ZMP
ADAM33
Ensembl ID:
Description:
ADAM metallopeptidase domain 33 [Source:HGNC Symbol;Acc:15478]
Human Orthologue:
ADAM33
Human Description:
ADAM metallopeptidase domain 33 [Source:HGNC Symbol;Acc:15478]
Mouse Orthologue:
Adam33
Mouse Description:
a disintegrin and metallopeptidase domain 33 Gene [Source:MGI Symbol;Acc:MGI:1341813]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34212 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34213 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27079 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10412 | Nonsense | Available for shipment | Available now |
sa18897 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34212
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 |
---|---|---|---|---|---|
ENSDART00000083255 | Nonsense | 16 | 944 | 1 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 61774411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 60993039 |
GRCz11 | 7 | 61303201 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGATGTATACCAAACACAGGCAGAAAAGCGGACACATTTCATCGACA[C/T]GATATGTGCTTGTAATGTTATCTGTTTTTCTGTTCAATGGCTTACTGGAA
Long Flanking Sequence:
CAAATTTATGAAAAATGTATAGTTTACTAATTGTATTTTTTTTATTCTGTGGAAATAGATTTCCATATGCTCTAGTAATATATATCTTGCCTCGCCAGGGAGACCCTCTATTTCAGACTAACAAACCAGTTTAGGCTGTTTTAAGCTGTTTTTTCTCCTCTCTCAGCAGGGGTCTGCTGAATACAGTGATCAATGAGTCATAAATTCACTATGCCCGGCAGGAAAGCCCTGGCAATGCGCGCGTGCTTTCAAGTGCCCAAGGCTTCTCGATTCGCATCCTTCGTGCTTATCTACTCTTTAGTAGGACAGTTTAACGAACATATGATGGTTCGCGCAAATCGAGAGGGCAGAGCTTAGCAGACTCAGTTCAGTTCCATCCATTTCTTATTTCCTCTCACGCTGGCGAGTGAACACAGTGCGAGGCGAGGCGGAGAACAGCACCGACCGCCACAGGGATGTATACCAAACACAGGCAGAAAAGCGGACACATTTCATCGACA[C/T]GATATGTGCTTGTAATGTTATCTGTTTTTCTGTTCAATGGCTTACTGGAATATGTAGGCGGAAATCCTCGGGAAGAAGGTAAGACACCGCTTTCTTACTTGGAAAGTTGCTCTCTTTTATCAACCAGTTGCGCGCATCCGTGAAGAAGTTTTTTTCAAGGCAAAACGCATTTGAAGCGTTTAGAAAAGTGCAGATTTGTTGCACAGATATGTCGTTTGCTTAGATTAATGTGTAAAAAAATGCATTTAAGAAATAATTCATGAGTGATTTTCTTTCTTTCCATGATGATGTCCACTAATGCAAGACTATAACCTCTCTGTTTTTAACAATCCTAATGTACACTTAAGAACATGCCAGCAGTTGTAGAAAGACCCGAAATACAAGAGCAGAATGAAAATTTGACATGAACTGGAACCTTGCGAATTGTTCAAGCGAACGGTACTACTGAAATTGAGACATAAAAGTTGATCCTCCGAAACCGGTTCGTTTTCACAGCTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34213
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 |
---|---|---|---|---|---|
ENSDART00000083255 | Nonsense | 190 | 944 | 6 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 61940256)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 61158884 |
GRCz11 | 7 | 61469046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGACCTGCCCATCAAAAGTGGCACCTGTGGACACAGCCATCACACTGGA[C/T]AAATGAGCCTGTTCAGTGGAGACTTTAAACCTTTGCATCAAAGGGTCAGT
Long Flanking Sequence:
TATAAATCACCCATGTCTTGAGGTAGTACATTATGATGTGATTTACCTTCTATGTGTGATTTGATTGGACAGGAATCAAAGGACTGATTTTTCTAATCCCCATAGACAAGAAAAAATAAAATAGTGAGTGCAGGTTCAAGGAAAGTACCGATACAGTACTAAAAATGTACTCTAGGGAGAGTAAAACTATTTTTTAAACATTTTTAAACTACTGAGTAAATTACAATTCCTGAGGAAAAACTACTCAATTACAGTAATATAAGTATTTGTAATTAGTTACTTTACACCACTGCTAATTGCTATTGACAGATCTGAAACTAGACAGCATTTAAACTAACATTCATCCAATTTTCCTCTGCAGAGGTCTGATTGTCTTAAACTCAAATGACACGTTCTACCTGGAGCCAATCAGAGGCCAGGAGGTTGTGCACCACGCCTTCTATCGCACTGAAGACCTGCCCATCAAAAGTGGCACCTGTGGACACAGCCATCACACTGGA[C/T]AAATGAGCCTGTTCAGTGGAGACTTTAAACCTTTGCATCAAAGGGTCAGTCGCAAATTCTTGTTATGGAATTCTCATTTTAGGGGGCTCATTCCCCAACGAATGTACAATAATAATAATAATAATAATAATAATTAAAAAATAATAATAATAATTATAATAAAATTAAAACAGTATACATTACATTACAATATAATGTTTAAACACAAATATTAGAAGCATTTTTACAAACCAAATTTTACTCTAAATTTTAGAACTTAAACTTCTTTTGTGTTTCTATTTATTAAAAGAAAACAAACAACTTTAGTACTTTTTAATTCAAAGTGACAATAAACTATATATATACATACATAAAGACTTTAGTCTAGCACAGTGTCTGAGAGATGCAATGCAATTAGATTCCAGCAACAAGCCCTGACTTGATACCAGACTTGGCAAGACAGAAATACAGAAATATTTAAATACCAGAGACATTCAGAAGCACAGAATCATGCACTGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27079
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083255 | Splice Site, Nonsense | 536 | 944 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 61966571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 61185199 |
GRCz11 | 7 | 61495361 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGCATGTGTCTGACCCATGAACAGCAGTGCCTGCAGCTGTGGGGTTA[C/A]GGTAAGATACATGCTGGCTGGCCGTGTGCCTTTAGTTTTCACAGAAATCA
Long Flanking Sequence:
TACACAAATATTAATTTCAACATTTAATAAAACTTCATTAAAATCAAATAATTTATCTACTAATGTTTAAACTGGGTATATTCTCTGAAGTCTGCTTATCATTTTACTTGCTACTTTATCACTTGCTCAGATTCAATGCTAGTAAGGCATTTACAGTAGTCGTCATCTTTGTTTCTGCATTCTAGAGAAACACCAGCGGCTACACTTTCATATCACTATGTTCTCTGTATGTAGTTTGCCCACCACCTGCTCTCTTCTTCTTTCATCAAAGTTCTCTAGTCTTCTTATCGTGCCCTCTGCCCACAGCTAAAGCAGGCTGGCACCATGTGCCGTGGACCAGCCGGTGCCTGTGATCTGCCGGAATACTGCACAGGAGGCTCTCCTTACTGCCCTTCCAACGTTTACCTCCTGGATGGGTCATCATGTCAGTATGGTCGTGCCTACTGCTATAATGGCATGTGTCTGACCCATGAACAGCAGTGCCTGCAGCTGTGGGGTTA[C/A]GGTAAGATACATGCTGGCTGGCCGTGTGCCTTTAGTTTTCACAGAAATCACATTTGAAAGTCATTTTATGGATTCATTCACTCACAGAAAAAAATGGTACAAAGTTCTCAGAAAAAAATGGTACTAAGTTGTACCAAAGAAGGTAAAAACCTTTGTCAGTGGGGCAGTACCTTTTTATGGGACAGAATTGTACCTTAAGACAAAGAAACTAATTTGTACCATTGCAGTTTGTACCATTAAGAACATGAATTGTACCATGGAAAACCAAAATATCCCTTTGGTGTTTAATACCTGCAGATACAATATTGTACCTTCATCAAAGGTACAAATCTGATCCATGAAGGTATACCTCAGTGACAAGATATTTTATACCTTAACAGTGTCAAAAATGCTCACCAAACATTTATTAAAATTCCTTAAATGTTTAGTTTACAATACCTGTAGTTTTGTTTTAACAGCTGTTTTGCATTATAGAACTTAATAATGAATGTTTATGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10412
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083255 | Nonsense | 934 | 944 | 23 | 23 |
ENSDART00000083255 | Nonsense | 934 | 944 | 23 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 62002515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 61221143 |
GRCz11 | 7 | 61531305 |
KASP Assay ID:
554-6160.1 (used for ordering genotyping assays)
KASP Sequence:
GAACCTAATGAGTGTTTTTTTTTTTTTTTTTCAGACCTGCTTCTGGACCC[A/T]AACCACTYATAGTTCCAGCCGTTTTCCGGAAATGACGCTTGCAGGATTTA
Long Flanking Sequence:
AGTTGCCTTTTCTAACCTTAAATGGGTTTAGACTCGGTTTATATTTCTGATGATATTGCTTAATCTCCAACAGTGAAGTGAATCGCTGATTCTCTGGCAAGTAATGGATCAAACTGAAAAATGAAAATCCACTATTCTACTTACGATCATTCTCATGCTCAAGTGCTTCCAAACCTTTATGACTTTCTTTATTCTGTTAAACACAAAAGAAGATATACTTCCAAACCATGACTACCATAGTAGGAAAAACATGTACTAATAATCATTCCGGCTTTTTTAGCATTCTTCAAAATAACTTATTTTGTGTTGAACAAAATAAAGAAAGTCAAACAGGTTTTGAAGAACATGAGGGTAAGGAAAAGATGACAACTTTCAGTTTCTTGGTTTTGTCAACCCCAAACTTGCTTTTAATATTGAGTTTGTTTAACTGGCTTTGTGGAACAGGTCTCTGAACCTAATGAGTGTTTTTTTTTTTTTTTTTCAGACCTGCTTCTGGACCC[A/T]AACCACTTATAGTTCCAGCCGTTTTCCGGAAATGACGCTTGCAGGATTTATTTTGAAAGACTGCAACCAGCCTATTTGCACTATAAAGCACCCTTGGCGACTGGTACTACATGGAAGTGTCTCTCAAGGGATGGAAGAGCTTGGTGCTATGGCCGTGAACGAGGCCTCTGAAACTGGCGTTCAACTAAAGCCGGGCACAGCAGAGATGACGCGGTTTTGCATGAACACATGCAGACTGAGAATGTTTTGGATAGACCATCACATTGCCAAAACCTCGACTTTTTATCACCTTGCAATTTTTTGTACTTATTTGTTGTTGCGTTTTAATGTTATGGCTCCGTCTTGTTTACATTTTTCATTCGACTATCATCTAATTGTCAAGTGCCAAAGATGTTGTTTTTTTTAATGCCTTGATTGTTTCATTTGATCTACTGTGCTGTTTCAGATTTTGTGTTTGGTACATTAAACGTTAAATCTTTTTAGTAAAGACTAAATGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18897
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083255 | Nonsense | 934 | 944 | 23 | 23 |
ENSDART00000083255 | Nonsense | 934 | 944 | 23 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 62002515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 61221143 |
GRCz11 | 7 | 61531305 |
KASP Assay ID:
554-6160.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCTAATGAGTGTTTTTTTTTTTTTTTTTCAGACCTGCTTCTGGACCC[A/T]AACCACTTATAGTTCCAGCCGTTTTCCGGAAATGACGCTTGCAGGATTTA
Long Flanking Sequence:
AGTTGCCTTTTCTAACCTTAAATGGGTTTAGACTCGGTTTATATTTCTGATGATATTGCTTAATCTCCAACAGTGAAGTGAATCGCTGATTCTCTGGCAAGTAATGGATCAAACTGAAAAATGAAAATCCACTATTCTACTTACGATCATTCTCATGCTCAAGTGCTTCCAAACCTTTATGACTTTCTTTATTCTGTTAAACACAAAAGAAGATATACTTCCAAACCATGACTACCATAGTAGGAAAAACATGTACTAATAATCATTCCGGCTTTTTTAGCATTCTTCAAAATAACTTATTTTGTGTTGAACAAAATAAAGAAAGTCAAACAGGTTTTGAAGAACATGAGGGTAAGGAAAAGATGACAACTTTCAGTTTCTTGGTTTTGTCAACCCCAAACTTGCTTTTAATATTGAGTTTGTTTAACTGGCTTTGTGGAACAGGTCTCTGAACCTAATGAGTGTTTTTTTTTTTTTTTTTCAGACCTGCTTCTGGACCC[A/T]AACCACTTATAGTTCCAGCCGTTTTCCGGAAATGACGCTTGCAGGATTTATTTTGAAAGACTGCAACCAGCCTATTTGCACTATAAAGCACCCTTGGCGACTGGTACTACATGGAAGTGTCTCTCAAGGGATGGAAGAGCTTGGTGCTATGGCCGTGAACGAGGCCTCTGAAACTGGCGTTCAACTAAAGCCGGGCACAGCAGAGATGACGCGGTTTTGCATGAACACATGCAGACTGAGAATGTTTTGGATAGACCATCACATTGCCAAAACCTCGACTTTTTATCACCTTGCAATTTTTTGTACTTATTTGTTGTTGCGTTTTAATGTTATGGCTCCGTCTTGTTTACATTTTTCATTCGACTATCATCTAATTGTCAAGTGCCAAAGATGTTGTTTTTTTTAATGCCTTGATTGTTTCATTTGATCTACTGTGCTGTTTCAGATTTTGTGTTTGGTACATTAAACGTTAAATCTTTTTAGTAAAGACTAAATGTTGT
Associated Phenotype:
Not determined