Busch Lab

ZMP

LOC555478

Ensembl ID:
ENSDARG00000036809
Human Orthologue:
ANPEP
Human Description:
alanyl (membrane) aminopeptidase [Source:HGNC Symbol;Acc:500]
Mouse Orthologue:
Anpep
Mouse Description:
alanyl (membrane) aminopeptidase Gene [Source:MGI Symbol;Acc:MGI:96749]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa15314 Essential Splice Site Available for shipment Available now
sa30626 Nonsense Mutation detected in F1 DNA Not yet available
sa34021 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15314
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
Order Allele From EZRC
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053444 Essential Splice Site 197 960 2 21
ENSDART00000053444 Essential Splice Site 197 960 2 21
Genomic Location (Zv9):
Chromosome 7 (position 16170551)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 15153430
GRCz11 7 15401717
KASP Assay ID:
2259-8540.1 (used for ordering genotyping assays)
KASP Sequence:
GACTAATTTTTCCATTTATTAATCATGTTGATGTGATCTCTTTTGTTTCC[A/T]GGATTATTGCCATCACTCAGATGCAGGCCACATWTGCAAGAAAAGCCTTT
Long Flanking Sequence:
CCCTGTATATGTATATATATATATATATTATTTCCTCTTGGTTTGATATTTTGGGTTTCAGGTAAAGCTATTAGATAAATTCAATCAGAAATATAAGCTATATCTTATAAAAAAAATAGTAAAATGTGAACTTACGGGGCGTCATGGTGGCTTAGTAGTTAGCACTGTCGCCTCACAACAAGAAGGTAGTTGGTTTGAATCCCGACTGGGCCAGTTGACATCTCTCTGTAGAGTTTGCATGTGGGTTTCCTTCAGTTTCTCCCACAGTCCAAAGACATGTGCTATAGGTGAATTGGGTAAACAAAATTAACCGTATTGTATAAGTGTGTGTGAATGAGGGTGTATGGGTGTTTCCCAGTGGTTGCACTGGGTTGCAGCTGGAAGTGCATTCGTTGTGTTAAACATATGCTTGAATAGTTGTTGGTTCATTCCGCTGTGGCGACCCCTGATGACTAATTTTTCCATTTATTAATCATGTTGATGTGATCTCTTTTGTTTCC[A/T]GGATTATTGCCATCACTCAGATGCAGGCCACATATGCAAGAAAAGCCTTTCCGTGTTTCGATGAACCTGGCATGAAAGCTGTGTTCAATATCATTCTCATCCATGACCGGGGAATGACAGCACTGTCAAACAGCCAAGAAATCAGTAAGACAATCAATCCATCACAAAGCCTATAACAGGTCCTCAACTAATCGCCTTGTATTTGTTGTCAATGAAAGACTAAGTGGGGGTTTTCACTCTTTAACAAATGGGCCACTGTTAACCAACATAATATCTGCATATAGAATTTTTTTTTTTTAAGTCTGCCAGCCTAAGCGCTTCTGGTGAACTGTCTTTCTATTACAAAATTGCATAAATACAATAATAAATTAATTTAATTAATAAATAATCAATACTCATAATAAGGTATATCTGCACACAGAACTTTAATTTTTTAAGTCTTTCTATTAAAAAATCACCACGTTCAAGATCTATTTCTTTAAAAATTACCAATCTTCACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30626
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053444 Nonsense 481 960 8 21
Genomic Location (Zv9):
Chromosome 7 (position 16160065)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 15142944
GRCz11 7 15391231
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTACATATGTTTATCATTACAGGGAGCTGCGGTGCTGAAAATGCTCTCC[G/T]AATTCCTGACGGAGCCTGTGTTCGCTAAGGGACTCAGTGTAAGTCTTGCT
Long Flanking Sequence:
CCAACCTGGTCTGAGCTGGGATTGAACCAGCGATTAGGCATGTGAGTTGGCTGCTCTAACAAGGAGTCTAAAGACAGTGGCCTTTAGCATCTGTCGCTAGAGCACCCTTAGAGGTCAGAGGAGTGAGGTTTTAGTGCACAGCACTTCACTTGCTGGCCTTCGTTACATGTTTTATGCTAATGATCAACCTAAAAGGACGTCATTTAGAATATTCTGAATTCACTGATTTCACATTACAGCGAGCTTAACAACAACATAAAAATGTATGTTTAAAAAAAGAATAACTTTAGAGCTGTTTTGAACATTTTTTTTCTATCTTTATGTTGGATCCATGTTAAGCACTGCCATTGTGGAATTTCGAAAGACCACCAAAAGCCCGATGCCTTGAGAGGATCGTAAATTAAGTCATAAAGCCGTCAGGCCAGCAACAGTCCAGTCAGAGATAAATGCATTACATATGTTTATCATTACAGGGAGCTGCGGTGCTGAAAATGCTCTCC[G/T]AATTCCTGACGGAGCCTGTGTTCGCTAAGGGACTCAGTGTAAGTCTTGCTGTCGTTTCTAATGTTAAAGAGTTCATGCAACTTTCGCTCTGTATTTCATGAGCAGTTAACGTCAGAATTATTAGCCCCCTTGTATTTTATTCCCCCCAATTTCTGCTTAATGGACATTTTTCAACACATTTCTAAACATAATGGTTTTAGTGACTCATTTCTAATCACTGATTTCTTTTCTCTTTGCCATGATGACAGTACATAATATTTGACTAGATATTTTTCAAGAAATTAGTATTCAGCTTAAAGTGCAGTTTTAAGGCTTAGGGTTAATTAGTTAAGTCCTTGTATATTGAGGGTTTGTTCTGTAGACAATTGAAAAAAGAATATTGCTTAAGAGCAATAATAATTTTGACCCTAAAATGTTTTTTTTTTTTAAATGAAAAACTGCTTTTATTCTAGCTAAAATAAAACAAATAAGACTTTCTACAGAAGAAAAAAAAATATTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34021
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000053444 Essential Splice Site 780 960 16 21
Genomic Location (Zv9):
Chromosome 7 (position 16153167)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 15136046
GRCz11 7 15384333
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAACCAAGAGCTGGTTTAAGAAATGGATGCAAAATCCTCGTGTCAACCC[G/A]TGAGTGCAAAACCTCAGAGGAAATTATGCAATTTTCTTTGTGGCCGGATT
Long Flanking Sequence:
TAGCTCCCTTAAATTTTCTTTCTCTCGATTGTCTATGGAAAAAACTATCGTTATATGATAACTTGCTTAATTACCCTAACCTGTCAATTTAACATAATTAACCCTTTAAAATTTACTTTAAGCTGAAGACTAGTATCTTAAAAAACATTTAGTAAAATATTATTTACAGTCATCATGGCAAAGAATAAATAAATCAGTTATTAGAAATGAGTTATTAAAACTATTATGTTTATAAATGTGTTGAAAAAATATTCTGTCCGTTAAATTGGGGGAATGCTATAGAAGGGGGCTAATAATCCTGACTTCAACTGTATGTCATATTTTTCACATTTTATTGAATTGATATTTAATACAGTTTTGGTTAATAATAAGGTATTTTCTCTCCTCAGGTTTACACAGATCATTGCGCTGTCTCTAGCCTGCGGAACAGGTGTAGAGGGATGCAGAGAAATAACCAAGAGCTGGTTTAAGAAATGGATGCAAAATCCTCGTGTCAACCC[G/A]TGAGTGCAAAACCTCAGAGGAAATTATGCAATTTTCTTTGTGGCCGGATTGTCATTATTTAGCAAGATGTTAGATGTTGGCAAATAAACCCCACAAGTTCCGTTTAAATGCCAGCTCTTCCCAATTTGGGTTAGGATGTCATATTTAGATGTTGACAAATAACCCCACAAGTTCCGTTTAAATGCCAGCTCTTCCCAATTTTGCTTAGTATGTCATATTTCCCATTTGTGTTTGATCATCATCATTGAGATATCTATTTCAAAACATTCGCACACACGCACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATACGAATTACAGGAGTTGCCCCATTGAGCTCAGAAATTATGGAAATCCATTTATACTGAAGAAACACATCCCTGTTATATGTTATCTCTTTAACAATATCTTTTTTTAAAGAACTAAGATGTTAATAAAAGTCAATCTGTTAAAAC
Associated Phenotype:
Not determined