ZMP
zgc:113006
Ensembl ID:
ZFIN ID:
Description:
amine oxidase, copper containing 3 [Source:RefSeq peptide;Acc:NP_001013573]
Human Orthologues:
AOC2, AOC3
Human Descriptions:
amine oxidase, copper containing 2 (retina-specific) [Source:HGNC Symbol;Acc:549]
amine oxidase, copper containing 3 (vascular adhesion protein 1) [Source:HGNC Symbol;Acc:550]
amine oxidase, copper containing 3 (vascular adhesion protein 1) [Source:HGNC Symbol;Acc:550]
Mouse Orthologues:
Aoc2, Aoc3
Mouse Descriptions:
amine oxidase, copper containing 2 (retina-specific) Gene [Source:MGI Symbol;Acc:MGI:2668431]
amine oxidase, copper containing 3 Gene [Source:MGI Symbol;Acc:MGI:1306797]
amine oxidase, copper containing 3 Gene [Source:MGI Symbol;Acc:MGI:1306797]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6037 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40100 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6037
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027258 | Nonsense | 459 | 754 | 1 | 4 |
ENSDART00000124160 | None | None | 223 | None | 4 |
ENSDART00000140117 | Nonsense | 451 | 746 | 1 | 4 |
The following transcripts of ENSDARG00000014646 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 33063142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32794452 |
GRCz11 | 3 | 32926166 |
KASP Assay ID:
554-3783.1 (used for ordering genotyping assays)
KASP Sequence:
ATRGCGAACAGCGCCCTGGTGATCCGCTCCATTACTGCTATAGGGAACTA[T/G]GACTACATATGGGACTTYATTTTCTATCAGAGTGRCTCAGTGGAGGCAAG
Long Flanking Sequence:
AGGGAAAAGCCTACTGGCCTAGGACCACAACAGTATTATCTTCAAGGTAAACGTTTCAGCGTTAAAAACAACCAGGTGGTTTATTTAGACTGGAACTTTGCATTTGGCATGAGCTCTCTGACTGGGATGAGAGCGTTTGATATTCGTTTTGAAGGGCAGAGGATAGCGTATGAGCTGAGCGTGCAGGAGGCGATGTCTGTCTACGGCTCCACCACACCTGGGATGATCCTCACCAAGTTCCTCGACTCCAGTATCGGAATCGGTCGCTTCGCTCACGAGCTCGTGCGCGGGATCGACTGCCCGTACGGGGCCACATATGTAGACACGCACCGCTACATCGACACGAACGTCACGCAGCGTTTCAGAAACTCCATCTGTGTGTTTGAGCATGACATCGGGCGACCTCTGCGACGACACTTCTCAGATTTCTTTCACAATAGTTACGGTGGGATGGCGAACAGCGCCCTGGTGATCCGCTCCATTACTGCTATAGGGAACTA[T/G]GACTACATATGGGACTTCATTTTCTATCAGAGTGGCTCAGTGGAGGCAAGAGTTCACGCCACCGGCTACATATCATCCTCCTTTTTGGTTGATGGAAATCTGAAGTATGGTCACCAGGTTGCAGAAAACGTCCTAGGAAACATCCATACGCATTTCATCAGCTTTAAAGTTGACCTTGATATCTTGGGTAAGTGTAGCACGTTGATTAGAGTTACAAAACATTTAATGTACTAAAATTAAATTACAGATACCTTTGATTTTTTTATGCGTAAACATTGGAGACTACAGAATGAATACTGAAAAAAACATTGAATACTGAAAACATTAAGAAATTAATTATTAGAATTTTTATTAACAATAATACAATTAAAGCCTGTTGAAATTGTGTGACAAGTTGCCCCCAAGTTGTCAAATATATTGTCATTAAAGATATAAGTGAGGATTATATTACTGTTTTCATTAAGCAATTAATCTTTTTATTTTAACATGTATAAATGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40100
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027258 | Nonsense | 723 | 754 | 4 | 4 |
ENSDART00000124160 | Nonsense | 192 | 223 | 4 | 4 |
ENSDART00000140117 | Nonsense | 715 | 746 | 4 | 4 |
The following transcripts of ENSDARG00000014646 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 33061685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32792995 |
GRCz11 | 3 | 32924709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACACTCACCTGATGGTGTGCATTTTATTCCGGGCTCTGAAAATGACTGT[G/T]AGTACAACAAAATGGCGTGTCTGGAAAAGGATCAGTGCACTTCCACACTG
Long Flanking Sequence:
TATTGTTTTGAGTCAGAATACTGAAACACATGCATGTTTTAAAAGAGCTGTTTATTGCTTTAACCTCTCTCATTTGCTTCTACTTTTTCAGGTATAAGGTTGCTATAACCAAGCATAAAGATGAAGAGCAGACCAGTAGCAGTCTATACAGTCAGAATTACATGTGGAAACCATTTGTGGACTTCAGCAAATATATAGAAGATAATGAGACAATCGACAACGAGGTATTAAAGCAGCGCTTCAACAGAATATCTTTAATTAGCAGGTGCTTTGATTTATTGCAAATAATAAAGTAATCTTCATTATGTCTTACTTAGGACTTGGTTGCCTGGGTCACTGCTGGTTTCCTACACATTCCTCATGCAGAAGACATACCCAACACTGTTACGGTGGGCAATGGTGGCGGTGTCCTCATTAGGCCACACAACTATTTCAATGAAGATCCGTCCATACACTCACCTGATGGTGTGCATTTTATTCCGGGCTCTGAAAATGACTGT[G/T]AGTACAACAAAATGGCGTGTCTGGAAAAGGATCAGTGCACTTCCACACTGGAGCCATTCACTTACCACGGCTTTGAAGGTGTTATGCAGTTTGAGTGAAAATTTTGATGCAAATTTCCATGTTGCTACAGATTTGCTAATACATTTGCAGTAGTATATCCTCACTCTCTGCTTTTTAGTTAATTGGAAAAAAGTATTTCCTGCTTTTGTAGCTGACTATGTAAATATTATTGATATTTTCTCATTTTCTGTTTACCAGAAGTGTGCTTTGTGAATTTTAGTTATTTTCATTTTTGTACATTTGGTGAACTTTTTGTAAATTGCTTCAAATGTATCATTTATTATCAAATCATATAATTTAGGGTATACCATAGCTCTTTAAGGCAGGGCTGTTTTTATTATACAATGTAAACTCTAAAGAGAGAGATTTCTAACAACTCTGAGAAATGCACTGATAAAACACCTCACAAAGTATACACTTATTTTTATAAACATTTTTAT
Associated Phenotype:
Not determined