ZMP
cherp
Ensembl ID:
ZFIN ID:
Description:
calcium homeostasis endoplasmic reticulum protein [Source:RefSeq peptide;Acc:NP_956368]
Human Orthologue:
CHERP
Human Description:
calcium homeostasis endoplasmic reticulum protein [Source:HGNC Symbol;Acc:16930]
Mouse Orthologue:
Cherp
Mouse Description:
calcium homeostasis endoplasmic reticulum protein Gene [Source:MGI Symbol;Acc:MGI:106417]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa29704 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa9494 | Essential Splice Site | Available for shipment | Available now |
| sa45752 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29704
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 |
|---|---|---|---|---|---|
| ENSDART00000028634 | Essential Splice Site | 9 | 909 | None | 19 |
| ENSDART00000110788 | Essential Splice Site | 9 | 532 | None | 18 |
| ENSDART00000125265 | Essential Splice Site | 9 | 255 | None | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 4630917)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 4605331 |
| GRCz11 | 22 | 4989706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTAGCCTGTATTGCTGAGAAATATGGATATTTCCACGCCTCCAGAAGG[T/A]AAAACTGCGCCTGCGCGTGTGCTGCAGCGCGAACGCTAGAGAAGTCACAT
Long Flanking Sequence:
TTAGCATCTTACAACTTATTCCACCTAACGGCACTTTTTCATTAGCATTAGCATATTTCGAGGCTAAACATCTTCAAAAAACTAAATTGCCTACAAAAATGTCTGTAGAACACGAAGATATACTAATGATTACTTACTGTTACGGTAATCAGCTTTCATATACAGAATAAAGTGTCACAATGTCAAAAAAAGAAGGGATAATTATCAAAAATCTTACAAATTTACGACCTCCCGACGGCAGTTGACGCTGTGACGAGACCTCTCTTCTTAACGTCACCAGAGCGCATGCGCCTCCCACGCACCGGAGGAAGTAGTGAAGATTCTGTTTCCTCTCGCTTCATCTTGAACAGAAACACAACAAACCCATGGAGATGTGGTCGTACATTTTTTAAAACTGGATATTTTTGTTTCGCGCTTCAGCGTGATGTCTTATAAGTGAATTCCTGGTCGTACTAGCCTGTATTGCTGAGAAATATGGATATTTCCACGCCTCCAGAAGG[T/A]AAAACTGCGCCTGCGCGTGTGCTGCAGCGCGAACGCTAGAGAAGTCACATTATAATCAAACAGACACAAATAGACACAATTGGTGTATAAAATGAGGATTTAAACTGCTGCTTTGTTTATTTTTGGCTGTTTAGTGTGGCTAGCAATGTGAAATGAAGTAGCCAAATATTCATCCACTGTATTAATTGAATGTACAACGTGTTTTTGCAATAATTGTCAATAGGATCAACGTTTTCAGCAAAAAGATTGTATTTAGTAGTTAATTTAGATGAAAATTTCATTATTATCTAAGTTAAGGCTGAACAGATTGAAAGATAGCATCAATATTATATATTAAGTATATCTCATGATTAATTTGGTCACACTTTTTTTAAAGGTACAATTCTCGCTATTATCAAATAATTAACTAAGAATTCTAGCTCAATAAACTGCTAATTTGCTGTTCTTTTTTGCAGTTAGTCAGATAGTTTGGTTTAGGTATCACTTTATAAGTGATAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9494
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 |
|---|---|---|---|---|---|
| ENSDART00000028634 | Essential Splice Site | 78 | 909 | 3 | 19 |
| ENSDART00000110788 | None | None | 532 | None | 18 |
| ENSDART00000125265 | None | None | 255 | None | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 4628653)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 4603067 |
| GRCz11 | 22 | 4987442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTCCTTTATAGATTCTGGCACTCATGATGATGAATATAATATGGAAG[G/A]TATTTATTAGACCGATGTTTCAGAAATGTTTCATTTTGCCTGGTATTCAT
Long Flanking Sequence:
CCCGAATTTGAGAAGATGACCATGGAGAAGCAGAAGGACAACGCCAAGTTCTCATTCCTGTTCGGAGGGGAATTTTTCGGCTACTACAAATATAAACTGGCCATCGAACAGCAGCAGCGTACGTGAAAGAACCGCAAGTCACATTTATTTACTAACTAGTGTTATTTTTAGTATAAGCTTTACGTAGGTGTATTTTTGCGATTTTTAAACTGGCTTGTTCCCATTGTAGTATTGAATATTATATTCATTTTTGAAAATGTTTGATAGTTTATATATTTAAATATTGCTTACTTCCGTTTTAAAAATTCATCTAACATTTGTTTGTTTGTTTCACTTTAAAGGAACTTTTTTTTTGTTTGTTTTCGCTAACATTAATAACCTTGCTGCTAACCAAAGATCTAGATTTGTCTGACAGCTGTGTTCTGCATATGTTCGTGTTTAAGGTGTGCTTTTCTCCTTTATAGATTCTGGCACTCATGATGATGAATATAATATGGAAG[G/A]TATTTATTAGACCGATGTTTCAGAAATGTTTCATTTTGCCTGGTATTCATGGAGTTCTTCTGCAACATCAGTGCTTAAAATCCTTATTTTGCTGTCAGATTATGTTATAAATGACATCTTTAAGTTAGCGTTCAACCTTTATAACTGGTTTAAATGCTATAAAACGGTTGCAAAAGCTTAACTGTTATTATTGCATTTATTTTGAGATTTAAAAGAAGCTTTCAAGCGAACTCTACTTTCTTGCACTGTTTTTTTTTTGCTACATAAACGATATGTAAGAATGTGCAGCTTTTTGTTTTGTACTTTCTGTTTGCAAATGTAAATATTATTGTTTAATATTTATTCAGCTTTTAAGGAAGCCACAAGCCAGCAGATTTTCTCTTTGGACTCTGGTTTCTTTTCCCCCGTAGCCTTAAATGTTTTTGCTTCCCGTTTGTTTGAGTTTTTTATGCTACAATCTCCAGACATGGAAAATCAGAGGAGAACAAACAAGCATGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45752
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 |
|---|---|---|---|---|---|
| ENSDART00000028634 | Nonsense | 610 | 909 | 12 | 19 |
| ENSDART00000110788 | None | None | 532 | 11 | 18 |
| ENSDART00000125265 | None | None | 255 | None | 6 |
Genomic Location (Zv9):
Chromosome 22 (position 4614061)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 4588475 |
| GRCz11 | 22 | 4972850 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTGGGCCTCCACCCCACGGCTTCAATGGTCAGGCTCCGCACATAAGA[C/T]GACACAACCCACCACACGTCAGTCAGGATGACCCTAGTCTCGTGCCCAAT
Long Flanking Sequence:
ATGCTTCTGTTGCCTTGCAACTTCCTACTGTCAAAAACAACTTTCTGTTGGTAAAAACATAACTTTGCTTCAGATATGTCCTTTAAAACAGCATATTCAGTGTTGCGAAAAAGATTTCTCTCCGGCTTGAAAAAGTGAAAATGAAAGTGAGTCGCAGCTGATCTAACATAGCCTAACTATATATTTTATAGTCTGTATTACCAAAAAGATCTATTTTTAGGGTGATGACTTAAATAAAAAAGGACAACAGAAATTTAAAGCTTAATTTTAATATCTCAAAAGAAGCTTTTAATGTAAATATGACATGACTATGTTTCTGTCTTCCTCTGCTTTTTCTTTAAAATGGCATTGTTTTCTCAGAGATTGGACCGCCGCCGCATCACCACCCGAACCAGCGGATTCCTCCTCCGGGATTGTCTGATCCTCCTCCATGGGGTGGGAACCAGCATGAGTTTGGGCCTCCACCCCACGGCTTCAATGGTCAGGCTCCGCACATAAGA[C/T]GACACAACCCACCACACGTCAGTCAGGATGACCCTAGTCTCGTGCCCAATGTGCCCTACTTTGACCTGCCCGCTGGACTTATGGCACCACTCGTGAAGGTCAGAGTATATTCAGCATCAATAAACAGTTTTCTAATCGTGATTAATTTGTACATTTTTTGCGACAAACATAATTATCGGGATAATATGAAATTGACGATACATGATATTGACCTTCAAAAAAAAGGTTACTTCAACAACCAAAATAACTAAAAATACTTGGCTTATTGCTTTATTGTTTCTGCAGGTTTAGAGTAAATAAATGTTTCAAACTAATTAAATAGCGAAAGGATAATAAAGTACAATAGTTAACACGTTACAATAAAGTCTTGTTATTAAATGTTGGTTAATGCACTCAAATTAACAGTGGGACAAAGATTTAATACATTTATTATGTTAATTTTAATTAACTAAAATATACTTAGTGTCACTTAACAATTTTCTTTTTGTGGTTAATTGTGA
Associated Phenotype:
Not determined