ZMP
apbb2
Ensembl ID:
ZFIN ID:
Human Orthologue:
APBB2
Human Description:
amyloid beta (A4) precursor protein-binding, family B, member 2 [Source:HGNC Symbol;Acc:582]
Mouse Orthologue:
Apbb2
Mouse Description:
amyloid beta (A4) precursor protein-binding, family B, member 2 Gene [Source:MGI Symbol;Acc:MGI:1084
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16258 | Nonsense | Available for shipment | Available now |
sa611 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16258
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 |
---|---|---|---|---|---|
ENSDART00000088750 | Nonsense | 589 | 890 | 8 | 15 |
ENSDART00000138796 | Nonsense | 564 | 863 | 10 | 17 |
ENSDART00000146232 | None | None | 138 | None | 3 |
The following transcripts of ENSDARG00000061880 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 18711676)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 19273510 |
GRCz11 | 1 | 19966447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGCTGTAAACAACTGCATYCGTCAACTGTCCTACTGCAAGAATGAYATA[C/T]GAGACACTGTGGGCATCTGGGGAGAGGTGAGCTACAGCTACACACACACA
Long Flanking Sequence:
TAACTCATATATAGGCATGGACAAGGAAATTAAAGAGCACTTGAAAACTCTCCTGGAGTACTGGAAGAGCATCCGCTGTGTAAAATATATGCTAGATAAGTTGGTGGTTCATTCCGCTGTGGCGACCTCTGATAAATAAAGGGACTAAGCCGAAGGAAAATGAATGAATGAACGAACGAAGGAATGAATATCATTTTGTTTTAATTTCTTGACATTAAAAATCAGGGATAGCTTGGCATATATTGGTATTGTGTTGTCTTAAAAAGTAATACAAATCCGTCTGAATATAACAATAGAGTATGTTTTTATCTTTTTTTTGGCAAAAAGGAAATTCTCTAAATGAAATGTTTCATCAGTGGGTGTGTTTTTTTTTATTCCAGTGTTTTGCCGTGCGCTCTCTCGGTTGGGTAGAGATGGCTGAAGAGGATTTGGCTCCGGGTAAAAGCAGTGTCGCTGTAAACAACTGCATTCGTCAACTGTCCTACTGCAAGAATGACATA[C/T]GAGACACTGTGGGCATCTGGGGAGAGGTGAGCTACAGCTACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAGAAACAAATACATTTCTAAAAATCTTTTGCACAATCTTTGCACAGTTTTACCAGAACCTTTGAAGTTTGAAATAGTTCTGCTGCTTTACACAAATATTTTTTTTAATATCCATATGCTGGGGCAAAGGAGTGGCGCAGTAGATAGTGCTGTCGCCTCACAGCAAGAAGGTTGCTGGGTCGCTGGTTCGAATCTCGGTTCTGTGTGGAGTTTGTATGTTGTCCCTGCCTTCGCGTGGGTTTCCTCCGGGTGCTCTGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTGTGTGTGTGAATGTGTGTGTGTGTGTGGATGTTTTCCAGAAATGAGTTGCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa611
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088750 | Nonsense | 837 | 890 | 15 | 15 |
ENSDART00000138796 | Nonsense | 810 | 863 | 17 | 17 |
ENSDART00000146232 | None | None | 138 | None | 3 |
The following transcripts of ENSDARG00000061880 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 18734009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 19295963 |
GRCz11 | 1 | 19988900 |
KASP Assay ID:
554-0521.1 (used for ordering genotyping assays)
KASP Sequence:
ATCCTCTCACTTTTTGACTCTTTTTCTCCTTTATGTCTGCAGTTGAGGTA[T/G]CAGAAGTGTCWGGTGGCGCGTCCTCCATCTCAGAAAGCCTGCTCACAGGC
Long Flanking Sequence:
CGCTTATCCGCACACCTCTCAAAAAAATTTAAACTACACGTCGCACAGGCTTTGTAATTGGTCAGTTTGACAGCAGTAACGGCCTGGATTAATTTGTTGTTCAATGTTGAAGTTTAATAAATAGTTTAATAAATAATCATAGACAGTAGATAGTGTGTGTTTCTATCAATTGTTTTAAAATCAAGTAATGCAACCTTCCTTAAAAAATCTCTCACTGGTAATATGTGAACTTATTTACTGTACAAAACCTGTCAGTGAACTATGAAGGCAAAAAAATAAAATAAAATAATTGTTCATTATTTATAATTAATACGAGTTAAAAGTATAATGTTTAGTTAAAGTATAATAAAAAGTACAATATAGAGTTAAAATGTTCAAGTAATCGAGATTTTGATAGGCCAAATCGCCCAGCCCTACAACCCAGCCTGTATTATTATACTCAACACATACATCCTCTCACTTTTTGACTCTTTTTCTCCTTTATGTCTGCAGTTGAGGTA[T/G]CAGAAGTGTCTGGTGGCGCGTCCTCCATCTCAGAAAGCCTGCTCACAGGCGGCCCCTGCTGATTCAGTCACCCGCCGCGTCTCCACCAGCGTCAAACGTGGAGTTCTGTCTCTCATCGACACGCTCAAACAGAAGAGACCCGTCACTGAGCTGCCTCAGTGATCTGACACGCACACTCACCGTCACGCTCTGCATGCTTATAACTATCCGAATGTCCTGTACATACCTGTCCGGTCACATGGTGGAGATGAAGAGGATCACAAGGATGAAAAATCAGAAAATAAAGCTGATGCCAAGAAAATACACCCTTTACTCACACACTCACAAGTACATCAGATCTACTATACAAGCCTCTCTCTCTTCCGATGTCAATCATGCATATATTTGCATGGGAAGCCACGCCTCTCCAGCATGACAGCAATCAACAGGCTCTGCCCACCTAGAAGAACCGCCTCATCTAGAATAAGCCTGATCAAAGAGAGAACTTGATTGGAAGAATG
Associated Phenotype:
Not determined