Busch Lab

ZMP

apbb2

Ensembl ID:
ENSDARG00000061880
ZFIN ID:
ZDB-GENE-090313-73
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
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