ZMP
zgc:112484
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC550361 [Source:RefSeq peptide;Acc:NP_001017668]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14740 | Nonsense | Available for shipment | Available now |
sa31337 | Nonsense | Available for shipment | Available now |
sa40093 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38399 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14740
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 |
---|---|---|---|---|---|
ENSDART00000055294 | Nonsense | 26 | 780 | 1 | 18 |
ENSDART00000055295 | Nonsense | 26 | 170 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 32422496)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32153806 |
GRCz11 | 3 | 32285520 |
KASP Assay ID:
2259-3645.1 (used for ordering genotyping assays)
KASP Sequence:
CATTTCAGTTCACCATCAGTCCTGAGGGGATCAACCTGCATCTGTCTTAC[C/T]AAGCCCTCAAWCAAATCTACCTCTCCGGATTGCGATCCTGGAAGAAGCGC
Long Flanking Sequence:
TGTATATATGTAATTAATGCAATTTTACATCTTCAATTCTCAGTTTTATATTCAAAACCAAAAGACCTTAAAGAAGATTCTTTTAAACTGTGTTCAACTGTACAATAAATGTCAATGGTTGTTGTACATAAATGCACCACTAGGTGTCATTGGTGTTTTAGTTGTGGCCTCAATTTGTTTCTAGACGTAAATGGTGTATCGACAGGAATTTACTTGAGAGGCCTTCCCTAAGATATTCATGTCTTTTACTCTGTTCCTCGTGTGTTTGCCTTAACAAACAGTGTAACCATTTCAAACAAAATGTAACAAAACTTTGTATTTTGAATGCTGTATTGAGACCAAATTACACAAGTGAAGTATACATGTTTCAGACAGAGTTTTTTGTTCATTTTGCTGATGATATTGTGTTGTTTGTGTCCACAGTGATGGCTGAGGCTCACCAAGCAGTGGCATTTCAGTTCACCATCAGTCCTGAGGGGATCAACCTGCATCTGTCTTAC[C/T]AAGCCCTCAATCAAATCTACCTCTCCGGATTGCGATCCTGGAAGAAGCGCATCAGCAGGATTAAGGTCAGTGAAAAAAATAATCATCAAACTCAGTGAACTCATAGAATTACCTAAAAAAAACAAAACTTTGTTTTTTTCTGTTGGGAAATAAAAAAAAAACAAAACTTTGTTTTTTTCTGTTGGGAAATTAAGCTAGTTATCTGCACAGAAGAGTTTTCTTCAATACATTTTCTGTGACATCATGAAGATCCTAATATAGTCAAATGTGCAACGTGTGTGCATGTACATAAGAGGCATTAATAATTATGAACTTTTTTGCTTTTCTGTGGACAGAACAGGATCATTAAGGGTGCTTATCCAGCTAGCCCCTCCTCGTGGCTTTTTATTGTCATTGCAATTCTAGCCACGATGTACATGCAGTCCGATCCATCAATGGGTCTCATCGCCAAGATCCAGGAACACCTGCCCCTTAGGTAACTCTTATGGTTAAGTTGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31337
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055294 | Nonsense | 138 | 780 | 3 | 18 |
ENSDART00000055295 | Nonsense | 138 | 170 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 32416423)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32147733 |
GRCz11 | 3 | 32279447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGAGGTTCTGCCTGAAGCTTCTCTTGTCCTACCACAGGTGGATGTTT[G/T]AACAACATGGTCATATGTCTACCAAGACCAAAGTGTGGGCGGTTAGTGCT
Long Flanking Sequence:
TCTAATTGTATTAGAGATTGGCAACTTGGTAAACGTGCACATTTTAACACTTTCATTTTTTTTCTGAAAGTCCAGTATTTGAGAAGTTTGTTTGTCACTTGAGTATTTTATTTTTATTTTTTACTTTTTATCGAAAAAACAAAAGAGATTCTGTGTTAACAAGAAAGATTATTTGTGTCTGATTCTGACTTGTTTCATTTCATTTATTATTAAAGCCCACTGTTTGCTCCACATTTGGTGTGTAATCATAAATCTGCATGCTTGAAAAAAGTCTAAAAATTAAGGTATAGTCATATTTGTGTTGTCTGCAGCTAATGTTGACCAAGAAGTGATGTTGCTGATTGTTTCTGCTGTGTTTGTGTACTGTCAGTCTGTCATTGAGTCCTCAAGGTCAGACCATGCTGTCGGCGCTGCTGTTCAGTACTCTGCTCTGGATGTCTCTCATTCTGACTCTGAGGTTCTGCCTGAAGCTTCTCTTGTCCTACCACAGGTGGATGTTT[G/T]AACAACATGGTCATATGTCTACCAAGACCAAAGTGTGGGCGGTTAGTGCTTCATTACTTTCAGCCTGGTTTAAAAAAATACATTTTCATTTTTTTTCTTAGTTCATTCTTTCTTGAAACAATAACAAAAAGGATTTGTGTTCTGAGCATGTGTTCAGATTTTTACTTGGCCTGCAATACAATACATTAATAAAGCATGCTTATATAGTAGAATTTGTATGTAATCTAATCTATATGTAATCTAGTTTAATATGTTACTTATTATTATGATTATTACTGAACACACATGCATGTACAGCTATCTTTATAAGGACTTCCCACAGATGCAATGCTTTTCATACTGCACAAGCTATATATTTTATCCCCCTAACCCCAATCCCCACCATAGTCCTAAACCCAACCCTCACAGGAAGCAATCTGCATTTTTTACATTTCCAAAATACTTTATTCTTTGTGGTTTATGTTTCATTTTCCAGATTAGGCTAAAAAAAATGTCCCCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40093
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 |
---|---|---|---|---|---|
ENSDART00000055294 | Nonsense | 352 | 780 | 9 | 18 |
ENSDART00000055295 | None | None | 170 | None | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 32398685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32129995 |
GRCz11 | 3 | 32261709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTTATCACAGAGGCCGTTACTTCAGATTATGGGTCTACCGAGCTGGA[C/T]GATTGCTTTCACCTAGAGAGATCCAATTTCAGATTCAAAGGATTTTGGAT
Long Flanking Sequence:
CTCGACTACTCCATGCTTTCCGCGCATGCGCCCCCCCCACTTGAACTCTTTTTTTTTTTTTTAACTAATGACTTAAAGAAAATACTGAGGACATTTAAATTTTTGCATTTTCATTTTATGCAGCGGTCTGTGATAAACTGTGTGCTGTGACAAAATTGGTGATTTATTGAGAATGAGCAGTATAGGGGAAAATGTGAATCAGTTTTTCTGTAATAATTGACATTATGACATGATTATTTCTTTAGAGTCGTATTCCTGGTACGGTCATACCGCTGTGTGCAGCTCAGTGTGAGCGCATGTTCAACACCACTCGAACACCTGGAGAAGAGACTGGTAAACGCACATTCATACAGACATGCAGACATAAATACGCATTAAGAAAATGGCCTTTGATGCAGTCTCTTTGTCTCTCAGATGTTCTGCAGCACTGGCAGGACAGCGAGTTTGTTGCTGTTTATCACAGAGGCCGTTACTTCAGATTATGGGTCTACCGAGCTGGA[C/T]GATTGCTTTCACCTAGAGAGATCCAATTTCAGATTCAAAGGATTTTGGATGACCCCTCACCTCCTTCTCCAGGAGAGGAGAAACTAGGAGCACTGACAGCAGGAAACCGGTTAGACACTCGTGTTTTTTTAAATTGGGGGGGTAATGTGTGGATTTATGTCAGCAGAACACTTTACTGTGAATATTTCCTAGATAGGTCTGATCATTCCAGAAGAACTTTTAGACAACATCCTCTGTGCATCGATTGTTGTGGTATTCTGTTACATTCAAATTTTATTAATATTAATTTTATTAATTCAAATAGTTGTCTTTGATTTTATAATTTTAGAGGTAAAGACTCATGGTGGAATATAAATTTTATGGGTTATCCTCCAAAAAAAACTAAAGTAATGATATTATAAAGGCTATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38399
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055294 | Essential Splice Site | 713 | 780 | 16 | 18 |
ENSDART00000055295 | None | None | 170 | None | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 32376344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 32107654 |
GRCz11 | 3 | 32239368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTAGTCAACCACCCAGAGTTCATCTCCCTGGGGGGAGGCTTTGGTCCT[G/T]TGAGTTACTGATCAACACACACATTATCTAAATGTAAATTCCACAAACTG
Long Flanking Sequence:
GGCCAGAAGATTTAATGAGACGCACAAGGTGACGTCAATAAAAAATCATTGATCCATTTACGCAGAAGTGACAAACTGCAAGTTTATATCTTCCTAATGGAACATTTTGGAGCATGCTAGTTTATAGATATTGTTAAAGTGAGTTGTATAGAGTGTAATTTTAAGGCTTGGATGTGTGTAAAAGATACAAATCAATGTGTGCTCATACTTCATTTGTAGAAACTAGGGTTAAGACTAACATACTGAAAACATCTCAAAATTTCTATTAGGATTTTACAGGGACTTTAAAAATGAAGTGTGACATTAAGGTAATTTATGAGTAGGAGATAATTAGCATGGATGTGAGGGCGTGAAGCTGTTTTTATATGCGTTTATGTGAACTGTAGGTTTTGTCAGAGCCCTGGCGCCTCTCTACATCTCAGACACCTGTGCAACAGATGGAGCTGTTTGATCTAGTCAACCACCCAGAGTTCATCTCCCTGGGGGGAGGCTTTGGTCCT[G/T]TGAGTTACTGATCAACACACACATTATCTAAATGTAAATTCCACAAACTGACTGCGGCTCTAATTTGATCACTGAGTTCATGGTTTGTTCCTGTTTAGGTAGCTGATGATGGCTACGGTGTGTCTTACATCATCATGGGAGAGGACATGATCAACTTCCATGTGTCTTGCAAGCACTCCTGCAAAGAGACAGTAAGAGCAAACCTAACAATTTAACAGCCACAATTTAAAACCTTGCTAAGCCTCCTGGTGACTGTTTGTTTGTTTGTTTATTTATTTATTTATATATATATATATATATATATATATATATATATATATATATATATACATACAGTATATTTATTGATTTATTTATTTATTCTTTTTTTTTACCATGAACCAATATGTGTATGGGCAGTATTATTATTATTATTATGAATATTATTATTATTATTATTATTTTAAACACTGAAGTAAAATTAAACTGAAAATAAAAATCATTTTCATATAGCAAAAAGC
Associated Phenotype:
Not determined