ZMP
zeb2a
Ensembl ID:
ZFIN ID:
Description:
zinc finger E-box-binding homeobox 2 isoform 1 [Source:RefSeq peptide;Acc:NP_001108023]
Human Orthologue:
ZEB2
Human Description:
zinc finger E-box binding homeobox 2 [Source:HGNC Symbol;Acc:14881]
Mouse Orthologue:
Zeb2
Mouse Description:
zinc finger E-box binding homeobox 2 Gene [Source:MGI Symbol;Acc:MGI:1344407]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34655 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16793 | Essential Splice Site | Available for shipment | Available now |
sa34656 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34655
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090028 | Essential Splice Site | 19 | 1196 | 2 | 10 |
ENSDART00000127834 | Essential Splice Site | 41 | 1218 | 2 | 10 |
ENSDART00000130059 | None | None | 370 | None | 3 |
ENSDART00000144499 | Essential Splice Site | 41 | 76 | 2 | 3 |
ENSDART00000146011 | Essential Splice Site | 41 | 204 | 1 | 5 |
The following transcripts of ENSDARG00000062338 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 26810688)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25966474 |
GRCz11 | 9 | 25777343 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTCCCCGGTGTAAGAGGAGAAAACAGGCCAATCCGAGGAGAAAGAACG[G/A]TAAGAAAGTGTCTCGTGTCGAAAAAACTTGTCTCCGGCTTGTTCTCGCGT
Long Flanking Sequence:
GGCACAAGCATCACTAAACACAAGTTGCAGAAAACTTTCATTGCTTTGCATTGTGTGAAATGCTCTATACGCACAGCACATGCTTTATGGTGACTTGAAGGTGTCGGTGTGTCCGTCCCCCTTCGTTCGCGCACTCACGCGCTGCTGTCCGATCACACACAGACACACACACACTCACACACACACTTCAAAAGATCAGACGACGCGCAGGACGCTCACGGTCCCTCCAAACAAACCCTCCTGGATAACTTCATTCGGACTTCTCAGTCACTCTACCCCCAAATATCATTTGCTCTCTCCTGTGAGCGACACACATCCTCCTTCCTGCCCTGAGAGTCCAATTGTTGCCGTGTGTGTGTTGGTTGCTAGATCTTGGATGAAGGAGCGGAGCCCATGCGGACTGCTGCCATCTGACCCACTCTTATCAATGAAGCAGGAGATCATGGCGGAGGGTCCCCGGTGTAAGAGGAGAAAACAGGCCAATCCGAGGAGAAAGAACG[G/A]TAAGAAAGTGTCTCGTGTCGAAAAAACTTGTCTCCGGCTTGTTCTCGCGTCTTGAAAACACTGTTAGATTTGGGTGAGATTGTGCGTTGTCAACTGAAGCGCTGTGTACAAGAGTACGGGAAACTCAACGACAGTGTGTTTACTTGTGTGCTTCAGACAGAAGTCTGCTGATTTAAAGAGTTTTTGTTGCTGTGGAAATATTTAAGTTGTAATAGAGTAGGAGTTACAGGGAGAGTTCAGATGTGTGAGCGTCTATTATCTCACAGCACAAAACCGTTATGTGTGTGTGAGCGCGTGCGCGAACGCGTGTCTTCTGCTGGACACAACATACTGCCCTAAAATACTTTTAAATACTTGCTGAAGTTGTTTTGCGTGGTTTGTCAAACTTTTACACCTTAGAGTTGTTGTGAACTTCTGTCTTTGGTGAAGTTGTGAAAGAGTGAAGTTCTGCTGTGTGAATACAGGTTATGTCTTTAGACACTTTTCGACACTTTCCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16793
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 |
---|---|---|---|---|---|
ENSDART00000090028 | Essential Splice Site | 92 | 1196 | 3 | 10 |
ENSDART00000127834 | Essential Splice Site | 114 | 1218 | 3 | 10 |
ENSDART00000130059 | None | None | 370 | None | 3 |
ENSDART00000144499 | None | None | 76 | None | 3 |
ENSDART00000146011 | Essential Splice Site | 114 | 204 | 2 | 5 |
The following transcripts of ENSDARG00000062338 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 26854673)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 26010459 |
GRCz11 | 9 | 25821328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATGGGGCAGGAGCCCATGTTTGGCGCCACGGGGAGCTGAATGGYTCAG[G/A]TAAGAGTTAGAAATGAGAATATCAGACTGAACTGTTGTATAAAGNNNTTTTTT
Long Flanking Sequence:
AACCACGCTGAACTGAACTGAACTGAACTGAACTTCAACTCTGAAAACTGGACTGACAAAGTTTCAATTCACTAGAACTTCTATGTTAAGCTGCTTTGACAATCAACATTGTAAAAGACCTATAGAAATAAACATATATTGAATGGATTAGCACATTATATCTAACATATTATCTTAATTTGCAGAAAGACATAGTGCAAACACTCTTTAAGACTGCACAAAACTCTCTTGAGATGTGGGTAAATCTGAATAATAACACCTAGCCTCTGTTCTGTCCTCAGTGCTGAGCTATGAAAACGTGGTGGATGCCGGTTCAGGGTCCGACGATGAGGACAGACTGCTGGGATCTGAGGGTGAAGGCAGTCCAGCAGGTGTCCCGAGTCTGGAGGCTTCACCCCGGGTAGCCCATGCCCTGCTCTCCTGCCGGGGTGACGAAGAAAATGAAAGCCAGGATGGGGCAGGAGCCCATGTTTGGCGCCACGGGGAGCTGAATGGTTCAG[G/A]TAAGAGTTAGAAATGAGAATATCAGACTGAACTGTTGTATAAAGTTTTTTTTTAGTCCAATCAAACTTGGATTTTTTTACTATGACCAAGACAGAGCAGCTTTATTTACCAGGCCAACACCTAGCAGCTGTTTGGCATTTTTGATGTAATGGCAACTTTTAGAGCATTAGCTCACTTTTCTACTTTGGTTTCCTACTTTTGTCACAAAGTAGGTTACACCTAATCTTCTGTGCCTCATCTCGGCCCCCACACCCCTTTCTTTCTGGATTCGTTTTGACTCACCCACCCAAAACCAAAAGCGATCTAGATCACGGACAAGACCCAAGCTAGTGAGGCTTTAAAGACAAATTTTCTTAATTAGGATCGCAGAGCTATCATTTAGCATGAGCCTGCCCTGCTGACGACTCATTAAAAGCCTTAAATGAAATTTTTAGCATTATGATGGCCATTTACATACATAATAGGCCCACAATTCCCTGGGCCTGGCTGACAGTTACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34656
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090028 | Essential Splice Site | 1002 | 1196 | 9 | 10 |
ENSDART00000127834 | Essential Splice Site | 1024 | 1218 | 9 | 10 |
ENSDART00000130059 | None | None | 370 | None | 3 |
ENSDART00000144499 | None | None | 76 | None | 3 |
ENSDART00000146011 | None | None | 204 | None | 5 |
The following transcripts of ENSDARG00000062338 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 26866765)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 26022551 |
GRCz11 | 9 | 25833420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTCCAGAAGACCAGTTCCCTCCTAAGACACAAATATGAGCACACAGG[T/C]ATATCACATTTAGACAACTCTTTTTTTTTTACCCTCGTCCATCCCCCCTC
Long Flanking Sequence:
AATTGTTTTATTTACAATTTGTTATTTATTGTTTTGGTTAAGATCACAAAATGCAGTATAACCTACTGTTATTTATATGAGTTCTTTCTACTCTGTTTACTGAACTGAAAGAACTCCTCTCAATATCAAGCCATATGTCCCTTTTTTGAGACATAAGATAAAGATCTTATACAGGTTACAGAGATAAGCTCTGTCCAGACTTGGGATCAAACATGGGGCAGGGGCTGCGGGGCTGTCTCTTCCTAGGTGGCAGGTTAAGATTAGGATTTGTGGCAGGTTAGGATTGTATGAAGTGTCTAAAATCTGTTTCTTTTGCAGGGGGATCTACTGGACAGTGCTGGGGACTATCTGTCAGGGCTAGAGGACCTGACAGACAGCGAGTCGCTTCTCGCCCGGAAGAAGATTAAGAAGACTGAAAGTGGTATGTACGCGTGTGACTTGTGCGACAAAACATTCCAGAAGACCAGTTCCCTCCTAAGACACAAATATGAGCACACAGG[T/C]ATATCACATTTAGACAACTCTTTTTTTTTTACCCTCGTCCATCCCCCCTCCAAAGTAATCCCTTTTTACCACATTGTGTTTTTTTCTTGTTTCTTTCATTCCTTTTCTGCTTTAATTTTTTTCATACCTACTTTTTTTCTGTCCATTGCCATATTTTTGTTGTACATTTCAAACCCATTACAAAGGTGTAACGGTTTTCTTCCTTTTGACAGGGGAAATATTTAAAAATTCAGCTAAAATATATATAATAATTACTCTTTGAGCTGCAGATACACACACATAAAAGATCCTCTATATATGTTTTGTTTAACGAAGCACTCTCGCACTGATTTTAAATGAAGCATTTGGACCATCAGTCGATATGGAGACACATTGTCAGTAGAGTTTGCTGGCATGCCAACATGGCGCAGTATGCCAGGTGTATGAAAGCCTGATGTGTGCGAGGCATTTCTATGCCACATTGTGACCTACCCTCCTGGGGGACTCCTCTCTTTCACACG
Associated Phenotype:
Not determined