Busch Lab

ZMP

appb

Ensembl ID:
ENSDARG00000055543
ZFIN ID:
ZDB-GENE-020220-1
Description:
amyloid beta (A4) precursor protein b [Source:RefSeq peptide;Acc:NP_690842]
Human Orthologue:
APP
Human Description:
amyloid beta (A4) precursor protein [Source:HGNC Symbol;Acc:620]
Mouse Orthologue:
App
Mouse Description:
amyloid beta (A4) precursor protein Gene [Source:MGI Symbol;Acc:MGI:88059]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa327 Nonsense F2 line generated Not yet available
sa34693 Nonsense Mutation detected in F1 DNA Not yet available
sa41475 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa327
Status:
F2 line generated
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
ENSDART00000077894 None None 362 None 11
ENSDART00000077901 Nonsense 142 694 4 17
ENSDART00000077908 Nonsense 142 751 4 17
ENSDART00000100684 Nonsense 142 660 4 17
ENSDART00000122679 None None 362 None 12
ENSDART00000122787 None None 83 None 3
ENSDART00000125536 Nonsense 142 694 4 16
Genomic Location (Zv9):
Chromosome 9 (position 36026372)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 35245883
GRCz11 9 35055068
KASP Assay ID:
554-3359.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGCGATGCCCTCCTCGTCCCAGATAAGTGCAAGTTCTTGCACCAGGAG[C/T]GAATGGACATGTGCGAGAGTCATCTACACTGGCATACAGTGGCCAAAGAG
Long Flanking Sequence:
TCTGTTCACTCGAACAACAATTTGTACCTTGTTTTGACTCCCACAGGTATACCCAGACCTCCAGATCACTAATGTAGTGGAGGCCAACCAGCCTGTCAGCATCCAGAACTGGTGCAAAATGGGTCGCCGCCAGTGCCGCAGTCACACGCACATTGTTGTTCCCTACCGTTGCCTGGGTATGTATGTGTGTGTTCACATAAAGAAAATCCTTCAACGTGACACTTACATCAGAACACTCTGCCACTCCTGGGGTATTAACCTGGATTTGTGGAACATTAAACTAATGCTTTTAGCACGGCTCTTGTTCGATTTCCTATCATCATTCTGCATCAGCTAAGATGAGATTCATTAAAACACCATCAAAATTTGCTCAGGATGCTTTACACATCAGCAGAAATCTATTTGAGCACCTGCTGAGCAAATGTTTGTTTATTTCAGTTGGGGAGTTTGTCAGCGATGCCCTCCTCGTCCCAGATAAGTGCAAGTTCTTGCACCAGGAG[C/T]GAATGGACATGTGCGAGAGTCATCTACACTGGCATACAGTGGCCAAAGAGGTCAGCGATCGCACCACATCACATTTACACTTTCACGTATTAATAACAGAAAAGTCAGATCAGATTTCTGTTTCTGGAACCGGCACCTATTTTAGTTTAGATCAATCTTTTGTGCTGCTGAAAATATGTTTGAAGGGACGGTTCATCTAAAAATAAAAATGACCTCATCATTTGCTCTCCCTCATGAGGTTTTAAATCTTTATGAGCTTCTTTCTTCTATTAAACACAAAAGAAGATGTGTTTTAAAATGCTGGTTGCTGGCACACATTGACTTTCATAGTAGGAAAACTATTGCTATGGAAGTCACTGGATGCTAGCATTTTTCAAAATATTTAATATATATACTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAGACTATATGTTTTGTTTAGGGATATATGTTTAGTTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34693
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077894 Nonsense 102 362 4 11
ENSDART00000077901 Nonsense 434 694 10 17
ENSDART00000077908 Nonsense 491 751 11 17
ENSDART00000100684 Nonsense 434 660 10 17
ENSDART00000122679 Nonsense 102 362 5 12
ENSDART00000122787 None None 83 None 3
ENSDART00000125536 Nonsense 434 694 10 16
Genomic Location (Zv9):
Chromosome 9 (position 36004688)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 35224199
GRCz11 9 35033384
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTAAAAATAATCCTGTCTCATACAGCCTCGGCAGGTGCTGAATCTGT[T/A]GAAGAAGTATATCCGTGCGGAGCAGAAGGACCGTCAGCACACTCTCAAAC
Long Flanking Sequence:
GCATTGTTGAGGATTTTGGATTTTGTTGGCCTATAAAATTGAAACCACGCTTCTTCGCCCCCAGCTGGCAGAAATTTTTTGACATTTTATTTATTAGACATGCTTATTTATTGCTTTTATTGTACGTGTTTTTTTGTTTGTTTGTTTTTTATCAGGTAATAGATTTTATTTATATAAAAGAAAGTTGTCTATAGAAATGAATAGTAATGAAATCATTCCGGAAATGTTCCCAATATTTACTGGTATTACTGTGTGAAAGTGGCTATTGTCTACATGAATACATAAAACTAGTTAAAATTGTGTTCTTTGCCCCCAAAAAACTACAAATCTTAATTTCATATCAGTTATGACTGTAAATTATATATAGAATACCTAGTAAATGTTGCCATAAATATAGCCTGTGCTTCTGATGTGATATTCAAACATAAATAAATAAACAAATTATAACATAAGCTAAAAATAATCCTGTCTCATACAGCCTCGGCAGGTGCTGAATCTGT[T/A]GAAGAAGTATATCCGTGCGGAGCAGAAGGACCGTCAGCACACTCTCAAACACTTTGAACACGTGCGGGAGGTCGATCCCAAGAAGGCTTCACAGATTCGGCCATTTGTAAGCTCCTGTCAAGCTGTTCGTTCCTGCTTTAATTATGATTTGTGTAAATGCTTTAGAACTTGATTTTGAGCCCCTGTGCTTTTAGGTGATGACCCACCTACGTGTGATTGAGGAACGCATGAACCAGTCTTTGGGTTACCTCTATAAAGTGCCTCAAGTGGCTAATGATATCCAGGATCAAGTGGGTGAGTTTTTTTAATCGCACTTCAGAGGCTCAAACTGTGCTGGAAATGGAATATGTTGTCACATAACATCATTTTATTTTGTTTTATTTTTAATGTTTTATTTTTTTGTTACTCAAAACTGTTTTACTGTACTTTTGTATATTTTTTGTGTAAAGCATTTTGAGAATTAAGTTTTAAAGGCGATATATATATATAAGTGATGTAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41475
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
ENSDART00000077894 Nonsense 121 362 4 11
ENSDART00000077901 Nonsense 453 694 10 17
ENSDART00000077908 Nonsense 510 751 11 17
ENSDART00000100684 Nonsense 453 660 10 17
ENSDART00000122679 Nonsense 121 362 5 12
ENSDART00000122787 None None 83 None 3
ENSDART00000125536 Nonsense 453 694 10 16
Genomic Location (Zv9):
Chromosome 9 (position 36004632)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 35224143
GRCz11 9 35033328
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTATATCCGTGCGGAGCAGAAGGACCGTCAGCACACTCTCAAACACTTT[G/T]AACACGTGCGGGAGGTCGATCCCAAGAAGGCTTCACAGATTCGGCCATTT
Long Flanking Sequence:
GCCCCCAGCTGGCAGAAATTTTTTGACATTTTATTTATTAGACATGCTTATTTATTGCTTTTATTGTACGTGTTTTTTTGTTTGTTTGTTTTTTATCAGGTAATAGATTTTATTTATATAAAAGAAAGTTGTCTATAGAAATGAATAGTAATGAAATCATTCCGGAAATGTTCCCAATATTTACTGGTATTACTGTGTGAAAGTGGCTATTGTCTACATGAATACATAAAACTAGTTAAAATTGTGTTCTTTGCCCCCAAAAAACTACAAATCTTAATTTCATATCAGTTATGACTGTAAATTATATATAGAATACCTAGTAAATGTTGCCATAAATATAGCCTGTGCTTCTGATGTGATATTCAAACATAAATAAATAAACAAATTATAACATAAGCTAAAAATAATCCTGTCTCATACAGCCTCGGCAGGTGCTGAATCTGTTGAAGAAGTATATCCGTGCGGAGCAGAAGGACCGTCAGCACACTCTCAAACACTTT[G/T]AACACGTGCGGGAGGTCGATCCCAAGAAGGCTTCACAGATTCGGCCATTTGTAAGCTCCTGTCAAGCTGTTCGTTCCTGCTTTAATTATGATTTGTGTAAATGCTTTAGAACTTGATTTTGAGCCCCTGTGCTTTTAGGTGATGACCCACCTACGTGTGATTGAGGAACGCATGAACCAGTCTTTGGGTTACCTCTATAAAGTGCCTCAAGTGGCTAATGATATCCAGGATCAAGTGGGTGAGTTTTTTTAATCGCACTTCAGAGGCTCAAACTGTGCTGGAAATGGAATATGTTGTCACATAACATCATTTTATTTTGTTTTATTTTTAATGTTTTATTTTTTTGTTACTCAAAACTGTTTTACTGTACTTTTGTATATTTTTTGTGTAAAGCATTTTGAGAATTAAGTTTTAAAGGCGATATATATATATAAGTGATGTAAGTGATGATTATTATTATGAAGAATTATGAAATGCTGTGTTTTGTGCAGCGGTGCTGG
Associated Phenotype:
Not determined