ZMP
zgc:162213
Ensembl ID:
ZFIN ID:
Description:
ceramide kinase-like protein [Source:RefSeq peptide;Acc:NP_001082943]
Human Orthologue:
CERKL
Human Description:
ceramide kinase-like [Source:HGNC Symbol;Acc:21699]
Mouse Orthologue:
Cerkl
Mouse Description:
ceramide kinase-like Gene [Source:MGI Symbol;Acc:MGI:3037816]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa45378 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15401 | Nonsense | Available for shipment | Available now |
| sa41544 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41543 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45378
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110411 | Nonsense | 62 | 577 | 1 | 13 |
| ENSDART00000147279 | Nonsense | 62 | 302 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 45355301)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 44487622 |
| GRCz11 | 9 | 44289364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGAAGCAAAGTCAGAAGCGCTCCGTTTCGGCCCCTCAGTTATGCCCC[G/T]AAGAAGACTACAAGGAGCGAGTAGAAACTAAATACAGACCGGACGAACCG
Long Flanking Sequence:
CCTATATATATTTTTAATTGTCAGTAGTAGACTACCTATTGATAATAAATCAAACGATTTATTACAGGCCTACAAGTATATAAAACGGATGATTAGAAATTAATATAGCATTTCACGTATATACACATTTGTTAAATTGCTTCAATAGTAGCCTAATAACAGGCAGTGAGGGCTGCGCGCGTGCTCGGCTGAGAAAGCTCGGCGGGCGCGCGCGCTGTAGAGGTGCATGGAGACGCGAGGAACTTCCTCAAGAGCCTAGCGACCGGGAGCGGTAAATTAATACACACAGGCGAGTTTGCCCTCAAAACATACACACTATGCTTGAATCCCCGTGTAAATCGATAAGTGTCCTCAACGCGTGGTCGGAGAGTCAGGAAGAGTTGCGCGAGACGCAACCGGTGTCTCCTCACGGGACGGAGAAGCGAGTAAAGACAAAAAAGAAAAAGAGAAAACAGAAGCAAAGTCAGAAGCGCTCCGTTTCGGCCCCTCAGTTATGCCCC[G/T]AAGAAGACTACAAGGAGCGAGTAGAAACTAAATACAGACCGGACGAACCGATTGTACGAGGAATCTTCCAAATTGAAAAAAAGAGCCACGACGTAGTTCTTACGACAACGCGGGTAACATGGACGCCCATTCAGCCCGAGACCCCTACAGGTGAGCAGCGATGCGCCCTGTTTACACCCGTTTCCAGGGGGACTGTACACTTGTGTTTACTTCCTGTGTGTGCGTGTGTGTTTGTGTGTGTGTGTGTGTGTGAGGCGCTTAAAGTCATCTTAGCAAGCAGTGTATTAATTTATCATGTTTATAGACACGGTTACGGCTTTGTGTACAAGACAGATACAATCTCAGCTATGGATAAAATGGTTCGCTGAGATTGAGACAAAAAGTAAACAATCAAACAATGCATAAATTAGAGTTTTAGAATGATACATTTTAGAAATATAATGTATTTCTCTATACTTCTGTTTGGTCACACTTTATTTTAAGGTACAATTCTCGCTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15401
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110411 | None | 180 | 577 | 2 | 13 |
| ENSDART00000147279 | Nonsense | 180 | 302 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 45315738)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 44448059 |
| GRCz11 | 9 | 44249801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RATCATGCCATCCATCTCAACAACCTGAGCGTGGACCACTGTGAGATCTG[G/A]TTCAAAACCCTCAAAGAGCTCCTCAACGGTACGTTCACATCMCAGCAGWT
Long Flanking Sequence:
TATATTTTGAGTAAATCCGATTTGCTTGGTATCTTAAAATACACTTGAAAAAAGTCTTTCACCGCATTTCAAAATTGGCATATATTAAAATTAAGCTGAAAATAATTTCAAACTATATATGAATCTTAGTCTTTAAATTTAACAAGACATTTTATTACACTTTAACTTGTTAAGTGTTGTTGTTATGTGTCATATAAAGGTGATTTTTTCCCACTTTTTTCTTTTTTTTAAAGGGAGGGGGATGGGGCATAGATATATAATATGAATTTTAAATGTCTCTTGTGTGTTTGTTTAGCTGACCGTGATCTGAAGAAGCAGGAGGAGTATGTGGACCTTAAAGACGTGTTTGCAGTGAAGGTAAAGCGGCGGCGGTCAGCTGGACAGCAGTCTGGTGGGACCCTTCTGGGAATCACACTCTTCCAATGCAAGAAGAAAGGCCTCAAACTGAAAGATCATGCCATCCATCTCAACAACCTGAGCGTGGACCACTGTGAGATCTG[G/A]TTCAAAACCCTCAAAGAGCTCCTCAACGGTACGTTCACATCACAGCAGATGCACAGACACTGAAGAATAGGTCACAAAGCAGGCATTTTAGCATTATTTTATCAGCTTGGAGCTTCAGTGAATTTTATGATACACATTTATGACGTGCAAACATTAACCTGGTCAACATTTGGCTCACTTTATATTTTATTGTGTTTGCTGACATTTATTGAATAAAGATTACCCATCCCAGTAATGAATCGGACACAATTGCTCTGTTCCTGAAACTAGTGAGTGTAGCATTTTAAGTGCACTCTTAATGCAAGGTTACCTCAAGATGTTAGGCAACATTATTATGTTATACTGAGTATATATTGTAATATTCTTCTAAGTCACTTTTTATAAGCTACGTGGCAGCATGTAATCCAGGTTAACACTGACTAACCATATTCCATACACAACGCTGTTCTGTACAGATTACCTTTTAACGTCAATTACTGAATAAATACTTACAGGTCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41544
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 |
|---|---|---|---|---|---|
| ENSDART00000110411 | Essential Splice Site | 387 | 577 | 7 | 13 |
| ENSDART00000147279 | None | None | 302 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 45175448)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 44307769 |
| GRCz11 | 9 | 44109511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGCCAGCGCCGCGAGTTCGCTCTCATTAAAACACTGGCAAAGCTCAA[G/A]TAAGCGCTCTCTCTTTCTCAGTTGTGTTGTCAGCTGTAGCTGTCTCTCAT
Long Flanking Sequence:
CGCCAGGGCAGCCAGAGCAAACTTTGATGCTCTTACCGCCTTCGGTGTGAACACACAATTAGACTTTGGGCTTAGATCGTTAAAATAGAGCCCAATTTGTGCTAGAAAAATAAAGACTGTAAATTTTGATTTCACGCAGACTTTAACTTGCAGTGCATTTGAGCTCTTAGTTACATTACAACACCTTAGTTTTGTAACAGAGATATATTCTACAGGTGTATCTTTTTATACTCTTTGTGGCTGCAGTGTGCTTTGTTGCTGGTGTTTTTGTACCCTCTGTAGGACACCTGATTTCTCTGACTGTTTTTGGTTGCTGTTCTAGGTCACCATCAGCCTGTGGACGTGTGCAGTTTCAGCTGTATGGGTCGTCTGCTGAGGTTCGGCTTCTCTGCCATGTTTGGTTTCGGTGGGCGGACACTCGCATTGGCAGAGAGACACCGCTGGATGCCACCCAGCCAGCGCCGCGAGTTCGCTCTCATTAAAACACTGGCAAAGCTCAA[G/A]TAAGCGCTCTCTCTTTCTCAGTTGTGTTGTCAGCTGTAGCTGTCTCTCATCTGGTGGGCTCCAAGGGACTGGCTGGTGCTCCATCAAATCTGGGATTAGTGTCAGAGCAGCCTGGCACAGCACACATGGGCACCGTCTCTTAGAAATCATCCTCTTCTTATCATAACACTCCATCTAACGTGTTTGTTCTCTTTCCTGGTGTCCGACTGATGGTGTTTGTGAAGACCTGAAGATTGTGAACTGTCCTTTTTAACCGCCAAAGGAGCTGAGGATCAGAAAAAGTGTGTGTTTTCAAGTTTGTTTGTTTTTTCATCCCTCATCCCCATCCAACTTTGAGCTTAATGATTTGAATGTTATTTTAAATATACCACCCCCTGTTTAATTGGCCATTGGAAAGAGATCAGATTGCTGAAGGTCACCCAGCTAATGCTAATAAGGCGGGCTGCTTCACACTGAGAGCAACCCATACAACTCTATTATTACTCAAATACAGATAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41543
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000110411 | Essential Splice Site | 551 | 577 | 13 | 13 |
| ENSDART00000147279 | None | None | 302 | None | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 45160551)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 44292872 |
| GRCz11 | 9 | 44094614 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATAAATCTGTGTAATGTTTAAATGTCCTGACAGAAGTGTTTATTTTCC[A/T]GAGTTCACCCTCAGCTCCTCACACTCTTTGGATCAGACGTGGAGGAGGCC
Long Flanking Sequence:
GAGATGTTTAACTTCACTTTCATGTTTATTAAACCACTCTGTGGTAAACTGATTTTTTTTACTCCATTCATATTTTCATTATGTATCACAGGAGACATTTAAAGCTTGATAACATCACGACATATCAAAAGCTGAAAATCTATGGCGAATCTAATGCATATTGCCTCTAAATATTTAAAATTTGCGTTCAATTCTGATATCGTATAATCGAGAAATCCTGAAAGCACTGGCTAACAGTAGTCAAGACAGCCACTGTGTGAATTCAGCAGATGAACTTCGGATGACCTGTGCAAACACAAGCCGTGTTGTTTTAACACACTCCAAACAATATACGAGCAGTACTTGATAAAAAAACTAAATTTATCTTTTCAAAGCTGCAGAAAAAGCGACAGAAGAATAAACAGAAGAGTGTGAGGTTCTGAGAAAGAGGGAGGGAGGTGTGCGGCTATCAGATAAATCTGTGTAATGTTTAAATGTCCTGACAGAAGTGTTTATTTTCC[A/T]GAGTTCACCCTCAGCTCCTCACACTCTTTGGATCAGACGTGGAGGAGGCCGAGGAGACGCCGGTGAAATGCAGCTGTATCTGAACACACACTCATACACACATGCACACAGAGAATTGCTATTAAGAACTCAACAAACAAACCGCACAGAGAAATGCTTTAACATGTAAAGAGAACATTTTATGACAACACAAAAACACACAGTACATTCCAGTGCATTACAACTTAAATAAACCAAAAGACAGTTTTTAAACAAATTTGTATCATTTTTAAAGACTTAACTTAATAAACATACACAGAAAAATAGCAATGTGCTTTTTTGCATTTGATTCCCTGAACTGTGGAGTTTTGTTTTGTTTTTATGTCTTAAAAAGAGCAGTGACAAGCAACCCATCTAATGTGTTTACTCAAAATAAAAAAAGACATCCCACATATTTAGTTTGAATTCTCACAGCATAGTTTGTGTTTACAAGCTCAATCATGCAGGAAAAAAAAAAAAGC
Associated Phenotype:
Not determined