ZMP
ampd2
Ensembl ID:
ZFIN ID:
Description:
Adenosine monophosphate deaminase 2 (Isoform L) [Source:UniProtKB/TrEMBL;Acc:B8JIS2]
Human Orthologue:
AMPD2
Human Description:
adenosine monophosphate deaminase 2 [Source:HGNC Symbol;Acc:469]
Mouse Orthologue:
Ampd2
Mouse Description:
adenosine monophosphate deaminase 2 Gene [Source:MGI Symbol;Acc:MGI:88016]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2452 | Nonsense | F2 line generated | Not yet available |
sa21296 | Nonsense | Available for shipment | Available now |
sa16131 | Nonsense | Available for shipment | Available now |
sa10749 | Essential Splice Site | Available for shipment | Available now |
sa872 | Nonsense | Available for shipment | Available now |
sa7613 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2452
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000045798 | Nonsense | 64 | 230 | 2 | 6 |
ENSDART00000093090 | Nonsense | 40 | 793 | 1 | 17 |
ENSDART00000121932 | Nonsense | 64 | 334 | 2 | 9 |
ENSDART00000143554 | Nonsense | 6 | 756 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26120861)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25248779 |
GRCz11 | 8 | 25267918 |
KASP Assay ID:
554-3166.1 (used for ordering genotyping assays)
KASP Sequence:
TAACCAAGCAYGGCCACATTGACCTACGCACCTCCATGGATGGCAAATAC[A/T]AAGAGATTGCAGAGGTAAACAAAGCACAAATCACAACACCGACTCTTGAT
Long Flanking Sequence:
ACTTTAGTAAACATTTTAGAAAACATTTTATAAACTGTGTTTTTACAGCGTGGGCGCTAGATGCATTTGGTCTTTACTTGCCCACAAGTTAAGTTGGCATTCTAAGACAAAGGCACAGCACACACTCACATATAAACTAATATCCTCCCACTTGAATGCTCCATTGTTTTTTGAGACAATTGGACAAACAGTTGCAGATCTTCGTCAGCTTTCTGACCCTGCCTTTCTCTGGACAGCAGAAAAACAACGCTATATATAATTGAACACAATCAATGTTGTCATTTTGGCTTAAACATTTTTCTCTATACTTACATCTTACAATCTGAATGTTTTAAATATGAAAACCATCTCAGTTAAAATATAAAGATGTCTTTCTCACTGTCTTATTAGTAGATCTCCGTGTTGGCAGACACCTTCTCACATCCCAGTATTCATTGCCTGGCAACCCTGTAACCAAGCACGGCCACATTGACCTACGCACCTCCATGGATGGCAAATAC[A/T]AAGAGATTGCAGAGGTAAACAAAGCACAAATCACAACACCGACTCTTGATGCCTTTGAATGCCACCCTGACCCAAATGTCTGGTGTTTTAGATTTATTATATATTTCTTTTACAATCTTTTTATTGACAATATGCAATAAAAAATATGACAATATAACATCACAATCATATTTACATCCTTGTTTTCAATTTAGAGGAAAAAACTAAAATATTGAGGAAACAAAAGCAAAAAAGGGATAAAAAAATTAATAAAAAAGGAAAAGGGGGGGGGGGCACAGGCTGTTTGAATAAATCTTTGGAAATCGGGGGAATATGTAGATAGGTAGTTTATTTTGTCTTTTCCTGTTTCATTAAATAAATTGCTGAAACTTGAGTGTCCACATTTTCTCAAAAACAGTAAGTTTGCATTTTGTATTTTGTATTTCTAACAATATCAGCAAAAAAAATGTGTAAACTAGTACTAGGTTTGTATAAATGTAAAAAGTGATAGAAAAAAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21296
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 |
---|---|---|---|---|---|
ENSDART00000045798 | Nonsense | 120 | 230 | 4 | 6 |
ENSDART00000093090 | Nonsense | 96 | 793 | 3 | 17 |
ENSDART00000121932 | Nonsense | 120 | 334 | 4 | 9 |
ENSDART00000143554 | Nonsense | 62 | 756 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26123658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25251576 |
GRCz11 | 8 | 25270715 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTTAATTAAATGCTTATTCTCTTGAGGTTTGAGCCTGATATCCTTCTA[C/T]GAGCCAAACAGGACTTCATGAAAACAGACAGCGCTACGGACCTGGAGTGA
Long Flanking Sequence:
TTCCATTTGCTAAAACACAGAGAGAGTTGTGCACAAATTAAGACTCAAAATTACTCCAGAGTGGATAAAAACATCCCCAAAAGCACACAAGGGTTAATCCCAAATTTCTTAAGCTAACAAATTGTTATGATCTCAGTATTTAACTAACAAAAATGTCTAGCTTAAAACTGGTGTAGAAGCAAAGTTTTGCTGGTAAAGTTCCAACTGGCTAACCAGAATTATTATAGCTAACTATTAAAAAACAATAAAACGTGTATATCTTTTGTTAAACTTTTTGAAAACCTGAATCTCAAGTTGTAGTCGAGCAGCCATACCAAAACACAACCTGAAAATCAGTCTAATGTTCATCTGCATTAGCTTTTTCAGCTGGGAATTTGAAATATACTCCTGAATGCATGAGCCAATGTTAGTCCAGCATTTATTGGACTGTATGCACATGTGAACCACAGAAAGTTAATTAAATGCTTATTCTCTTGAGGTTTGAGCCTGATATCCTTCTA[C/T]GAGCCAAACAGGACTTCATGAAAACAGACAGCGCTACGGACCTGGAGTGAGTGCCTTTAACATCTTCTGTGATGATCGCTGTTTGTTGACTAATCCACTAGATAAGTCTGACATCACATGCCATAGTTTCTGGGTCCAAAATCGACAACAAATGGTAGTAACCTAGCTAACAGGAAACATTCTGTAACCTTTGATAAAGGTTTTCTAAGTTTTAATTTGTAATGTTATTAAAGTTGTGCATTTGGAACCATTCTTGTAACATTGATAGAAAAACGTTCCTAAAACATTAATATGATGTGGAAGAAATGTTCGAATAACCTTTTAAATAATGTTGTAAGAACATGAAAAGAACATGAAACCTTATGAAAATGCTGAGAATAATGTTATTATAATAAAAAAATTATGTTATTTACATAATCTAAAAGATTGATCTTTTGAACCTACTAAGAACAATTGAAAAATGAATTATATATAACTAAATGAGAACATTAAGAGAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16131
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045798 | Nonsense | 148 | 230 | 5 | 6 |
ENSDART00000093090 | Nonsense | 124 | 793 | 4 | 17 |
ENSDART00000121932 | Nonsense | 148 | 334 | 5 | 9 |
ENSDART00000143554 | Nonsense | 90 | 756 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26124472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25252390 |
GRCz11 | 8 | 25271529 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTCAGGTATATGAAAGAACAGAGCCAGACACCCATAGAAAACTA[T/A]CCCGAGAGAGAGCTYATCCCRGAGAGAGAGTACCAGAGAGTCACTATCTC
Long Flanking Sequence:
ATAACCTTTTAAATAATGTTGTAAGAACATGAAAAGAACATGAAACCTTATGAAAATGCTGAGAATAATGTTATTATAATAAAAAAATTATGTTATTTACATAATCTAAAAGATTGATCTTTTGAACCTACTAAGAACAATTGAAAAATGAATTATATATAACTAAATGAGAACATTAAGAGAGTGTTTTTTTGCAACCTTAAATTGTTAGCAGGAAGTATATACTTACAGTTTGGTGTGCATAATGTTTATAACCATGTCTAATTTCAAATGGTCCATATTTTGTAAATGGGTTGAGCAAAATCATCATAAAGATTTGCTTAAATGTGTCTATGACTACATGACTAAACAGTAGTCATAAACGGCTATGGGCTATTGAGATTTTTAATTCAAATGAGTACTTAGAGTATTTCATGGATCAAAACTTAACAAGCACATTGTATCTCTTGTTTTTTTTTCAGGTATATGAAAGAACAGAGCCAGACACCCATAGAAAACTA[T/A]CCCGAGAGAGAGCTTATCCCGGAGAGAGAGTACCAGAGAGTCACTATCTCTGGAGAGGAGAAGTGTGGGGTACAGACAGACCTCTTCAGCTTTGTTTATTACACTAAAACAAGATGTTGTTGAGAGAACTGGAGTGGACACTGCAGACATTACATAAACTCCTCAGGGAGAAATATTTCTCACACATACACACACACACACAAATACACAAACCCCAGCGGAAACAGGCTGACAGCAATGCAGCTGAAGAGTTTTCACATAAACTTATGAAGAAAAATGAGCAGAAAAGTTTTTCTTTTATATTTATATATATTCATAAAACTAAAATCATGTTTGACTCGAATAAAATTGACATATATTAGACAAATATAATACATATAAAGCAAAAATAAGATAAATCTGGATTTTAAAATCCAATAAGGATAAAATACTTTAAAAAAATTATGAAATCAGATTAAAACAAATGAATTCATGCAAAATTTCGCCAAAATAATCTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10749
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045798 | None | None | 230 | None | 6 |
ENSDART00000093090 | Essential Splice Site | 590 | 793 | 14 | 17 |
ENSDART00000121932 | None | None | 334 | None | 9 |
ENSDART00000143554 | Essential Splice Site | 553 | 756 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26136682)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25264600 |
GRCz11 | 8 | 25283739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTTAGATMACTTGAGGATGAGTAAACTGCATTATTTATGTCTCTCAAC[A/T]GGCAAAGAAACATGAATTCGTTCGTGTTRCGYCCTCACTGTGGAGAAGCA
Long Flanking Sequence:
GTTGGGTTTGACAGTGTGGATGATGAGTCCAAACCTGAGCATCACATCTTTAACCTGGACAGTCCAAAACCTGTCAACTGGACGGATGAAGACAATCCTCCATACTCTTATTATCTGTACTACATGTATGCAAATATGACTGTACTCAACCACCTGCGCAGGTATTTAATCCACGCTTTGCATATTTCACATTGATTTGAGACTAAGATTTTGGGACATAAACAGCTAAACTTAAATTTAAAAAAATGGGTTAAAGGGATAGTTCACGCAAGATTGAAAATTCCTTCATTATTTATTACATCTCTCCCTCAAGTGGTTACAAACATGTTTGAGTTTACCTTCTTTGGTTGAAAACAAAACAAAAAAAACATACTTTGAAAAATGCTGGAAACTGGCCATTTTTTCCACTTATGAAATTCAATGGCTGAACAGAAGAAACAAAGTCATAAAAGTTTAGATCACTTGAGGATGAGTAAACTGCATTATTTATGTCTCTCAAC[A/T]GGCAAAGAAACATGAATTCGTTCGTGTTACGTCCTCACTGTGGAGAAGCAGGGCCGATTCACCACCTTGTGTCTGGATTCATGCTGTCAGAGAACATTTCCCATGGCCTACTTCTCAGAAAAGTAAAGACACTCTTGATACTTTTACTGGCTCACGGTCACCTCAGAAATCTGTTCTGCACAGATTTAAAGCATGCTATGTGTATTTATTTATTTTTTTACATGTCATTTTTTTGTGTTAGACCAAGGCCACATCGCACTTTTGAGCAGTGTCACACACTTCATTTTCTCCATCAAACACCTTCAACTTAGATTTTTCAGTCAGTCCTTGAAAGCAATATCAGATCAATCTGTGTCCCAGTTTAGAAGATCTTGTTATGTGTAACATTTTTTGAAAATTAAAAAAGAGACTGCTTAGATTGTGTTTCTGTACTGGTTTAGGCCGGTCATGGATAGAAATCCATTTCTAGTACAGTTGATTTAATTTTAAAGATTGCAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa872
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045798 | None | None | 230 | None | 6 |
ENSDART00000093090 | Nonsense | 636 | 793 | 15 | 17 |
ENSDART00000121932 | None | None | 334 | None | 9 |
ENSDART00000143554 | Nonsense | 599 | 756 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26141845)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25269763 |
GRCz11 | 8 | 25288902 |
KASP Assay ID:
554-0774.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTTGAGTGATATGTTGCTGTATTTCCCACAGGCTCCTGTACTGCAGTA[T/A]CTGTATTATCTGGCTCAGATTGGCATTGCTATGTCGCCGCTCAGCAACAA
Long Flanking Sequence:
CCTAATGTTTTAGATCAGGGTGTCCGCAGAGTCTTAAAAAGTACTTAAATGTCTTACATTTTAAGCCTTAAAAAGTCTTACATTCACTGAAATATTGTGTTGTAGGTTTTAAATAATTTTAAACAGGTCTTAATTTACGTCAAGGGTCAACTACCTGATCAGGCTGACACAAAACACAACTTTTTTTTATATTTAAGTCTTTTATTGCAAAGAAATGCAATTCAAAACAGCTATTAAGACATTTAAAGGAAATTCTCCTAATTAAATTCCCCAATCGGGAAAAGAAAACTAAAGAAACAGATCCCTTTACAAAAAAAATACTAAAACTTTTTACGGATGTAACTGGGCCATTAGAAAATATCCTTAATGTTTAGCCCTGTATAAGTCTAAAATTTCATTCATAATGATCTTAAAAAGTCTTAAATTGACTTGAAGAAACCTGCAGAAATCCTGTTGAGTGATATGTTGCTGTATTTCCCACAGGCTCCTGTACTGCAGTA[T/A]CTGTATTATCTGGCTCAGATTGGCATTGCTATGTCGCCGCTCAGCAACAACAGCCTCTTCCTCAGCTACCATCGAAATCCACTGCCTGAATATCTGTCCAGAGGCCTCATGGTGTCTTTGTCCACTGACGACCCTCTGCAGTTCCACTTCACAAAGGTTAGAAGTCAAACCACATCATCTGATATGAAGTGTTTTTACTTATTGTGTGGATAAATGTGTTTGACCGAATATATGTGTGGTTTGTTTAGGAGCCACTGATGGAGGAGTACAGCATCGCCGCTCAGGTGTGGAAGCTGAGCTCATGTGACATGTGTGAACTGGCCCGAAACAGTGTGCTCATGAGCGGATTTTCAAACCAGGTGCTCACAGCTACACTTACACTTCTATTCAAGCACTTTTGGTTCTTTTTTGTGACATTTGACAGTAAGTTAATGCATCAGTTAATGTATTTTAAAGCATAATCTAACAAAAAGCCTAAAATGTTATAGTAATGTAGCTTT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa7613
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 > C
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045798 | None | None | 230 | None | 6 |
ENSDART00000093090 | Missense | 730 | 793 | 17 | 17 |
ENSDART00000121932 | None | None | 334 | None | 9 |
ENSDART00000143554 | Missense | 693 | 756 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 26144192)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25272110 |
GRCz11 | 8 | 25291249 |
KASP Assay ID:
554-4216.1 (used for ordering genotyping assays)
KASP Sequence:
GCGCATTTATCTGACCTATTCAAATGTCTTCTGTGAAGGTGAAAAGCTAC[T/C]GGTTGGGGCCGCATTAYATAAAAGAGGGACAAGAGGGCAATGACAWCMGA
Long Flanking Sequence:
TCTCCCTCTACTTATTATGTGGTTTCTGTCGCCATTTTGTGGCAGAACGTCGATCACCACTGTCGACCGATGCACCGAATCTCCGAAATGATATTTTAAAATAGGCACTATCCTTATAAATAAACTGCATAGTTGCGATCTAAACTATTATATTCTCAACTAAAAAAGCCTTAAAAGTACATTATGTTGTATAACTGCAGCAAAATTTATTAAACTGTAGAGTGTCCTTTGCTTGTCGCTGTATGTGGGCAAAGTAATACACAAGGGTGATAAGGCTGTACGAATACTGGCCTTTAAAGAATATCACTTGATTATCAGCCAAGAACAAGACAGAACTGTTTTTAATATAAATCTATATATATTTCTGAATTATTGGCTGCCATTCAATTTTAGCACTGTATTTAGCCACCACTGTTGACACAGATGATTTAAATACAATCTACCAGAGACGCGCATTTATCTGACCTATTCAAATGTCTTCTGTGAAGGTGAAAAGCTAC[T/C]GGTTGGGGCCGCATTATATAAAAGAGGGACAAGAGGGCAATGACATCAGACGTACCAACGTTCCTGATATCCGTGTGGCGTATCGCTTCGAGACTCTGTGTGAAGAACTGAATCTGATCACACAGGCAGTGCGGTCAGAGGAGCTGGAGACGGTCAAAGAGGAGGGATCCCTGTGCATGGCTTCAATACGCTAACAGTGTTTCACACTTTCAATTATTCAACCAGTGCAGAGTGTGAGTAAAAGGTTAATCAGGGAAATGTGGGACTGACTTTCTGTCCACAGGTATTCACCTAAACCCAATTGATAGTAATGTTTTGTAATTCATTTGGAAGCATTGTGCAGTTTTAAAGGGATGGTTCAGTCATAAATGAGAATGTGCTAATTTACTCACTCTCAGGTTACGGAAGATGTAGGTGACTTTTTCTTGAAAGTTTTTAGCTGAAACTGTGGTCGTTGGTGATTCACATAAAGTAGTTTAACAGTTACCAGCAATTTAATG
Associated Phenotype:
Not determined