Busch Lab

ZMP

adam9

Ensembl ID:
ENSDARG00000010070
ZFIN ID:
ZDB-GENE-040912-127
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

This allele has been removed from public view.

Allele Name:
sa27265
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
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 60 271 2 10
ENSDART00000132297 Essential Splice Site 60 816 2 23
ENSDART00000132810 None None 73 None 3

The following transcripts of ENSDARG00000010070 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 48079933)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 45918191
GRCz11 8 45926070
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCGAGACGCATCAGCAGACAGAGGAGAAACCAGGACAGTGCAGATAAG[G/A]TAAACATTTAGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC
Long Flanking Sequence:
ATACCCTAATTATGAAATGTTCTTTCTCCCATGTCCTCTTTATCCTTTTTGGGAAACCAGCACAGGAAGTCTCATCCAGCTTTCTAAGTGATGAGTCAGGAGCGGCTGGAAAACTTCAGCTTCCTGAGGTCTTTCTCACTCCATGATATCCAACGCTGCAGTATTTTATTACTGGAGCATTTGGCACTTGAACCAGTCAACTGCACTCACTCTAATTACCCATGATTACAGTAGAAGTGCTTATTTACAGATAAGCATGTTGAAGTGAGAGGAGCAATAGATGGAGAAATAGACCATAACTGCTGGTAGATTCAGTGCAGGTTTTCTTGCTTTGCTTGTGTAGTTCATCATGTTGGTTGTTATGGGTAGACTATATTGTGACTGAAGTGTCTCTGTTTGTAGGTTCAGTAACCCAGCAGACGTCTCAGCTCTCTTCATATGAGGTGACGGTACCGAGACGCATCAGCAGACAGAGGAGAAACCAGGACAGTGCAGATAAG[G/A]TAAACATTTAGCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTAGTTTCAAGCTTTAAATTGGAAAATTATCAAAAAATAAAATTTTTGAGCAAGGTGCTAATGGTCCAATTCGATTCAATTATTTATGCTAAGCTTAGATAAAAGTGACACCTAAATGCATTTAGAAATGGTAAAACACAACCGTTTACCTCTTGGTGACTTATAAAATGAGCTTATTTCCCACCCAAAAAGTGGAGTGTTTCTTTTAAGCTGTAGGGAAAGTAAAGAACTAAAAAGTTTTAAAGCCGTTTACACCAGGGCTATTCGATTAGTTTGTCATGGGGGACAGTTCTTGAAAAGTGTCCCTAATGAGGGGCCAGAGAGATCTGACTTGCAATATGAGTGATGACACAACAGCAATATAAGTTGTAAGCTATATGTTGTATTTTTGCTCCTTTCTACCTTAACATGTTAA
Associated Phenotype:
Not determined

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.
Availability:
Order Allele From ZIRC
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

This allele has been removed from public view.

Allele Name:
sa27264
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000040066 Essential Splice Site 106 271 4 10
ENSDART00000132297 Essential Splice Site 106 816 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 48060925)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 45899183
GRCz11 8 45907062
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTATGCCAAAGATGGCTCGCTGGTCACGGAGAAATTAAATACGACTG[T/C]AAGTCTGAAAATGAATGATCTTTTTAGCCCACAAAGAACTTGCTTTTTAA
Long Flanking Sequence:
CTACCTTGTTAAATCATTGTTGACAACTACTGTGTGAAATCATTAACATGATCAATGTCTTCACAGAGATGAATATTATTAATTATTAATAACAACATATAATTAAAAGTAAAATACAAAAAATCTGTTATTTAATAACTGGTAGCCCTTCACACTAATCGGTACCCAAGAAGTAGCTCTCAGTTTCCAAAAGGTTGGTGACCCCTGAGTTAGACTTTACAATTTAGACTTAACACTGAGTTCAAAAAGGTCAACCCAAACACCAAGCATTTCAAATTTTTGTTAACAAAATACATTTCAGACTGTAAGTAGGTGCACTACTATTCAATATAAGCTGACTGTGTGTGTTTGATGCGAGACTGTTATATTTCTGCAACAACGAATGCTCACATAGTTTTATGTTTGTTTGTTTTTTCCTAGATTGCTACTTCCAGAAGACTTCACTGTGTACTCTTATGCCAAAGATGGCTCGCTGGTCACGGAGAAATTAAATACGACTG[T/C]AAGTCTGAAAATGAATGATCTTTTTAGCCCACAAAGAACTTGCTTTTTAATACAAGTATCCAACAGTATCAGTTGTCTAGATTTACCTATATCTGTACGTCTTTCAGATGTGCACTGCAAAAAAAGTCTTCTTACATAGATTTGTTTTCTTGTTTCTAGTCCAAATATCTACAAATCCTTAAATCAAGAAGCATTTTCTAGACAAGCAAAACATATAATCTTGTTTTAAGAAATAATATGCCAAAATGAAGTGAGTTTTTCCTCAAATCAAGCAAAATAATCTGCCAGTGGGGTAAGCAAAATAATATTGTTTTTCGATTTGTGATAAGATTATTTTGCTTACCCCATTGGCAGATTATTTAGCTTGATTTAAGGAAAAACACTTCATTTTGACATATTATTTCATAAAACAAGACAATATGTTTTGTTTGTCTAGTAAATGCTTTTTGATATAAGAACTTTTAGATATTTGGACTAGAAACAAGACAAAAAGTCTAAGT
Associated Phenotype:
Not determined

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.
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