ZMP
zgc:136652
Ensembl ID:
ZFIN ID:
Description:
2-hydroxyacylsphingosine 1-beta-galactosyltransferase [Source:RefSeq peptide;Acc:NP_001037790]
Human Orthologue:
UGT8
Human Description:
UDP glycosyltransferase 8 [Source:HGNC Symbol;Acc:12555]
Mouse Orthologue:
Ugt8a
Mouse Description:
UDP galactosyltransferase 8A Gene [Source:MGI Symbol;Acc:MGI:109522]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18467 | Essential Splice Site | Available for shipment | Available now |
| sa39599 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8667 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39598 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa11773 | Nonsense | Available for shipment | Available now |
| sa38257 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18467
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054510 | Essential Splice Site | None | 542 | None | 7 |
| ENSDART00000124770 | Essential Splice Site | None | 541 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 19374928)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 19900687 |
| GRCz11 | 1 | 20593624 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGGGACGTCAGTTTCACACTCATTCGGAMACCGTGTTCACCTGGACAGG[T/G]AAGCGKTCRAGGGCGGCGTTTCCGATWAGCAACAGGTGTTCCGCRCTACT
Long Flanking Sequence:
ATCGTCGTATTTATTGTCTAGATGACGTGAAAGCTGAATTATCCCCTTTTATGATCTTCGGAAGTTGACTCAGAGATCTCTCCCGGTCTTTATATCGTCGTATTTATAGCGCAGCTCTGCCTAAATAGAAGCGCAGCGGTGACGCGCCTTAAATGCAAATATACCTGTGTCGAAAGAGCAAACAACGCACCTGACGCTTCCCATGGGATGCGAGGGAAGGCCGAAGTCTCTCTTTAGTTCTGGCGTGCACTCTGCCTCGGCTCGACCACTCCCTGCACTGACTGTGAATTGAGTTTTCGCAAATCCCGCCCTCCCCGGAGTTCTGACACACAACGCCCCATCTCATAGCCATTGGAAAAACCACCTCGCCTGTTGTGGCAAGCGGGTAGTTTTAACCGGCAAACACCATTTGTGGATATATGTAAAAGTGTCAGAGGCTCGGGAGAGCGAGGGGGACGTCAGTTTCACACTCATTCGGACACCGTGTTCACCTGGACAGG[T/G]AAGCGGTCAAGGGCGGCGTTTCCGATTAGCAACAGGTGTTCCGCGCTACTGTACATTGAGCGACCGCGCAGAAATTAGCGCTTGCTTTTTAAAGGTAGATTAGACTCTGGTGTGTTTTTCTTATTTTCGTGTTGATATTGTGGAGATGGTGACATTTAAAAGTTACTCGCCCGCTACTGCTCCTTATGACTTAACTTGCTTTAATGATGGGTTCTTGATGATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATGATACGAATGAATACCTATCATGTGCTGTATTTAAAGCCTGAACAATGAGTAAGTGAGCGGTTTGGGACCTGATCTAAAGATTTTACCTGCTCACTTTTCCCGGCCCCCTTCATCTATTTTTAACTGGAGAGTGATAGTTTAGCAGGGGGGATGTTGCAGGAAGACTGACATCCAATTCCTGATGATGCTAATGTCAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39599
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 |
|---|---|---|---|---|---|
| ENSDART00000054510 | Nonsense | 13 | 542 | 2 | 7 |
| ENSDART00000124770 | Nonsense | 13 | 541 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 19363173)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 19888932 |
| GRCz11 | 1 | 20581869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCTGCAGTCATGAAGGCTTTTTTTGTGCTTGCCACATTGCTGTGGTG[T/A]TTAGCGACAAGTTTATCCTGGGCAGCCAAGATTGTGGTAGTTCCTCCAAT
Long Flanking Sequence:
GTCAGATTTGTTTAATGCAACAGTAAAACATGTCTCTTCACTTTCAGAAATTGCAGTGATTTTTTTATTGACCCTGAAAAAGATGTAAAACATGTTGGTTATGGATATATTTTTTTAAAATATTGTAATGCATAATGAATGTCCCATTATTTAGCTTGCTAGAACATAACCCATTTTTCTTCAAAATCACACAACCTTTCTAAATATGTGTCATATGTTGATAAATTGAGAAGTATTACTCAGGGCAATTCTGAAGTTGTGCTAAAAACTAAAATAAAAGGCAAACAAAAAATACTACAAGGCTTAAAGATTAGGAATAGAGTTCCTTAACACTGATAATATTGGGCTATCAGTGACGTTTAGATGTGCAACACAAAGTATTGATTTATGCAGCTGCACAGTACAAGGGTTAATATTTGACTAAAACTGTCTCTAATTGCTTTTTTCTCTCTTTCTGCAGTCATGAAGGCTTTTTTTGTGCTTGCCACATTGCTGTGGTG[T/A]TTAGCGACAAGTTTATCCTGGGCAGCCAAGATTGTGGTAGTTCCTCCAATCATGTTTGAGAGCCATCTATATATCTTTAAGACTCTGGCTTCGGCTCTCCATGCCGAGGGCCATGACACCGTCTTTCTGGTTTCAGAGGGCCGTGAGATCCCACCTTCCAACCATTATCGTCTCCAGCGATACCCTGGGATTTTTAACAGCACTTCAGCTGATGACTTCCTCCAATCAAAAGTTCGCAACATCTTCTCAGGGCGTCTCACAGCACTGGAGCTTTTTGACATCTTGGACCATTATTCTCAAAACTGCGATGCGGTTGTAGGAAGTACTTCTGTCATGGAGCAGCTAAAACGTGAACATTTTGACCTGTTGCTCGTCGATCCCAATGAGATGTGTGGATTTGTCATAGCTCACATTTTGGGTGTCCAGTATGCAGTATTTAGCACAGGACTGTGGTACCCTGCTGAAGTTGGGGCACCAGCTCCCCTATCTTATGTCCCGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8667
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 |
|---|---|---|---|---|---|
| ENSDART00000054510 | Nonsense | 193 | 542 | 2 | 7 |
| ENSDART00000124770 | Nonsense | 193 | 541 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 19362635)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 19888394 |
| GRCz11 | 1 | 20581331 |
KASP Assay ID:
2259-0469.1 (used for ordering genotyping assays)
KASP Sequence:
CTTATGTCCCGGAATTTAACTCTCTACTAACGGACCATATGTCGTTGTTT[C/T]AAYGGGYAGCTAACACAGCRGTGTACCTAGTTTCCAGGTTTGGTGTCCAR
Long Flanking Sequence:
TAGTTCCTCCAATCATGTTTGAGAGCCATCTATATATCTTTAAGACTCTGGCTTCGGCTCTCCATGCCGAGGGCCATGACACCGTCTTTCTGGTTTCAGAGGGCCGTGAGATCCCACCTTCCAACCATTATCGTCTCCAGCGATACCCTGGGATTTTTAACAGCACTTCAGCTGATGACTTCCTCCAATCAAAAGTTCGCAACATCTTCTCAGGGCGTCTCACAGCACTGGAGCTTTTTGACATCTTGGACCATTATTCTCAAAACTGCGATGCGGTTGTAGGAAGTACTTCTGTCATGGAGCAGCTAAAACGTGAACATTTTGACCTGTTGCTCGTCGATCCCAATGAGATGTGTGGATTTGTCATAGCTCACATTTTGGGTGTCCAGTATGCAGTATTTAGCACAGGACTGTGGTACCCTGCTGAAGTTGGGGCACCAGCTCCCCTATCTTATGTCCCGGAATTTAACTCTCTACTAACGGACCATATGTCGTTGTTT[C/T]AACGGGTAGCTAACACAGCGGTGTACCTAGTTTCCAGGTTTGGTGTCCAGTTCCTGGTTCTACCTAAATATGATCGCATTATGAGGAAGTACAACATCCAGCCATCTGTCTCCATGCACGATCTGGTTCAGAACAGTCGACTCTGGATGCTGTGTACTGACATGGCACTGGAGTTCCCACGACCAACTTTGCCACATGTTGTCTATGTAGGGGGCATCCTCACTAAACCTCCCAGCCCATTACCACAGGTAAGAAACCACTGCTATTATATTTGAAAATTTTTTAAAGGGGTCCTTTCCTTTTTCATTTTAGGATGGTAAAATGTTGGTAAAGCTCAATGCAAAGGGTGATATTTTCTATTACAGAATCCACTTTAAAAGGCAGAACACAAACAGCTGATAGGGTCTACAGCAAGCTTTTTTTCTGACTTTATAAGACCACAATCCTAAAATGTACATAAACCCTTCCTCTTGGCATGATACTTCCAGACAAAAATGGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39598
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 |
|---|---|---|---|---|---|
| ENSDART00000054510 | Nonsense | 253 | 542 | 2 | 7 |
| ENSDART00000124770 | Nonsense | 253 | 541 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 19362455)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 19888214 |
| GRCz11 | 1 | 20581151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAACAGTCGACTCTGGATGCTGTGTACTGACATGGCACTGGAGTTCCCA[C/T]GACCAACTTTGCCACATGTTGTCTATGTAGGGGGCATCCTCACTAAACCT
Long Flanking Sequence:
TCCTCCAATCAAAAGTTCGCAACATCTTCTCAGGGCGTCTCACAGCACTGGAGCTTTTTGACATCTTGGACCATTATTCTCAAAACTGCGATGCGGTTGTAGGAAGTACTTCTGTCATGGAGCAGCTAAAACGTGAACATTTTGACCTGTTGCTCGTCGATCCCAATGAGATGTGTGGATTTGTCATAGCTCACATTTTGGGTGTCCAGTATGCAGTATTTAGCACAGGACTGTGGTACCCTGCTGAAGTTGGGGCACCAGCTCCCCTATCTTATGTCCCGGAATTTAACTCTCTACTAACGGACCATATGTCGTTGTTTCAACGGGTAGCTAACACAGCGGTGTACCTAGTTTCCAGGTTTGGTGTCCAGTTCCTGGTTCTACCTAAATATGATCGCATTATGAGGAAGTACAACATCCAGCCATCTGTCTCCATGCACGATCTGGTTCAGAACAGTCGACTCTGGATGCTGTGTACTGACATGGCACTGGAGTTCCCA[C/T]GACCAACTTTGCCACATGTTGTCTATGTAGGGGGCATCCTCACTAAACCTCCCAGCCCATTACCACAGGTAAGAAACCACTGCTATTATATTTGAAAATTTTTTAAAGGGGTCCTTTCCTTTTTCATTTTAGGATGGTAAAATGTTGGTAAAGCTCAATGCAAAGGGTGATATTTTCTATTACAGAATCCACTTTAAAAGGCAGAACACAAACAGCTGATAGGGTCTACAGCAAGCTTTTTTTCTGACTTTATAAGACCACAATCCTAAAATGTACATAAACCCTTCCTCTTGGCATGATACTTCCAGACAAAAATGGACATGAATAGGCTTCATACGGCTTCACACTGCCATTAAGGGAAACTTTAACAGTGGTGTAGAATAAAGGTAAATAATGTGTTTTTTTAGAAGAATAGACATAATAAACACAGCTCATAAACATTATCAGGGCTTTAAAAAAATGATGGTTTACAACCCCTTTAAAAAATACACCTACTGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11773
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 |
|---|---|---|---|---|---|
| ENSDART00000054510 | Nonsense | 318 | 542 | 3 | 7 |
| ENSDART00000124770 | Nonsense | 318 | 541 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 19357675)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 19883434 |
| GRCz11 | 1 | 20576371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCAGATGACATTGCTCAGAAACTCGCTGGAGCCTTGAGCCGTCTGCCC[C/T]AGAGAGTCATCTGGAGGTACTGCCATTCATTCGTTCTCTCATGTGATCAC
Long Flanking Sequence:
TCACTTGTGTGGTATTGAAAAGTCAAAAGTTGTACCTTGAAGCCTTGGACAAACTAGGTTAGAAATTGCTAGTGAACATGTATAATATGTTGCATTTCAGCCATTTTGTTGTATGTTTACAAGAACACAAGTTTATAAAACAGGCGTTTAGTAATGTGTCTGTAACAAACTTCCTGTTCTGTTCGAAGTTCTTTGTACATATATGGTCATAAAAAATACTGAATGATAATGCTTCTACTTTATTCTTCCCTTTTTTTTTCAAGCTGAGTAAAAAAATAATAATTCAGATGCTACTTCATCCACCATGAACCATACAATCCTATAAATTGTTTCATTGATAGTCAGACTGCGCTGTAATTGATCTGTGTTTACAGGAGTTTGAAACCTGGGTGAAGGACACAGATGAAGATGGTTTCGTGGTGGTCTCATTTGGTGCAGGAGTGAAGTATTTGTCAGATGACATTGCTCAGAAACTCGCTGGAGCCTTGAGCCGTCTGCCC[C/T]AGAGAGTCATCTGGAGGTACTGCCATTCATTCGTTCTCTCATGTGATCACTGATCCATTTTTCCAGCAGATCAAATCACCTGCGTCTCAGTCCATTATGGTTTTTTCTATCACAGAGTATCCAATGGCAACTGGCCTGTTGTGGCAGGTGGCTTAAAAGCCATTCATTCTAAATTATCTGATCGTTTGCTAGACTTTCCAGTGGTTTCTAAATGCAAAATGACACTAATTTGTCTTGAACTATAGCATTTCCATACATCATGTATAGATACACTTTATACACTATACTAGGAGTGTTCGATCATGTGATAAATCTGTGTGGAGACACTATTAACAATAAAACTCAATACATATTTTAATTGTTCAGGGAGGAAGTATACTGCATCCTTTGAGATGGTAGACACTTCAAGAGCCATGGGTCCCTCTTTATATTAGGATTGTTTTACTCATACAATTTTGTATATATATATTACTTATTCTATACCTATAGTGTTCATGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38257
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000054510 | Essential Splice Site | 349 | 542 | 4 | 7 |
| ENSDART00000124770 | Essential Splice Site | 349 | 541 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 19350845)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 19876604 |
| GRCz11 | 1 | 20569541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAACAATACTAAACTAGTGGACTGGATGCCACAGAACGACTTGCTGGG[T/C]AAGTATTCATTCTATCACTTTTACAGATCGATAGAATTTTTATTTAAATT
Long Flanking Sequence:
AAATCTTTATTTGTTAACAATAATATTTAAGTATTACGAAAAAAAATAAAATAACAAACAAACAAACAAACCAAGAAATATAAAACGCTTACAAGCTCTGAAGAAATCCATGTTGTTCTGCAATGACACTGGTTGAATCTCTTTCATCATTTGCATTTTTTTTTTTCTGAATGTAGGCATAGTTTTTAATCTGATCTATACATGCAAAATATTTGGCCTCTGTCTCTGTCACACAATTTAGTCTCTTAATGTGTTTTTTTTTTCTTTCCAGCATACCTCATTTCCCTGCAGTCATGGTGTATTTATGATAATATTTTTGATAAATGATTGTCATCTTAGCTCTAGATGATAAGCTTTTTACTGTTTTTGAATATTTTCTAGAATGAGACATCTGTATCTTACTTTGTTTAATCTCTCTGCAGGTTCTCTGGAGTTCCTCCATCAAATCTTGGCAACAATACTAAACTAGTGGACTGGATGCCACAGAACGACTTGCTGGG[T/C]AAGTATTCATTCTATCACTTTTACAGATCGATAGAATTTTTATTTAAATTATGTTTTGTTGGCCGTGTTCGCGTGAGTTTCCTCCAGGTGCTCCAGTTTCCCCCACAGTCTAAAGACATGCGGTACAGGTGAATTAAATAAGCTAAATTTGCCATAGTGTATGTGTGTGAATGCAAGAGGTTATGGGTGTTTCCCCATGTTGGGCTGCGGCTGGAAGGGCATCCACTGCGTAAAACATATGCTGGATAATTTGCCGGTTCATTTCACTGTGACGACCCCTGATTAATAAAGGGATTTAGCCGAAAGGAATATGAAAAAATATATAATGTTATATAATATATAATAATGTTAAAAAAAAAAAGGTCAGGAGAAGGATTTCTTCAATGTCATTAATATTAGTCATTTATTAGAAACAAATGAATAATTCGATACACAGAGCTCTGGGGGTGGCGTTACACCAATGCAATGCAAAAATGACATTCAGAAGGTTCGCAACCACA
Associated Phenotype:
Not determined