ZMP
adamts13
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate ADAM metallopeptidase with thrombospondin type 1 motif, 13 (ADAM
Human Orthologue:
ADAMTS13
Human Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 13 [Source:HGNC Symbol;Acc:1366]
Mouse Orthologue:
Adamts13
Mouse Description:
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 13 Gene
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5819 | Nonsense | F2 line generated | Not yet available |
| sa16863 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5819
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110085 | None | None | 1332 | None | 32 |
| ENSDART00000110310 | Nonsense | 705 | 1318 | 20 | 33 |
| ENSDART00000142300 | None | None | 357 | None | 9 |
| ENSDART00000146364 | None | None | 400 | None | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 47273256)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 45241957 |
| GRCz11 | 8 | 45249836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAATAAACACAGGTTATCAGCTCCTTTAACATCTTCACAATGCACCTG[C/A]ACTCTGGACAGATGCTGTCTTTAAGGCCGTACTCACACTAGGYACAGTTG
Long Flanking Sequence:
GTCACAGATCAATCTTGCAGTGTAAACAAAGCAGCGACGAAGCGCTAGCCCAGATAGTCATGCTGTGTGAAAACATCTGTGACACGATTACTTTGAAAATCATGCATAACTCGGCATAAGTTAAAGGACAGTAAGTGAGTGAGTAAACTGTATTTTTAACATTCATTATTTTGTCTTACATGGGAGCCTCATTAGTGCCATACCCTAAATAATCATACACTGTCATGCAGGAGACCCAGCTAATGGTTGCTCAGGCTTCAAAATGTGTACAGGTAGCACACACAGCTCTCTTGTTCTGAATTACAACCACTTCGATATAATTTATCCTTCCTCAGTGGCCAACTTAACCATGCAATGCCTACAAATATACCGGCCTGTGAATCTACTGCATTGAAACATTCATGGGCCGGCAGGTGGCCCAACACCAGACATGAATCAATTGATTAAAGTTCAAATAAACACAGGTTATCAGCTCCTTTAACATCTTCACAATGCACCTG[C/A]ACTCTGGACAGATGCTGTCTTTAAGGCCGTACTCACACTAGGTACAGTTGCCTCGAACCGGGCAAAAGCACGCTTGTCCCCCCACCCATCTCCCCCGACGGCCCGCACTCACACCACAATCGGGCCTGGGCATGCTTACGTCATCGCTGCTGCGCTGTTCAGTGAGAAGCGCTGTCACTCAGCAGCACAGTGGAGATTTCTCTAGTTATATCATTTCAGTCGTTTGATATGCAGTGACATGCAGTCAAATATTTCGCCAAACAGTCCTTAGGGATGCGTTGACACGCAGTCAGATATTTTGCCGAACAGATCGGCCACTTTTGGCGCTCATAAACAATCATAAACCCCTCGTGCTGCAGGAATGAGGAGGTCTGCTGAAGGTACGCAGCTGTCGTGCATTGAGAAGTTTGCGTATTTAATAAACTACGACAGTTTGCGTTCACTGAACAGTAAGAATGATTAATAAATCCATATGAAATAGTCCCTTAAAAGTCACGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16863
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 |
|---|---|---|---|---|---|
| ENSDART00000110085 | Essential Splice Site | 1159 | 1332 | 29 | 32 |
| ENSDART00000110310 | Essential Splice Site | 1152 | 1318 | 30 | 33 |
| ENSDART00000142300 | None | None | 357 | None | 9 |
| ENSDART00000146364 | None | None | 400 | None | 9 |
Genomic Location (Zv9):
Chromosome 8 (position 47288415)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 45226798 |
| GRCz11 | 8 | 45234677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGGTYATTCAAATCARAATTATTTCCAGTACCCTTAACTGCCAGCAAA[G/A]TAAGTGCTAATCTTTCATTGCTTACAGACAGGGGAATCTGTAATAGCATG
Long Flanking Sequence:
CAGCCGCGCTGACTTGACACCAAACACCCGCAGCATTCAGTCTCCCATTAGCGGCGCTGCAATGCTCACGTAAAAGGCTGACGCAGCCTTGTATTGACCGCAACTGTAGAGAGAGAGAGGGACAGGAAGGAAACTTTTCCCCGACATTGATGCTGACCGTTACCGGTAGCAAACGAGCCTGCTGAAACAAAGACTCCCCAAAGAAACACAGACGTGCATAGTGCGGTGTCAAAGCAGTCTTTTATACACCCTGAATACCCTAAGAAATTTATAGATGTATAGAGTTTGGGGATTAATATGTGAACAGATGAATGAACGTGGGGAAAAAACTAAGTCATCCACTCTCGTTTCAGGTATCTGTGGGCAACTCCTGCTTCAAGACTCAGGAAATATTGATCTCCGCAATGTCACTGAGAGGAGATGCATATTTGCTATTGGCCGACCTCTTGATGAGGTTATTCAAATCAGAATTATTTCCAGTACCCTTAACTGCCAGCAAA[G/A]TAAGTGCTAATCTTTCATTGCTTACAGACAGGGGAATCTGTAATAGCATGGTGAATTGTGTGCATATTTGTGTGTTCTTTTCAGAGGAGAATATAGCCCTGTATGACAGACTTGTCCTTATGCGTCTTTGTGAGAGGATGACTGGTAAAATGGTCAAATCACGAACAAATGTTCTTTTGGTACGCCAAAACCGTCTCACCTCTGGCAATGGAGTGGTACTATTTTATCAAAGTGTAAAGACGAATAAAGGCTACAATAGAGGTGAGTCATTACAAACAAACCATGAATCTAATACTTTAAAATGCATGCTGTAGTCTACTATTGTCAGGATTATGCCACTTTGGTTTTGTCAATTGTAAAGTATTTTAACCCTGAAATGAGAGAAACTCTGGGTTTTCCGTTTCAAAATGACAGGTTTATCAAACTCAAGAAAGCAGGGTAAGTCAAGCCTGTTTCTGAAAGAGGGGTAACTTTAACTCAAAGTCAGTTACTGTGGTAAC
Associated Phenotype:
Not determined