ZMP

si:ch211-271f14.1

Ensembl ID:

ENSDARG00000076560

ZFIN ID:

ZDB-GENE-091118-127

Human Orthologue:

APBB1

Human Description:

amyloid beta (A4) precursor protein-binding, family B, member 1 (Fe65) [Source:HGNC Symbol;Acc:581]

Mouse Orthologue:

Apbb1

Mouse Description:

amyloid beta (A4) precursor protein-binding, family B, member 1 Gene [Source:MGI Symbol;Acc:MGI:1077

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9076	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa21692	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa9076

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
ENSDART00000115130	Essential Splice Site	656	710	12	13
ENSDART00000136709	Essential Splice Site	637	681	12	13

The following transcripts of ENSDARG00000076560 do not overlap with this mutation:

ENSDART00000141652

Genomic Location (Zv9):

Chromosome 10 (position 16021609)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	16034916
GRCz11	10	15993035

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGATCCAAATGCAGCCAGTCTAAGTGAGGCCGTACAGGCTGCCTGCATG[G/A]TGAGCAAGGAATACCTAGTACATTCTTTACATACTTGCCCATTACTATAC

Long Flanking Sequence:

TTATCTGTGACTGCTTAAAATACCTGTTTATATTTTTAACTGAAAGTTAGTTCTCTGAAATAAGCTTGTCGTGTTGGTTTTGTTATTTGAAGGGATGGAAGTTATTAATGTAGCACTGGAGACTGCCCTGAACAAAGACAAGGAGGATTGGACACCTGTGACTGTAAACGTGGCCTCTGCTACGCTTACTGTTCTAACATCTGAGGTCAAGTTTTTTTTTTTTTACACTTAAGTATTATTAACTTGAATACCCAATTCTTGATTTTAAATGTCTGCTTAGCTTTGTTAATTGCACTGAAGTTCTATCTTTTTTTCGCAAACAGACAGAGGAAGTTCTCTCTGAGTGTCGTGTGCGTTTCCTGTCATTTATGGGAGTCGGGAAAGACGTTCACACCTTTGCGTTCATCATGGCAGAGGGACCTGGAGACTTTATATGTCACATGTTCTGGTGTGATCCAAATGCAGCCAGTCTAAGTGAGGCCGTACAGGCTGCCTGCATG[G/A]TGAGCAAGGAATACCTAGTACATTCTTTACATACTTGCCCATTACTATACTATACAATTAAATGAAGTTGCCCCAGATGTGGATGAGACTGAAATATTCACGTGCTGCTTGTAAAACTAGCATTACATTTTTAGTTCAAGCAGCTGTAAAACTGTTGTTAGAGGAATGAGTATCATGCAGGTGGAACACAAAATAAGATGAATAAATTGTTTATGCTTTTCATACAATGATACTATAGTTTCACAATACTTTGAGCTAAATATTTCCACAAAAAAGCACTGTAACACTATTTTGACATTAGCCCTTTTCATACCAGCAATGAACGGAACGGAACGCGCGTCAAGCGCGAGTGATTTACATGTTAAGTCAATGCAAACGCGCGAATAGACATCCTGTGGCGCGATACGAGCGAATGGCACGGCACGAATGACGAGAATTGCGCGGTGCGCATGGCGCGAATGGCGTGGCGCGAATTGAGCGTTTTGCGCGTTTGACACGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa21692

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115130	Essential Splice Site	656	710	None	13
ENSDART00000136709	Essential Splice Site	637	681	None	13

The following transcripts of ENSDARG00000076560 do not overlap with this mutation:

ENSDART00000141652

Genomic Location (Zv9):

Chromosome 10 (position 16021610)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	16034917
GRCz11	10	15993036

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGATCCAAATGCAGCCAGTCTAAGTGAGGCCGTACAGGCTGCCTGCATGG[T/C]GAGCAAGGAATACCTAGTACATTCTTTACATACTTGCCCATTACTATACT

Long Flanking Sequence:

TATCTGTGACTGCTTAAAATACCTGTTTATATTTTTAACTGAAAGTTAGTTCTCTGAAATAAGCTTGTCGTGTTGGTTTTGTTATTTGAAGGGATGGAAGTTATTAATGTAGCACTGGAGACTGCCCTGAACAAAGACAAGGAGGATTGGACACCTGTGACTGTAAACGTGGCCTCTGCTACGCTTACTGTTCTAACATCTGAGGTCAAGTTTTTTTTTTTTTACACTTAAGTATTATTAACTTGAATACCCAATTCTTGATTTTAAATGTCTGCTTAGCTTTGTTAATTGCACTGAAGTTCTATCTTTTTTTCGCAAACAGACAGAGGAAGTTCTCTCTGAGTGTCGTGTGCGTTTCCTGTCATTTATGGGAGTCGGGAAAGACGTTCACACCTTTGCGTTCATCATGGCAGAGGGACCTGGAGACTTTATATGTCACATGTTCTGGTGTGATCCAAATGCAGCCAGTCTAAGTGAGGCCGTACAGGCTGCCTGCATGG[T/C]GAGCAAGGAATACCTAGTACATTCTTTACATACTTGCCCATTACTATACTATACAATTAAATGAAGTTGCCCCAGATGTGGATGAGACTGAAATATTCACGTGCTGCTTGTAAAACTAGCATTACATTTTTAGTTCAAGCAGCTGTAAAACTGTTGTTAGAGGAATGAGTATCATGCAGGTGGAACACAAAATAAGATGAATAAATTGTTTATGCTTTTCATACAATGATACTATAGTTTCACAATACTTTGAGCTAAATATTTCCACAAAAAAGCACTGTAACACTATTTTGACATTAGCCCTTTTCATACCAGCAATGAACGGAACGGAACGCGCGTCAAGCGCGAGTGATTTACATGTTAAGTCAATGCAAACGCGCGAATAGACATCCTGTGGCGCGATACGAGCGAATGGCACGGCACGAATGACGAGAATTGCGCGGTGCGCATGGCGCGAATGGCGTGGCGCGAATTGAGCGTTTTGCGCGTTTGACACGCTT

Associated Phenotype:

Not determined