ZMP
adamts8a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ADAM metallopeptidase with thrombospondin type 1 motif, 8 (ADAMT
Human Orthologue:
ADAMTS8
Human Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 8 [Source:HGNC Symbol;Acc:224]
Mouse Orthologue:
Adamts8
Mouse Description:
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 8 Gene [
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14348 | Nonsense | Available for shipment | Available now |
| sa40460 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13542 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14348
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:
Founder:
SL4_06_B12
KASP Assay Location:
Unknown
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098300 | Nonsense | 193 | 884 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 31815411)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29576241 |
| GRCz11 | 5 | 30176394 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCACAGCGTCTTTGGTCTTTGATCAAATGAAAGTTGACAGTCTTGTGAAA[G/T]AGAGCAAACTGAACTCCAGTGAAGATGAAGACRGCAACATGAGACGCGCA
Long Flanking Sequence:
AAGAAGAGACTGTGTTAGTAAACCGTACATTTAGGAAAGGTCTTTTTTGGAGAAGTGAAGAGAGACAGCATTTTAAGCTCAGTGCGTTTGGCCACCTTTTCCTGCTTGACCTGTCTCCGGACAGCAAGTTCGTGTCTCCAGTTTTAAACGTCCAGCGCATTAAAGCAAAGAATCTCCGCTCTGTCCTGGACGCCTCCAGGAGCGGGGGTGCTCTCAGGGATGCCACCCTTTACCCAGACAGCGGTGCGGACCTCAGAGACTGCTTCTACACCGGCACGGTAAACTCTGAAAAGGAATCTGTAGTTGCTGTCAGCTTGTGCCACGGCATCCACGGCACCTTCATAACACAAGGGGTCGAGTACTTTATTCACCCTAAAGCAAGTGTCCAGACCACCGGGAAACATTTTCCGCAGGTGCACGTCATCAAGAGGAGAGCTGTTTCCAACAGTCGCACAGCGTCTTTGGTCTTTGATCAAATGAAAGTTGACAGTCTTGTGAAA[G/T]AGAGCAAACTGAACTCCAGTGAAGATGAAGACAGCAACATGAGACGCGCAAAAAGATTCGTGTCCGCTGCGAGATACATCGAGACACTGGTAGTGGCCGACGCGTCCATGACACGGTTCTATGGGGATGAGATAAAGGTGAGTTAAGGGTCAGGGGAAATGGTTAATGGTTGTTATTAGTTATGCGCCTAACTTTATTCAACGCGTTTTTCAGTCATCTGATTCATTCTGAAAATGTTAACAATTCCTGAATCGACTGCTAATCATTTGAGAGGCTTTAAAACCTGCTGTAACAAGTGTAGACAGTATCCTTTATTATTATTATTATTATTATTATTATTATTGTTGTTGTTGTTGTTGTTGTTGTTTTTGTTGTTGTTATTGGTGTAGACCAATTTCATATCAAATAATGGTAAAAGTGATAATATTAAATATCTGTAAAAATGTTTTCTATATTTATATTAAAACCTAACTCTGCCAAAAAAGTGGCATAATCTACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40460
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
Founder:
SL7_03_C5
KASP Assay Location:
Unknown
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098300 | Nonsense | 588 | 884 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 31798761)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29559591 |
| GRCz11 | 5 | 30159744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGTGTCCTTTTTTTAATCCACAGGAAAAAGCTTCAGAGAGGAGCAGTG[T/A]GAGAAGTATAACAGTGACCGTTACATGGACATTAAAGGGAACATAAAGCA
Long Flanking Sequence:
AAACAAAATTTGTTATATATAAACAATATATATATAATTTACAATATCATTGTACTGTATTTTGTACTTTGTTACATTTTATTGTGAAATCTAACAGCCTCTATTTTGTGTCCCAGGTGCCCGTCAATGGTGGATGGGGAGAGTGGGGCCCTTGGGGGCCATGTTCACGAACATGTGGTGGGGGTGTGGAGTTTTCCCATCGAGAGTGCACTTCTCCTGTACCACAGAATGGAGGATTGTACTGTGTGGGACAGAGGGTCAAATACCAGTCCTGCAATACTCAGACCTGCCCAGAAGACCATGGTAACATTTTATAAATAAACCTCCATACTCACTTTAGATAGCATAGGTCGCATTATTGAGGGTTAGAGAATGAGTGAGTGGAGAGAATGAAGCCATGAGGTCAAAAGACCGTGCAGTTTTCTTATAACATTTATTCTCAGAGATGCACCTGTGTCCTTTTTTTAATCCACAGGAAAAAGCTTCAGAGAGGAGCAGTG[T/A]GAGAAGTATAACAGTGACCGTTACATGGACATTAAAGGGAACATAAAGCAGTGGATCCCCAAATATTCTGGTGTCTCTCCACGAGACCGCTGCAAACTTGTCTGCCGAGCCAAAGGAAGCAATGAATTCAAAGTGTTTGAAGCCAAGGTGCACATCCATTGAAGACATTTTACTTTTAATCTAATCCGATCAGCAATAAGAACGATATGTGAAATTAATTTTAGTCTCTGCCTGCTCTAAAGCTTTACTAAGATGTCAGACGGTCGCTCTCTTAGACTTCCCTCTCGCCACATGCCCATTGATATCTTTACACTCCCACTAAACTCTCATGCATGAAATATTTTCCCTGTTGTAAAATGTGAAACCTGAGCACCCCAACCCTACAGTCCAGCTACTTGCTTAAGCTCTTGAGTGCACCTCTGTAACTGATATTTCAGATACAGCTGAAATGTTGTTAGTTTTGCATCATCAGCCCAGAGTTCTGGCGATTCTGCTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13542
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:
Founder:
SL4_06_F1
KASP Assay Location:
Unknown
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098300 | Essential Splice Site | 696 | 884 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 31797946)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29558776 |
| GRCz11 | 5 | 30158929 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTGATGGTACAACCTGCAGGAAAATAAGTGGTTCGCTAAACAAAGCTAC[G/T]TAAGTGAAAATCATATTTTTAAGCAATTCATTTAAAAAAAAWNKAAATATA
Long Flanking Sequence:
CCCACTAAACTCTCATGCATGAAATATTTTCCCTGTTGTAAAATGTGAAACCTGAGCACCCCAACCCTACAGTCCAGCTACTTGCTTAAGCTCTTGAGTGCACCTCTGTAACTGATATTTCAGATACAGCTGAAATGTTGTTAGTTTTGCATCATCAGCCCAGAGTTCTGGCGATTCTGCTTTATGTGGAATAGCCATTATGTGAGAACAGAATACACTGGAGCACTTAGGCTGCCATTGCAATAAAAATACACATTATTTCTTGAAACATTTGTTGAAGGTTTCTGTCTATTCTGACACTCGTCTTTTCTATATGCTGGGCAGGTTGTGGATGGCACCACCTGTGGGCCAGATACCACATCCATCTGTGTTCAGGGCCAGTGCATCAAAGCCGGATGTGACCAGGTGATAGGTTCCAATGAAAAGCTGGACAAGTGCAGTGTTTGTGGAGGTGATGGTACAACCTGCAGGAAAATAAGTGGTTCGCTAAACAAAGCTAC[G/T]TAAGTGAAAATCATATTTTTAAGCAATTCATTTAAAAAAAAAGAAATATAAACACTGGGAAAGGCGAGAGCTGCTGATATAACTGATATGAAATTCTGATTTTAGGCATCAGGGTACCATATTTCAGTGTGAGAAATGGCTATTCACTTTGAGATTTGCTAAAAAATTAGTTTTGTTAGTAGTTTTAAAGATTAACTTTGGTAAGTGTTTAAGGAAAAATGTAAATGTTGATGATGGGCTTAAGCAATTAATGACCCACTATGAGTTAATATCTGTTAATACATCCAATATTCAGAATTGTGTTCTGGAAGAACCATTTGTATGGGGCCCACCATCATAAAATCATCAGTGAAAAGTTCTTAAAAGGATTGATCACTCAAAATTCAAATTTAATGTTAATAAACTCACCCTCAGGCCATGCAAGATGGAGACAGTTTGTTTTCTTCAGGAGAGCCTTCAAGAAGAGCTTGAGCTAAAACTGTGGTCCTTTCAGAGAGTGT
Associated Phenotype:
Not determined