ZMP
si:dkey-45m5.4
Ensembl ID:
ZFIN ID:
Description:
A disintegrin and metalloproteinase with thrombospondin motifs 10 [Source:RefSeq peptide;Acc:NP_001
Human Orthologue:
ADAMTS10
Human Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 10 [Source:HGNC Symbol;Acc:13201]
Mouse Orthologue:
Adamts10
Mouse Description:
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 10 Gene
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38685 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34374 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa18917 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9421 | Nonsense | Available for shipment | Available now |
| sa31645 | Nonsense | Available for shipment | Available now |
| sa7130 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38685
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 |
|---|---|---|---|---|---|
| ENSDART00000113910 | Nonsense | 87 | 1108 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 20909904)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20339801 |
| GRCz11 | 8 | 20371886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCGGCGCAGCACCGAAACACAGAGCGCTCCAGAGCCGCAGCTGTACTA[T/A]CAGCTCTCCACTTCCAGCACTGATCTGCTGCTCAACCTCACGCTGCAGGG
Long Flanking Sequence:
TTGTAGTGCTATATGTCGGCACACTTAACCACTAGGCTATTGGTGCCGACTGGGGTACTCTTTTAAATCTGGAAGCATTAACAACTTATATCAAAATATATATCGTTATCGTTCAATATGGAAAATAATTATCAAGATTGCATTTTTTCCATATCACCCAGCCCTAATTTATGCATAAAATAATATCTCCACTGAGATATTAAACACTTAAGGTTTTATTAAACCAAATAAAAGGCTTTTTAATAAGTAAATATCCGTACACACATTTAATAGCCAAATAAGAGATCAATTTAAACTGAACATCCATCAGTTTCACGGATATTGTTTTTTTGTTTTTCCACAGCTGAGTTTCTGTCCAGCTTGGGCCAGTATGAGATTGCCATCCCAGTGCGTGTGGGGCCTCATGGGGAAACTCTTTCGGAAGAGGAGACGTCTCACGGGACTGTCCGCCACCGGCGCAGCACCGAAACACAGAGCGCTCCAGAGCCGCAGCTGTACTA[T/A]CAGCTCTCCACTTCCAGCACTGATCTGCTGCTCAACCTCACGCTGCAGGGAGGACTGCTCTCGCGCCAGTTTCGTGTCGAATACTGGAAGAGGGGCCGCTTGGCCTGGAGCCACCCATACTTGCCCAGCTGCCACTATGTGGGTCACCTGCAGCACCAGCCGCACTCCAGTTCTGTTGCTCTCAGCAACTGTAACGGACTGGTGAGCTCCAGTTTACTTCTGTAGCAAACACTCAAATGATGCACAATTATATTCTTAACATAATCAATCCACTGAGGAAATATGGTGATAAATATAAGTTATTTTTACTCCATTGACTTGCAGTATCTTGCCTTAAAGGGATGTTTTAGGTTCATAAAAAAGTCAAGCTTAATCAACCTGTGGTTCTCACCATGTAGGAAAGGCAGGCAATATTGAAGAATCCAGTCATAAAAGAGAATTAGCTGTGTAATTTCATACAATTTGGCATATTTTGGATGAATACATTAGTTAATTAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34374
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113910 | Essential Splice Site | 208 | 1108 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 20906930)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20336827 |
| GRCz11 | 8 | 20368912 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTCGTCTCTGAGATATCAGAACATGGACCAGTCCTGTGGAGTTATCGG[T/G]AAGAACCAAAAAGTTTGTAAGTTTTAAATGAAATTTGTTTGCCAACCTGT
Long Flanking Sequence:
AGCATGCCTTAATTCTTCAGGGGACGCTCAGTGTGTCCACAAGACCGTCACTAAGCATATTACAGGATTATATGTACACTTGTAAAGTGTGATTAAGAGAGATGAAGAGAGGAACATGCTAATATCCTTTGACCTGCTACCATTAGTTCCTATTTCATCCGGGATTATTTGCCCAGTACATGCTCATTATTTTAAAAGCAAATCTAATGATGGAATGGTTTGAAAGTATTGTCTGTGTATGTACAATGTAAAATGATATCCACAATGAGGATTCATGCTCAAAAAAAGCATTTAATTCATGTTAACTTGGAGCAAAAAGAAGCAATTTTTTTTTTCCAGCAAGGGGTCATTGTAGCAGGAGGTGAGGAGTACCTTATTGAACCCCTGGTTTCTGCTAAAAACTTGACTAATGAGGATGGCAGAGAAGGGCGACCACATGTTGTGTACAAACGCTCGTCTCTGAGATATCAGAACATGGACCAGTCCTGTGGAGTTATCGG[T/G]AAGAACCAAAAAGTTTGTAAGTTTTAAATGAAATTTGTTTGCCAACCTGTTTTGTTGAGTCTTTTAATATGTGTATAGTATCCTATTTATTCATTATATGTCAGTCCTCCAGACGTCAAATTAAATAAAAAAATAAATGAATGTTTTGAGTGTTAGCATGTATCTATATATTGGTTATAAGTTTATCAATAAGCTGTTGTGGACTAAAACAATGACACATTTTTACTTTGAATTTAGGTTTGTACCGATATGAACATTTTGGCCAATAATATAAACCGTTTATAATTGAAACTAACAAAAAGGCGATAAAAATCTTGATGTAAATTTTTCTAAGCCTCATTACAAAAAAAAAATTTGATTAACTGGATTAACGAACGTAACCCTCATTCCCCGAATAGGGAACGGAGACGTGTCTGGAAGACACTTTGGGAGGATACTAGCTGACAAAAGTGTCTTCCAAACACATTTCTGTGTATTCATGAAGGGGAACATCTTGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18917
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 |
|---|---|---|---|---|---|
| ENSDART00000113910 | Nonsense | 495 | 1108 | 10 | 24 |
| ENSDART00000113910 | Nonsense | 495 | 1108 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 20886702)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20316599 |
| GRCz11 | 8 | 20348684 |
KASP Assay ID:
2260-0458.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGCAGACGAGCAGTGCCGCTTCCAGTACGGAGTGAAGTCTCGTCAGTG[T/A]AAATACGGGGTACTTGCATCACTACGTGTAACAACAGCTCTTTTTTCCAA
Long Flanking Sequence:
ATGGTGTTGGCAATGCATGCGGGGTGCGCAGTCAGGAGACCGCCAAACTCATGGCTGCCCACATTACCATGAAGACCAACCCGTTCGTCTGGTCCGCCTGCAGCCGCGATTACATCACCAACTTCCTCGAGTGAGTGTGTCTGCTGCATGAGTCTGAGATCTGTTTTCCACCAAGTCAAATATTGACTGCTGAAATACTGAATTTCAGTTAGATTGTAATAATATATAAATTATAACCGATAATAAGAGTAACGATTAAAATAAATATTTAATGAGCTATACTGAGTTAACAAATAGGCTGTTAAAATTCGAATTAAACATCCATACTTTTTAACACAGCTATTCTCTTTTTTATGATTATTTCTTAGCTCTGGCATGGGTTCCTGCCTCAATAATGTGCCCCCCAAGCAGGAGTTTGTGTACCCCACCACAGCCCCAGGCCAAGCTTATGATGCAGACGAGCAGTGCCGCTTCCAGTACGGAGTGAAGTCTCGTCAGTG[T/A]AAATACGGGGTACTTGCATCACTACGTGTAACAACAGCTCTTTTTTCCAAGAAAGAAAATTATCATTGTTGATTAATGTTGCAGATTAGAATGATTTAGAAAATAATTTTATACTACCTTTCTAATGTTTAGTTTTTCAGTGTTTTAAATATATAGAAAGACATCAGTGTGAGCATATCAGAGGATATCCTGAAGCCAGATCAAGCCAAACATAATAGAAAAAGTAAACCGAATAGGCACACTGTCACTTTAGCTCTTAAAAGGCAATTTAATTAAACAATGTTTCGACCTACAAGGTCTTCATCAGTGTTTTAAAGGGCACCTATGATGAAAATCATCTTTTGTAAGCATTATGAGACATCTATGCGCAAGTGGCGTCTTTTTCTATATGAATTGTTGGTTAAGTCCTGTCCAGGCTGCCTTTATATCTCTACAGTAAATCATTTAACACTCACTCTCTCTCTCTCTCTCTGTAAATCTGCACCAGATGGTAGCTGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9421
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 |
|---|---|---|---|---|---|
| ENSDART00000113910 | Nonsense | 495 | 1108 | 10 | 24 |
| ENSDART00000113910 | Nonsense | 495 | 1108 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 20886702)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20316599 |
| GRCz11 | 8 | 20348684 |
KASP Assay ID:
2260-0458.1 (used for ordering genotyping assays)
KASP Sequence:
GATGCAGACGAGCAGTGCCGCTTCCAGTACGGAGTGAAGTCTCRTCAGTG[T/A]AAATACGGGGTACTTGCATCACTACGTGTAACAACARCTCTTTTTTCCAA
Long Flanking Sequence:
ATGGTGTTGGCAATGCATGCGGGGTGCGCAGTCAGGAGACCGCCAAACTCATGGCTGCCCACATTACCATGAAGACCAACCCGTTCGTCTGGTCCGCCTGCAGCCGCGATTACATCACCAACTTCCTCGAGTGAGTGTGTCTGCTGCATGAGTCTGAGATCTGTTTTCCACCAAGTCAAATATTGACTGCTGAAATACTGAATTTCAGTTAGATTGTAATAATATATAAATTATAACCGATAATAAGAGTAACGATTAAAATAAATATTTAATGAGCTATACTGAGTTAACAAATAGGCTGTTAAAATTCGAATTAAACATCCATACTTTTTAACACAGCTATTCTCTTTTTTATGATTATTTCTTAGCTCTGGCATGGGTTCCTGCCTCAATAATGTGCCCCCCAAGCAGGAGTTTGTGTACCCCACCACAGCCCCAGGCCAAGCTTATGATGCAGACGAGCAGTGCCGCTTCCAGTACGGAGTGAAGTCTCGTCAGTG[T/A]AAATACGGGGTACTTGCATCACTACGTGTAACAACAGCTCTTTTTTCCAAGAAAGAAAATTATCATTGTTGATTAATGTTGCAGATTAGAATGATTTAGAAAATAATTTTATACTACCTTTCTAATGTTTAGTTTTTCAGTGTTTTAAATATATAGAAAGACATCAGTGTGAGCATATCAGAGGATATCCTGAAGCCAGATCAAGCCAAACATAATAGAAAAAGTAAACCGAATAGGCACACTGTCACTTTAGCTCTTAAAAGGCAATTTAATTAAACAATGTTTCGACCTACAAGGTCTTCATCAGTGTTTTAAAGGGCACCTATGATGAAAATCATCTTTTGTAAGCATTATGAGACATCTATGCGCAAGTGGCGTCTTTTTCTATATGAATTGTTGGTTAAGTCCTGTCCAGGCTGCCTTTATATCTCTACAGTAAATCATTTAACACTCACTCTCTCTCTCTCTCTCTGTAAATCTGCACCAGATGGTAGCTGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31645
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 |
|---|---|---|---|---|---|
| ENSDART00000113910 | Nonsense | 818 | 1108 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 20847797)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20277694 |
| GRCz11 | 8 | 20309779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAATGTGTGGCAGGTCTTGGTCCGTGAAGAGAATCCAGGAATTCTATA[T/A]CGATTCAACCCTCCAGTCAGCAGAGATCCTCTGAGCAGTTACTCTTGGCA
Long Flanking Sequence:
ATGTCAAATTCAGTCGCACTAGAATAAATGTTTTGTATTAATAATAAATTCTTCTTGACATGATGCTGACAACATCAATCAACTACAGTGTTTTAAGGGCGTGTCAAATTAGGCATTGTTTGCAGGCAGGCAGCGAATAAAGAGGACAGGCTGACCTTATGCAAATTGCTTACAGAGCTTTATAGATTAGGTACAGAAGCGAAACTCTAATTACGGACTCGTCTCAGCAGTTCACAATGGACTCTTTCTTTTTGGAGATCAAACTAATTTGTGCACTTTGATCTTTAAATTTTAGCAGGCATTTCATTCATAAACAGTTATAGTGCATTTTGCAGCAGATGAAAAGTAAAATCGGAACAAGCATACAGTATTAAGGTCCCTTTAACAATTCAGCTTCAGATATGAATCAAAATGATTGAAGGTCAGATAAATTTGTTAAATCCTGCGTTGTTTAATGTGTGGCAGGTCTTGGTCCGTGAAGAGAATCCAGGAATTCTATA[T/A]CGATTCAACCCTCCAGTCAGCAGAGATCCTCTGAGCAGTTACTCTTGGCATTATACATCCTGGTCCCGCTGCTCTGCACTGTGTGCTGGAGGTAAGGAGTTTTCTGGTCACTAACTAGCATATTACAATCATTGACACAAGAAAATGCCACTTAAAGGCATAGATAACCTTTAAATAAAAATGTTAAACCTCCTATCTACTTTCAAGATTTGTGTAATATGTTTTTTCTGCAGAACTTTAAAAACGTTTTTATTTTGTTGTTGATAAAAGTCATGGTCTTTGGTGATTTATTAACTGCAAGTAAACTATTAATGTCACTTTTTAAAAGTCAAAAGCATGCACTGAAAAAAGGTAATTAACCCTTGTGTACTGTCCAAATTGACTAGCCTTTAGTTATGTTCATGGCTGTTTTTTTCCAATTGACTTCCATTATAACAACACTTTTGAGCCATAACACCAAATGACAATAATTGAACACAACAATTTTTGATTGTTGGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7130
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 |
|---|---|---|---|---|---|
| ENSDART00000113910 | Nonsense | 1062 | 1108 | 23 | 24 |
Genomic Location (Zv9):
Chromosome 8 (position 20839202)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 20269099 |
| GRCz11 | 8 | 20301184 |
KASP Assay ID:
554-4688.1 (used for ordering genotyping assays)
KASP Sequence:
TGCCCTGAGTCTCATCGTCCAGCCTTCATGCAGCAGTGCAAGAGCAAGTG[C/A]GACCACAGCGGCCCTACAGACAACCCTGAAGGTCAGAGGTCAAACAAAAG
Long Flanking Sequence:
CTTTAATTGAAATCTGAAAATGCACTTCCTGTTTGTTTGTTCTGTTAAATTCTCAGTTACTTTATATTGAGGTATTGGACTAGGTTAACATACCACACCCCTCCAACTGTCAGAATTGAAGGAGGTGTCTGTTAGATAGTTGTAACTCTCCCCAAACCCTTTTCCTGGTATTTCTAAATGAAATGCCTACTGTACTACATCCATTCAGCTCGCAGTAGAAAAAACAAGCCAAGGCCATTGTTTTCTCATTCAATATTCACTATACGAGAAAAAAAACTGTTGCAGCTTCTGGTTCATGATATGTTAAGTTCCTTGAAAACAATTTATTTTCTCATACCTGTTGGTGCCTGTGTGTATGTTTGTGTGTTGTAGTGTTCTGCGAGGTGTGGAATGGGTCAGGAGATTCGTTTTGTTCAATGTCTGACACACACTGGCCAGCCGTCCAATGAGTGCCCTGAGTCTCATCGTCCAGCCTTCATGCAGCAGTGCAAGAGCAAGTG[C/A]GACCACAGCGGCCCTACAGACAACCCTGAAGGTCAGAGGTCAAACAAAAGCACACACACACACGCACATGCTCACTGTTCACATGCTGTCCTGAATGAAAACTCATAATAATTAACTTTTTCCAAATGTGTGTTAAAAGGATGTGTCTGTCAAAGATTTTTTGGGTAAATATTTCCCATAATGGGTGACGCAGGGGCACAGTAGTTAGTGCTGTTGCCTCACAGCCAGAAGGTCGCTGATTCGAGCCTCGGCTGGGTCAGTTGCCGTTTCTGTGTGGAGTTTGCATGTTCTCTCTGCATGGGTTTCCTCCGGGTGCTCCGTTTACCCCCACAGTCCTAAGACATGTACTACAGGTGAATTGGTTAAGCTAAATTGTCCGTAGTGAATGAGTGTGTATGGATATTCCCAGAGGTGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATATGGTGGATAAGTTGGCGGTTCATTCTGCTGTGGCGACCCCAGCTTAATA
Associated Phenotype:
Not determined