Busch Lab

ZMP

ampd1

Ensembl ID:
ENSDARG00000033832
ZFIN ID:
ZDB-GENE-040426-1906
Description:
AMP deaminase 1 [Source:RefSeq peptide;Acc:NP_957187]
Human Orthologue:
AMPD1
Human Description:
adenosine monophosphate deaminase 1 [Source:HGNC Symbol;Acc:468]
Mouse Orthologue:
Ampd1
Mouse Description:
adenosine monophosphate deaminase 1 Gene [Source:MGI Symbol;Acc:MGI:88015]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa21209 Nonsense Available for shipment Available now
sa7609 Missense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa21209
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042755 Nonsense 294 717 7 15
Genomic Location (Zv9):
Chromosome 8 (position 11610667)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11058457
GRCz11 8 11096162
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGCCTGCATGAACCAGAAGCATCTCCTCCGCTTCATCAAGAAGTCCTA[C/A]CGTGTGGATGCAGATCGGGTGGTGCATGTTTTGAAGGGCAAAGAAGTGAC
Long Flanking Sequence:
AAGGAAAATGAATGAATGAACTATTATGTTTAGAAATGTGTTGAAAAAATCCTTGTTGTCTGTTAAACAGAAATTGGGGGAGAAATTTACAGGGGGCTAATAATTTGGCAACTTTTACGTTCTTGAAGAATGTTGATGTGCATTGTTCCTTTTTTAAAAAAGAGGATTAATTATGCTGTTGATTTTCTTGCTGAAAATCTCAGTGTCTTTTCTCCCTCAGAAAGACCTACACTCACCGCCGCCTGAAGTTCCTCATGTCAAAGTTCAACGTGCATGAGATGCTGAACGAGATGGAGGAAATGAAAGAGCTGAAGAAAAATCCCCACAGAGACTTTTACAACTGTAGGAAGGTGTGATTCCAATCAGCCACGTCATTTATTAATTTCCAGCTAATTTTCACAGTCATTACCGTTGTTGTTGTTGTTGTAGGTTGATACTCACATCCACGCTGCCGCCTGCATGAACCAGAAGCATCTCCTCCGCTTCATCAAGAAGTCCTA[C/A]CGTGTGGATGCAGATCGGGTGGTGCATGTTTTGAAGGGCAAAGAAGTGACCCTGAAGGAGCTTTTTGCATCTCTTAACCTGCACCCTTATGACCTGACTGTAGACTCCTTGGATGTGCACGCTGTAGGTATCATACAACACATACATATTCATTCATTTATACACATACAACACATCCATGCAGCTTCTTAGTGCCTTCCCAACTAAAATGGGAAGAATATGGGTTTAGGAGGATTATATTTCACCACATATGGTTTGGAATAGAAATAACTGTCTTTTATGATATTATTTACGAAACAGTATTACTTGACAGTTGGCCGCTAATTAAAAAAAACAATATTTCTAGTAATGCCTGAAATTGTCACATGGTTTAGTGTGATAATCAGCTTGCAGTTATGTAAATATGTAATTGTAAATGCAGTACTGTGATCTGTTTACATAAGCAGCTCTCGGAGCAACTCAACTAAATAATTATCTCAAATATATATATATATATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7609
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000042755 Missense 645 717 14 15
Genomic Location (Zv9):
Chromosome 8 (position 11623467)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 11045657
GRCz11 8 11083362
KASP Assay ID:
554-4110.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGGAGCCACTGATGGAGGAGTACGCCATCGCAGCRCAGGTGTTCAAGC[T/G]CAGCACCTGTGACATGTGTGAGATCGCCAGAAACAGTGTCWTGCAGAGCG
Long Flanking Sequence:
TTTTTTTATTATTATTATTGTTATTATTATTATTATTATTATTTAAGCAAATAAGAATGCTATATATATATATATATATATATATATATATATATATATATATATATATACATATACATATATATTCAAGTTAATATGAAAATGGTCATTAAATCATGACAGAAATACAGCAGCCAGTGTGTCCTTATGTGTTCTCAGAGTCCAGTCCTGCAGTACCTGTATTACCTGGCTCAGGTGCCCATCGCCATGTCTCCTCTGAGCAACAACAGTCTGTTCTTGGAGTACAACAAGAATCCCCTGCTAGAGTTTCATAAGAAGGGCCTAATGGTCTCTCTGTCCACCGATGACCCCATGCAGTTCCACTACACCAAGGTATGCAGCTTTCCTGATGCTTGTCATGCATCTGTTTTCTTTGATTTGATGTGTTTATTTTTTTATGTGCACTCATGAACAGGAGCCACTGATGGAGGAGTACGCCATCGCAGCGCAGGTGTTCAAGC[T/G]CAGCACCTGTGACATGTGTGAGATCGCCAGAAACAGTGTCTTGCAGAGCGGCCTTTCTGCTGAGGTGAGGCCAGCTCAACTGAACATCACTTCGCTTTCAGATGTACATTTACACACAGTGGGGTTTTGGTTATTACACAGCAACTGTTATGTTTATTGAACTAATAGTGCACAGTGTAAATGTTTAAGGATTACAAATTACATCTCTAACTGTGACACGCCTTTAAATGTTTACACTATAGTTTCATAATGTATTTTAAGTATGTTTTAATATAAATGTGTGCAAGTATTATTAATATTATATAATGTAATAAATATTATTTTGAATATTATTTTTATAGCTTTTTTGCATGAAAATATTTAGATTTAGTGTTATGTATTATTAATATTTTTGTTTTATTTCTAACTAAAAACTTATTTGTAATATAATAATAATTATTATTAATATTATTTTTATAATTATTGTTATTATTATATTAAAAAAATAAAAATTAATATAT
Associated Phenotype:
Not determined