ZMP

si:ch211-51e8.2

Ensembl ID:

ZFIN ID:

Human Orthologues:

EBF1, EBF2, EBF3

Human Descriptions:

early B-cell factor 1 [Source:HGNC Symbol;Acc:3126]
early B-cell factor 2 [Source:HGNC Symbol;Acc:19090]
early B-cell factor 3 [Source:HGNC Symbol;Acc:19087]

Mouse Orthologues:

Ebf1, Ebf2, Ebf3

Mouse Descriptions:

early B-cell factor 1 Gene [Source:MGI Symbol;Acc:MGI:95275]
early B-cell factor 2 Gene [Source:MGI Symbol;Acc:MGI:894332]
early B-cell factor 3 Gene [Source:MGI Symbol;Acc:MGI:894289]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa8686	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa8686

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
ENSDART00000140184	Essential Splice Site	172	195	6	6

The following genes are also affected by this mutation:

ENSDARG00000069196

Genomic Location (Zv9):

Chromosome 21 (position 32938983)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	33938676
GRCz11	21	33973166

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATGCACAATACTGCTTTCTTAGCTAATTTTGTTTTGTTGTTGTCCTTTTA[G/A]TCGATGCTGCGACAAAAAGAGTTGTGGAAACCGCAATGAGACACCCTCTG

Long Flanking Sequence:

CGTTCTGCTAGACCTTCACAAATGGGAATTCTTGATCAACTTGCAAGCAAGCAGTACTGTTAAACACAAATATATGCAGTTTTGTGTTTTTGTGGTGGTGTAGTGCTAAAGTGAGTGATATAAAATAAATGTAAATGTCAGCAAGACAAAAGAAAAATCCTTCTTATCTTCCATTATTGATGTTTCTATTCTTGCAATCCATCACGACTCGTCTGTTAAAATATTAAGAAGAAAAAAGTCTTTTGTCTTTCATATTTTAGTCAATGTCACTTGCTCTGCCTCTGAAGGAACTTTCCTATTTTATTGATGTCATTTCACCCTCTTTTAAGCCACTCCCCTTTAACATCTATCTGAAACTAGTTTTCTGTGTTGAATTAAAATACTGTTGTGTTTAGTTTAGCTTTCATGAACATTGATTTGTAAAAATAAAACCCTAAAATGCCTTATTGAATGCACAATACTGCTTTCTTAGCTAATTTTGTTTTGTTGTTGTCCTTTTA[G/A]TCGATGCTGCGACAAAAAGAGTTGTGGAAACCGCAATGAGACACCCTCTGATCCAGTCATCATTGACAGGTAGGTACTTGTGTGTCTAAAAACATTTGATACCTTTGTTTTTATAATCTCACAAAAATAGAGTCTGTGGTTGAAGTTTTCGTGACATGCTGAAGTAATCACGGTCTGCTCCGTGTGTGTTTAAGTCACTTGTTAGTGAACTGCTCTGTCAAATATTTTTAAATTTTGTTGTGGCGTTAGGATTGGCTGAGCACAAACACTTGATATTTATGTGCTTTTTTATTGCTGTCTTTGCTTAGGTAAATTATTGGCATAAAGTCTTTAGACATAGCTTTTGTTAAAAGTGTTTATATAATTTCTCTTGAAAAGATGTTAGCGATTGAGATAATATCTACATGGTATGTACTTCAAATTGATATCTGGCCTGGTTTTGAATTTTGGTTCCCTTTGAATTATGGTACAAAAGACAGTGTTCTTGGTCCCTTTTGTTC

Associated Phenotype:

Not determined