ZMP
cerk
Ensembl ID:
ZFIN ID:
Description:
ceramide kinase [Source:RefSeq peptide;Acc:NP_001099056]
Human Orthologue:
CERK
Human Description:
ceramide kinase [Source:HGNC Symbol;Acc:19256]
Mouse Orthologue:
Cerk
Mouse Description:
ceramide kinase Gene [Source:MGI Symbol;Acc:MGI:2386052]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20295 | Essential Splice Site, Missense | Available for shipment | Available now |
| sa33481 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa26314 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa18020 | Essential Splice Site | Available for shipment | Available now |
| sa10769 | Nonsense | Available for shipment | Available now |
| sa33482 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33483 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20295
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, Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000100453 | Essential Splice Site | 183 | 568 | 5 | 13 |
| ENSDART00000146099 | Missense | 264 | 649 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 4 (position 27222044)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 27936105 |
| GRCz11 | 4 | 27925393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTATCATCAACCTGGTAACAATGGCTTTTCCCTTTTTGTTTCTATA[G/A]TTACAGAGCATGCAAATCATGCCAGAGACCACTTGAAGGCAGAGGCTGAT
Long Flanking Sequence:
GGAAGACCCTGGCTTTGTGTGAAAATTGGCTGAGGCTTACAGGCTGGCTCAGCAGTTGCTTGAGGGTGTTCTTTTTTACGACCACGCGAACATTTCGTAAATGGTAAAGTACATGTCTTGCTGGACAAATACCATTCAAACCAAATCATTAGAGGAGCCAAACAAGATGTTCTGCCGACGGTTTAATAAGCTCCATACATCACCTTTGGCATATATCATCAGCGTGATCCACAGGGCTCGGTCCTAGGCCCCATTCATTTTCAGCGCATCCCTCCGAGTTACGCTTTTACATCATCGCTGATGGTAAAGAACCGGTAATGAAATGTACCGGGGATTGTTTTTCACCACGAGTTCAGCTTCATCATCTGATGCAGCTGATTGATGGTCTCCATCAAGCTAGCAGAAAAATGCAATTTAACTGCCAGATGAACATAATGATGTTTCTCCCCCCTCTCTATCATCAACCTGGTAACAATGGCTTTTCCCTTTTTGTTTCTATA[G/A]TTACAGAGCATGCAAATCATGCCAGAGACCACTTGAAGGCAGAGGCTGATCTGAAGAAGTATGATGGGTAAGTGGATGTCCTGCTGTGGGATATCACGGTCACTGTGCTGCAACTCTTAATTTGCACAGCTAAGATTGCATCTTCCGCAGCAAAGCTCAGATTAACATTTGCGCATTGATTCTGTCTGCTGGAATAACAGGTGACTGTTCCTGGCATTTAAGGAAATGACGATTGAAAGTGGCTTTTAACAATGACAACATCAATGCATCTTTAAAGCTGGCGCTAAATTCACATATCTCTGTTTACTTTTGTATCTTTTTTCTGTATTTCAGAAAGGAGGTTTAAGGGATTTAGGTGATTGTCCTCAGAAATGATTTTTGTTTTATTAATCTGGATGATTTGTTATCATTAAATGAAGTTCTTCACATGTATTTGTATTTTATTATTCAGTGGAAGGTGTAGGACCAAAAAAAGGTGTAGGACCAAAAAAAGTTAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33481
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000100453 | Nonsense | 203 | 568 | 5 | 13 |
| ENSDART00000146099 | Nonsense | 284 | 649 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 4 (position 27222106)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 27936167 |
| GRCz11 | 4 | 27925455 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAATCATGCCAGAGACCACTTGAAGGCAGAGGCTGATCTGAAGAAGTA[T/A]GATGGGTAAGTGGATGTCCTGCTGTGGGATATCACGGTCACTGTGCTGCA
Long Flanking Sequence:
AGGGTGTTCTTTTTTACGACCACGCGAACATTTCGTAAATGGTAAAGTACATGTCTTGCTGGACAAATACCATTCAAACCAAATCATTAGAGGAGCCAAACAAGATGTTCTGCCGACGGTTTAATAAGCTCCATACATCACCTTTGGCATATATCATCAGCGTGATCCACAGGGCTCGGTCCTAGGCCCCATTCATTTTCAGCGCATCCCTCCGAGTTACGCTTTTACATCATCGCTGATGGTAAAGAACCGGTAATGAAATGTACCGGGGATTGTTTTTCACCACGAGTTCAGCTTCATCATCTGATGCAGCTGATTGATGGTCTCCATCAAGCTAGCAGAAAAATGCAATTTAACTGCCAGATGAACATAATGATGTTTCTCCCCCCTCTCTATCATCAACCTGGTAACAATGGCTTTTCCCTTTTTGTTTCTATAGTTACAGAGCATGCAAATCATGCCAGAGACCACTTGAAGGCAGAGGCTGATCTGAAGAAGTA[T/A]GATGGGTAAGTGGATGTCCTGCTGTGGGATATCACGGTCACTGTGCTGCAACTCTTAATTTGCACAGCTAAGATTGCATCTTCCGCAGCAAAGCTCAGATTAACATTTGCGCATTGATTCTGTCTGCTGGAATAACAGGTGACTGTTCCTGGCATTTAAGGAAATGACGATTGAAAGTGGCTTTTAACAATGACAACATCAATGCATCTTTAAAGCTGGCGCTAAATTCACATATCTCTGTTTACTTTTGTATCTTTTTTCTGTATTTCAGAAAGGAGGTTTAAGGGATTTAGGTGATTGTCCTCAGAAATGATTTTTGTTTTATTAATCTGGATGATTTGTTATCATTAAATGAAGTTCTTCACATGTATTTGTATTTTATTATTCAGTGGAAGGTGTAGGACCAAAAAAAGGTGTAGGACCAAAAAAAGTTAAAGTTAAAACAAGCCTATCATAAAGTCCGAACATTATGATAGGCTGTCCTGTCTGCCTGTTGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26314
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 |
|---|---|---|---|---|---|
| ENSDART00000100453 | Essential Splice Site | 279 | 568 | 7 | 13 |
| ENSDART00000146099 | Essential Splice Site | 360 | 649 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 4 (position 27233762)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 27947823 |
| GRCz11 | 4 | 27937111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGTTGGCTCAAATGACCCCGTCACCTCAGCGCTGCACATGGTCGTGGG[T/A]AAGTGAGCATCTTCATATTAGCTGTATGAGACGCGTTTAGTTATGCATAT
Long Flanking Sequence:
AAAAGAAACATCATTTAACAAACAGTAGTGTAACTGTCAGTATGTTTTTAAACCTTAAACCTTTTGCTGTTATATAAGCAATTTGAGGATGAGGAATTAGATTAGCAGACAGCGAATAAGAGATAGGAGGGCTGAACTCATCTGAAATCTCATCTCTCTATATAACAATGCTTCAGTCATTTTGAAGAATGAAAAAAAAAAAAAAACTTTCTTATTCTCACTAGGAGCGAAAACTCCACTGGCCCTGGTATGTTTGGTTAGCGCTCACAATTGAAGGTTAGATTGCGGCGGCTCCCTGTACGCCGGCGAAATTGAAAATGAAAGTGTGATTTTCATACGTTAACCTTTTCAGAGTGAATTATGAAGAGATAGACGTGGGCCGTTTCTGAACCCCTGACCCGTGAAATGTGTTTTTGAAAAACAGGTTCCACTGACTGTATATGCTATGCCACGGTTGGCTCAAATGACCCCGTCACCTCAGCGCTGCACATGGTCGTGGG[T/A]AAGTGAGCATCTTCATATTAGCTGTATGAGACGCGTTTAGTTATGCATATGTATGTTTCTGGAAAGTCTTATGCTGCATGGGTGTACAAAGTATGGGTCAGAATTATGTAGATATATTAAACATTTTTTTTTTTTATTGGTAGTATGCATAGCTAAAATATTTAAGACCAATTTCTCAATTTTTATTCAGTTTTGTTTTGTTTATCTTATGTTTTGTTTTATATTGTTTTTGCTTTGTGGTTTATTTTGATTTTGTCTTGTTTTATTTTATTTTATGTTGTGTTGTTTAGTTTTGTGTTTTTTATTTAGTTTTGTTTTATTTGACCTTGTTTTGTTTTTTTGTTTTGTTTTGTAATTTATTTTATTTTGTTTAGTTTTATTTTACCTTGTTTTGTGGTTTTGTTTGTTTAGTTTTATTTTACCTTGTTGGGTTTTACCTTGTGTTTTGTTTTGTTTTATCATGTTGTGTGTCATGTCATGTTGTCTTGTTTTGTTTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18020
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 |
|---|---|---|---|---|---|
| ENSDART00000100453 | Essential Splice Site | 279 | 568 | 8 | 13 |
| ENSDART00000146099 | Essential Splice Site | 360 | 649 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 4 (position 27235157)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 27949218 |
| GRCz11 | 4 | 27938506 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TYTGTGTTTTGTTTTGTGCTTTCCATAAATYCATTCTGTCATTTTCCAYA[G/A]GTGATTCTCAACCAATGGATGTCTGCTCAGTGCACAGCGATGATCGTTTC
Long Flanking Sequence:
TTTTGTTTCATTTTATCTTGATATAATGTTTTATGTATTTTAATTTTGTTTTGTTTTAGTTTGTTTTATTTTAGTTTGTATTTTTGTTTTGTTTTATGATTTAAAATATTTATCTTGTATATTTTTGTTTTGTCTTGTTTTATATTTGTTATTTTATTTTAACTTATTTTGTTGTATTTTGTGATGTTTTGTTTTTGTTTTTTGTCTTTTTGTTTTATTTTAGATCCCTATATTTAATTCCACTATTTAGTTTTTTTTGTTTGTTTTGTGATTTGTTTTGTTATGTTTTATCTTGTCTTGTTTTTTGTTTTAGTTTTAGTTTTGTTGTGTGTTGTTTTTATATGTACATTTAATTATTTTTTTGTGTTTAGTTTAGTTTTGTTTACTTTTATTTTTATGTTTACTATTTATTTTTATTAGTTATTTTATTTTGTTTTTATTCTTTTTTCTTCTGTGTTTTGTTTTGTGCTTTCCATAAATCCATTCTGTCATTTTCCACA[G/A]GTGATTCTCAACCAATGGATGTCTGCTCAGTGCACAGCGATGATCGTTTCCTGCGTTACTCTGTCTCACTGTTGGGTTATGGTTTCTATGGAGATGTGCTAAAAGACAGCGAGAGGAAGAGATGGATGGGTCCTGCTCGTTACAATATCTCAGGTCACATAAAATGTCGTAAAAAATAAAATAGCTAATTTATTTCTTTCAATTGTCCTGAATTTTTTGTTATTGTCATTTATCAGGGGTTAAAACGTTTCTGTCACATCGCTACTATGAGGGAACCGTGTCTTTCCTACCTGCAGAAGAGAACTTGGGAACTCCAAGAGACAAAGTGCAGTGTCGATCTGGGTAAATGCTATACTTTGTTCCATGTTTAAGCATAATATGATCACAATAATTTATTGGAAAAATACAAATCTAGCCAAACATTAGCACAAACCTATCCAGAATTATCAAAAAAGACAAACAAAAATATCACATGGTCCTAAGTCTTCAGACTCTTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10769
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000100453 | Nonsense | 303 | 568 | 8 | 13 |
| ENSDART00000146099 | Nonsense | 384 | 649 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 4 (position 27235230)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 27949291 |
| GRCz11 | 4 | 27938579 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCTCAGTGCACAGCGATGATCGTTTCCTGCGTTACTCTGTCTCACTGT[T/A]GGGTTATGGTTTCTATGGAGAWGTGCTAAAAGACAGCGAGAGGAAGAGAT
Long Flanking Sequence:
GTTTGTATTTTTGTTTTGTTTTATGATTTAAAATATTTATCTTGTATATTTTTGTTTTGTCTTGTTTTATATTTGTTATTTTATTTTAACTTATTTTGTTGTATTTTGTGATGTTTTGTTTTTGTTTTTTGTCTTTTTGTTTTATTTTAGATCCCTATATTTAATTCCACTATTTAGTTTTTTTTGTTTGTTTTGTGATTTGTTTTGTTATGTTTTATCTTGTCTTGTTTTTTGTTTTAGTTTTAGTTTTGTTGTGTGTTGTTTTTATATGTACATTTAATTATTTTTTTGTGTTTAGTTTAGTTTTGTTTACTTTTATTTTTATGTTTACTATTTATTTTTATTAGTTATTTTATTTTGTTTTTATTCTTTTTTCTTCTGTGTTTTGTTTTGTGCTTTCCATAAATCCATTCTGTCATTTTCCACAGGTGATTCTCAACCAATGGATGTCTGCTCAGTGCACAGCGATGATCGTTTCCTGCGTTACTCTGTCTCACTGT[T/A]GGGTTATGGTTTCTATGGAGATGTGCTAAAAGACAGCGAGAGGAAGAGATGGATGGGTCCTGCTCGTTACAATATCTCAGGTCACATAAAATGTCGTAAAAAATAAAATAGCTAATTTATTTCTTTCAATTGTCCTGAATTTTTTGTTATTGTCATTTATCAGGGGTTAAAACGTTTCTGTCACATCGCTACTATGAGGGAACCGTGTCTTTCCTACCTGCAGAAGAGAACTTGGGAACTCCAAGAGACAAAGTGCAGTGTCGATCTGGGTAAATGCTATACTTTGTTCCATGTTTAAGCATAATATGATCACAATAATTTATTGGAAAAATACAAATCTAGCCAAACATTAGCACAAACCTATCCAGAATTATCAAAAAAGACAAACAAAAATATCACATGGTCCTAAGTCTTCAGACTCTTTACTACGTATTTAGTAGAAGCACCCTTTTGATCCAATACAGTCATGAGTCTTCTTAGAAAAGATGCAAAAAGTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33482
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 |
|---|---|---|---|---|---|
| ENSDART00000100453 | Nonsense | 363 | 568 | 9 | 13 |
| ENSDART00000146099 | Nonsense | 444 | 649 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 4 (position 27235492)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 27949553 |
| GRCz11 | 4 | 27938841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTACCTGCAGAAGAGAACTTGGGAACTCCAAGAGACAAAGTGCAGTGT[C/T]GATCTGGGTAAATGCTATACTTTGTTCCATGTTTAAGCATAATATGATCA
Long Flanking Sequence:
TTTTATATGTACATTTAATTATTTTTTTGTGTTTAGTTTAGTTTTGTTTACTTTTATTTTTATGTTTACTATTTATTTTTATTAGTTATTTTATTTTGTTTTTATTCTTTTTTCTTCTGTGTTTTGTTTTGTGCTTTCCATAAATCCATTCTGTCATTTTCCACAGGTGATTCTCAACCAATGGATGTCTGCTCAGTGCACAGCGATGATCGTTTCCTGCGTTACTCTGTCTCACTGTTGGGTTATGGTTTCTATGGAGATGTGCTAAAAGACAGCGAGAGGAAGAGATGGATGGGTCCTGCTCGTTACAATATCTCAGGTCACATAAAATGTCGTAAAAAATAAAATAGCTAATTTATTTCTTTCAATTGTCCTGAATTTTTTGTTATTGTCATTTATCAGGGGTTAAAACGTTTCTGTCACATCGCTACTATGAGGGAACCGTGTCTTTCCTACCTGCAGAAGAGAACTTGGGAACTCCAAGAGACAAAGTGCAGTGT[C/T]GATCTGGGTAAATGCTATACTTTGTTCCATGTTTAAGCATAATATGATCACAATAATTTATTGGAAAAATACAAATCTAGCCAAACATTAGCACAAACCTATCCAGAATTATCAAAAAAGACAAACAAAAATATCACATGGTCCTAAGTCTTCAGACTCTTTACTACGTATTTAGTAGAAGCACCCTTTTGATCCAATACAGTCATGAGTCTTCTTAGAAAAGATGCAAAAAGTTTTCACACCTGGATTTGGGCATCCTCTTGCAGATTTTCTCCAGTTCTGTCTGGTTGGATGGTAAACATTAGTGGACAGCCATTTTTAGGCCTCTCCAGAGATGCTCAATTGGCTTTAAGTTAGGGCTCTAGCTGGGCCATTCAAGAACGGTCACAAAGTTTTTGTGAAGCCGCTTCTTCGTTATTTTATCTAAGTGCTTAGGGTGCTTTCTCATCATCTTTGAGTCCTTCACCTGTTTTTTTAGCAAACTCCATGCAGGCTTTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33483
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 |
|---|---|---|---|---|---|
| ENSDART00000100453 | Nonsense | 451 | 568 | 11 | 13 |
| ENSDART00000146099 | Nonsense | 532 | 649 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 4 (position 27242728)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 27956789 |
| GRCz11 | 4 | 27946077 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCCTCGTCAGAAAGTGCTCCAGAGTCGACTTCCTGCGACACCTGCTG[C/T]GACACACCAATAAGAAGGACCAGGTTAATATCTCAACAGAATAAATCATT
Long Flanking Sequence:
CTGAGCAGTAGTTTACCAGTAATTTCTGAACACTTTTAGATTGTAGGGCATGAAAAAAAAAAAAAGAGTAAAATGATGTAAATATGAAAGTAAGTCAAGCCCCATTTTTCAGCGAGGGCTTTGAGATTTACATTAACCTCACTTTGTTTATTCTAACTAGATTATAACTTGATTTTTAGATCTTCAAAACATGTTCATTTAGCAGAAGCTCCAATGTAATTTATGTAAATAAATTACTTATCCAGATGGCCAGAGAATAGTACACTTTACCGTGCAGTGTTTTACTAGTGTTAACACAATCTTGTTGTTTTGTTTAAGATTGCCGGGACACCTGGACGGTCATCAGGGGGAAGTTCTTGGCCATTAATGCCGCCAACATGAGCTGTGCATGTCCTCGCAGTCCTAAAGGTCTGTCGCCGTCCGCACACCTAGCAGATGGAACGACTGACCTCATCCTCGTCAGAAAGTGCTCCAGAGTCGACTTCCTGCGACACCTGCTG[C/T]GACACACCAATAAGAAGGACCAGGTTAATATCTCAACAGAATAAATCATTTTTTGTGTGTGTGGAAGATAGAAACGTTTATGAACACTATAGTAACCACCAAAGTTCAAAAAGCATCACAGCTGACCAGCAAATGGTTACTGTATATTTTATAATAGTATAAATTCATATCTAATTTTAATTAACTGTAATTTTGTTCATTTTTTAAGGAAATGAGCTGCAAATCTACTTCTTTGAAGTGCATAGTCACAGCAGGGGTTTCCTGTTCATGAAGAACTTCAAAGTCATGGGAATATTTCTGCCTTTTTTTTTTTTTTTTTTGCCTAACTCCTAAATCATTTAATTGACTAGAAATGCCACCTTCTGAGAGCAATCTCTGTAAATGTATCATCTTAGTAATTACAAATGTTTGGAAATGTCACAAAAGTAAGCAACTTTGTAAAAGTCCATATTTAAAATTATCCAGAAACCAGAAATATTAAAGCTGATTTCTAACTATGG
Associated Phenotype:
Not determined