ZMP
si:ch211-236l14.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate carnitine palmitoyltransferase 1A (Liver) (CPT1A) [Source:UniPro
Human Orthologue:
CPT1A
Human Description:
carnitine palmitoyltransferase 1A (liver) [Source:HGNC Symbol;Acc:2328]
Mouse Orthologue:
Cpt1a
Mouse Description:
carnitine palmitoyltransferase 1a, liver Gene [Source:MGI Symbol;Acc:MGI:1098296]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38079 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14518 | Nonsense | Available for shipment | Available now |
| sa38080 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38081 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38082 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa24683 | Essential Splice Site | Available for shipment | Available now |
| sa25226 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38079
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089199 | Nonsense | 151 | 774 | 3 | 18 |
| ENSDART00000137612 | None | None | 584 | None | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 24326445)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 23505558 |
| GRCz11 | 25 | 23603106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGGATGTTTAACCAGCATGGAACTCTGTCCTTAAAAACAAAGATTTG[G/A]TTGGTAAGTGTGGAGAAACAGATAGATAATCCATCTCTTAATGTAACAAT
Long Flanking Sequence:
TCTTGAAGTTATTATGAAATGTTGCAGCCGTTTATGAACCATATGTAACTACAGAGGTTATAATGACAAATCATTACATAGTGTTGCATAACAAGTTTTGGTAAAGTAGCCATTTATTTTAATCAACATTATTATTAAATAAATATGTGAGTAGTGAAATGAAGTCAATGAATTCAAATTTCGGCAGCTTCATTAACTACTTATCAACAATTAACTGATTTTAATTAGATTTTTAATTGGTGTTTTTATAGTATTGCGCTGTGTTGTTGAAATCTCTTACAGCGTCTATAAGGGCACTGCAGTTGTCACCTAACAGCTTTGTTTCCCTGCAGTAAATACATAACAGAAGATGGCCAACGTATTGTTGGTGGTGTGCTTGTTGGCACGGGACTGTGGATTGCTGTGACTTTCGTTATGAGGAACGCTCTCAAGTACTTGCTGTCCTGGCATGGCTGGATGTTTAACCAGCATGGAACTCTGTCCTTAAAAACAAAGATTTG[G/A]TTGGTAAGTGTGGAGAAACAGATAGATAATCCATCTCTTAATGTAACAATTCACCCATTATTTGGCACCTTGATTGTTAAATGAAATCTAAATTTATTATTAAGTATTATTGATTATTGATTATTTAATGACATGAATGTCTAAATGACAAATAGACATTAACGTCAAAAAAGTGTCAAAAGCGCTAAAGGATTTGATGTCAAAATCTTGGCGTCTATTAGACATCTGCACATTAATGCCCTTTTGACCACCAAAATAATCACACAAAGTGTTATAATATAATGAAATTATATTATAATGAAAAGTTTTACTCATCTGAAAGCTTCAATTCCAATTGAACATGTCAAAAATTTATTAAAAGACAGTTCTGAAATCAATTTTTGATTTTTGACTTCAATTTTAGATAGAAATTTAATGTTGTTTAGATTGACATCAAATTGATAAATGTTCTTGACACATTTTTATTTAATTTTGACATCAAGGTGCCCACAGAGTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14518
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089199 | Nonsense | 166 | 774 | 4 | 18 |
| ENSDART00000137612 | None | None | 584 | None | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 24327289)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 23506402 |
| GRCz11 | 25 | 23603950 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGCTCAGGTGTTGGTGAAGTTATTTTCTGGGCCAAAGCCAATGCTGTA[C/A]AGCTTCCAGAGTTCACTACCACGGTTGCCAGTGCCTCCTGTAAAAGACAC
Long Flanking Sequence:
TCAAAAATTTATTAAAAGACAGTTCTGAAATCAATTTTTGATTTTTGACTTCAATTTTAGATAGAAATTTAATGTTGTTTAGATTGACATCAAATTGATAAATGTTCTTGACACATTTTTATTTAATTTTGACATCAAGGTGCCCACAGAGTTTTTTTAGAGTATCATTTTTAAGGTAAACAATTCATTTAACTTGCTTTAAGTAAACCAGCTTAGTAAATATTTTCCTAACTCTATATCCAGCAAGAGTCTAAAGTCTTAATGCACTTGTTTTATAACATAATCTTAGCACTGTTCCGGTTTTAGCAGGTTTTTATTGAATTTAGCTTTCTCTATGTAATTGTGTCAAAGTGATTGCGATATATCTCTTCACTAGAAAAGGCTTGGCTTTATCATTGGAAAGTATTCCGGCTGGTCTCATGTTTGACTCTTGACCCAATGCTATCGCTATCTGCTCAGGTGTTGGTGAAGTTATTTTCTGGGCCAAAGCCAATGCTGTA[C/A]AGCTTCCAGAGTTCACTACCACGGTTGCCAGTGCCTCCTGTAAAAGACACCGTTAGAAGAGTAAGTCACATCTTAACTTTATACAGTTTATTAAAAGATCAAATATGATGTTTATTAGAAATGCACTGATTGACAGGCCAGAAATTGTTGTCTATCAGACCCACAATTGGCATATTTTTGATTTTATTATAAGAAATTGTGATAGTCTCTCTGTTCCTAATGCTAACAGGGGTCTCAGACTGCGGGCCCTCCTCCTCCCTCTGGCCTGCAGTTGACATCAAAATAATACTAGATTCAGCCTGCCAAAACAGATTTTTTTGTACCTCTATCATTGTTGTGCAGTTGTTTCAGGCCACTTGTGGTTTTTACCCGCCACCTAGTCGACATTTAAAGCACTGCATTCATATTACTGCATTACAGGCTTACTTTCATTTTCTCTCAGCGTGTGGTCGAGAGTAACACACATGTGTTTTAATTTTATGGCTGATTTTAACGTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38080
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 |
|---|---|---|---|---|---|
| ENSDART00000089199 | Essential Splice Site | 232 | 774 | 5 | 18 |
| ENSDART00000137612 | Essential Splice Site | 46 | 584 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 24332536)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 23511649 |
| GRCz11 | 25 | 23609197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAACTTCAGTGGTACCTGAAGCTGAAATCCTGGTGGACTTCCAATTAC[G/A]TAAGATCACTCAATGTTTAATGTTTAATCGCATTGTCAAACTATTATTCT
Long Flanking Sequence:
ATACATATGTGTGCTCTGGTTCTTTACAGTACTAACCAAGAAAATCACAATTATTCCTGCTTGCCTTTAAGTGTCACCTATAGGCAGAAAGTGAATCTGCATTTTTCATTCAATACGTCAACTGTTTTGTATGCATCATGTAGGATAATTCCAGAAAGCTAATGTCAAATCATTCTGTGATTAGTTTTAAACATTTTTACCATATATTTATATTTAACATATATACTTTTCAACATATGTTTAGATTTTTAAAACCATAAAAACATAATCATTTGAAAAAGGACATCGGTACCATGATTTAATAAATTGGAATCAGCCTAAAGCCTACCTCACCTATTCACATATGTATTGTTTTTTTTCAGTACCTGGAGTCGGCACGTCCTCTGATGGATGATGAACAGTACAAACGTATGGAGGGTTTAGCAAAGGACTTTGAGAAGAATTTGGGCCCCAAACTTCAGTGGTACCTGAAGCTGAAATCCTGGTGGACTTCCAATTAC[G/A]TAAGATCACTCAATGTTTAATGTTTAATCGCATTGTCAAACTATTATTCTACAGGCATTCTTATCTCATTAGAACTGATTCCGTAGCGAAAGGCAATAGAGTTCAATGCTAAAAGTGATTTTGAGGTCTGCTTTTTTTAGATTATCTTTTTGGTTGAGCAGTAGTTTGACAGAAGGCAAAGTTGAAGTGGGAGAAAGGGACAGCACTGGGAAATATCCATGATGCAGGAATCAAACTCAGAACAATTGAAGCGCAGTTGAGCTATTGGCGCAAACATAGTTTTTTTTAAACTTTAACAAGAATAATAAAATTGCGTTTGTTTCTTAACTCTAACAAATTAAATACGCTTTTTAAATCCTAACATTTAATGACAGCAATAAAACACAATACAGAAAAAAATGGAATCCTGAAATTGTTAAGCATTGTTTTATCGAATTTGGGAAATTAATTAAATAAAATTGAAAAAAATCTTAGGTCCTTAATGGTATAAAATTATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38081
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 |
|---|---|---|---|---|---|
| ENSDART00000089199 | Nonsense | 239 | 774 | 6 | 18 |
| ENSDART00000137612 | Nonsense | 53 | 584 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 24340290)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 23519403 |
| GRCz11 | 25 | 23616951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACTTTAAATAAATTTGTTTCACACTTTCAGGTCAGCGACTGGTGGGAA[G/T]AGTACATTTACCTCAGAGGTCGAAGTCCAATCATGGTCAACAGCAATTAC
Long Flanking Sequence:
AGCATCATACAGTAAAAATCCGTCATCTTGACATGCAACACTTTCTGGTTCAAAGCGTGTAAAGATTTTGGACATCTTCTTAGACACTTTTAATGCTTCTAAACAGTATGCTGCAATTATAAAGTGCCCATGTCTTGAGGTAGTTCAGTATGATGCGATTTACCTATGTGCGATTTAAATTGACAGGAATCACATGACTGATTTTGCTAATCCCCGTAGACAAGAAAAAATAAAGTAGTGACTGCAGGTCGAAGGAAATAGTGAAGTAAAAGTACCAATACAGCCCTAAAAATGTACTCAGGTGAAAGTAAAAGTACACCGTTTTTAAAACTACTTATTCCTGAGAAAAACTACTCAATTACTGTAGTGAGTATTTGTCATTTGTTATTTTACACCACTGGCCATACTTTAAATAATACATACATTAAATAATTAATAATACATTAAATAATACTTTAAATAAATTTGTTTCACACTTTCAGGTCAGCGACTGGTGGGAA[G/T]AGTACATTTACCTCAGAGGTCGAAGTCCAATCATGGTCAACAGCAATTACTATGCAATGGTAAGGCTGCTATGCACTCCATAAGCTCACTGACACGAAAACAGTTGATGGGGTATACAACTTGTAAATTATTCAGTCACAAGATTATGCCAAACAGTCAAAAACGCATATCAAATGACAGCAATTACTCAAATGCCCACAAACGTCTAAACAAAGAGTCGCTGTCATTTCTGAAGGAGATTCGCCAGCATGACCAAGTTGTGGATTACTTCAGAAGACTAACTCAATCTGACGATGCATTATTTAGAGGATGATAAGTCATCCAAAGAATCCAAAAGTAATCCATCATAATATGAGAGAAATCAACAGTTTTATGTTGGTGTCACATTCTTTTTGTGTAGTGATTTCTAAAAAATGTTGTTTGCGTTTTTGTTTTTATAAGGACTTCCTGTATGTGAATCCCACTTCACTCCAAGCTGCTCGAGCTGGTAATTCCATCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38082
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 |
|---|---|---|---|---|---|
| ENSDART00000089199 | Nonsense | 256 | 774 | 6 | 18 |
| ENSDART00000137612 | Nonsense | 70 | 584 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 24340343)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 23519456 |
| GRCz11 | 25 | 23617004 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATTTACCTCAGAGGTCGAAGTCCAATCATGGTCAACAGCAATTACTA[T/A]GCAATGGTAAGGCTGCTATGCACTCCATAAGCTCACTGACACGAAAACAG
Long Flanking Sequence:
AGCGTGTAAAGATTTTGGACATCTTCTTAGACACTTTTAATGCTTCTAAACAGTATGCTGCAATTATAAAGTGCCCATGTCTTGAGGTAGTTCAGTATGATGCGATTTACCTATGTGCGATTTAAATTGACAGGAATCACATGACTGATTTTGCTAATCCCCGTAGACAAGAAAAAATAAAGTAGTGACTGCAGGTCGAAGGAAATAGTGAAGTAAAAGTACCAATACAGCCCTAAAAATGTACTCAGGTGAAAGTAAAAGTACACCGTTTTTAAAACTACTTATTCCTGAGAAAAACTACTCAATTACTGTAGTGAGTATTTGTCATTTGTTATTTTACACCACTGGCCATACTTTAAATAATACATACATTAAATAATTAATAATACATTAAATAATACTTTAAATAAATTTGTTTCACACTTTCAGGTCAGCGACTGGTGGGAAGAGTACATTTACCTCAGAGGTCGAAGTCCAATCATGGTCAACAGCAATTACTA[T/A]GCAATGGTAAGGCTGCTATGCACTCCATAAGCTCACTGACACGAAAACAGTTGATGGGGTATACAACTTGTAAATTATTCAGTCACAAGATTATGCCAAACAGTCAAAAACGCATATCAAATGACAGCAATTACTCAAATGCCCACAAACGTCTAAACAAAGAGTCGCTGTCATTTCTGAAGGAGATTCGCCAGCATGACCAAGTTGTGGATTACTTCAGAAGACTAACTCAATCTGACGATGCATTATTTAGAGGATGATAAGTCATCCAAAGAATCCAAAAGTAATCCATCATAATATGAGAGAAATCAACAGTTTTATGTTGGTGTCACATTCTTTTTGTGTAGTGATTTCTAAAAAATGTTGTTTGCGTTTTTGTTTTTATAAGGACTTCCTGTATGTGAATCCCACTTCACTCCAAGCTGCTCGAGCTGGTAATTCCATCCATGCCATGATGATGTACAGGAGAAAACTGGACAGAGCACAGATCAAACCTGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24683
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 |
|---|---|---|---|---|---|
| ENSDART00000089199 | Essential Splice Site | 626 | 774 | 15 | 18 |
| ENSDART00000137612 | Essential Splice Site | 436 | 584 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 24359359)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 23538472 |
| GRCz11 | 25 | 23636020 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCAAATTTCAGTAATCATTCTATTTCATGAATCTTTTTTTTTTCCTC[A/T]GAGAGAAGAGAGACTGAAGCTGCTGAAGGCGGCCACAGAAAAGCACCAGA
Long Flanking Sequence:
TATTTAACCGACTATATTTTCGATGCAGTAAAAGATACTCCATGAACTTGAAAATAGCCAATCTTTTGCCGGACGTGTTCAGTTGCTAAACAGCACTTCTGTGCATATAAACCAATTCATAAATAAGAACACGGTTTACATAAGTTCTGCTTGGCTAAAATAGTTTTAAAACATACCTGTCTAAAAGAAGTACTTCAGCCAAGTTGTGAACCTTCAGATCGTTGTTTTGAACTGCATAGCGTCATTTCTGTCCAGCCTGCAAAAGTAATTCTGATATTGATCCTGGTTGATGCAAGTTAAACCATTCTAAGAAAAGAAAAAGTCAAACATATATATTTTCTTAATAGATCTATCATGATGCATGCAGTAGTTAGTATTCTGAATGATCCTCGTTACCTGGGGATAAACTTGCCTTGCTACTGTACAGTAGTTCTAGTGAGTGTGTTTGTTTCTGCAAATTTCAGTAATCATTCTATTTCATGAATCTTTTTTTTTTCCTC[A/T]GAGAGAAGAGAGACTGAAGCTGCTGAAGGCGGCCACAGAAAAGCACCAGAATTTATACAAACTGGCCATGACTGGAAAAGGCATTGACCGTCATCTTTTCTGCCTCTACTTAGTGTCCAAGTACCTCGGTGAAGATTCACCTTTCCTCAAAGAGGTTTGTGAGCGACCTGTAACAAAACAATCTGCAAATCTATCAGTTTTGTAGCCTAGAAACATTACATAGTCTGTAACGAGCTGGGTTTGATCCAGGTTTTGTCAGAGCCCTGGAGGTTGTCCACCAGTCAGACTCCTCTCCAGCAGATGGAACTCTTTGACTTGAAGAAACATCCAGAATATGTCACCAGTGGAGGTGGATTTGGACCTGTAAGTTCATTTTGTATCAATATTTTATCCTGCCTAGACAAGGTGCAATGACAACTGGTGTTCAGATTATTCTTCAAAAGTGTTGTTTTTTTTTTTTTGAAAGGAAACAGACGCATTGCAAGTTTTTATTGTTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25226
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 |
|---|---|---|---|---|---|
| ENSDART00000089199 | Nonsense | 643 | 774 | 15 | 18 |
| ENSDART00000137612 | Nonsense | 453 | 584 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 24359413)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 23538526 |
| GRCz11 | 25 | 23636074 |
KASP Assay ID:
554-7594.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGAGAGACTGAAGCTGCTGAAGGCGGCCACAGAAAAGCACCAGAATT[T/A]ATACAAACTGGCCATGACTGGAAAAGGCATTGACCGTCATCTTTTCTGCC
Long Flanking Sequence:
TAGCCAATCTTTTGCCGGACGTGTTCAGTTGCTAAACAGCACTTCTGTGCATATAAACCAATTCATAAATAAGAACACGGTTTACATAAGTTCTGCTTGGCTAAAATAGTTTTAAAACATACCTGTCTAAAAGAAGTACTTCAGCCAAGTTGTGAACCTTCAGATCGTTGTTTTGAACTGCATAGCGTCATTTCTGTCCAGCCTGCAAAAGTAATTCTGATATTGATCCTGGTTGATGCAAGTTAAACCATTCTAAGAAAAGAAAAAGTCAAACATATATATTTTCTTAATAGATCTATCATGATGCATGCAGTAGTTAGTATTCTGAATGATCCTCGTTACCTGGGGATAAACTTGCCTTGCTACTGTACAGTAGTTCTAGTGAGTGTGTTTGTTTCTGCAAATTTCAGTAATCATTCTATTTCATGAATCTTTTTTTTTTCCTCAGAGAGAAGAGAGACTGAAGCTGCTGAAGGCGGCCACAGAAAAGCACCAGAATT[T/A]ATACAAACTGGCCATGACTGGAAAAGGCATTGACCGTCATCTTTTCTGCCTCTACTTAGTGTCCAAGTACCTCGGTGAAGATTCACCTTTCCTCAAAGAGGTTTGTGAGCGACCTGTAACAAAACAATCTGCAAATCTATCAGTTTTGTAGCCTAGAAACATTACATAGTCTGTAACGAGCTGGGTTTGATCCAGGTTTTGTCAGAGCCCTGGAGGTTGTCCACCAGTCAGACTCCTCTCCAGCAGATGGAACTCTTTGACTTGAAGAAACATCCAGAATATGTCACCAGTGGAGGTGGATTTGGACCTGTAAGTTCATTTTGTATCAATATTTTATCCTGCCTAGACAAGGTGCAATGACAACTGGTGTTCAGATTATTCTTCAAAAGTGTTGTTTTTTTTTTTTTGAAAGGAAACAGACGCATTGCAAGTTTTTATTGTTTTATAATATTGGTGTAAATGTTTTTTTTTTTTTATTTAAATACAAATTTATATAATAT
Associated Phenotype:
Not determined