ZMP
adam9
Ensembl ID:
ZFIN ID:
Description:
a disintegrin and metalloproteinase domain 9 [Source:RefSeq peptide;Acc:NP_001004678]
Human Orthologue:
ADAM9
Human Description:
ADAM metallopeptidase domain 9 [Source:HGNC Symbol;Acc:216]
Mouse Orthologue:
Adam9
Mouse Description:
a disintegrin and metallopeptidase domain 9 (meltrin gamma) Gene [Source:MGI Symbol;Acc:MGI:105376]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1421 | Essential Splice Site | Available for shipment | Available now |
| sa41289 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1421
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 |
|---|---|---|---|---|---|
| ENSDART00000040066 | Essential Splice Site | 80 | 271 | 4 | 10 |
| ENSDART00000132297 | Essential Splice Site | 80 | 816 | 4 | 23 |
| ENSDART00000132810 | None | None | 73 | None | 3 |
The following transcripts of ENSDARG00000010070 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 48061006)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 45899264 |
| GRCz11 | 8 | 45907143 |
KASP Assay ID:
554-1342.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGCAACAACGAATGCTCACATAGTTTTATGTTTGTTTGTTTTTTCCTA[G/A]ATTGCTACTTCCAGAAGACTTCACTRTGTACTCTTATGCCAAAGATGGCT
Long Flanking Sequence:
TTAAAATTACTTTATGTTAGTTTTTAAAAAAACCTTTAAAAATAATTTCAGACAAATGAAGTGTTGCATATTGATATTTATCTACCTTGTTAAATCATTGTTGACAACTACTGTGTGAAATCATTAACATGATCAATGTCTTCACAGAGATGAATATTATTAATTATTAATAACAACATATAATTAAAAGTAAAATACAAAAAATCTGTTATTTAATAACTGGTAGCCCTTCACACTAATCGGTACCCAAGAAGTAGCTCTCAGTTTCCAAAAGGTTGGTGACCCCTGAGTTAGACTTTACAATTTAGACTTAACACTGAGTTCAAAAAGGTCAACCCAAACACCAAGCATTTCAAATTTTTGTTAACAAAATACATTTCAGACTGTAAGTAGGTGCACTACTATTCAATATAAGCTGACTGTGTGTGTTTGATGCGAGACTGTTATATTTCTGCAACAACGAATGCTCACATAGTTTTATGTTTGTTTGTTTTTTCCTA[G/A]ATTGCTACTTCCAGAAGACTTCACTGTGTACTCTTATGCCAAAGATGGCTCGCTGGTCACGGAGAAATTAAATACGACTGTAAGTCTGAAAATGAATGATCTTTTTAGCCCACAAAGAACTTGCTTTTTAATACAAGTATCCAACAGTATCAGTTGTCTAGATTTACCTATATCTGTACGTCTTTCAGATGTGCACTGCAAAAAAAGTCTTCTTACATAGATTTGTTTTCTTGTTTCTAGTCCAAATATCTACAAATCCTTAAATCAAGAAGCATTTTCTAGACAAGCAAAACATATAATCTTGTTTTAAGAAATAATATGCCAAAATGAAGTGAGTTTTTCCTCAAATCAAGCAAAATAATCTGCCAGTGGGGTAAGCAAAATAATATTGTTTTTCGATTTGTGATAAGATTATTTTGCTTACCCCATTGGCAGATTATTTAGCTTGATTTAAGGAAAAACACTTCATTTTGACATATTATTTCATAAAACAAGACAAT
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:
sa41289
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 |
|---|---|---|---|---|---|
| ENSDART00000040066 | Nonsense | 114 | 271 | 5 | 10 |
| ENSDART00000132297 | Nonsense | 114 | 816 | 5 | 23 |
| ENSDART00000132810 | None | None | 73 | None | 3 |
The following transcripts of ENSDARG00000010070 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 48051931)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 45890189 |
| GRCz11 | 8 | 45898068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTTTCTCTCTATTTTTCCCATCAGGATCATTGTCATTATAGTGGTTA[C/A]ATAGAGGATGTGGAGGGCTCTTCTGCAGCACTCAGCCTGTGCTCTGGGTT
Long Flanking Sequence:
AATCAATGCTTTTTGCTTTTGTATTTCTGAACTGATTTTCTCGAGCTGCTCCGTGTCTGATGTCACAGTCTGATTCATTTGCTCTGAAAAGGGCTTGTTTTCTGGCCACACTCACATTTCACCATGAACACACAGCATTAAAGAAACACATGACTCATTGTTATATGTGCTCGCTAATGCATTCAGAAAAGTATAACGATTAGCAGTTATTGAATGCTAAAGCAGACAGAATTGAAGTGTGTATGTTTTCTTTAAATCAGTGTGTTAGTCTATAACAGTCTAGTTCGCCTCTAGTGGAAAACTGCTGCTTTCTAGCTACGGTTTGTTACCTGAAGAGCAAACACCCTGAGCTGCATTTAGGTTCTGAATGCTAAGAATGTTGCTGGTTGTTATTGAAGACATTGAATTTTTATTATATTTTTTTAATTCTTGATTTATTTTACTGAGGTGTATTTTTCTCTCTATTTTTCCCATCAGGATCATTGTCATTATAGTGGTTA[C/A]ATAGAGGATGTGGAGGGCTCTTCTGCAGCACTCAGCCTGTGCTCTGGGTTAAGGTGAGATCACTTTAAATGGATAGAGGGCAAAACTGTTGCTTTAAAAAAAACATTATTAAATGTCTTAAGTTTTATGTTTGTACAACTCATGTTATTAAACTCAGATAGTATTCTTGCATTAAAACAAATGCAATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATTATATAATATAATATTATATAATATAATCAATTATTTATTTATTTATTTATCTATTTATTTTTACTTATTTATTTATTTTAATCTCATAATAACAGTAATAATAAAAAAAATAGTCGCATTTTCATAATCTAGTCAGATCTCAGTGGATAAATTAAATGAAAATAAATGACTGTCTGTCTTGGATTGGATTGTGACATTTTTAACATTTTTGTAACGTCTTTAAATTTTGAATGCATTTAATATTATT
Associated Phenotype:
Not determined