ZMP
adam8b
Ensembl ID:
ZFIN ID:
Mouse Orthologue:
Adam8
Mouse Description:
a disintegrin and metallopeptidase domain 8 Gene [Source:MGI Symbol;Acc:MGI:107825]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10008 | Nonsense | Available for shipment | Available now |
sa41968 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6236 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22036 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10008
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 |
---|---|---|---|---|---|
ENSDART00000066471 | Nonsense | 241 | 819 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 9879416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 9087371 |
GRCz11 | 12 | 9125214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTWGATNNNNNGAAACAYACTAAAAACATMAKTCTTTTCTCAGTTGTA[T/A]CGATCTCTTAATATCCGAGWGATGTTGGTGGGTCTTGAGGTCTGGATGAA
Long Flanking Sequence:
ACATTTAGTAGTTTTGATCAGGACTGAGGTTGATTTATGCAACAAAAAAAAGGGAAAAATATGTGTGTGATGCATTTTTACTGCAATTTAATCCAGTGGACGTTTTCATTCCTAACATAACAAAAGGGTAGTCAATTTGAACAGTGCACAAGGGTTAAAGTTTGTTGGCCAATTGTATTAATTTCAAAACAGATATTGCCTGTTTGATTGACTTGGACAATATTTTATCTAATTGCTAATATTTCTACATTATAGATTGACCAAAAAAATATTGTAAATGTTAAGTTATGTTTTACTCTTATAGTACAGAAACTTTGGCTCTAGCATGGATTCTATCAGAGCCAGGATGCTGGAGGTGGTAAATCACGTTGACAAGGTATAAGTTCTTTTTTTTTTTTTTCAAATAGAGTCAATGCTAAATATGTTAAGTCATTAATAATTAATATAAATATTTAGATTTTTTGAAACACACTAAAAACATAAGTCTTTTCTCAGTTGTA[T/A]CGATCTCTTAATATCCGAGTGATGTTGGTGGGTCTTGAGGTCTGGATGAAACAGGACCAGATTGTGGTCAGTGTGAGTTCTGATGACACTCTCAGTCGCTTTATAGAATGGAGGAAGAGCAATCTGCTTAAAAGGGTCAAACATGACAACGCTCAGTTTGTGACGTGAGTATGACCTAATTACCTATTTACTCGGCCGGATGACTGAGATCATTCGCTACACTATAGCAGAGCCTAATGTACTGCACTTTAATATAATGCCCACACTTTACACTAATGTTTTAATGGTTGTCACTTGTTAACTACTAACTAAACTTGCACTTATTTATCACATTAAAGCTATGGTCTCAAACTGAATTCCTGGAGGGCCGCAGCTCTGCATAGTTTAGCTCTAACCACCTCCAACTCACTCCTGCTTAATCGTCTTTAGTAGTCTTGAACAACTTGATTATTTGGATCAGCTGTGTTTCATTAGGGTTGGAGCAAATCTGTGCAGAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41968
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066471 | Essential Splice Site | 324 | 819 | 11 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 9876994)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 9084949 |
GRCz11 | 12 | 9122792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATTGTTTTTTGTTTTTAAAGACAATTACACAATATGCTGTTATTTTC[A/C]GGATCATAATCAGAACCCACTGGGCCTGGCATCCACAATTGCACATGAGA
Long Flanking Sequence:
CGCAATAGTCTCTGTGGCAAGGGGGCAGGGCCCAGAGCCGTGGGAACGTAATGAGACTGCTGTGTAAGTGGATTCACCTGTAGCGCGCACTGGTCTCGAATCCTAAGGAAGGAGCTCTGGACTTTAAGAGGAGGAACGATGGCAAAAGTAAAACAATCTGTTTGGGCCCGGTCCACTCTCGGGTTCCTCGGCCATCGTTCCTCATCTGGTGAAATTGTATTTAGATTGCAATATATATTGCAAAATAAAAAAAAATCTCAATATCGTGCAGCCCAACTATTAACAGTTTTTTTTTTTTTCCTCTAGTGGAATTGATTTTTTGGGTGACACAGTTGGGTTGGCAAACAAATTTGCAATGTGTGCCGAAAGCTCAGCAGGAGTCAATCAGGTATTCATTGCCTAAATTTGCGATGATTTCTGGTATCAAATTAAATCACGATTTGGAACAAAAGGATTGTTTTTTGTTTTTAAAGACAATTACACAATATGCTGTTATTTTC[A/C]GGATCATAATCAGAACCCACTGGGCCTGGCATCCACAATTGCACATGAGATGGGTCATAACATGGGCATGTCCCATGATGAGGATCACTGCACGTGTGGCTCGTCAGTGATCAGTTCCTTCTGTATCATGACAGAGCGTGTGGGGTAAGCAGTATTTGTGTAATATCATACTGTTTTCATTTGTGCTTTGGTTAGAAGTCAGATCTCTCTGTCTAGTAGCTGGCTACCAGAAATTAAGGCAACATAGGCTCATTTTGAAAACGTAGCCCTATATATATTTCTGGAGATTGTGAATTATGTAGCAGAAGGCATGTATGGCTGCATTTCATCTTTGAAACGAATGCTACGAGGGTGATATGACACTGTTCCTTGTTGTGGTTACCAGCCGACCACTTAGCTCCGATTAGACAGCTTTCCCACTGTTACCAGTTAGTCCAGTTAGCTCGTCATGTATGTCAGAGGACTTGAGATGCAGAGAGAAGTTGGGGTTCGAGTCCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6236
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066471 | Nonsense | 638 | 819 | 17 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 9859021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 9066976 |
GRCz11 | 12 | 9104819 |
KASP Assay ID:
554-5369.1 (used for ordering genotyping assays)
KASP Sequence:
ATAAGTGCCAAGAMTTGAACATTTATGGTWGCATTGAAGRCTGTTCACTG[C/T]AGTGCAATGGTCGAGGGGTGAGATCAAAYCTYCTATTATTATATTTATAA
Long Flanking Sequence:
TTCATTAAAAAGTGAATGTTATATATATAACATCATTCTTCAAACTACTTTACGTAAATATTACTGTTTATTCTTCAAAAATGGTGTTTTACAAAAACGAAAATACTTTTACTGCCTATTTACAGCACATCCATGTGCTCTTTCTCCATCATGTTGACATAATTATCCTTTCCCCTCATATAGAAACATGTTTTGTGGAAAGATCTTTTGCAATGAAGGAAATGAATTCCCCGTTACTGGTCAGAAAGCGGTCATAGTAACATTAAGAGGACAGTGCAACGTAGCAGGGGACCAAACAGAGGAGGACGCGCTCAGCATGGTTCCAACTGGCACAAAATGTGGGCATAATAAGGTAAGCATGTAGGAATGCTACTTGGACTTGCTGTTGGAATTTATTCTTAGGCACAAAATAAGTAGTCTCGTGCTTGTTTTAACAGGTTTGCTATGATTATAAGTGCCAAGAATTGAACATTTATGGTAGCATTGAAGGCTGTTCACTG[C/T]AGTGCAATGGTCGAGGGGTGAGATCAAATCTTCTATTATTATATTTATAATTCATAGCATAAAAATACATAACTAGATTGTTACTGTTTGTTGTTTTTGCAGATTTGTAATCATAAAAAACAATGCCACTGTGATCCAGGCTGGGCACCACCTTACTGTAATGTCAAATATTCTGAATTGTCATCTGGTAAATGTTCTATTTTTCTGAAATGTCTTAAACATGTTTAAATAACCTGTAATGTTTTGACACGTTTTACTCTTCTTTCCAACAAGCAAAGACCATTGGCATCTCAGTAGCTGTTGCAGTCGCTGTGCTTGTGGTAATATGTGGAGCCGTGCTTTATCATAAAAAAAGAAAAGCCATCAGCCGCCACAAGACGTGAGTTATATTATTGACATTTGAGCTGAATACTAGTGTCTTGAAAAATCTCTAGTCAAATATTATGTACTGTCATCATGGCAAAGATAAAAGAAATAAATTAATAGAAATGAGTTAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22036
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 |
---|---|---|---|---|---|
ENSDART00000066471 | Essential Splice Site | 672 | 819 | 19 | 23 |
Genomic Location (Zv9):
Chromosome 12 (position 9858748)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 9066703 |
GRCz11 | 12 | 9104546 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTAAATAACCTGTAATGTTTTGACACGTTTTACTCTTCTTTCCAACAA[G/A]CAAAGACCATTGGCATCTCAGTAGCTGTTGCAGTCGCTGTGCTTGTGGTA
Long Flanking Sequence:
GTGCAACGTAGCAGGGGACCAAACAGAGGAGGACGCGCTCAGCATGGTTCCAACTGGCACAAAATGTGGGCATAATAAGGTAAGCATGTAGGAATGCTACTTGGACTTGCTGTTGGAATTTATTCTTAGGCACAAAATAAGTAGTCTCGTGCTTGTTTTAACAGGTTTGCTATGATTATAAGTGCCAAGAATTGAACATTTATGGTAGCATTGAAGGCTGTTCACTGCAGTGCAATGGTCGAGGGGTGAGATCAAATCTTCTATTATTATATTTATAATTCATAGCATAAAAATACATAACTAGATTGTTACTGTTTGTTGTTTTTGCAGATTTGTAATCATAAAAAACAATGCCACTGTGATCCAGGCTGGGCACCACCTTACTGTAATGTCAAATATTCTGAATTGTCATCTGGTAAATGTTCTATTTTTCTGAAATGTCTTAAACATGTTTAAATAACCTGTAATGTTTTGACACGTTTTACTCTTCTTTCCAACAA[G/A]CAAAGACCATTGGCATCTCAGTAGCTGTTGCAGTCGCTGTGCTTGTGGTAATATGTGGAGCCGTGCTTTATCATAAAAAAAGAAAAGCCATCAGCCGCCACAAGACGTGAGTTATATTATTGACATTTGAGCTGAATACTAGTGTCTTGAAAAATCTCTAGTCAAATATTATGTACTGTCATCATGGCAAAGATAAAAGAAATAAATTAATAGAAATGAGTTAATAAAGCTATTATGTTTATAAATGTGTTGAAAAAATCTTCTATCCGTTAAACAGAAATCAGAAAACAGAAATTGGTTAATCATACCAAATCACCGTATCCTACAGGGGATAGTTCACCCAAATTAAAAATTCTGTCATCAAAATTCTATCATTTATTCACCCTTCACATGTTCAAAACCTATTTGACTTTCTTTCTTATATTGCTGGTCACTGGAACCCACCCAGCTGGCGTGGCCCCTCTGTACTCCAACGTCATGGGACGTTGCATTTTGTTTGA
Associated Phenotype:
Not determined