ZMP
zgc:152925
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC767754 [Source:RefSeq peptide;Acc:NP_001070189]
Human Orthologue:
CENPE
Human Description:
centromere protein E, 312kDa [Source:HGNC Symbol;Acc:1856]
Mouse Orthologue:
Cenpe
Mouse Description:
centromere protein E Gene [Source:MGI Symbol;Acc:MGI:1098230]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24832 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32570 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19390 | Nonsense | Available for shipment | Available now |
| sa32571 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24832
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092584 | None | 21 | 317 | 3 | 10 |
| ENSDART00000111806 | Nonsense | 66 | 2690 | 3 | 58 |
| ENSDART00000133431 | None | None | 171 | None | 5 |
| ENSDART00000148172 | None | None | 170 | None | 4 |
| ENSDART00000148261 | None | None | 199 | None | 4 |
The following transcripts of ENSDARG00000063385 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 137422)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 267552 |
| GRCz11 | 1 | 262731 |
KASP Assay ID:
554-7286.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCTCGTGTGTTTCAGACCGTGTGTTCAGTGCGGCAGAGTCCACTGCT[C/T]AACTCTATCAGGACATCGCGAAGCCTCTGGTCGTGTCTGCAGTTGAAGGT
Long Flanking Sequence:
TGACTTTGGAAACAGTGTAAAATCCCTGTCTAACACTGACTAGAAGAAATTCCTTTTCTTACTTGAAGTCTTGTTTCCAGTCCAAATGTTTTTAAAAAATCTAGACAAGCAAAAAATATTTTCTTGTTTTAATAAATGAAATAATGATGATGTTGATAATATTAATAATAATAATCATCTGCTAATGGGGTAAGCGAAATAATCTTGTTTTTGCATTGAAATAACATTTAGCTTACCCAATTAACAAATTATTTAGCTTGTTTTAATGTAAAGCTCACTTAATTCCTGAAAACAAGACAATATCTTTTCTAGTCTATTTATTATTAAGATAATATTATTATTATCATCATTATTATTATTATTATTATTTGGACTAGAAACAATACAGATTCTAAGTAAGAAAACAATCTTTTGCAGTGTGCTTTGACTTTGGCTAGCAGGTTAATGCGCTGTCCTCGTGTGTTTCAGACCGTGTGTTCAGTGCGGCAGAGTCCACTGCT[C/T]AACTCTATCAGGACATCGCGAAGCCTCTGGTCGTGTCTGCAGTTGAAGGTTATAACGGTGAGTCCAGAAATGAAGATTTATTTTTTCCAGCACAGCAAAGCACAGACACACGGGTGATTTACTGAAATGTAGGGTTGAATGATCCAGAGTACAATAACGTGACAAATAAAAATGATAACAGTAGATAAATGAAAGACCTTAAAGACTAAATAGATTTTAAAAGGGTTATTTTTTTCATGAATGTTTCAGGAAAGTTGTTCTGTTTTAAAAAGGCAAGAAAAAAAACACTCCAAGCATATATTATTATACACATGTCTCGTCTTTCATGAGGTCAGATATTTGCCTTCCTTAGTAGCTTTCTGTATCAAATTACACTAGCATGTGTTTTCATCTACAAGGAAAGATTATTAAAGTGAAAAATAATCCTGAAATGCTGTAAATTGCACTGTATTTTGTGTATTTGTATACTGCATATACAGTATACTCTTAAATGTAATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32570
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092584 | Essential Splice Site | 35 | 317 | 3 | 10 |
| ENSDART00000111806 | None | 80 | 2690 | 3 | 58 |
| ENSDART00000133431 | None | None | 171 | None | 5 |
| ENSDART00000148172 | None | None | 170 | None | 4 |
| ENSDART00000148261 | None | None | 199 | None | 4 |
| ENSDART00000092584 | Essential Splice Site | 35 | 317 | None | 10 |
| ENSDART00000111806 | None | 80 | 2690 | 3 | 58 |
| ENSDART00000133431 | None | None | 171 | None | 5 |
| ENSDART00000148172 | None | None | 170 | None | 4 |
| ENSDART00000148261 | None | None | 199 | None | 4 |
The following transcripts of ENSDARG00000063385 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 137466)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 267596 |
| GRCz11 | 1 | 262775 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCTCAACTCTATCAGGACATCGCGAAGCCTCTGGTCGTGTCTGCAGT[T/A]GAAGGTTATAACGGTGAGTCCAGAAATGAAGATTTATTTTTTCCAGCACA
Long Flanking Sequence:
AGAAATTCCTTTTCTTACTTGAAGTCTTGTTTCCAGTCCAAATGTTTTTAAAAAATCTAGACAAGCAAAAAATATTTTCTTGTTTTAATAAATGAAATAATGATGATGTTGATAATATTAATAATAATAATCATCTGCTAATGGGGTAAGCGAAATAATCTTGTTTTTGCATTGAAATAACATTTAGCTTACCCAATTAACAAATTATTTAGCTTGTTTTAATGTAAAGCTCACTTAATTCCTGAAAACAAGACAATATCTTTTCTAGTCTATTTATTATTAAGATAATATTATTATTATCATCATTATTATTATTATTATTATTTGGACTAGAAACAATACAGATTCTAAGTAAGAAAACAATCTTTTGCAGTGTGCTTTGACTTTGGCTAGCAGGTTAATGCGCTGTCCTCGTGTGTTTCAGACCGTGTGTTCAGTGCGGCAGAGTCCACTGCTCAACTCTATCAGGACATCGCGAAGCCTCTGGTCGTGTCTGCAGT[T/A]GAAGGTTATAACGGTGAGTCCAGAAATGAAGATTTATTTTTTCCAGCACAGCAAAGCACAGACACACGGGTGATTTACTGAAATGTAGGGTTGAATGATCCAGAGTACAATAACGTGACAAATAAAAATGATAACAGTAGATAAATGAAAGACCTTAAAGACTAAATAGATTTTAAAAGGGTTATTTTTTTCATGAATGTTTCAGGAAAGTTGTTCTGTTTTAAAAAGGCAAGAAAAAAAACACTCCAAGCATATATTATTATACACATGTCTCGTCTTTCATGAGGTCAGATATTTGCCTTCCTTAGTAGCTTTCTGTATCAAATTACACTAGCATGTGTTTTCATCTACAAGGAAAGATTATTAAAGTGAAAAATAATCCTGAAATGCTGTAAATTGCACTGTATTTTGTGTATTTGTATACTGCATATACAGTATACTCTTAAATGTAATTCAATGTATTTTGCACTGTGTTTAGCCTGCACTCAAGCTTTTCCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19390
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000092584 | None | None | 317 | None | 10 |
| ENSDART00000111806 | Nonsense | 389 | 2690 | 13 | 58 |
| ENSDART00000133431 | None | None | 171 | None | 5 |
| ENSDART00000148172 | None | None | 170 | None | 4 |
| ENSDART00000148261 | None | None | 199 | None | 4 |
The following transcripts of ENSDARG00000063385 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 142648)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 272778 |
| GRCz11 | 1 | 267957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGACTCAAACCACAGCGACCGAGCGAGAGTCTCTCTGTCAGCTCCTG[C/T]AGGAGAAAGACCAGCTCCAGAGAGAGCAGGAGGACCGCATCAAGAACTTG
Long Flanking Sequence:
TGTCAGGGACGGACTGTACCTTGTGTTCGTTTCATACAAAAAACAAAACCGGAGAACAATTGTTTATTAAGCCAAAAACATCTGTTTGTAGTTTGTTTAAGAGTAGGGGTTTGAAGCTTTCAGTGGATATATTTCTCCCGTGTTTGAAGCATGTATTGGCTGAGATTCCAGTGTGTTTGCTGACCCCAGAGCATTCATAATGAAGCTGCAGAAACTGTCCTAAACACATGTCTGCACTGAGACCCTCCCCTGGAGAATCCTCACTCTATAGTGATCAATGATTGGCTCCTGCACCAGAATGCAGGACTTTACTAGCCATATTGACTGTTAACACATTTTTCCCATTCAGAACTGTACGAGTGGCTTGTCTTGTGTATTCTAGTGTTTGTCATAACTCAACCCATCCTCTCCTCTCCTCATGTGTTTCACTCCTGACTGCACAGGTTTCGTCTGTGACTCAAACCACAGCGACCGAGCGAGAGTCTCTCTGTCAGCTCCTG[C/T]AGGAGAAAGACCAGCTCCAGAGAGAGCAGGAGGACCGCATCAAGAACTTGACCAAGTTACTGGTTACTTCCTCCAACATTGCGCTCATCCCGAAGGTAACAGATGACAGCAGTTTACTCAGAACCTTTGTTTCTTTCTTCTGTTGAACACAAATGAAGATATTTTAAAGAAAGTTGGAAACCTGTAACCATTGACTTCCAGAGTTTTAGTTTTTTTCTACTATGGAAGTCGATGGTTACAAGTTTTCAGCATTCTTCAAAATATCTTAAACTGGTTTGGAAACACTCGAGGATGAGTGAATAGCGAATACATTTTTGCCTGATCTTTCCCTTTAAAGTCAAAGTTTGCAGTGTTTATTTTGGTAGCTCGCGTTATTATTTTAAATGGAATAATCTGTGCGAGGTCATCCACTGACATTTTGTTTTGGTAATCTTAAAGTTTGATCATTTGTGTTACTTTAACTACTGTTAGATGCATGAACGCGCTGTTTATTTTAGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32571
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 |
|---|---|---|---|---|---|
| ENSDART00000092584 | None | None | 317 | None | 10 |
| ENSDART00000111806 | Nonsense | 561 | 2690 | 16 | 58 |
| ENSDART00000133431 | None | None | 171 | None | 5 |
| ENSDART00000148172 | Nonsense | 125 | 170 | 4 | 4 |
| ENSDART00000148261 | None | None | 199 | None | 4 |
The following transcripts of ENSDARG00000063385 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 144437)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 274567 |
| GRCz11 | 1 | 269746 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGAAGCTCTCGCATCTGCAGAACATGCTGGAGGCTCAGTCTGCACCAT[C/A]ACACGAGGAGAAAAACACCATCTCTGAGCTGGAGAAGCAGATGGAGGATC
Long Flanking Sequence:
AGTTTGTGCTTTTCTTGAATTATATAATACTGTGTTGTAATTTTGTTGTTGTGTTCAGATATGGATGAGTTTGACAGCCGCTTCGACTTCACTGCTATGGAGGAACCCAACATGGACATGGAGATGAGCAGCATCACTGTCCGCAGCTCCTCGGAGGGGTGAGAAAAAGCTCTATTAGGTTTAAAATAGCTCTTATGTCCAGTGTTGTTCATATTTATGATTGTTTATTTATGTAGCATCGTGTTCCTGTGAGACAGAGTTTTATTCCACTGTATGTCCACTTGTAGTGCAATGACAGTAAACCTCATCTTCATTTCCTCTGTTCAGGAGTCATTTTCTGGACTCTCCCCGTGCGAGCGAGCTGATGCAGAAGGTGTCGTCTCTGGAGAGTCAGCTGGAGGCCGAGACTCAGAGCAAACAGATAGCAGAAGAGATGAACGCTGAGCTCCAGATGAAGCTCTCGCATCTGCAGAACATGCTGGAGGCTCAGTCTGCACCAT[C/A]ACACGAGGAGAAAAACACCATCTCTGAGCTGGAGAAGCAGATGGAGGATCTGCAGCGGAGACTGGAGACGGAGGTTCAAGAGAGACAAACCGCTGAGGAGAAGAGCATCTCACTGGAGCTGAAGGTGGCAGAGCTGGAGAAACCATCAGAAGAGCTGCTGCACTCACAGAACACGTGCGAACGGGTACAGCTGCTAATACTACAGCTTATGCAGTGTCTGCCCATCTGCTTTCACTCTGGAACAGCAGTCCATTGACCCTAACTGGGTGAAATATGCTTAGCCACGCCCCTTCCCCAGTATGCTGCGAGTGCAATATGCAGTCTTTTTATTATTTTTTGTTATTACCTGCCTATTATTAAGATATTAAGTGTACATTAGTAGTTATACATAATCTCATTCTGCAACTCAAAACCTAAACCAAACTTCTACCTTATTAATTAAAGGTTTAATAATGTAATCTATTAAGCTAGTAGTGTTTGTTAATGCCAGGAGTTGAGAC
Associated Phenotype:
Not determined