ZMP

A0PJR1_DANRE

Ensembl ID:

ENSDARG00000062000

Description:

LOC100007078 protein [Source:UniProtKB/TrEMBL;Acc:A0PJR1]

Human Orthologue:

ABTB2

Human Description:

ankyrin repeat and BTB (POZ) domain containing 2 [Source:HGNC Symbol;Acc:23842]

Mouse Orthologue:

Abtb2

Mouse Description:

ankyrin repeat and BTB (POZ) domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2139365]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9010	Nonsense	Mutation detected in F1 DNA	Not yet available
sa7531	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9010

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
ENSDART00000089113	Nonsense	450	1032	4	17

Genomic Location (Zv9):

Chromosome 25 (position 25429410)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	24608523
GRCz11	25	24706071

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGTGATGATGTCAGACAGACAGCMCGACTACTCCTGCCTGGGCTKGACTG[T/A]GAGCCCAGACTGCTGAAGTAAGACAACCAACGARAAAAAGCTAGTCKGAC

Long Flanking Sequence:

ATTAACATCCAAGTCCATGCTTGTTAACATTAGTTAATGCACCATGAGTTAACATGAACTAACAATGAACTACTGTATTTTCATTACCTAACGTTAACTAATATGAACAAATACAGTAGTAAATGTATTGTTCATTGTTTGTTCATGTCAGTAAATCCATTAATTAACATTAACTAAAGAACCTTAATGTAAAGTGTGACCTATTCTAATCCACACCATAACACTAAAAAAAAAAATCATATACAATATATATATATATATATATATATATATATATATATATATATATATATATATAAATAAAAAGAAAAAGTTTCAGTATTCGTAACATAAAAAATCATACTCTTTTCTATTGCTATTCCCAGGCCTTTCCTGCTCCTCCCCCCTTTAATGGAGTGGATGCGTGTAGCCATTGTTCATGCAGAGCATCGGCGGAGCTTATTGGTGGACAGTGATGATGTCAGACAGACAGCCCGACTACTCCTGCCTGGGCTGGACTG[T/A]GAGCCCAGACTGCTGAAGTAAGACAACCAACGAAAAAAAGCTAGTCTGACTGACAACCAGCAAGCTTTTTCACTGGGTGGCTGATAATCAAGTAAAGAAAATCTTGTAGACATGCACTAAACACTTACACATCTTGGATATATACATACATAGTCTTGGATAGAAAGTGCCCTTCCAAAATGATCAAAAGTGCCCCCGTGACGCGGCACACCTTCGGTCCCGCCCTTCAGTAGGCGCGCGACAACACCCCTCTTGAGTACGAGAGATCTGCAGATCTGCACAAATTGCCCCCACCCCCCGCTCTTCCAAAAATTTATCCCGCTCATGCCCTTTGGACGGTCTCTGCACGGGCCTGTGTAGCGTACAAAACTAGCACCCTGTCGGAACAGCTTAGCAACTGTATAACAGTGCCCAAGCACCCCATTCAGAACACTTTAGCAATACATAGAACAGCTTAGCTAATGCACACTAATGCTTCAACAATCACTCTGAGCACCAGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7531

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:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000089113	Missense	975	1032	17	17

Genomic Location (Zv9):

Chromosome 25 (position 25446394)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	24625507
GRCz11	25	24723055

KASP Assay ID:

554-4146.1 (used for ordering genotyping assays)

KASP Sequence:

GATCCTAATTTGTCNNTGTGTACAGGCTAATGGTGCAGTGGAGCTCAGTA[T/A]AWACTGTGAAGGTTAYTTCCTGCAGAACATGGCARTTCTGTTGGAGAGAGAA

Long Flanking Sequence:

CATTTACACATTACTATTGAACTGTGAAGAGACTTTTAATTAGCACAACAAAAATGTTTCTGAAGACAATAACCTCTTCACCTTTTATCCCAATTTCTCGATTTCAACACAAGGACAGAAGAGATGTCAGACAATAAAGTGGAAAACTTACTTGTCCTAATTTAAAACTAAAAAGAAAATAATACTTCAAAAATGTAATATGTTTTCTTGGTAATAAAAAGTAATGGGTTACTGAGCATACAACTCACATTACTCATAGTGGATCACACAAAACACTGATAATTAGGTATATAATAAAAGTTAATTTTTTATTTTTTTAAATAACATACTATACAATTTTATAGGCCAAAAAAAACCAAAAAAAAAACATGTAAAGGTGGTTCAGTATTACCATGTTACAGCTTCGTTTGTTAAAGTTACACTAACAAAGTTTTTTTCTGTAGTAAGTATGATCCTAATTTGTCTGTGTACAGGCTAATGGTGCAGTGGAGCTCAGTACA[T/A]ACTGTGAAGGTTACTTCCTGCAGAACATGGCAGTTCTGTTGGAGAGAGAAGCCTTTCGGGTGATGATCCTGGGGTCTGGGGCAAGGAGCGGATCTGGGAAAGACTCTCTTTTGGAAGCGCTGGAAGCAACATTAGTGCGCAGACTGCGTTCGCTGCTGGTGACATCTCGCGTGTGAAAGGAAAAGAATGAAAACTAGAAAGAAATACACAGAGTGAATGTGATTCTAAGACTGTGAGGAAAGTATGAAGAATAATCAAAACAAGATGGAATGATGACTGAACATGAGCTTTAGGGACAGTTTCCTGAATTAAAAAAGCTTAAAGGTTACAAATGATGTGTGGCCAAAGCTATCAGAACTTATATATGTTAAGAGTGCGGACAACAGTTATCCCACAGTTAAACAGATGCCATTTTGTACAGTTGTTGGCTAAAGTGGGAGGCTAGAGTGTATCTTTATCTTTTTTTTTTTCCTCCATAGTTGTTTTATTTTAAGCTATCA

Associated Phenotype:

Not determined