ZMP
adamts15a
Ensembl ID:
ZFIN ID:
Description:
a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 15 [Sour
Human Orthologue:
ADAMTS15
Human Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 15 [Source:HGNC Symbol;Acc:16305]
Mouse Orthologue:
Adamts15
Mouse Description:
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 15 Gene
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10262 | Nonsense | Available for shipment | Available now |
| sa420 | Nonsense | Available for shipment | Available now |
| sa20449 | Nonsense | Available for shipment | Available now |
| sa31450 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10262
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098294 | Nonsense | 33 | 935 | 1 | 9 |
| ENSDART00000134624 | Nonsense | 33 | 958 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 31818123)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29578953 |
| GRCz11 | 5 | 30179106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAGTGGAGAATTGTGAATTCAATGCAGAGCCAGTTATGCGTGCCCATC[A/T]GAATGGATCATGTAAAGAACAGTTTAGTCGATGATGAGGACAGTATTTTG
Long Flanking Sequence:
TCATACAAGTCACTGTTGGATGCTGTGAATGAGTGGGAGGGAAACCCGGCTCTTGGAGCGCTGCAGGCTGATGATGCGGAGCGCAAAAAGCCACAAGTAGTTGCGGGCTTAACCTTGAACTGAGAGGAATACCCAATGAGCGCACTCGAGCACCTCCCCAAAATCTTCTGATTACAAGCGCGAGATGTTTACACATGACGCGCGAGCATAAAGCCGACAGATGAACACAACCGCTTCAATATACAGGTACAAGAGAGAGATGGAGAACAGACCGGCGGATTTCACACTTTGTGGACGCGCAAAGGCAACATTGTAGTGCAGCAGCATCCTGGATTATTCTTGCAGTCACATCTCACTGTGTCAATTTGCGCTTCACAAGTCAAACCCATTTCAAGCGCATAAACATGTTTTTGTTGCTAAGGTCAGTTCTTCTTGTAAACGTGTTCTACGCTCAGTGGAGAATTGTGAATTCAATGCAGAGCCAGTTATGCGTGCCCATC[A/T]GAATGGATCATGTAAAGAACAGTTTAGTCGATGATGAGGACAGTATTTTGCCGCGCAAGGCTGTATTTAAAATAAGTGCGTTTGAACAAGATTTTGTACTCGAATTGAGGTCGGACTCCAGCTTCATTGCTCCAGGTTTCTCAGCGCGCACAGACTCAGCTGCGCACAATTCCGCGCACGGTGAAGATCTGAGCCGGTGTTTTTATGCCGGTGAGGTGAATTCTGATCCCTATTCCTACGCTGCGCTCAGCTTGTGCAAGGGTCTCCAGGGCGCATTCGGATACGACGGCTGGGAATATTTCATCAAGCCGGCTTCTAACAATACCGACCGGGACAACGAAGCCGCGCATCTCATCAGACGCAGATCTAACGCCGATCTGAGTGGAAACTCCACGTCAAGGTGCGGCGTGGACAGCAATGCGACTCAAACCGTTGCACAGTCCCTAGCGAAGTTTAAGCACCTGAAGGAACAACACATGAATAACGTCACTATGTCATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa420
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098294 | Nonsense | 119 | 935 | 1 | 9 |
| ENSDART00000134624 | Nonsense | 119 | 958 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 31818381)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29579211 |
| GRCz11 | 5 | 30179364 |
KASP Assay ID:
554-0281.1 (used for ordering genotyping assays)
KASP Sequence:
CCGGTGAGGTGAATTCTGATCCCTATTCCTACGCTGCGCTCAGCTTGTGC[A/T]AGGGTCTCCAGGGCGCATTCGGATACGACGGCTGGGAATATTTCATCAAG
Long Flanking Sequence:
GATGGAGAACAGACCGGCGGATTTCACACTTTGTGGACGCGCAAAGGCAACATTGTAGTGCAGCAGCATCCTGGATTATTCTTGCAGTCACATCTCACTGTGTCAATTTGCGCTTCACAAGTCAAACCCATTTCAAGCGCATAAACATGTTTTTGTTGCTAAGGTCAGTTCTTCTTGTAAACGTGTTCTACGCTCAGTGGAGAATTGTGAATTCAATGCAGAGCCAGTTATGCGTGCCCATCAGAATGGATCATGTAAAGAACAGTTTAGTCGATGATGAGGACAGTATTTTGCCGCGCAAGGCTGTATTTAAAATAAGTGCGTTTGAACAAGATTTTGTACTCGAATTGAGGTCGGACTCCAGCTTCATTGCTCCAGGTTTCTCAGCGCGCACAGACTCAGCTGCGCACAATTCCGCGCACGGTGAAGATCTGAGCCGGTGTTTTTATGCCGGTGAGGTGAATTCTGATCCCTATTCCTACGCTGCGCTCAGCTTGTGC[A/T]AGGGTCTCCAGGGCGCATTCGGATACGACGGCTGGGAATATTTCATCAAGCCGGCTTCTAACAATACCGACCGGGACAACGAAGCCGCGCATCTCATCAGACGCAGATCTAACGCCGATCTGAGTGGAAACTCCACGTCAAGGTGCGGCGTGGACAGCAATGCGACTCAAACCGTTGCACAGTCCCTAGCGAAGTTTAAGCACCTGAAGGAACAACACATGAATAACGTCACTATGTCATTTCTGAGAAACCGCTCGAAAAGATTCGTCTCCATTCCGCGTTATGTAGAGACATTAGTGGTGGCCGATGAATCCATGGCCAAATTCCACGGTGACGACCTCAAGCATTATGTGCTGACCTTAATGTCTGTGGCGGCGAAGCTTTACAAGCACCCCACCATTCTCAACTCCATCAACATCGTGGTTGTCAAGTTTATGGTGATTAACGAGGAAGAGAAAGGACCCAAGGTTTCCGGGAACGCGGCGATGACCCTGCGTAAC
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa20449
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 |
|---|---|---|---|---|---|
| ENSDART00000098294 | Nonsense | 290 | 935 | 1 | 9 |
| ENSDART00000134624 | Nonsense | 290 | 958 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 31818894)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29579724 |
| GRCz11 | 5 | 30179877 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGGTTTCCGGGAACGCGGCGATGACCCTGCGTAACTTCTGCACCTGG[C/T]AGAAGAAGCTGAACAAAAACAATGACAAGCATCCGGAGTACTGGGATACG
Long Flanking Sequence:
GCGCATTCGGATACGACGGCTGGGAATATTTCATCAAGCCGGCTTCTAACAATACCGACCGGGACAACGAAGCCGCGCATCTCATCAGACGCAGATCTAACGCCGATCTGAGTGGAAACTCCACGTCAAGGTGCGGCGTGGACAGCAATGCGACTCAAACCGTTGCACAGTCCCTAGCGAAGTTTAAGCACCTGAAGGAACAACACATGAATAACGTCACTATGTCATTTCTGAGAAACCGCTCGAAAAGATTCGTCTCCATTCCGCGTTATGTAGAGACATTAGTGGTGGCCGATGAATCCATGGCCAAATTCCACGGTGACGACCTCAAGCATTATGTGCTGACCTTAATGTCTGTGGCGGCGAAGCTTTACAAGCACCCCACCATTCTCAACTCCATCAACATCGTGGTTGTCAAGTTTATGGTGATTAACGAGGAAGAGAAAGGACCCAAGGTTTCCGGGAACGCGGCGATGACCCTGCGTAACTTCTGCACCTGG[C/T]AGAAGAAGCTGAACAAAAACAATGACAAGCATCCGGAGTACTGGGATACGGCGATCCTCTTCACTAAACAGGTAAGGTGTAACGCGCGCTTCCCCCATAGAGGGCAGCATGAGAAGCAGAGAATCATCAGGCTAATGTATCTGGTGGTAATCATATCAAGATGGTTAGCAACATGAAACAAAACTGCACACCAGACAGGCGACTGCAATTTACTTACCCAATAATCAAACCAATTTAGACATGATTTACGCTGACATTGTAATCACAGCTTTTAAATCTAAAGGTAGGCTCCATACGCATAAATATGCTGTTTTAATCATGTGTTTGTGGGGAAACAAATGCACAATGGGATGATGTAATAAAACAAAAAGAGCTTGAATTGGGGTAACATCTGAACACATATTTGTGTATTTAGCTTGGTTAGATGCTGAACTATGTCTTGTGTCTCACAGAGTAATGGGCAGGCTGCAACAAGAGCAGGCTCTCCTGTTAACCTGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31450
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 |
|---|---|---|---|---|---|
| ENSDART00000098294 | Nonsense | 390 | 935 | 3 | 9 |
| ENSDART00000134624 | Nonsense | 390 | 958 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 31837349)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29598179 |
| GRCz11 | 5 | 30198332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTTTTTGGAAAGCTGCAGGACAATCACATGATGTCCCCTACTCTAATC[C/T]GAATCAATCGCACCAGTCCATGGTCCCCATGCAGTGCTGCCATTATCACA
Long Flanking Sequence:
GGTCATGTCAGCATCCAAAATCATTTGGAGAGTCTCCACAACAATGTTCCTGAGGTGATGTTCACTCTGTTCAGATCAGCCCGGTGGAGCAGCTGAGGAAAGATAAGCTCTATCGAAGTGGTTTGTTTCCCCGTAGGAAGCCTCATAGGCGGTTTTGCAAACGTTTCCTCCAAGGGCAGGGAGGAAATGTGGGGAGTTGTTGGAGGTATTGTAAAAGTGACTAAGCATAGCTGTGGTGCATTTGCTGACAGGAAAATTGCATTGGAATAATTCTAAAGTAAAAATCTAAACCTACATTTGAATAATTCCAAGAGATCGTGCCTTCACATCAGCATGGAGTGCTGACATATTTTGTTTGTCTCTTGTCATTTCTGACTTCTTTTCTGTCGTTTCTCTCTGCTACAGGACATGTCTTCAATATGCCGCATGATAATGTTAAGGCATGTGAGGAGGTTTTTGGAAAGCTGCAGGACAATCACATGATGTCCCCTACTCTAATC[C/T]GAATCAATCGCACCAGTCCATGGTCCCCATGCAGTGCTGCCATTATCACAGACTACCTGGACAGTGGACATGGTAAGTCAAAGAAAGCCATACAGTAGAGATGTGAACCTACACTGGTCTCACGGTTCAGTTCGGTTACAATCATCATGCCATCGATTTGGTTCAATTTGATATCTCGGTGCATCATGGTGCATTTGAAGATGCTTTCTATACACAATTTTATATTTTACACAGCACAAGAATTCTTGTATTAAAACATATCATTTTAAAATACATTTTATATGTATTTGTAATACAATCCTGTTCTTACTTACAAGCAACCATATATATGAACTGTACCTTAAATTTTACCAGCTCAAAGAAAACACTCTGCATCAAACAAAACTCAGGCACAGAACAACATGAGCATTTATAGCAAAGAAACAAATGTAAATATTATTCTGCTTTCTTCTTAAGCAAGTTGTTAAATGCCTATGATTGGTCAACAAAACAGATTGCTT
Associated Phenotype:
Not determined