI Symbol;Acc:MGI:1920740]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32126 | Essential Splice Site | Available for shipment | Available now |
| sa36335 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36336 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2915 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa32126
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105266 | Essential Splice Site | 66 | 223 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 10183443)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 10261881 |
| GRCz11 | 17 | 10417915 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTCTCTCTCTTCCCCTCTCTCTCTCTCTCTCTTTTTTTTTTTCTCTC[A/T]GTGCTAGTGGAGGAAATCTATAAGGCTCAGAGGGAGAGAGACCAGGCTGT
Long Flanking Sequence:
GTCAAACACAGCCATGTTTGTCCTCCTATATGAGGATGTTTTTCGGTTGCTTTCTGACATCCATGAGCCTGGTGTAATTGCTTGCGGTTCCCGTACAATGTTGATAAACCAGAGCGTTTCCATGCTGAAATTTCATAAATAAAATGTCTCCGCAGTCTCCAAGAGCCTGGAACTCTGACTTCAGGGTGTTGCTGCTGTTTTTATTGCTCTGGGCGCTCGTGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAGACCTCCCCCGGGGAAACTGTCTTCTCAAAATAAGGCTCACTTAGAGTTATTAATACTTATGCCATAGTGTTTCAACTGCAATAACCTCTTTCCCGAGGAGCTTAGCCTTGTTATTGTGCAGCTGGAGCTCTGGAGTGCAATACCAGAATAATAACCTCCCTCCCTCTCTCTCTCTTCCCCTCTCTCTCTCTCTCTCTTTTTTTTTTTCTCTC[A/T]GTGCTAGTGGAGGAAATCTATAAGGCTCAGAGGGAGAGAGACCAGGCTGTGATGGCCAGACTGCGGCTGGCGAACGAGGAGAGGGATGAAGCTTTACTTCGGGCCAAGAAGCTTCAGGAGGCGACACTGGAGTATGTGCTGTTCAAACCTCTTCCAAAACAGAGCTTTTATTCAGCTTGTCCAACTACATGCTGCTCTAATCATTTCTGTCCTCTGAAAGGAGCTCGTAACAAAATGAAAATGTGATAATCTGGATTTGCAGCATTTATTTTTTATTTTTGCTTAGGTCAGAAAATAACACTCTAAATAAAATATACAGTATATAGACAGCAAATATACATTAATGTACCAGCCAGATCTCACGAGGAAACCTAACTTTTATTTATTTTTTTACGTTTTCTCAATTTAGTGGCTAATTCATATGAGTTCAGTCATACAAAATTGTATGATTTTTAAAAAAAACCTCTAAACCCAACCATCACTGGGGCGTAAACAAATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36335
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105266 | Nonsense | 139 | 223 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 10196015)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 10249309 |
| GRCz11 | 17 | 10405343 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGAGCTGTTGAACCGGGTGAACAGTGCAGAATCTGCCCTCGCTATT[G/T]AACAGAGCGGAGCGGCCATCATTGAACAGATCCAAAGGGCCAGAGAGCGA
Long Flanking Sequence:
ACACGCAAGTGAATGCTGCTCTCTCATTGGCTGTAGGCGATGGCTGATGTTATTTTCAGTCAAAACTCAATTCACACAGAATGATTTGCATCGCCGACAGCTCCAGATATTTAGCATGCCAAATATCTCGCAGGCATCGGCGACTCATCGGCGATTCTCTCAGATCGCGTCTTTGATAGTTCATACTGTGTGATTGTCACTCACATGCACGAGCAACGATTTGCCTGTGATTTCAGGCATTTGTCGGCGATTTCTCAAAACCTGTCGGCGAGCCAAAATCGGGGCTAAAATCACGCAGTCTGAACTAGGCATTAATTGAACCACTTTAAATCATAAATAATTACATTTATGCTGGTTAAGTTAAATTTTAGTAAGGTTTCTTTTGAAAAATGTATAAAGCAGACCCCAGGGTTGCAAATGTAAATGTATCTGTATGTTCTGTTCAGGATCTGGAGGAGCTGTTGAACCGGGTGAACAGTGCAGAATCTGCCCTCGCTATT[G/T]AACAGAGCGGAGCGGCCATCATTGAACAGATCCAAAGGGCCAGAGAGCGACGTTCCCAGATCACCTCAGAGGAGATGAAAACAGTCATCCAGGAGCGAGACGCTGCTTTAACCAGGGTACAAACCCACAGCACACACTCAAGGGTCAATCCTAACACACACCAGCCCTAAATGCTCCTCTCACAGTAGTTGTGTACTGAGCCAGAAACCTTTACACCATAGAAAAAAAAAAATCAAATACGACTCTCTAAATATTGACTATCTCTCCTCCTCCTGCGTTTTTGAACTCCTCTGCAAGACGACTTTGATTATTGGTCTATTAAAGCACATACATCTTGTGTTTATTCACAGATCCGGCACTGATTTAAGAATCAACACACACCAGCCACCTAATTCACATGTCGGGACAAATATTGCTGCGTAACCTCAAATATTTGGTATATGGTTCCTACACACATAATTCAATCAAATGAAAACAAACAAGCAGGTAGCTAAATATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36336
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 |
|---|---|---|---|---|---|
| ENSDART00000105266 | Nonsense | 148 | 223 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 10196042)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 10249282 |
| GRCz11 | 17 | 10405316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCAGAATCTGCCCTCGCTATTGAACAGAGCGGAGCGGCCATCATTGAA[C/T]AGATCCAAAGGGCCAGAGAGCGACGTTCCCAGATCACCTCAGAGGAGATG
Long Flanking Sequence:
TGGCTGTAGGCGATGGCTGATGTTATTTTCAGTCAAAACTCAATTCACACAGAATGATTTGCATCGCCGACAGCTCCAGATATTTAGCATGCCAAATATCTCGCAGGCATCGGCGACTCATCGGCGATTCTCTCAGATCGCGTCTTTGATAGTTCATACTGTGTGATTGTCACTCACATGCACGAGCAACGATTTGCCTGTGATTTCAGGCATTTGTCGGCGATTTCTCAAAACCTGTCGGCGAGCCAAAATCGGGGCTAAAATCACGCAGTCTGAACTAGGCATTAATTGAACCACTTTAAATCATAAATAATTACATTTATGCTGGTTAAGTTAAATTTTAGTAAGGTTTCTTTTGAAAAATGTATAAAGCAGACCCCAGGGTTGCAAATGTAAATGTATCTGTATGTTCTGTTCAGGATCTGGAGGAGCTGTTGAACCGGGTGAACAGTGCAGAATCTGCCCTCGCTATTGAACAGAGCGGAGCGGCCATCATTGAA[C/T]AGATCCAAAGGGCCAGAGAGCGACGTTCCCAGATCACCTCAGAGGAGATGAAAACAGTCATCCAGGAGCGAGACGCTGCTTTAACCAGGGTACAAACCCACAGCACACACTCAAGGGTCAATCCTAACACACACCAGCCCTAAATGCTCCTCTCACAGTAGTTGTGTACTGAGCCAGAAACCTTTACACCATAGAAAAAAAAAAATCAAATACGACTCTCTAAATATTGACTATCTCTCCTCCTCCTGCGTTTTTGAACTCCTCTGCAAGACGACTTTGATTATTGGTCTATTAAAGCACATACATCTTGTGTTTATTCACAGATCCGGCACTGATTTAAGAATCAACACACACCAGCCACCTAATTCACATGTCGGGACAAATATTGCTGCGTAACCTCAAATATTTGGTATATGGTTCCTACACACATAATTCAATCAAATGAAAACAAACAAGCAGGTAGCTAAATATTGACATCCAGATATTCGGCTTCATCATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2915
Status:
F2 line generated
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105266 | Essential Splice Site | 177 | 223 | 5 | 7 |
| ENSDART00000105266 | Essential Splice Site | 177 | 223 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 10196133)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 10249191 |
| GRCz11 | 17 | 10405225 |
KASP Assay ID:
554-3055.1 (used for ordering genotyping assays)
KASP Sequence:
AGAGGAGATGAAAACAGTCATCCARGAGCGAGACGCTGCTTTAACCAGGG[T/C]ACAAACCCACAGCACACACTCAAGGGTCAATCCTAACACACACCAGCCCT
Long Flanking Sequence:
CCAAATATCTCGCAGGCATCGGCGACTCATCGGCGATTCTCTCAGATCGCGTCTTTGATAGTTCATACTGTGTGATTGTCACTCACATGCACGAGCAACGATTTGCCTGTGATTTCAGGCATTTGTCGGCGATTTCTCAAAACCTGTCGGCGAGCCAAAATCGGGGCTAAAATCACGCAGTCTGAACTAGGCATTAATTGAACCACTTTAAATCATAAATAATTACATTTATGCTGGTTAAGTTAAATTTTAGTAAGGTTTCTTTTGAAAAATGTATAAAGCAGACCCCAGGGTTGCAAATGTAAATGTATCTGTATGTTCTGTTCAGGATCTGGAGGAGCTGTTGAACCGGGTGAACAGTGCAGAATCTGCCCTCGCTATTGAACAGAGCGGAGCGGCCATCATTGAACAGATCCAAAGGGCCAGAGAGCGACGTTCCCAGATCACCTCAGAGGAGATGAAAACAGTCATCCAGGAGCGAGACGCTGCTTTAACCAGGG[T/C]ACAAACCCACAGCACACACTCAAGGGTCAATCCTAACACACACCAGCCCTAAATGCTCCTCTCACAGTAGTTGTGTACTGAGCCAGAAACCTTTACACCATAGAAAAAAAAAAATCAAATACGACTCTCTAAATATTGACTATCTCTCCTCCTCCTGCGTTTTTGAACTCCTCTGCAAGACGACTTTGATTATTGGTCTATTAAAGCACATACATCTTGTGTTTATTCACAGATCCGGCACTGATTTAAGAATCAACACACACCAGCCACCTAATTCACATGTCGGGACAAATATTGCTGCGTAACCTCAAATATTTGGTATATGGTTCCTACACACATAATTCAATCAAATGAAAACAAACAAGCAGGTAGCTAAATATTGACATCCAGATATTCGGCTTCATCATAAGAGTTCAAGTGTGGGGCAGTGGATGTATTTGCGGGGATTTCTTTGTTGATGAATGCCGCCTTGCGTTTCATAATTGCGGCTGATTGCACTA
Associated Phenotype:
Not determined