ZMP
LOC100333601
Ensembl ID:
Human Orthologue:
MMP25
Human Description:
matrix metallopeptidase 25 [Source:HGNC Symbol;Acc:14246]
Mouse Orthologue:
Mmp25
Mouse Description:
matrix metallopeptidase 25 Gene [Source:MGI Symbol;Acc:MGI:2443938]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41941 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35194 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41942 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22003 | Essential Splice Site | Available for shipment | Available now |
sa22004 | Nonsense | Available for shipment | Available now |
sa22005 | Essential Splice Site | Available for shipment | Available now |
sa41943 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41941
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081382 | Nonsense | 6 | 573 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 4941311)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4224028 |
GRCz11 | 12 | 4260796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGTGAATAAAGGTCTCCACCAGCACACACATGAGTTTCTCAGGATA[T/G]CTTGGTCTGGTTTACCTGACCTGCCCTATGCTTGTGTTCTTCTCTGCGGT
Long Flanking Sequence:
CAAATTTTTGAAGAATGTTGGATGAAAAAAAAAACATTCATCTAATTTTTTTCCCCTATTGATTGGCTACATTCTTCACAATATCTTCCTTTGTGTTCAACAGAAGAAAGAAACGCATGTAGTCCTCACTCGTTTTTGGGTGAACTGTCCCTTTAAATCAAGTTACAGCTGAATAATTAATGTTAATATTGATTATGTATTTTAATCCAGTTAAGCAATGTTTATTGAATCTTTAGGGAGTAAGAGATTCTCATAGAGAGGATTTTTTCTGAGTAAAGCATATGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGACTCATTGATTGGTTCAGCCCTGCCTAGTCCTAAAGAGACAAACTGAAGAAGCCAGAAAGACGCATATAACGGTGTGAAAGCATAAAGGCAACACTCATCTGTGAATAAAGGTCTCCACCAGCACACACATGAGTTTCTCAGGATA[T/G]CTTGGTCTGGTTTACCTGACCTGCCCTATGCTTGTGTTCTTCTCTGCGGTTCATTCGGCTCCGGTAAAGGATCAGTATTCTCGGGGTGTGGTGAGTTCTTTACTCTGATTTTCTATAAATTGAACACTTTTACAGATAGACGAACAAACACTGTATAAGTGGATCTGGTTGATGTATTATAAGTAGTGCACTTTTAAAAAAGGGGGGAGGACAACATAATTGTTTTATTTTCAATCCACTTTAATTTGTACAACAACAATTAAACTGTTAACTTTATAAATTTGTGTTGGGACAACGTGGAGTTGTGTGGAACATTTTTACAGTGCATGTTATTAGTTCAAATCCCTGTGTGACAGATTGTTAGTGGAATTATAAGGATTTTATATATTATTTTTGAAGAAACTACTGTACAGTAACTAGCTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35194
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081382 | Nonsense | 75 | 573 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 4943415)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4226132 |
GRCz11 | 12 | 4262900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACGGCATCGAGAGAGCCATTAGAGAAATGCAGAGATTCGCTGGACTC[A/T]AGGAAACAGGCAAACTCGGTACATAATTCTGATCACACATAATTACCTGT
Long Flanking Sequence:
CACCAAACATCTTTAGAAATAGAAGATAACACATTTTAATTCATGCAAAAATATAGCAATTTCCAAGCAAGTATGCCTACTTTTCATTTCTCTTGATTTTTTTTCTCTTTTTACATTTTTTTTATTTAATATTTTTCCCTAACATACAAATTTTGGTGTTTTAATTTTTGGATAATACGCTACTCTGTTAAATAAGCTTCAGATTTTGCTTCAGTATTGACTAATCTAATATATATGCACAAATATCATTTTGTAAAGCTTCCTATAGAAAATATTAATTTAAAAGAGTGATTTGTGAGGGGTGTACTCGTTTATGTTGAGCACTGTACATTGAATTATTGATTATCGGCATATGTCTAGTCACATGGTATTTCTCTGACCTGTAGGACTGGTTGAGCCGGTATGGATATCTGCCTCCTCTAGACCCGCGCACAGGACAGCTACAGAGCAAAGACGGCATCGAGAGAGCCATTAGAGAAATGCAGAGATTCGCTGGACTC[A/T]AGGAAACAGGCAAACTCGGTACATAATTCTGATCACACATAATTACCTGTAAAAGAGCTTGCAAATCTATTCACTAACACCATCTTGTTATTCAGTTGTACCAAAGATTGTACCCTTTGCGATTGCACCCCTCCCCTCTTTTTACAGTAATAAACGTTAATTTCAAAAGCGTTTAAGTACTTTTGCATTTGGCTGTAAATTTACAGTATTTTATTAAGTGTACACTGTAAAGAACATCCTTAAATTAGCAGTTTTTCATATTTTGTGCTTCATGTTTTTATTTTTTATGTTTATTTATGCTTTTAAACTGCATTATGGGACCTTGGACTTTTTTTTACAACTTCTAACCTTGAAAAGTTGGGAAAAAAGTGACTTTTAGAAACATTTTTAATAGTTTAAAGTGATATATTGTGTGCGTTGGTGTTGTAATTACACTACAAAAACCTTGTAATTAGCTGCCAGTACATTTTCTGTTATTCTACAGACTTATTTCTCTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41942
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081382 | Nonsense | 109 | 573 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 4946788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4229505 |
GRCz11 | 12 | 4266273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGTTCTCTGCCAGACATCATAGGCATTGAGGACAAGCTGAAAAAGCGC[A/T]GAAGGAAAAGATACGCAACCACTGGGCTCCGCTGGACAAAGTCTGACATT
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTAGATAGATAGATAGACAGAATAGATAGATAGATAGATGGATAGATAGATAGATGGATGGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATATGTAAACTGTAATTTGATATATGTAAATGTAATAATGAGACTTTTTATTCCTAATTCTGTGGTTGCTGGCTTCAGTAAATCTCTTCTAGAGAAAGAGTTCTTCCATTGTCCCTCCTCCTCCTCCTCGTGTGGGTTTTATTACATGTTCTGAAATGGGCTCTGTGTCTCTGAAGTCTATATATTGATCCGGTACCTTCTGCCGTTGTGTTTCCAGACAGTGACACTCTGACGCTGATGAACACACCACGATGTTCTCTGCCAGACATCATAGGCATTGAGGACAAGCTGAAAAAGCGC[A/T]GAAGGAAAAGATACGCAACCACTGGGCTCCGCTGGACAAAGTCTGACATTACATGGAGGTCTGTATGATCGAGATATGATCACCGCTAACCAAACTAACAAGCATGACTAACTGAAAATCAAGCACTTTATATATGCAAAATATTACTCCAGTAAAAGTAGAATGATGGAGGCACGGTGGCTCAGTGGTTAGCACTGTCACTTTACAACAAGAAGGTCACAGGTTTAAGGGCCAGTTGGCATTTCTGTGTGGAGTTTGTATGTTCTCCCAGTGTTGGTGTGGGTGTCCTCCGGGTGCTCCAGTTTCACCCACAGTCCAAACGCATGCGCTATAGGTGAATTGGATAAACAAAATTGGCCGTAGTGTATGAGCGTGTGTGGGTGTATGGGTGTTTCCCAGTACTGGGTTGCAGTTGTAAGGACATCCGCTACATAAAACATATGGTGGAATAATGGGGTCGCCACAGTGTTAAATAAGGGATAATAATGTTAAATAAGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22003
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 |
---|---|---|---|---|---|
ENSDART00000081382 | Essential Splice Site | 225 | 573 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 4949219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4231936 |
GRCz11 | 12 | 4268704 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCAGCCACTTATCTACACATGTCCTGTTCTTATTCTCTGTATATTTTC[A/T]GATGAAAGCGGCACTGATTTGTTTGCGGTTGCGGTGCATGAGTTTGGTCA
Long Flanking Sequence:
CTAGTTCACCTTATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTAAAAAATATCAAGTAAAATATTATTTACTGTCATCATGACAAAGACAAAAAAAATCTGTTATTAGAAATAGGTTTTTAAAACTATTATGCTTATAAATGTGCTGAAACAATCTTCCCTCCATAAAACAGAAATTGGAGAAAAAAGTAAACAGGGGCACTAATAATACAGGGGGGCTAATAATTCTGACTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTACATTTATTTACTAATGTTATTTATTTATTATTAAATTAATAAGTAAATGCATACAATAAAAGTTATTGTGAACCAGCAACTGTTGGGCTACCAAGACTTTCTCAAATTTGTATTTATTTATTTATTTTGTGCTCAGCCACTTATCTACACATGTCCTGTTCTTATTCTCTGTATATTTTC[A/T]GATGAAAGCGGCACTGATTTGTTTGCGGTTGCGGTGCATGAGTTTGGTCATGCTCTGGGTCTTTCTCACTCCTCCTCTTCCCCCTCCATCATGAAGCCCTATTATCAGGGCTCTGTTGGAGATGTAGGATCCTACATTCTTCCGGACGATGACCGTGAGGCCATTCAGTCACTCTACGGTATTTTTCTTTTCCCTAATATATGTTTAACGGGAAAAAAAAGGTTTTCAACACATCTCTAAACATCATAGCTTGTTCTGTAGACAATCAAAACATATATTGCTTAAGGGGGCTAATAATATTGAGAAATTTAAACTGCTTTTATTCTAGCTGAAATAAAACAAAATAAAACAAATAAGACTTTTTTTCAGAAGAATAAATTTGATAGGAAATACTGTGAAAAAAATCCTTGCCTTGGTAAACATCTTTTGGAAAATATCTGAAAAAGAAAATTCAGAGGAGTCTAATAATTTAGACTTCAACAGTTGGTGGTTGATCCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22004
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081382 | Nonsense | 258 | 573 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 4949321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4232038 |
GRCz11 | 12 | 4268806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTGGGTCTTTCTCACTCCTCCTCTTCCCCCTCCATCATGAAGCCCTA[T/G]TATCAGGGCTCTGTTGGAGATGTAGGATCCTACATTCTTCCGGACGATGA
Long Flanking Sequence:
ACAAAGACAAAAAAAATCTGTTATTAGAAATAGGTTTTTAAAACTATTATGCTTATAAATGTGCTGAAACAATCTTCCCTCCATAAAACAGAAATTGGAGAAAAAAGTAAACAGGGGCACTAATAATACAGGGGGGCTAATAATTCTGACTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGTACATTTATTTACTAATGTTATTTATTTATTATTAAATTAATAAGTAAATGCATACAATAAAAGTTATTGTGAACCAGCAACTGTTGGGCTACCAAGACTTTCTCAAATTTGTATTTATTTATTTATTTTGTGCTCAGCCACTTATCTACACATGTCCTGTTCTTATTCTCTGTATATTTTCAGATGAAAGCGGCACTGATTTGTTTGCGGTTGCGGTGCATGAGTTTGGTCATGCTCTGGGTCTTTCTCACTCCTCCTCTTCCCCCTCCATCATGAAGCCCTA[T/G]TATCAGGGCTCTGTTGGAGATGTAGGATCCTACATTCTTCCGGACGATGACCGTGAGGCCATTCAGTCACTCTACGGTATTTTTCTTTTCCCTAATATATGTTTAACGGGAAAAAAAAGGTTTTCAACACATCTCTAAACATCATAGCTTGTTCTGTAGACAATCAAAACATATATTGCTTAAGGGGGCTAATAATATTGAGAAATTTAAACTGCTTTTATTCTAGCTGAAATAAAACAAAATAAAACAAATAAGACTTTTTTTCAGAAGAATAAATTTGATAGGAAATACTGTGAAAAAAATCCTTGCCTTGGTAAACATCTTTTGGAAAATATCTGAAAAAGAAAATTCAGAGGAGTCTAATAATTTAGACTTCAACAGTTGGTGGTTGATCCACACAGAACAGCGTATAGACTTAAAGGGGTAGTTCAAAGATAAAATTAGAAATCTGTCGTCATTCACTCATCCTTTATAGGTTTCTGTAACACTTTAGTTTAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22005
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081382 | Essential Splice Site | 341 | 573 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 4953378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4236095 |
GRCz11 | 12 | 4272863 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTTTGATGCAGTGGCGAACCTCAGAGGAGAAGTTTTCTTTTTTAAAG[G/A]TACAGTGCAATAACAATTTCTACAATGTAGAGATTTTGTAAACCAGGGGT
Long Flanking Sequence:
CATCTCTGGGAAACATATTACTCATTTTTTTATTTATTAATTAATTTATCATTTAGTAATTTTGTTCTAGAAAATAAAGCAAATCAACACCAAATTTAATAAATAATGCATCATTTAGAAAATTTCTAAAAGATTAACAATCTTTGCATTTCCTAATGTAATCAATCGGCTGCATGGGAATATAATGTGATAGCGATTTTTTTTTACTAAATTCACCTGAAGTGTATTGCATTACATCAAAAAAGACAGAAAAATTTACATTGTACCATAATATTTCAAATTCAAATGAAATAGTTTTTAAATTTCTATCAGTTTTTATAGCGTTTAAAAAACAGCAACATTTTTGCACTTTCTCAAACACTCAATACTATCCAGTTAAAAGTATTAACAAATTCTCTGACCTTTCTGTTTGTCTAGACCTGATCCGTCAATCCAGAATCGCTGTGAGGGAGGTTTTGATGCAGTGGCGAACCTCAGAGGAGAAGTTTTCTTTTTTAAAG[G/A]TACAGTGCAATAACAATTTCTACAATGTAGAGATTTTGTAAACCAGGGGTGCGTTTTCGAAAACCATCATTAGCCAACTAAGGTTGTTATAAACATAGTTCATTGATTTGGCGTTTCCCAAATCCATCGTTTCAACGAACATTCGCAAACTGCGTCGCAAACTTGTACGCTTGCAACTACACCTCTGGAGCTGTAGTTAGAAACATAGTTCCTGGCTATGTGCTATTCCAAGTTATCCCCCCTATGCCCTATTTGTTTAGAACATTTTAACATTTAAACTCTTATTGGAATTTTTTGCCAATTCCATGCGTGTTCAATAAGAAAAGGTCTGGAGAGGGTTTTCTTCAATGCCAAAAATATTAGTAATTTATTAGATACAAATGAATAATTCGATGACAGAGCTCTGGGTTACGTTACCCCAATGCAATACAAGACTTACATTTAAGAGGTTCGCAACTAACATGCATTTCCTAACTCCAGCATATATACACAACTGATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41943
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081382 | Essential Splice Site | 392 | 573 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 4956290)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4239007 |
GRCz11 | 12 | 4275775 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGCAGTCTATGAAAGAAAGGTGGACAACGCAATCATCTTCTTCATAG[G/A]TTGGTCTCTCTTTATTTGCAGTGAAAAATATATGGAACAATTGATTTGAA
Long Flanking Sequence:
TGGAGTAAAAGCTGTCCATTGGATCTCATTACTGTCGTGATGGCAAGCAGCTGCTTTGTTTTTTATTTATTTATTTTAAAAGGGCATTAAAGCTGAGATACAACCTGAAAGACGACAATACAGCACTTACTATCACAATCATCAACACTTTTAATAGTTTATTTTACAGACTTATAATACGCTCTTGTTCTATTGGAGTTTTCATTCTAAATGGCCGCCGCACCATCTAGTGGCTGTTTCCCAAATTACACTAGAGTGTCGCCTCTTGGTCATTCTAAGCTCTTTGGCTCAATGTTTAAACTTGCTTGTGGAAAAACATTGTGTTGTTACTTGTTGCTCTTGCCCAGGTCCATATTTCTGGCGAATCCAGCGGACGGGTTCTCTAGTGTCCTTTCAGCCTGCTCACATTAAGAACTTCTGGATGGGTCTTCCTCCAACCACCAATAAGGTAGATGCAGTCTATGAAAGAAAGGTGGACAACGCAATCATCTTCTTCATAG[G/A]TTGGTCTCTCTTTATTTGCAGTGAAAAATATATGGAACAATTGATTTGAAAATTATTTTTAGTAAGTTATGCGTAACTTTTCCCACATAGGCTCACAGTACTGGGTATTTAAAAACACGGAGGTGCTTCCTGGCTATCCACGTCCATTGTCTGACTGGGGAATGATCACTCAAGATGGAAGGAAGGTGATGAGAGTGGATGCAGCCTTTATTTGGGCTCATAATGGAAAAACCTACATTTTCAGCGGTGGAGAGTTCTGGAGGTTCTCTGAAGGCAGGGAGACTGAGCTGCGCGGTCCGGACACAGGCTATCCCAGAAACACCAACCTCTGGAAGGGGGCGCCAAGTAACCCGGATGACGTCATCACCTGGGGACAAGGTAAAGTAATAATATAGAGGAAATCAGTTTGCCTCAAACGCATTTTCTAAGGTGAAACAACATTTAAGAAATTTATTCAGTGCTGATTCTGTGATTTTCTAAATTTATCACTATTCTCACTT
Associated Phenotype:
Not determined