ZMP
si:ch73-38f1.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate early B-cell factor 3 (EBF3) [Source:UniProtKB/TrEMBL;Acc:B8JKJ0
Human Orthologue:
EBF1
Human Description:
early B-cell factor 1 [Source:HGNC Symbol;Acc:3126]
Mouse Orthologue:
Ebf1
Mouse Description:
early B-cell factor 1 Gene [Source:MGI Symbol;Acc:MGI:95275]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35725 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35726 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35725
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000006698 | Essential Splice Site | 45 | 591 | 2 | 17 |
ENSDART00000134114 | None | None | 335 | None | 8 |
Genomic Location (Zv9):
Chromosome 14 (position 36183736)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 34685064 |
GRCz11 | 14 | 35025378 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATAAATACATCCATCATCATTCTGTCTGTCTTTCTTCTGTGTGTTTAT[A/T]GTGGAGTGGGTCTTGCTCGAGCACACTTTGAGAAGCAACCTCCTTCAAAC
Long Flanking Sequence:
GCAAGTCACATTTAAACTATTTAAAAAATATTTCTTCTGACATTATTATTTTAGCCTTAAAATAGCGGCTGCTTTTTAATGACTTTGCAACAGTGCGTTGATTTATTTGCCCTAAAATATGGAGTTTTAAAGAAAATAAATACCAGTAGCCTAGCTTACTTGTTTGTTCAAGTATAGATTTAGAGCAATTAAGCTACTTTATGATTTATCACAATTGCCAATAGTATGTTAAATGGAATATATGTTGTTAAAGACTAGCATAACTTTTTAAGTGATTGTGTAAAACACAAAGCTATATTTCAAGTTGTTTTCTTAAACTAATAAAGCAATTCACGTGTGCTATTTCAGGGCTTTCCCGTTGCACATTTGAACTAAAATTAGCCTATTTATTTTTAATATTTTGAGACAATTATAATAAATCACAAAATAGGCTATAATTGTTGCTTTTAATTATAAATACATCCATCATCATTCTGTCTGTCTTTCTTCTGTGTGTTTAT[A/T]GTGGAGTGGGTCTTGCTCGAGCACACTTTGAGAAGCAACCTCCTTCAAACCTTCGTAAATCCAACTTCTTCCACTTCGTATTAGCGCTATACGACAGACAAGGACAACCCGTGGAAATTGAAAGAACATCTTTTGTTGGATTTGTTGAAAAAGAAAAGGCAAGTCAAACGTTATCCTTTACACATATCGGTTTTGCAAATTTGAGTGAAAATGGTTTATCAACTCTGATAATTATTAATGTTGGGCTTAAGTCGAAAGAATTATCATTATTATTATCATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATGATTATTATCATTATTAGCTACATGTTCAAGTAGTAAGCTATAATTTCACTGAAGCTTTTTTACCCTTCAATACTTTGTACATTTACTAATGTATAATTTTCAGATAAGTTACAGTGATAAGGATGAATTTTCCTTTTTAAAATGTTATATTAGTAAATGTATTATTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35726
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 |
---|---|---|---|---|---|
ENSDART00000006698 | Nonsense | 263 | 591 | 9 | 17 |
ENSDART00000134114 | Nonsense | 82 | 335 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 14 (position 36342979)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 34844307 |
GRCz11 | 14 | 35184621 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCCTCTGTCTGACTCTTTTCTTTTGCTCTTTCTAACAGCTACTCCTTG[C/A]ATTAAGGCCATCAGTCCCAGTGAAGGCTGGACGACAGGGGGTGCAACAGT
Long Flanking Sequence:
ATCATTGATGTATATTTAATGTTATCTTACTGCAAATCATATCTTGTATCTCATTTTCGTATCTCATTCCTACAATTTAGTACGATTTGCTAATCACCCAATGACAGTTGGGTTTAGGGGTGGGGTTTGGTGCCAAGTTTCTTTTTAAAAATTATACATTTTTGTACTACAAATTTGTACTAATTAGCCAATAAACTTGCATGTGTCTTTTCATGATGTTTATTGTATATGACAGCCTCTGTCTGACTAGAATTCAAGTTATTATTTGCTGTTCATATATCTCATTTTCATATCTCATTCGTACAATTTAGTACGATTTGCTAATCCCCCAATGATGGTTAGGTTTAGGGGTGGGGTTTGGTGCCGCACCTCCTTTTAAAAATCTACAAATTTGGTACGAATTAGCCACTAAACTAGCAAATGAATTTTCAAGATGTTCATTGTATATGACTGCCTCTGTCTGACTCTTTTCTTTTGCTCTTTCTAACAGCTACTCCTTG[C/A]ATTAAGGCCATCAGTCCCAGTGAAGGCTGGACGACAGGGGGTGCAACAGTCATCATTATTGGTGATAACTTCTTTGATGGCCTACAAGTCATCTTTGGCACCATGCTGGTCTGGAGTGAGGTTGGTTACCTTTCTATTTGAGTTGCCATTGGTTTTGTGAAAAAAGTGCAGCTGAAGCATGTTGAGGGGATGCTGTTTTAGGCTCTTGGAAAGAGACCAGATGTCAGGGTTCACACAGGTCATGGAATTTCTGGAATATCATGTCAATTTAAAAGGTCTGTCCCAGATGTTGGAGGTATATATTCTAATGGAATGTATATATTTTTGACATAATCATGGATTATCAGGGATTTTTTTTTTACTTCCCATTCATGTGAATTTAGTACATTGTTTCACAAGTGTCTCCCGATTGTTATGGTTAGTTTTTTTGTCACTGCTATTTTATTCCTTTCTCACTTGTCAGCCAGCAATCAAATGCAGTCACCTCACCTGGCTGTACC
Associated Phenotype:
Not determined