ZMP

cbfa2t2

Ensembl ID:

ENSDARG00000074337

ZFIN IDs:

ZDB-GENE-060929-236, ZDB-GENE-070209-1

Description:

hypothetical protein LOC767652 [Source:RefSeq peptide;Acc:NP_001070060]

Human Orthologue:

CBFA2T2

Human Description:

core-binding factor, runt domain, alpha subunit 2; translocated to, 2 [Source:HGNC Symbol;Acc:1536]

Mouse Orthologue:

Cbfa2t2

Mouse Description:

core-binding factor, runt domain, alpha subunit 2, translocated to, 2 (human) Gene [Source:MGI Symbo

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa33986	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa33985	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa33986

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
ENSDART00000083807	Essential Splice Site	50	568	1	10

Genomic Location (Zv9):

Chromosome 6 (position 57604960)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	57658022
GRCz11	6	57654886

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCCGTCAACCCCAGCGGACCTCGTCCCGCAGCCTTCTCCACTACTGCAT[G/A]TGAGACTCACACACACACTTGTATAGCTATCTTTATGGGGACTTCTCTTA

Long Flanking Sequence:

TATGTTCAATTGACCTAAATTTGTAAAAGCGATACATTTAACTTGAACAGTTTGTGTTGGGTCAACATCTTGAAATTCTGTGTGGTGTAATTTACACCTTAGGATTGAAACATGCCATTAATTTGTGTGCACGAAAGTGGGACAGTTTGCAGATGATGAACTTTTGGTGAGCTCTCCTCCCTCAGTGTCTTAATGTCAGACAGAATGAGATCAGAGATGTTCTGCTGCCACCGATCTGCCACGTTGATTGGGTTTTAATGGAAATCTCCACATGCACAAACAGAACCGTTGGTGATTAGAGGGAAATCAGTGATGTGTCAGTCTGAGCTCATTCTGTGTCTGGCTCTGATTTGCAGACAGTGCAGAGAAGAAGGTTCCTGCCATGCCCGGTTCCCCAGTGGATGCAAAGACTCATTCCAGACCGACCGTCTCCGTCATGCCACCGCTGCCCTCCGTCAACCCCAGCGGACCTCGTCCCGCAGCCTTCTCCACTACTGCAT[G/A]TGAGACTCACACACACACTTGTATAGCTATCTTTATGGGGACTTCTCTTAGCTGTAATGTTTCTACTGTACAGACTGTGTATTCTTTACCTCCAAAACCCAATCCTCACAAGACACAATCTGCAGTTTTACAAAACTCTGTGTGATTTCTGAGCTGATTTCCTCATGTGGACAAAAAAATGTCCCCGTAAGGTAGAAAAAAAATACTGGTATTGCTATACTTGTGGGGACATCTGATCCCTACGACTTAAAGAATACAAAGTACAAACACACACACACACACACACACACACGCACACACACACACGTTTGTTTTTGTGAAAAGTGGGGACATTACATAGGTTTCCATTCCTTTTATACTGTCCAAACCGTATATTATATTGCCCCCACCCGACCCCACCCCTAAACCCAACCATCACAGGAGACTGTGTGCAGCTTTACTCTCTGATTAAACTCATTCTGTAGGATTTATAAGCATTTTGAGAAATGAAGACGTCACCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33985

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000083807	Essential Splice Site	329	568	6	10

Genomic Location (Zv9):

Chromosome 6 (position 57592090)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	57645152
GRCz11	6	57642016

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGACTGACGGAGAGAGAGTGGGCTGAGGAATGGAGACATCTGGATCATG[T/A]AAGTCTACGCTTATGGAGAATCTGCTAACATCTTTAAAGAGCCATGAAAC

Long Flanking Sequence:

ATACACACAAACATACACAGACACAAACATACACACACACATACACTATTAAAGAAGATGTGCCCATGACTCACAGCTACACACAGTTCAGTTATTAGATCATTACCAACCAAACACAACTCACAGAAGTCGGGTGGAAACTATGCTAATGTAGGACTGTCAATCATTAGCAATGGGCGGGGCTTAAACAATGTGACATCACATTGCTTAGAAAATCTAAACTGCGTGTCTAATGAGACTCGACTTAACGTGACATCTGATTTAATGTGGATTAGAAAATAAGGAGTGGGTGGATTTGATCAGTAGAAGGATGCCAACACACATTTATGTCCAAACACCACACAGCAGAGAATCTTACATAATATGTGTCCTTTAAAGAGATTTCTGACACACTTTTGTGCTGATGTGTTCAGGCAGTAACGGAGGCTACCGAGAGGAGCCTGTAGACCACAGACTGACGGAGAGAGAGTGGGCTGAGGAATGGAGACATCTGGATCATG[T/A]AAGTCTACGCTTATGGAGAATCTGCTAACATCTTTAAAGAGCCATGAAACCCCCTTGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCAGCTTTGTTTAGGGGGGAGTGTCGGAGGAACTAAAGTGGGATGGTGTGGGAGTGTCTATTTGGGCACGCGCTGACTTTCAGAGTCAAAACACACACAAACACGGGAGAAAGTGACTGTGTTTACATGGACATCTGTAGTCGAATTATTTGGCAAATTATTAAATGGTGGACTTTAACTGCAGTTCGGCTCTTTCATTCAGGGAATTCATTCATGTCCCTCGCGACAAACGAGATATTTGATTCGAGGAGCTGCTGTAAGCGTGTATTTTTCATGCAATGTTTGATACCGCACGGCGAATGAGAGAAAAAAAACCCTCCGCATTTCCCGGAAACTTAGATGCACACGGCAGGTAGCGTCAGAAAGCCGCGTGTGTTATTCCGGTC

Associated Phenotype:

Not determined