ZMP

coe2

Ensembl ID:

ENSDARG00000042525

ZFIN ID:

ZDB-GENE-990715-11

Description:

Transcription factor COE2 [Source:UniProtKB/Swiss-Prot;Acc:O93375]

Human Orthologue:

EBF2

Human Description:

early B-cell factor 2 [Source:HGNC Symbol;Acc:19090]

Mouse Orthologue:

Ebf2

Mouse Description:

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

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa2249	Essential Splice Site	F2 line generated	Not yet available
sa20582	Essential Splice Site	Available for shipment	Available now
sa44626	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa2249

Status:

F2 line generated
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
ENSDART00000014822	Essential Splice Site	136	578	5	16

Genomic Location (Zv9):

Chromosome 5 (position 70394648)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	66719792
GRCz11	5	67398161

KASP Assay ID:

554-3310.1 (used for ordering genotyping assays)

KASP Sequence:

TCGTTCTGATTTTTAATGCATYGATTCGCATTGCTGTTTTGCATGGTTCA[G/A]CCCATATCATATGAAGGGCAGAACAAGAATCCAGAAATGTGCCGCGTTTT

Long Flanking Sequence:

GCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTCAAATATTATTTACTGTCATCATGGCAAAGATAAAATAAATCAGTTATTAGAGATGAGTTATTAAAACTACTGTGTTTAGAAATGTGTCGAAAAATTCTTCTCTCTGTTAAACAGAAATTGGGGGGAAAAATAAAGGGGGCTAATAATTCTGACTTTAACTGTGTATTCTGTGTAAATATTATCCTTTATTTAGATTCAGTGGCCAAATTTGAACTCTGGTTTAATTACCAATCCTCTATATAGTGACATCAGTAAGTTTATGTGTTGTTTTTGTTCACAGGCGTCCGCACTGAACAAGACCTTTATGCTCGTCTCATTGACTCGGTCACTAAACAGGTAAAACACTGCTATCCTTTTCTGAGGTTTGAATTCTTCTAGCCAAAATAAAATGCTTGCTTCGTTCTGATTTTTAATGCATTGATTCGCATTGCTGTTTTGCATGGTTCA[G/A]CCCATATCATATGAAGGGCAGAACAAGAATCCAGAAATGTGCCGCGTTTTGCTGACTCATGAGGTCATGTGCAGGTGAGTACGTTTTTGATATGTACAGTTGAAGTCTGAATTATTGGCTCTTCAGAATTATTAGCCCAGCTATATATTTTATCCTCAATTTCTGTTTAACGGTAAGAAGATTTCAGCACATTTCTAAACACAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTAATTTTTGTCATGATGACTACAGAATATTTGACTACATGTTTTTCACTAGTATTCAGCTTAAAGTGACATTTAAAGACTTAATAAGGTTAAGTTAGGGTAATTAGGCAGGCCATTGTATAACAGTGGCTTGTTCTGTAGACAATTGAACAAATATTGCTTAAGGGGGTTAACAATATTGAGTTTCAAAATGTTTTTTTAAAAATACAAAATTGCTTTTATTCTAGCCGAAGTAAAACAAATGAGACTTTCTCCAGAAGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa20582

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000014822	Essential Splice Site	302	578	10	16

Genomic Location (Zv9):

Chromosome 5 (position 70428500)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	66753644
GRCz11	5	67432013

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGATTGTGTAACAAACTTTAACAACTTGTTTTTCTCTCATTATTCGTGCA[G/A]TTGATCACACCTCATGCGATTCGAGTTCAGACTCCACCTCGACACATTCC

Long Flanking Sequence:

GAAAAATATGATGAATATACTATAACAATTGTGTACTCTCAGAAATAAAGGTAAGGAAGCTGTCACTGGGGCAGTACCTTTTTAAAGGATACATATTTGTACGCAAATAGTCCACAGTGGTACTTAAAAGGTGCATATTAGTCCCCAAATTTACCTAAAGAAATACCTTTGAGGTACCATAATAGACCTTTCAGGTACAAACATGTACCTTTTGAAAAGGTACTGCCCCCGTGACAGCTCCCGTACCTTTATTTCTGAGTGTCGAAGGTTAGCATTTTGCTAAAGCTAAAATTGTGGAAAATGTCAGCTCTGTTACTGTCAACTCTGTTAGTCTATTAATTATTTAATAATATATTTGTTTAATATCGCTCCAGTTTAAAGTAAATGAATGGGAAATATTTGAAATGTACCATGTAGTGTCAAGTTAACTGGCTTTGAAATTAAGGACCAAGATTGTGTAACAAACTTTAACAACTTGTTTTTCTCTCATTATTCGTGCA[G/A]TTGATCACACCTCATGCGATTCGAGTTCAGACTCCACCTCGACACATTCCAGGTGTTGTAGAAGTTACACTGTCCTACAAATCTAAGCAGTTTTGTAAAGGAGCTCCGGGACGTTTCATTTATACAGGTAAACTCATTCCCAGACACCTACGCTCATGCAGAAGCGCAAACTTTAAGACAAAGGGAAACATGTTAGAGTGGCACATTGGCTCAGTGGTTAGCACTGTGGCCTCACAGCTAGAAGGTCGCTGATGTGAGTCCCAGCTTGGCCATTTGGCATTTCTGTCTGGAGTTTGCATGTTCTCCCTATGTTGGTGTGGTTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCCAAGACAAGTGCTATTAGTTAATTGGATGAACTGAATTGGTCGTAGTATATGTGTGTGTGTGTGTGAATGAGTGTGTTTGGGTGTTTCCCAGGGTTGTGGCTTGAAACATATGCTGCAGGAGTTGGTGGTTGGCAGCCCCTGATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44626

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000014822	Nonsense	352	578	11	16

Genomic Location (Zv9):

Chromosome 5 (position 70429527)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	66754671
GRCz11	5	67433040

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTCATTTGATTTGGTTTTCTCTAGCACTGAATGAGCCTACTATTGACTA[C/A]GGCTTCCAGAGGCTCCAAAAGCTCATCCCTCGACATCCCGGTGACCCCGA

Long Flanking Sequence:

GAATGAATGAATGAATGAATGAATGAATGAATAGTTTTAGCATTAGATAAAAAACAGCTTTTTTTTTTTGTATTTTTATGCCAAAAATCATTAAGATGTTAAGTAAAGATCATGATGAAAGTAGATTTGTTGTCAATTTCCTACTTTAAATATATCAAAACTTAATTTTTGATTAGTAATATGCATTCCTAAGCATTTTATTTAGACAACTTTAAAGATGATTTTCTTAATATTTAGATTTTTCTGAACCCTCAGATTCTCCATATAGTTGCATTTCAGTCAAACATTGTCCCACACTAGCCATACATCAGTGCAAAGCTTATTTATTCAGCTTTCATGTGAAGTGTATTGACTCGTCACTGCTTTTGGGGTCTAGGATCATAAACCTTATGTAATATGGGATTTATGCAGCTTGTAAAATACTTGGATGTTTTAAAGACAGAAATGGAGTCTCATTTGATTTGGTTTTCTCTAGCACTGAATGAGCCTACTATTGACTA[C/A]GGCTTCCAGAGGCTCCAAAAGCTCATCCCTCGACATCCCGGTGACCCCGATAAACTGGCCAAGGTTAGTTAATACTTATGCTTTTAAAAATTAATATACACACTTAGAACTTGAGATAATTTATATTTTCTACTCTATTTAAATTTTAGGAAATGTTACTTAAAAGAGCGGCAGATGTTGTTGAATCCCTCTATGGAAATACCACCAGCAATCAGGTAAATAACCACTGAACTGAAGCACTGGGAAATGAAAATATTGGGAATGTTTAACGTGTATTGGGGGTCAGGTGTTTAAAATCACTTGCAAACATGCTGCTATTTTATAATTTCGTTTTTTCTTATTCCAAATTTCACTATCAGCATAATAGTTTAAAGTCAAATGAAACAGAAATGTTAGAAACATAGAAACATGTTAGCCACCCTGTGATATTTTAATTGTTTGTTTTTATTTTAAGTGATGTTAAACAGAGCATGATGTTTTCACAGTACACTGATAAAAAA

Associated Phenotype:

Not determined