ZMP
ampd3
Ensembl ID:
ZFIN ID:
Description:
AMP deaminase 3 [Source:RefSeq peptide;Acc:NP_956142]
Human Orthologue:
AMPD3
Human Description:
adenosine monophosphate deaminase 3 [Source:HGNC Symbol;Acc:470]
Mouse Orthologue:
Ampd3
Mouse Description:
adenosine monophosphate deaminase 3 Gene [Source:MGI Symbol;Acc:MGI:1096344]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36613 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36612 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36613
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 |
|---|---|---|---|---|---|
| ENSDART00000048722 | Nonsense | 12 | 779 | 2 | 16 |
| ENSDART00000093095 | None | None | 196 | None | 15 |
| ENSDART00000145546 | None | None | 188 | None | 4 |
| ENSDART00000148222 | None | None | 196 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 16454109)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 16805875 |
| GRCz11 | 18 | 16794941 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCTGTGCTGTCAAAATGAGCAAAAAAGGAACCCCTCTGTCTAAGCAA[C/T]AATCAACACCCAACTTTGGGAGGGGTAAGTTTGGCACAGTGTATGATAAT
Long Flanking Sequence:
GAGTTTTATCAGGGGTGGTACCATTTTTAAAAAAAATGTTGAGGCATTTCCTTATTTAGAACTGCATGGTGTATCTGTTCTTGCAGATAAGCTAAAACCTTGTAACTTCCTAGCATTTTACACAAGCTGCTTCACATGCTACAAGACACGCTCAGGAGGATCAGTAAATACATAGGGGGAATAACTATATCGTACATGCCTTTGAGGATGCAGAAACAGTGAACTGTTAGAAGTCTTCTTATGAATTTCCTTTTTCCTGTTTGTGAAAACCACACATACACACACGATTGGTAGTTAGCATTCATCAGCTCACTGAGAGGTAAACAACCCATGCTCTAATAACCTTATAACAACAATTGTGGTGCTTTTACTGTGTATTTGTTTTAGGATTATGCAATGCATTTAAGAGTTTACTTCTGTCCCTCAGTTGAAACTTAACTGGACATCGTGTCTGCTGTGCTGTCAAAATGAGCAAAAAAGGAACCCCTCTGTCTAAGCAA[C/T]AATCAACACCCAACTTTGGGAGGGGTAAGTTTGGCACAGTGTATGATAATCCTATATCTTAAGAGTCATGTTAACTTGTTTTTTAGCCAGTTTTGTGCTTGTTAAAGGCAAGTATATGTGCAGACCCATTGAAACAAGCTCCTATAAAGTGGCATGAGGACATAACGTCTGCTATTGTCTCTCTCAAAGTAGGTTAAAGTCAAGGTGTCCTTTACATTCTTTACAAGCATGTCATAAAGTGCTCTATCAAAAGAGCGCTGGATGTTTCTAAAAATAGCTGATTTGCAACGAAGCACTTTCCTCATGACAAGTCTGATGAGTTGTGCAACAGCTTTTGCAACAAGTTGTTTTCATTTGAAACCCAAAGAACTATAGATGCAGGTATTTTAATTACACGCTAATGACTTTTATATAAAATAAATAGTATAATATAACTGTATGTGAATGACAAAAGAGTGAAATGCTGGTTACATGTAAAATGCTATTTTGTAAAGGGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36612
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048722 | Essential Splice Site | 208 | 779 | 5 | 16 |
| ENSDART00000093095 | Essential Splice Site | 196 | 196 | 4 | 15 |
| ENSDART00000145546 | None | 188 | 188 | 4 | 4 |
| ENSDART00000148222 | None | 196 | 196 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 16439675)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 16791441 |
| GRCz11 | 18 | 16780507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGAGTGCCAATAATGAAAAGTGGAGTGAGGATGAAGAAGTGCTGCCAG[G/A]TATGTTGTGGTTGGCAACAGTTCATGCACAATGCACAATTAACTGTCTGA
Long Flanking Sequence:
AAACCATTTTAAGGTCAATATTATTAGCCCCCACAAGTAATATTTTTTTCAATTGTCTACACAACAAAGTATTGTTATACAATGATTTACTTTACCTAATTACCCTATTTTGCCTAACTAACCTAGTTAAGTCTTTAAAAAAACTGTAATTCTTAGTTGTAATAATACTATGCCATATTGCTGTTTTACTGTATTTATGATTAAATAAACATAGCGTTTGTGAGCATAGAAGACCTCAAATCTTACCAGCTTAAACTTTCAAACCGTAATGAATAATGAGCATGCTATGTGAACTCCTAAAATATGTTTATTAACCTATGTTGATTTCTGACAGATAACGGTTGAGGATTATGAGCAGGCAGCAAAATCTCTGTTGACAGCGCTTTTCATCAGAGAAAAATATTCCCGGCTGGCATATCACCGCTTCCCCAGGACCGCAGCCAAGTTTCTACGGAGTGCCAATAATGAAAAGTGGAGTGAGGATGAAGAAGTGCTGCCAG[G/A]TATGTTGTGGTTGGCAACAGTTCATGCACAATGCACAATTAACTGTCTGAAGCAAGACACTACAGGTGAATAGAGTAAACACGCAGTGCTTTCCCAAACTGTTCCCCCTTACTGTTTTCTAGAATATTTTGTTATATGCAAATATATAAAAAGAATCAACAAGTGGTTAAAAAAGTTTTTCAAAATTGACAGAAAAAGACAGAAATGGATGTAGCTCAATTTTGATGAAAGACTTCAAATGTTGACTACTTTATTTATATTTCTAGCACACAAATCATATATAAAATAATAAATACTACCCTGACACCCTGAAATATATCACCCTGCAGCCCAAGACTGGTTACTCACTGAAGCTAAGCAGGGCTGAGCCTGGTCAGTAGCTGGATGGGAGACCACATGGGAAAACAAGGTTGCTGTTGGAAGTGGTGTTAGTGAGGCCCATCTAAGTGGATGCTGCACAACGGTGTTGGTGTGGAAAGACTCCTCTCTTGATTGTGAAG
Associated Phenotype:
Not determined