ZMP
zzef1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2CES1]
Human Orthologue:
ZZEF1
Human Description:
zinc finger, ZZ-type with EF-hand domain 1 [Source:HGNC Symbol;Acc:29027]
Mouse Orthologue:
Zzef1
Mouse Description:
zinc finger, ZZ-type with EF hand domain 1 Gene [Source:MGI Symbol;Acc:MGI:2444286]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2251 | Nonsense | F2 line generated | Not yet available |
| sa5742 | Nonsense | F2 line generated | Not yet available |
| sa428 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2251
Status:
F2 line generated
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000141463 | Nonsense | 906 | 1300 | 14 | 23 |
| ENSDART00000146476 | None | None | 453 | None | 8 |
| ENSDART00000141463 | Nonsense | 906 | 1300 | 14 | 23 |
| ENSDART00000146476 | None | None | 453 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 32691696)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 30452526 |
| GRCz11 | 5 | 31052679 |
KASP Assay ID:
554-3373.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGATGTGGACCCYGCAGAAGCTGTTGGAGAGCTCTGTAGACATTTATG[T/A]CAAGGTGAGACCAATGTGCAAGTTAYAGGGAGGSTGTGGGGGGATTGACC
Long Flanking Sequence:
GTAACCATAAATGGTGTGTTTCCTTCAATTATGTTAATATTAAAAGATAAGAAATGTACTCTTTCAAAAGCATGCCTCGCTTTTAATCGATGAGTGTTTACACTACAACCTTTTAATGAACTTTTTGAGGGGCAAAATACAATTTACTACAAAATAATCCCATAATAATTGAACTCGAGGCTATCGAGGATTAGATTATTGAGTCATATAGTCCAGCCCAGTGTCCTTTGTTAAAATACATGCTGACTGCACAGTTTTTGTCTGTTCTAATGCATCTTTGTTGCGTGTTTGTGTGTATGTTTGTACACTCTCAGTGAAGGAGAAGAGGCCATAAAGACAAGAGTTCTCCTTCTTCAGCTGCTCCAGAACTGCTTCCCAATGTTGCCCAGTCCGACCGAGTCCCAGCCGTCAGATCTCTCAGCATCAGCCTCAGCATCGCCTTCAGGCAGCTCAGATGTGGACCCCGCAGAAGCTGTTGGAGAGCTCTGTAGACATTTATG[T/A]CAAGGTGAGACCAATGTGCAAGTTACAGGGAGGGTGTGGGGGGATTGACCCCCTTAATTAATGCTTGATCCCCTCTGAAGGACATCAAAACAGCATGTATGGGGGATCACTTCTTTAATACTGATAAATAATTTGTTCTGCTTTGTATTTTAAATAATAATGTCAATAATTGAAATTAATACAAGCAATCAGGTTAATAATATAAATATGCATTTGACCACCCCTATAATGGTTCATATCGCACCAATCAGTCTGCGAGCAAAAACTCATTCAACAGTCTGAAACCAGCAGATCTAGAGCACCAATAGGCAACGTAAATGTTCACAAGACTGTTTTCTAGTAAAATAGCTGTTTGTTTCTACATATAGCCTAAAAGTAAAGTCAGATTAAATGCATAGTTTACTAACATTAACTTCAAAAGTAGCTAATCCGATACTGTAGGACAGAATACACAAAATATCCCACAAAACACTGAAAACTTAAATACATTTTATTAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5742
Status:
F2 line generated
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000141463 | Nonsense | 906 | 1300 | 14 | 23 |
| ENSDART00000146476 | None | None | 453 | None | 8 |
| ENSDART00000141463 | Nonsense | 906 | 1300 | 14 | 23 |
| ENSDART00000146476 | None | None | 453 | None | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 32691696)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 30452526 |
| GRCz11 | 5 | 31052679 |
KASP Assay ID:
554-3373.1 (used for ordering genotyping assays)
KASP Sequence:
TCAGATGTGGACCCYGCAGAAGCTGTTGGAGAGCTCTGTAGACATTTATG[T/A]CAAGGTGAGACCAATGTGCAAGTTAYAGGGAGGSTGTGGGGGGATTGACC
Long Flanking Sequence:
GTAACCATAAATGGTGTGTTTCCTTCAATTATGTTAATATTAAAAGATAAGAAATGTACTCTTTCAAAAGCATGCCTCGCTTTTAATCGATGAGTGTTTACACTACAACCTTTTAATGAACTTTTTGAGGGGCAAAATACAATTTACTACAAAATAATCCCATAATAATTGAACTCGAGGCTATCGAGGATTAGATTATTGAGTCATATAGTCCAGCCCAGTGTCCTTTGTTAAAATACATGCTGACTGCACAGTTTTTGTCTGTTCTAATGCATCTTTGTTGCGTGTTTGTGTGTATGTTTGTACACTCTCAGTGAAGGAGAAGAGGCCATAAAGACAAGAGTTCTCCTTCTTCAGCTGCTCCAGAACTGCTTCCCAATGTTGCCCAGTCCGACCGAGTCCCAGCCGTCAGATCTCTCAGCATCAGCCTCAGCATCGCCTTCAGGCAGCTCAGATGTGGACCCCGCAGAAGCTGTTGGAGAGCTCTGTAGACATTTATG[T/A]CAAGGTGAGACCAATGTGCAAGTTACAGGGAGGGTGTGGGGGGATTGACCCCCTTAATTAATGCTTGATCCCCTCTGAAGGACATCAAAACAGCATGTATGGGGGATCACTTCTTTAATACTGATAAATAATTTGTTCTGCTTTGTATTTTAAATAATAATGTCAATAATTGAAATTAATACAAGCAATCAGGTTAATAATATAAATATGCATTTGACCACCCCTATAATGGTTCATATCGCACCAATCAGTCTGCGAGCAAAAACTCATTCAACAGTCTGAAACCAGCAGATCTAGAGCACCAATAGGCAACGTAAATGTTCACAAGACTGTTTTCTAGTAAAATAGCTGTTTGTTTCTACATATAGCCTAAAAGTAAAGTCAGATTAAATGCATAGTTTACTAACATTAACTTCAAAAGTAGCTAATCCGATACTGTAGGACAGAATACACAAAATATCCCACAAAACACTGAAAACTTAAATACATTTTATTAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa428
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000141463 | None | None | 1300 | None | 23 |
| ENSDART00000146476 | Essential Splice Site | 127 | 453 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 5 (position 32707137)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 30467967 |
| GRCz11 | 5 | 31068120 |
KASP Assay ID:
554-0376.1 (used for ordering genotyping assays)
KASP Sequence:
TGTTTCTAATGTCCCAAATCATTGTGATTTTATCTTTATCTGTCTTTCTC[A/T]GCTACTTTTCTCAGCTTGTGGGCAGCGGGCAGGAGATGAGGGAACGGGTC
Long Flanking Sequence:
TTCAGGGTATTTCAGGATTTGTTGCTCCATTTATGTTTATTGTGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTATGTGATGGCCGGATGAGCAGTAATGATGTGTGTTTGTGTTTGTTCAGTGTTCTTCAGACTCTGGCTCTGAAAAAGGCACAGGCTGTAAGTGTGTGTGAGGTACTGGAGCTCGTGCAGCAGTGTATTCTCACCCTGGGCAAACCGCACCTCTTCCAGGCACCCTGCATTTTGTTTCTCCAGGAACTCTTGGCTTGCCAGAAAGATTTCACCAAGTATGTAATCCAAATTTAGTTGTAATTTTGGATGTTTCTAATGTCCCAAATCATTGTGATTTTATCTTTATCTGTCTTTCTC[A/T]GCTACTTTTCTCAGCTTGTGGGCAGCGGGCAGGAGATGAGGGAACGGGTCAGACACTCGTATCATCAGCTGGTTCTCATGCTAGTTGAAGCTGTGCAAGGCTTCAGTGCCCTGAACGAAAAGTGAGTTCTCTCTCATCTGGTTTTAAGCATTTGATCTACAATATACAATACAGAGTTGATGTTTAAACGTGATTTGAAGCAAGTGTGTTCTTCAGAAATAACACGACTAATACATTTACTTTTGCATTTAATTATTTAGCACATGCTTTTTTTGTCACTTACAAAGTACATTTTTTGCTAATTAAGACAAATTCTAATCTTTTATAGCCTACAGCTGTTTGTCCTATATGTATGATGTTCATTGTGTGTGTGTCCTCAGGGTTCTGCTTCCTGCACTATCATGCGTTCAGACTTGTCTGCTGCATTTGCTGGACATGAGCTGGGAAGCTGAAGACTTGTCGCTGTTTCTTGATATTAAACTGCCGGATCTCCTGCTTGC
Associated Phenotype:
Not determined