ZMP
appbp2
Ensembl ID:
ZFIN ID:
Description:
amyloid protein-binding protein 2 [Source:RefSeq peptide;Acc:NP_997798]
Human Orthologue:
APPBP2
Human Description:
amyloid beta precursor protein (cytoplasmic tail) binding protein 2 [Source:HGNC Symbol;Acc:622]
Mouse Orthologue:
Appbp2
Mouse Description:
amyloid beta precursor protein (cytoplasmic tail) binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa4606 | Nonsense | F2 line generated | Not yet available |
sa1303 | Essential Splice Site | Available for shipment | Available now |
sa16354 | Nonsense | Available for shipment | Available now |
sa15168 | Nonsense | Available for shipment | Available now |
sa13157 | Essential Splice Site | Available for shipment | Available now |
sa22644 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa4606
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002824 | Nonsense | 45 | 446 | 1 | 11 |
ENSDART00000110234 | Nonsense | 45 | 586 | 1 | 14 |
ENSDART00000137569 | None | None | 246 | None | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 23296064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 24007251 |
GRCz11 | 15 | 23942516 |
KASP Assay ID:
554-3526.1 (used for ordering genotyping assays)
KASP Sequence:
CGACGGGACATCCGATCTCTCCCCGAAAATATACAGTTTGATGTGTACTA[C/A]AAGGTAAGAAGCACGATGATGGAGTTYAGGGCGGAACAGCCGTCAAAATC
Long Flanking Sequence:
ACAGTCAGAAAGGTTCTGTCACAAACCTTTAATCACTTCTGAGAGATTTCTTCTGTCCTCCCAGCGGCAGTTGTTTTGAACTGCAATCAAATGCGCGTTCACTGAGTGCAAGCGCTACGTCATTGCCTAAAGTGTCATAGAGTGGGCGGGGCATCTCGATCGGGGATGAGCTTTAAACATGAGAGCATAACCAGGGGGTTGTGTTCTCTATCATAACAGCCCATTTCAACCTCAAAAAGCGCTTCCAGCCGCGGGGGTGTATGAGGAACACCAGAGTAAAGCGTTTTACCTCGATCAGGTAGCGAAGGAGGTGAAAGTAGGAGTGGAAGAGGGGGGCTGTGGTTGGATTTAGTGAAAGAAAACAATATGGCCGCGGTGGAGCTGGAATGGATCCCTGAGACCCTTTACAACACTGCTATTTCAGCCGTGGTCGACAACTACGACCAGTCGCGACGGGACATCCGATCTCTCCCCGAAAATATACAGTTTGATGTGTACTA[C/A]AAGGTAAGAAGCACGATGATGGAGTTCAGGGCGGAACAGCCGTCAAAATCATCTGACACTTTTTTACTAGCAGTTAGGCTAACAAAAACTGAATCAACCTCTCAGTGGAGCACTGGTTAGGAGAAATTCGAGCTACGAGACCATTTAACCTGGTTAAATCCTGGTTTACGAGTACATTCATATTTCTGTGTGGCAGTTAGACTGTTAAAACCTAAGTGCCCACTGTTTAGTTATCCTAGCTTGTAGCTTATCTACTACTGTATGAGATACAGCTCTCTGGGTCAACACTAGTTAACCATACAGTACCATGACATTTCACTTTTTACCCTTTTAACCTATTTATGATTACTAGGTCAGTGTAATATTATGGGACGTTTAACCAAACCCGTGTTTTGAACGAATTTGGCGAGTGTCATCTGTAAAAACGGTTTGTTACCAACTGCTGTGAATACAATAAATGACCACTGTAACGTTACAGTAAGATAAAAACAGCAATGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1303
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002824 | Essential Splice Site | 224 | 446 | 5 | 11 |
ENSDART00000110234 | Essential Splice Site | 224 | 586 | 5 | 14 |
ENSDART00000137569 | Essential Splice Site | 193 | 246 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 23285437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23996624 |
GRCz11 | 15 | 23931889 |
KASP Assay ID:
554-1218.1 (used for ordering genotyping assays)
KASP Sequence:
GTATGGAGAACTGTGTGCCCTGCTTTTTGCCAAAAGCCACTATGATGAGG[T/C]GAGTCCCCTTGCAACTGTCCCAGAAGTCTGTTTGGAGAAGGCCTGTTCTA
Long Flanking Sequence:
AATTATACGTATACTGTATCACTGAGCACTGTATCATCCTCAGTTATTTTAACCATGACTGTATATCCAATAAAACGATCAAAACAATTTAAAAGCCCAATAACTAATATCATTATTATTATTATTATTATTATTTAGAATTTTACATTTACTGTGTTAATTACATAGTTTTTATGGTCATTAGATCTTGGTTGTAAAAAAGCAGAAGAGTGTGTTACTTTGATATGTATTTATATGATATTGTATTAGTTCAAAATGTTAATCAATATTTTTGTAAAAAATAAACATTTTGACATGCAAGCTAATTTTATGCTGATTCTTATGTGCCAGGTTACTTCATGTGCGTAACGGCAACTGCAAATACCACCTGGGAGAAGAGACTTTTAAACTAGCCCAGTCTTACATGGACAAACTAGCCAAACACGGACATCAGGCTAATAAGGCTGCCTTGTATGGAGAACTGTGTGCCCTGCTTTTTGCCAAAAGCCACTATGATGAGG[T/C]GAGTCCCCTTGCAACTGTCCCAGAAGTCTGTTTGGAGAAGGCCTGTTCTACATTAATGTTTTCCTTGTGCATTTCAGGCCTATAGGTGGTGTATAGAAGCTATGAAAGAGATCACAGTCGGCTTACCTGTGAAAGTAGTAGTTGATGTTCTCAGACAAGCCTCAAAGGTCTGTTATTGTTGGATGTTTGAGTTATTCAATGTTTCTAATAATGAATCTAAAAAAGTGTCTACATTGATCTCTGCAGGCTTGTGTTGTTAAGCGGGAGTTCAGGAAAGCTGAACAACTGATTAAACACGCAGTCTTCTTGGCACGGTAAGAAATATCATGTGTAGTGAGAACTATCAACTTGAAATAGTTCAGTTTGACACTTCTGAAATATGTTCACATTTTTTTCAGGGAACATTTTGGGCACAAGCATCCAAAATATTCAGATACACTACTAGATTATGGGTTTTATCTCTTAAACGTGGATAATATCTGTCAATCTGTGACCATTTA
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:
sa16354
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 |
---|---|---|---|---|---|
ENSDART00000002824 | Nonsense | 287 | 446 | 8 | 11 |
ENSDART00000110234 | Nonsense | 287 | 586 | 8 | 14 |
ENSDART00000137569 | None | None | 246 | None | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 23285008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23996195 |
GRCz11 | 15 | 23931460 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGTTCACATTTTTTTCAGGGAACATTTTGGGCAYAAGCATCCAAAATA[T/A]TCAGAYACACTACTAGATTATGGGTTTTATCTCTTAAACGTGGATAATAT
Long Flanking Sequence:
TCAGGCTAATAAGGCTGCCTTGTATGGAGAACTGTGTGCCCTGCTTTTTGCCAAAAGCCACTATGATGAGGTGAGTCCCCTTGCAACTGTCCCAGAAGTCTGTTTGGAGAAGGCCTGTTCTACATTAATGTTTTCCTTGTGCATTTCAGGCCTATAGGTGGTGTATAGAAGCTATGAAAGAGATCACAGTCGGCTTACCTGTGAAAGTAGTAGTTGATGTTCTCAGACAAGCCTCAAAGGTCTGTTATTGTTGGATGTTTGAGTTATTCAATGTTTCTAATAATGAATCTAAAAAAGTGTCTACATTGATCTCTGCAGGCTTGTGTTGTTAAGCGGGAGTTCAGGAAAGCTGAACAACTGATTAAACACGCAGTCTTCTTGGCACGGTAAGAAATATCATGTGTAGTGAGAACTATCAACTTGAAATAGTTCAGTTTGACACTTCTGAAATATGTTCACATTTTTTTCAGGGAACATTTTGGGCACAAGCATCCAAAATA[T/A]TCAGATACACTACTAGATTATGGGTTTTATCTCTTAAACGTGGATAATATCTGTCAATCTGTGACCATTTACCAGGTGAGAAAATAATCGCTTTAAATGTGGGTGTGTAAATAAGCCACTTTCTCATTTGTTTGAAAGACTAAAGGCATTTCATTTGTTATTCAGACTGCATTAGATATTCGGCAGTCAGTGTTTGGAGGAAAGAATATTCATGTTGCGACTGCGCATGAAGACCTGGCGTATTCATCTTACGTCCATCAGTACAGCTCTGGTAAATTCGACACAGCACTGTGAGTATATCATTTCTGTCTAGAGAATTATGAACTAATATTCAGCACATATGCTTGGATGTTTTTTAATGCAATCTCAGAGCAGTTAATAACCTTTTAATTTACTGGCAATTGGTATAACATTTAATACTAAATTACATTTTAGTACATTATGCTCATCCTCCAATGAGAGGCGTGGTTTGGGGTAGGCCTGTCACAATAAGGAATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15168
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 |
---|---|---|---|---|---|
ENSDART00000002824 | Nonsense | 306 | 446 | 8 | 11 |
ENSDART00000110234 | Nonsense | 306 | 586 | 8 | 14 |
ENSDART00000137569 | None | None | 246 | None | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 23284953)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23996140 |
GRCz11 | 15 | 23931405 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AYACACTACTAGATTATGGGTTTTATCTCTTAAACGTGGATAATATCTGT[C/T]AATCTGTGACCATTTACCAGGTGAGAAAATAATCGMTTTAWATGTGGGTG
Long Flanking Sequence:
AGCCACTATGATGAGGTGAGTCCCCTTGCAACTGTCCCAGAAGTCTGTTTGGAGAAGGCCTGTTCTACATTAATGTTTTCCTTGTGCATTTCAGGCCTATAGGTGGTGTATAGAAGCTATGAAAGAGATCACAGTCGGCTTACCTGTGAAAGTAGTAGTTGATGTTCTCAGACAAGCCTCAAAGGTCTGTTATTGTTGGATGTTTGAGTTATTCAATGTTTCTAATAATGAATCTAAAAAAGTGTCTACATTGATCTCTGCAGGCTTGTGTTGTTAAGCGGGAGTTCAGGAAAGCTGAACAACTGATTAAACACGCAGTCTTCTTGGCACGGTAAGAAATATCATGTGTAGTGAGAACTATCAACTTGAAATAGTTCAGTTTGACACTTCTGAAATATGTTCACATTTTTTTCAGGGAACATTTTGGGCACAAGCATCCAAAATATTCAGATACACTACTAGATTATGGGTTTTATCTCTTAAACGTGGATAATATCTGT[C/T]AATCTGTGACCATTTACCAGGTGAGAAAATAATCGCTTTAAATGTGGGTGTGTAAATAAGCCACTTTCTCATTTGTTTGAAAGACTAAAGGCATTTCATTTGTTATTCAGACTGCATTAGATATTCGGCAGTCAGTGTTTGGAGGAAAGAATATTCATGTTGCGACTGCGCATGAAGACCTGGCGTATTCATCTTACGTCCATCAGTACAGCTCTGGTAAATTCGACACAGCACTGTGAGTATATCATTTCTGTCTAGAGAATTATGAACTAATATTCAGCACATATGCTTGGATGTTTTTTAATGCAATCTCAGAGCAGTTAATAACCTTTTAATTTACTGGCAATTGGTATAACATTTAATACTAAATTACATTTTAGTACATTATGCTCATCCTCCAATGAGAGGCGTGGTTTGGGGTAGGCCTGTCACAATAAGGAATTTTTGTTGTGCGATACACAAGCGATATTATTGTCATTTTGAGATTTTATGCCACTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13157
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002824 | Essential Splice Site | 313 | 446 | 9 | 11 |
ENSDART00000110234 | Essential Splice Site | 313 | 586 | 9 | 14 |
ENSDART00000137569 | None | None | 246 | None | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 23284843)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23996030 |
GRCz11 | 15 | 23931295 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCAMTTTCTCAWTTGTTTGAAAGACTAAAGGCATTTCATTTGTTATTCA[G/T]ACTGCATTAGATATTCGGCAGTCAGTGTTTGGAGGAAAGAATATTCATGT
Long Flanking Sequence:
TAGAAGCTATGAAAGAGATCACAGTCGGCTTACCTGTGAAAGTAGTAGTTGATGTTCTCAGACAAGCCTCAAAGGTCTGTTATTGTTGGATGTTTGAGTTATTCAATGTTTCTAATAATGAATCTAAAAAAGTGTCTACATTGATCTCTGCAGGCTTGTGTTGTTAAGCGGGAGTTCAGGAAAGCTGAACAACTGATTAAACACGCAGTCTTCTTGGCACGGTAAGAAATATCATGTGTAGTGAGAACTATCAACTTGAAATAGTTCAGTTTGACACTTCTGAAATATGTTCACATTTTTTTCAGGGAACATTTTGGGCACAAGCATCCAAAATATTCAGATACACTACTAGATTATGGGTTTTATCTCTTAAACGTGGATAATATCTGTCAATCTGTGACCATTTACCAGGTGAGAAAATAATCGCTTTAAATGTGGGTGTGTAAATAAGCCACTTTCTCATTTGTTTGAAAGACTAAAGGCATTTCATTTGTTATTCA[G/T]ACTGCATTAGATATTCGGCAGTCAGTGTTTGGAGGAAAGAATATTCATGTTGCGACTGCGCATGAAGACCTGGCGTATTCATCTTACGTCCATCAGTACAGCTCTGGTAAATTCGACACAGCACTGTGAGTATATCATTTCTGTCTAGAGAATTATGAACTAATATTCAGCACATATGCTTGGATGTTTTTTAATGCAATCTCAGAGCAGTTAATAACCTTTTAATTTACTGGCAATTGGTATAACATTTAATACTAAATTACATTTTAGTACATTATGCTCATCCTCCAATGAGAGGCGTGGTTTGGGGTAGGCCTGTCACAATAAGGAATTTTTGTTGTGCGATACACAAGCGATATTATTGTCATTTTGAGATTTTATGCCACTGATTATATAATGATTATATAACAGCATAATAATTCAAATAGCCATAAACACTTATCATGAAAATACTTATAAAGCTTAGGGTTATTTATTTAAATTCTATAATTATGGTGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22644
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002824 | None | None | 446 | None | 11 |
ENSDART00000110234 | Nonsense | 543 | 586 | 13 | 14 |
ENSDART00000137569 | None | None | 246 | None | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 23276733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23987920 |
GRCz11 | 15 | 23923185 |
KASP Assay ID:
2260-8481.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTGGAAACTATGAGAAGGTATTTGAGTATCACAATATTCTGTCCAACT[G/A]GAACCGTTTAAGGGACAGGCAGTTTGCCGTAGCCGATGCGCTGGAGGACG
Long Flanking Sequence:
CTGAGGACCACAATGCAAACTTTTGGAAATGGAAATTGATATTTTTTGTATTTCAATTTTGACAGTTTTTAAAATATGTATGAGTTATTCCTATTGGCCTGTCAAATAAAAACAAACAAAACAAATATAGAGTCATTATGGTCAAAATAATTGGTCAAATTAATAAAATCAAAGATGTCAAAAAGTAAAGTAAAAAAATGGTTCATGTTTCAACTTCAGAAGTCATTCTAATTAGATTTTTTTTCTGAATGTTTAATTTAAGTTTCAAAAGAACATTTAAAAAAGTACCAAGTGTCTGTTCTGTCATTTTTAATGACTTTACCACATGTTTAAAATAGCAACCCCAGTCATTTGAATCTATCTGTTGTTTCCTTCAGGCAAGAAGCTGTTTGGGGAGGGTTACAGTGGACTGGAGTATGACTACAGAGGCCTGATAAAACTGTACAACTCAGTTGGAAACTATGAGAAGGTATTTGAGTATCACAATATTCTGTCCAACT[G/A]GAACCGTTTAAGGGACAGGCAGTTTGCCGTAGCCGATGCGCTGGAGGACGTCAACACAACCCCCCAGTCCACAGAGCAGGTGGTGCAGTCTTTCCTGCTTTCCCAGAGCCACGGAGCCGGACGCTTGGGCTAACACACCCAGCGTTCACTTTAAAAACACATAGATGTGCACAGCCACCCCCATTTCACACATTCACACCCATTTATTCACAAGTAGTCAAGGCAAGGAGGGGAAGTTTGGAGAGCTCTTGAACTGTCAGTTCACAGTTCCCATAGGCCCATTTTCCTTGAAGTGGGAACATAAACATGACCATGCTTAAACACTCACCATGGACAAGAAACCATTCTTCAAAGAACCATTGAATTATAAAAATAAAATAAAATGAAAAAGGAGCGAGGATGGAAATCTTCGAACCACCGCTTTTTTTTATTTTGTATTCGAAGGAGTGTTGCTCCACATACAGGAATACCTATCACTGCATCTGCTATTTGTGAAGAAA
Associated Phenotype:
Not determined