ZMP
abp1
Ensembl ID:
ZFIN ID:
Description:
amiloride-sensitive amine oxidase [Source:RefSeq peptide;Acc:NP_001071066]
Human Orthologue:
ABP1
Human Description:
amiloride binding protein 1 (amine oxidase (copper-containing)) [Source:HGNC Symbol;Acc:80]
Mouse Orthologues:
1600015I10Rik, Abp1, Doxl2, Svs1
Mouse Descriptions:
RIKEN cDNA 1600015I10 gene Gene [Source:MGI Symbol;Acc:MGI:1917011]
amiloride binding protein 1 (amine oxidase, copper-containing) Gene [Source:MGI Symbol;Acc:MGI:19237
diamine oxidase-like protein 2 Gene [Source:MGI Symbol;Acc:MGI:3618290]
seminal vesicle secretory protein 1 Gene [Source:MGI Symbol;Acc:MGI:2682321]
amiloride binding protein 1 (amine oxidase, copper-containing) Gene [Source:MGI Symbol;Acc:MGI:19237
diamine oxidase-like protein 2 Gene [Source:MGI Symbol;Acc:MGI:3618290]
seminal vesicle secretory protein 1 Gene [Source:MGI Symbol;Acc:MGI:2682321]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44196 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12589 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44196
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 |
---|---|---|---|---|---|
ENSDART00000087422 | Nonsense | 178 | 742 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 24 (position 41580286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 40119480 |
GRCz11 | 24 | 40007327 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATAAGATTCTGCAGGAGAGCACCGGGTTTACTTACGGCAACTGCACT[A/T]AACGCTGTCTGACCTTCTCTGATATCGCTCCCCGCGGGCTAACGTCAGGA
Long Flanking Sequence:
CTCTGGCTTCATCCTCCGCTTCATCACGAACGCGGGAATGGGCTCATCACGGGGCGATGATGTTTGCTGACCTCACTCCGCAAGAAATGTACGCGGTGAGGGATTACCTGTACTCCTGCAGCGAGCTGGGCCTCACCTCAGCACGGGGAACATCCCTCAAGAAGAACAGCATCCTCCTCATGGAGCTGCATGTTCCCCGAAAGCATGAGGCGCTGCGTGCACTGGACAAAGGACAGGCCAAACCATCCCGCCAGGCACGTGTGGTGGTGCAGTTCGGCAACCAAGCGGTGCCAAATGTCACTGAATACATCGTTGGCCCACTTCCATTCCCGAAGACTTACCATCTGAAAACATTCAAGAACAACAAGAACATCCGCTTTGAGTCCCGGCCGATCTCTGCAGTGGAGTACGAACACCTAAGTGGGGTTTTGGACAAAGTGGGATCTAAAGTGAATAAGATTCTGCAGGAGAGCACCGGGTTTACTTACGGCAACTGCACT[A/T]AACGCTGTCTGACCTTCTCTGATATCGCTCCCCGCGGGCTAACGTCAGGAGAGAGGCGGACCTGGATCATGCTGCAGAAGTTTGTGGAAGGATACTTCATCCATCCAGTAGGCTTCGAGGTCCTTGTTAACCACAAAGATCTGGATCATGAAAAGTGGACGGTGGAGAAGGTGTGGTACAACGGGCAGTATTTCGACAGCTTGGATGAATTCGTGGAGAAGTATGAGAAAGGGACGGTGGATAAAATCAAGCTTCCGGAGCATGATGAGGAGGATCTTTTCTCCACTTACATTCCCAGGGGAGACATGAACACACGGACCAACATCCATGGAGCAAAGCTTGTTGAACCACAAGGGCGCAGATTTCAGGTGGATGGGAATTTCGTGGAGTATGCCGGATGGTCCTTTGCTTATCGGGTTCGCTCTTCAGCTGGTTTGCAGATCTTCGATCTTCGCTACAATGGAGAGAGAATTGCTTATGAAATCGCTCTTCAGGAAGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12589
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087422 | Nonsense | 295 | 742 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 24 (position 41579935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 40119129 |
GRCz11 | 24 | 40006976 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGACATGAACACACGGWCCAACATCCATGGAGCAAAGCTTGTTGAACCA[C/T]AAGGGCGCAGATTTCAGGTGGATGGGAATTTCRTRGAGTATGCYGGATGG
Long Flanking Sequence:
CATTCAAGAACAACAAGAACATCCGCTTTGAGTCCCGGCCGATCTCTGCAGTGGAGTACGAACACCTAAGTGGGGTTTTGGACAAAGTGGGATCTAAAGTGAATAAGATTCTGCAGGAGAGCACCGGGTTTACTTACGGCAACTGCACTAAACGCTGTCTGACCTTCTCTGATATCGCTCCCCGCGGGCTAACGTCAGGAGAGAGGCGGACCTGGATCATGCTGCAGAAGTTTGTGGAAGGATACTTCATCCATCCAGTAGGCTTCGAGGTCCTTGTTAACCACAAAGATCTGGATCATGAAAAGTGGACGGTGGAGAAGGTGTGGTACAACGGGCAGTATTTCGACAGCTTGGATGAATTCGTGGAGAAGTATGAGAAAGGGACGGTGGATAAAATCAAGCTTCCGGAGCATGATGAGGAGGATCTTTTCTCCACTTACATTCCCAGGGGAGACATGAACACACGGACCAACATCCATGGAGCAAAGCTTGTTGAACCA[C/T]AAGGGCGCAGATTTCAGGTGGATGGGAATTTCGTGGAGTATGCCGGATGGTCCTTTGCTTATCGGGTTCGCTCTTCAGCTGGTTTGCAGATCTTCGATCTTCGCTACAATGGAGAGAGAATTGCTTATGAAATCGCTCTTCAGGAAGCCATAGCCTTCTACTCCGGAGATACTCCAGCAGCCATGCAGACCAAATACATTGATGCCGGGTGGGCGATGGGGACGTCAGATTATGAATTATCACCTGGGATCGACTGTCCAGAAATTGCTCACTTTGTTGACCTCTACCATTACTACGACACAGACAAACCTGTGCGCTACAGAAACGCACTCTGCATCTTTGAAATGACCACTGGCATTCCTTTAAGGAGGCACTTTAATAGCAACTTCCAAGGGGGCTACAATTTCTACGGAGGCCTGGAAAATCATGTTCTGGTGATCAGAACTACATCTACAGTCTACAATTATGATTACATCTGGGACTTTGTCTTCTACCAGAAT
Associated Phenotype:
Not determined