ZMP
ebf3
Ensembl ID:
ZFIN ID:
Description:
transcription factor COE3 [Source:RefSeq peptide;Acc:NP_001074071]
Human Orthologue:
EBF3
Human Description:
early B-cell factor 3 [Source:HGNC Symbol;Acc:19087]
Mouse Orthologue:
Ebf3
Mouse Description:
early B-cell factor 3 Gene [Source:MGI Symbol;Acc:MGI:894289]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18240 | Essential Splice Site | Available for shipment | Available now |
sa22167 | Essential Splice Site | Available for shipment | Available now |
sa35372 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35371 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18240
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085381 | Essential Splice Site | 297 | 548 | 10 | 16 |
ENSDART00000138241 | None | None | 128 | None | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 44171339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 42392450 |
GRCz11 | 12 | 42547739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTGGTGCAGTTTGCAAGRTCCTAACCAAGTTTATCYATTCTCTCCTAT[A/G]GCTCATTACACCCCATGCCRTCCGAGTGCAGACCCCTCCRAGACACATCC
Long Flanking Sequence:
GGTCTTGCAAAACAATTGAACAATTAGGGGTGAAATATCTCAGAGGGGGAAAAGCCGAGCGAGGGAAAGCAAGGAAAACAGTGAAGGAAAGACATATGGAGATGATTTTCGCAGGACTCCTGCCCCTTGGCCTTTCCTGGGCTCAGTGAAATCCAAGGTCTATTTGCTGACGTTAACTCTGAAGCGGAGAGGGGGAAACAAAGAAGGTTTGCAGGTTCGGTTAGGAATGGCCTCTGTTTGACAGGTTATTTTACCAGTTGGGCAATTGCAGATATGCAACAACTCTAAGCAAGCTTGTCCACAGTCTTTATAAGTTGGTAAGGTCCCAATTCTGAGACTTAAGTCAGTTCAAATTATCCATGAACAAGACACATGGAAATCCCCCACTTGGGCGTTAGTTTCTACCTGAAAGGCTGCAATTTCTTTGCCAGGTGTTGAAATGCATGCAACATTTGGTGCAGTTTGCAAGGTCCTAACCAAGTTTATCCATTCTCTCCTAT[A/G]GCTCATTACACCCCATGCCATCCGAGTGCAGACCCCTCCGAGACACATCCCGGGCGTTGTAGAAGTCACCCTGTCCTACAAGTCTAAGCAATTCTGCAAAGGTGCACCGGGCCGATTTGTGTACACAGGTGAGTTGCAATTGGATCAGTTGAACTGTGCGCAGCTTCCATCCATTCAAGTGTTTGGCTCCATCCTTAAGTACTGAACCCCGACCAGTGTGAGATGCATGCCTCTGTAACCCTATATCTCCTCCATCTAAGGCAGGGCAATGGAGTTGGGGGCAGCTGCCAACTCCAGTTAATCTCAAACCTTGACAACACATTTTAGACTCCTGCACTCAGTCCTCTCCTGTGCACAAAAACACTAGTGCTTCTTGTCGCCCAAGTTACTCATGTGTGCATATGTATGTGTGACCAGCATTGTGGATCTCGGACTAATCTTTCCCTCGGTACAGCTGATACTGGAGGTTACACGGTCACACCATGTTTGACCTGGAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22167
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085381 | Essential Splice Site | 368 | 548 | 11 | 16 |
ENSDART00000138241 | None | None | 128 | None | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 44151775)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 42412014 |
GRCz11 | 12 | 42567303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGAAGGTCATTCCCAGACATCCAGGTGATCCGGAGAGGTTGCCCAAG[G/A]TCAGTGATCCTGTGTGTGTGCGTGCTTGTGTGAAGCAGCTATTTATCATA
Long Flanking Sequence:
GAAGGGTTGCAATAGCCAGACATATGTCATCATTGCCCGTTGCCCATAAATCCAGCGGGTGCTTCAGGAAGTGGGACTGATGCAGACTTCACAGGGTTGACAGTCGCAATCGAGCGTGTGTGTTGTGTTTCATTCATAATGCATCCGCTAACTTCTTTAAATTTATCTGATCAATTATAGCCTAGTTTTTTTTCCAAATAGGAGAGGTGATAGATGCGACTCTACATGGAGTATTTCACACCACGTTATTACCTTTTATTCAAATGCTCAGACCTATCTGGAATAAAATGCATGACGGGTGCAGGAGCGAATGTAATAACATTTATGATGGCGCATATGAAAACACAAATCTCTTCATTTGTTTTGCCTGGGCAGGATGCTAACCGATGGCTTTCTTGTTTTGCGGTTTAGCACTGAACGAACCAACTATTGACTACGGCTTCCAGAGACTGCAGAAGGTCATTCCCAGACATCCAGGTGATCCGGAGAGGTTGCCCAAG[G/A]TCAGTGATCCTGTGTGTGTGCGTGCTTGTGTGAAGCAGCTATTTATCATAGAAATGTCAAAATGGGGAAACAATTCACTGGCTTAGATGAGCAAACGCATACAATCGCTTTTGGCAAGTCATCACTATGCAATCCGGCGTGTTTGGATTCCGCCGGAATCGCGCAAACTTTCAGCCCATCGAAATGGTTCAATTAAGTGTTTTTCCACCCCAGTAGGCAGTGGCGATTGTAATCTAAGCGGAGGCCCTTTTTCAGATGTGTGATTATTTTGGTCTTGTTTTCCTTTCATTTTCCAAAGCTAGATCCAGTTTAATCTTTTGTTTACAGAGCTTCCCGTTAAAAGTCCTTGTCTTAGCAGGTTAATAAATGAGTTTTGCACACGTTAATATGGGCAAGCCCTCTTTCTGGGCTTTTTAGCTCCATTTATTTATTTTTCCCCAGCCTAAATTCCACAAATCATGCAGTTTGCCTGCGGTTCCCATGTGGTCGACACGTATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35372
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085381 | Essential Splice Site | 369 | 548 | 12 | 16 |
ENSDART00000138241 | None | None | 128 | None | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 44146878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 42416911 |
GRCz11 | 12 | 42572200 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTGATGGTGTTTATATGTCTTTATGACTGATTATGTTGCATATTGC[A/G]GGAGGTGTTGCTAAAGAGAGCCGCTGACCTTGTGGAAGCGCTGTACGGGA
Long Flanking Sequence:
TTCACTTTATTGTCCTAAAGAAAGAGGAATGGGCATTGAACTCTTCTGCAAATTTGGGGCACGAATTAGGGGTGAGATGTTGTCTTTGAGGACTCTGCCAGTTTAATTAAGATATGGAAAATGACTCATTGTTCTTCTGAGCTAAAGTGCGTGGAATTAGCAGCCGAACGTGGCGTCTGTGTTTGACTCAGTGCCGCGTGCTAGTGTTTGTTTGTTTAATACACGCAGGGCCTTATGTTGACTCATTTAGCTTAAGTTACACATCACTTCACTAGTCTAACTAAGTCAAATGAAATGTGACTAAGAAATAAAAGAACGCATTCGATAAAATATAATTAAAAAAGTGGTTTGTTTCCACTCGTCCGCTTGTGTATTCTTTCCCCAACCGGAGATAAAAGGCTTATGATTTACCTAGACCCACATGCACGCTTATTGTTCATGTGCAATGCACTGGCTGATGGTGTTTATATGTCTTTATGACTGATTATGTTGCATATTGC[A/G]GGAGGTGTTGCTAAAGAGAGCCGCTGACCTTGTGGAAGCGCTGTACGGGATGCCACACAACAACCAGGTACAAACTCATGCTAATGAAGCACCTTTGCTTTTCCCTTCCTTTGCATGGTGGCAGTAATTAAATCAGCATTCGTCTCCTTTTGCAACATTCCTGTATGTTTCAAAGCTTGCTGGGGGCCTTTGTACTGTAGCTGGGTGAAAGCTTTTTCTTCTTCACACTTTCATTCACTGCTGCGACTCTTGGTGCGAAGTGATGAGTTAATCACTCAAAACGCATGCACGCAGCCATATACAGGCTTACTTAAATGGGAGGATAACCTTGAACTTGGCCCTAAAAGGTGCACTTCTAGAATATATTCCACAGAGCGGTCCAGCTATGCTTGAGAGGTCTAATACATATTCAGAAGAAATGATCCATTACATTATTTTCCCCTAGCCGAGTAGCACAGAGGTGAAGACATTGCAATACAACTATTGCGAAACGTGCTGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35371
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000085381 | Nonsense | 507 | 548 | 14 | 16 |
ENSDART00000138241 | Nonsense | 51 | 128 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 12 (position 44144779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 42419010 |
GRCz11 | 12 | 42574299 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACCTAGTTCACCGGGCTTCTTAAATGGCTCCTCTGCGAACTCTCCCTA[C/A]GGCAGTAAGTATCAAGGTAATGACGAGCTCCCCGCTCTCTCTGTCCCCAC
Long Flanking Sequence:
TTGAGTAAACCTGGCCGTAGTATATGTGTGTGAATGAGTGTGTTTCCCAGTTCTAAGTTGCAGCTGGAAGGACATTCGCTCCCTTAAAGTACAAAGTGTATTGGTGTTTCCCAATACGTGCTAGGTTGTGCATCCACTATGGAAAACCTATACCAGAGTAGTTAGTTCAGTCCTCTGATAAATCAGAGACTAAGCCGAAGGAACACGAACGACTATATTTCACTTTTAAATAAACACACATGCTTATAAATTGTTTCATCTTGTTGTACATAATGCAAATTGTGGCAGCTTTTAACCAAAGTCTTTCTATCCACAGTGGGCTACAGTCGCAACACGAGCAGTGTGTCACCTCGCGGTTACGTGCCTAGCAGCACCCCGCAGCAGTCCAACTACAACACTGTCAGCAACAGCATGAACGGCTACGGCAACACAGGGATGCCCAACTTGGGTGTACCTAGTTCACCGGGCTTCTTAAATGGCTCCTCTGCGAACTCTCCCTA[C/A]GGCAGTAAGTATCAAGGTAATGACGAGCTCCCCGCTCTCTCTGTCCCCACCTGTGCTTCCCTTTCTTTTCGACACTCCTTTGTTGTTGTTCTGTTGGTTGTTTGTTTGTTGGTTTGTTTTGTTATCTTTTGGGAATGTGTGCTACTGGATAAAAGGAGGGGTGACTCTGGAGGCTGAACAACCGAGACATTTAGCAAATCCGACCAATCAAAGCAGCTGATTGAAACCAACAACAAAAAAAAAAACTGCAATTATAAAGCAGGCCACCAAAACAGCACTCAAAATCAAAAAAAAAAAACCCAAACAATTAAAAATCTCAAATGTTTTCGGCAAAGTGACCCAATCAGAGTCGATAAGAACGCCTATTATCCAGAAAGTGGCCAAGGCAGGACATCTCTCATCCCATTTCAACTCCATTTACCTGATTGATTTGCTCGTTTGTTTTTAGTCCCCCCCCCAAAAATGACCCAAATTTTTTCCCTCATAACCATTTCTCCCTG
Associated Phenotype:
Not determined