ZMP
adamts22
Ensembl ID:
ZFIN ID:
Human Orthologue:
ADAMTS2
Human Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 2 [Source:HGNC Symbol;Acc:218]
Mouse Orthologue:
Adamts2
Mouse Description:
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 2 Gene [
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32352 | Essential Splice Site | Available for shipment | Available now |
sa1626 | Nonsense | Available for shipment | Available now |
sa13856 | Nonsense | Available for shipment | Available now |
sa29631 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32352
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114158 | Essential Splice Site | 158 | 1295 | 3 | 22 |
ENSDART00000147203 | Essential Splice Site | 123 | 1257 | 2 | 21 |
The following transcripts of ENSDARG00000075930 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 31381524)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 32580994 |
GRCz11 | 21 | 32614252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTACCTGTTTTTGAAAAAGCCTAATCTCTGCCTCTCCTTCAAACCCTTC[A/G]GGCGGGGATGATCCGCGCAGGTCAGGAGGAGTTTTTTATCGAGCCACTGG
Long Flanking Sequence:
GCGCCCCTGGCAATGGACGCGGCCCATCAGTCAAAGCCAACGAATCTCAACTCGACACAGCGAGAGCGCAACATGAGCTGTCAAGTGTATCTGTCAGTGAGTTTGTTCACTCTGGCAGAAAGATTTGTATTGATCTTCGCTCGTGGTTTGGATTTCCCTCTTTGCCCTCATAGACTATTCCTCCTTAAATGGTATAAACAAGACAATGTCACATTTTCTTCCTAAAAGCGTCAGGTTGTTCAGAAACATTAGTGAAGAGTTTGTTGTTTTGCTTCTGACAGGCAATGTCACAGAGTTTCAGAGATGGCCACACGAGTTAGAAAGAGGAGCGATCGATTCAGAGATCAGGTTGCCCGAGGGTTTCTTCCAAAGCTGATGAAAACATGATATAGCAGGCGCACAGAAATAGCCCTGATTCGCTTAATGGACTTGATTGTGCAAGCTTTGTGTTCTACCTGTTTTTGAAAAAGCCTAATCTCTGCCTCTCCTTCAAACCCTTC[A/G]GGCGGGGATGATCCGCGCAGGTCAGGAGGAGTTTTTTATCGAGCCACTGGAGAGAGGAGGCGACATGACAGGAGAGGAGGAAGGAGGACCCGGGCGTCATCACATCGTCTACCGCTCCTCTGACATCAAGAAGCCGGCCGTCAATCAGCCCGCTGACTTTCACCCCAGAGGTCAGACCACCTTTATGACACCAGCTCATCATGGAGCGCTGCCGAGAGCTTTCACATGCATGCTGATGACTATAGAGAGAGATGCTGAGTTTCATGCGGTTGACACTACAAAATTATTTGGCTTTCTGAATTATTAGCCCCCTTGGATATTCTTTTGTCACCCAATTTTTGTTTAATGGAGATATTTTTTTTCACATTTCTAAACATAACAGTTTTAATAACTCATTTCTAGTAACTAATTTATTTTATCTTTGCCATGATATTTGACTATATATTTTTCAAGGTACTAGTATTTAGCTTATGTGCAATTCAAAGGGTTTACTTGGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1626
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 |
---|---|---|---|---|---|
ENSDART00000114158 | Nonsense | 592 | 1295 | 12 | 22 |
ENSDART00000147203 | Nonsense | 557 | 1257 | 11 | 21 |
The following transcripts of ENSDARG00000075930 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 31316423)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 32515893 |
GRCz11 | 21 | 32549151 |
KASP Assay ID:
554-1567.1 (used for ordering genotyping assays)
KASP Sequence:
GCCAACGGAGGGCGCACTTGTTATGGAAACAACTATGAGTTCCAGTTATG[T/A]AACACGGAGGAGTGCGCAGAAGCCCTGGTGGACTTCAGAGAGGAGCAGTG
Long Flanking Sequence:
CCCCTGAGACCTTCGTTTTTCTACAGAACACAAATTGAGATATTTTAGATGAAGTCCAAGAGTTTCCTCGTCCTCCATAGACAGCAAGGGATGTGAGACGTTCAAAGTCCAAAAATATATAAAAAACATCATCAAAACATTCCATATGTCTTCAAGGGTTCAACTATTATCATAAAAATCTCCAAGAACACCTTTGTGCAGCCAAAAACTGTAAAATTGCTGTCTTTGGAGGATGAGAAAGCTCTCATATTTCATTTAAACAAATCTTCATTAAGATTCCAAAGATTAATGGAGGTCTTGGAGGACTAGAATGATACAAAGGTTTGTAATTAATAACAGAATTTTCATATTTGGTTAAACTAACCCTTTAAACCCTTCAAAGAACCCCTGAATAACCTATTTTGTGTGTATGTGTGTGTGTGTGTGTGTGTCTGTGTATGTTGTAGTCCAGCCAACGGAGGGCGCACTTGTTATGGAAACAACTATGAGTTCCAGTTATG[T/A]AACACGGAGGAGTGCGCAGAAGCCCTGGTGGACTTCAGAGAGGAGCAGTGCAAGATGTGGGACCCGCACTTTGAGCATGAAGGAAACAAACACCACTGGCTGCCCTACGAGCACTCTGAACGTGAGTGATGATCAGAAAAATGGTTTAGTTTTATTAATTTTCAAATCAATTTTCAAATTTTTTCCAGTCTAGTTTTATGCTGTCGCTGTCATCACGTTTCATTTTAACACGTCCTGATGTTCGCCATATGTGTTGGAACATCATCTTTAAATGTTATCCTTCCATAAGAGTGATAAAATATTTTCCTGACCTCTGTATTTTATGTTGAAGTAAACAGTTTTTTACATTCTAGACAAAACAAGAGTGGTGTAGAAATTATTTTTACTTTACAGGCTTTACAGGGTTGACTAAGGGTGTATTCACACCTGCCACTAGAGTTTGTTTTCCCTCTTGGTGCGGTTTGTTTGGGCAGGTGTGAATGTAGCAATCGCACTTGAGT
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:
sa13856
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 |
---|---|---|---|---|---|
ENSDART00000114158 | Nonsense | 676 | 1295 | 13 | 22 |
ENSDART00000147203 | Nonsense | 641 | 1257 | 12 | 21 |
The following transcripts of ENSDARG00000075930 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 31303732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 32503202 |
GRCz11 | 21 | 32536460 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCGCTGTTCCTACAAAGACCCCTACAGCGTGTGTGTKCGTGGAGAGTG[T/A]GAGGTAAAGGTTATTCAAACACACCCATCCCTCCAGTTCATCCTCCAAAA
Long Flanking Sequence:
TTACCAGGTTACATAGGCTGAAGCAAGCAGGGAAGTCCTCACTGTGCTGTCGTGTTTTAAAATGGTGGCCTCGTGAAATAAGCGTATAGGTGAATTGGATTAACTAAAATGGCAATGTGTGTGTGTCTGTGAATGAGAGTGTATGGGTGTTTCCCAGTACTGGGTTGCTGTGGAAGGGCATCCACTGCATAAAACATATGCCGGAATAGTTGGCGGTTCATTCCGCTGTGACGAACCTTGATAAAATAAGGGTTAAAGCTGAAGGAAAATGAATGAATGAATAAAATATAGCAATTGCAGTGTTTTTGTCGTTTAATCATCTAATGTGCAAACCGTTACCTTTATGAGTTTGTCTGTTTATTTTGTCCAGCTGATGAAAGATGTCAACTGTACTGCCAGTCAAAAGAGACCGGAGACGTGGTGTCCATGAAGAGGATGGTGCACGATGGCACTCGCTGTTCCTACAAAGACCCCTACAGCGTGTGTGTGCGTGGAGAGTG[T/A]GAGGTAAAGGTTATTCAAACACACCCATCCCTCCAGTTCATCCTCCAAAATGCCATAGAATGAATAATATCAGGCCTAATCAGACTTCTTTCCACTTCTCACTGCCAGGTACGGTGTTGATTTACTAAAATCGAAAGGCCTGTGTTTTGATTTGTTCTGTTATGGCTGGAAAACATGACTGCGAAATTTGATTGACGAACTACATGCCGTGTTTTGCTACTGGAACTAAAAGATAAAGTGCATTCCAGGATGTATTGCTTTTTAATCTGAGAGGGATATGAATGTCTGGAAAACCATGGGTCTGAAAGTGAATTGGCACTCAGCAAGGGAAAGATTGTTTCCATGCATTTGTGTGCGTAAGAGTGTTTCCTAGGTGAACGTCTTACATTTATATTGATGTGTATTGTTTTTAATGCCAAATAGAGATACTGGTAGGGATTCGGATTGAGAAATGTTATACTAAAGGTGCTGTTTGTAAGGTTTTGACTCTTCTAAATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29631
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 |
---|---|---|---|---|---|
ENSDART00000114158 | Essential Splice Site | 1035 | 1295 | 21 | 22 |
ENSDART00000147203 | Essential Splice Site | 997 | 1257 | 20 | 21 |
The following transcripts of ENSDARG00000075930 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 31287804)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 32487274 |
GRCz11 | 21 | 32520532 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCTCTCCAGAGCAGACCCAGAGTTCCCGGCACCAAAGATCTCCTCAA[G/A]TAAACGTCCCGTTTCCAGTCATCAGCCTGCCGTGTGCTGCATGGCCGCTC
Long Flanking Sequence:
GAATTTACAGCATAACCTAAAAATAAACAGATCATTATCAGTCTTCTGTGTGGACACAAATATATTTATCATTACTGTATATTTATATGTATCATTATCATGCTTCGTGTGAATAGGCCTTAAAGGTGCAGTATTTAAGTTTGACACTCAGTGGTTGAACTAGGTATTGCACCCCTGGTACAAAACACATGCAAGCGCAGGTTGCCAGATTGACAGCTTGCCTGACTATTGAGCATAAAAGCTGATTTAAGTCGTGTTCTACATAAAAGCAACATCATGCAATAGAACGAAGATTTCCCATACTAAAACGATTTGTGATTCGGGCATAAAGAAATCTCTGAAGGATGAGTAAATAATGACCAATTTTTCACTTTATTTGGCTCAACTAACACTTTAAATCATCTCTCTCTCCCCCAAACTCACAGATGACAGAGGCAACTTCCTGATCCAGTGGCTCTCCAGAGCAGACCCAGAGTTCCCGGCACCAAAGATCTCCTCAA[G/A]TAAACGTCCCGTTTCCAGTCATCAGCCTGCCGTGTGCTGCATGGCCGCTCGCTTCTGGACCCTGCCTCTGTCTCTTACGCTATGGCTCTGTTACACTCTGTCCTGACCGCTTCTCTGTCCTTCTCAGAGTCTTAACTTTCCCTTCATCCAAGGGAATTCTGTGGGCTATTTCTTTCCTCTGCCCTTGTTGGCTCTTCTGCAGGGCTGAGGGCTAAACGCGGCCTGAAAGTGCATTGAAAGGGGGCAGTATAGGTGCCTGTGAAGAAGAGGCCTTGTTTTGAGAAGCTGTGACGGTTGTGCTACGTCAGGTAATATGGATATGACTGTTGTGACGATTTCCAGGGTGAAAATCACTCAGTGACACAAACTCCTCTGGGAAGGTACCATTGTGGTACCATTGGAGCATTTAGTGAGTTTGTTCCCCAAATAATTATACAATATAAAATAATATATCACTAAAATAACAATGTGAGCCATAACCCTTATTTATTTTCCCTGTC
Associated Phenotype:
Not determined