ZMP
hhat
Ensembl ID:
ZFIN ID:
Description:
protein-cysteine N-palmitoyltransferase HHAT [Source:RefSeq peptide;Acc:NP_001108362]
Human Orthologue:
HHAT
Human Description:
hedgehog acyltransferase [Source:HGNC Symbol;Acc:18270]
Mouse Orthologue:
Hhat
Mouse Description:
hedgehog acyltransferase Gene [Source:MGI Symbol;Acc:MGI:2444681]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9470 | Essential Splice Site | Available for shipment | Available now |
| sa19176 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa36421 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9470
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113846 | Essential Splice Site | 150 | 494 | 5 | 12 |
| ENSDART00000113846 | Essential Splice Site | 150 | 494 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 17 (position 25667328)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 25807247 |
| GRCz11 | 17 | 25825638 |
KASP Assay ID:
2261-1110.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCTTGCTSCTCTCCACWCTTAATGTCAGTGCCCTTCAAGATTTACAGG[T/A]GTGTGTATGGGTTTGTCTGTCTRTCTGTAAYTKCATGTWTGTGAGACCAA
Long Flanking Sequence:
GGTTCCTGTTTCATGCTCAGTTATCAATTTCCTTTTCTACAGATGTACAAAACACACACACACATTCTCTCTCTTATTTTCTGTAATTGCATGTTTTTCTGTCTGTGATTTTAGGACCCTACTGATTTTGAGTGGAGTTTTTGGAATGAGTGGGCGTGGCGATCTCTTCTCTGGTCTCTGATTGGCCATGCTGTGGTGTCCAGGCTGGCATATTATTATCTGCCTCAGGTAAGTTTAATTTAAAAGCAAAGTAATCAAAATGGGCACAGGCTTGTTCATCTTTCTCTGTGCTCTTGTGTTACAGTATCGACTGGCAGTCTTTGCGATGTATGGTTTGATCTCAGCTGGTTGGATTCTCGGGGTGAGGGGTGTGATTGTTTTGATGCTGCATCTGAGCATCTCATTGGTGGTTGCTCAGCTACGTAGCCCCGTCCTCTCGTGGTTTTGCTCCCTCTTGCTGCTCTCCACTCTTAATGTCAGTGCCCTTCAAGATTTACAGG[T/A]GTGTGTATGGGTTTGTCTGTCTGTCTGTAACTGCATGTATGTGAGACCAAGAAGTAGCTCTTTCTCTGAGAAGAAATTGCACAAAAGTGTCCAATTTAATGGGTTGTTCTCCCAAAAATGAAAGTCTGGCCTCATTTACTTACTTTCATATCATTTCAAGTTCTTGCTTTTTTCTACCCTTTGCAACACAAAAGAAAAATCTGAATGATGTGCTAGTTGCTTTCTTCCCTAGCAATTACCATGAATAACAGCTAGATATTTCAAGCTTCAAAAAGGACACTAAACCACTATAAAAGTATAGTGAATATGGTCCTGTGCCTTACTTCACATTCATGAAGGAAGTAGCAGAACCTGACTAGAACAAATAGTTTTTTTTTTTGTTTTTTTTTGAGTCAAATTGTTTGTGAGATTTATGTGCATTCAACATATTTTAACACCAAATAGCTTCTCAAAGAGAGTCTAAATAATTTGTTTCATGATGTGTTGTTTTAAACTCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19176
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 |
|---|---|---|---|---|---|
| ENSDART00000113846 | Essential Splice Site | 150 | 494 | 5 | 12 |
| ENSDART00000113846 | Essential Splice Site | 150 | 494 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 17 (position 25667328)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 25807247 |
| GRCz11 | 17 | 25825638 |
KASP Assay ID:
2261-1110.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTTGCTGCTCTCCACTCTTAATGTCAGTGCCCTTCAAGATTTACAGG[T/A]GTGTGTATGGGTTTGTCTGTCTGTCTGTAACTGCATGTATGTGAGACCAA
Long Flanking Sequence:
GGTTCCTGTTTCATGCTCAGTTATCAATTTCCTTTTCTACAGATGTACAAAACACACACACACATTCTCTCTCTTATTTTCTGTAATTGCATGTTTTTCTGTCTGTGATTTTAGGACCCTACTGATTTTGAGTGGAGTTTTTGGAATGAGTGGGCGTGGCGATCTCTTCTCTGGTCTCTGATTGGCCATGCTGTGGTGTCCAGGCTGGCATATTATTATCTGCCTCAGGTAAGTTTAATTTAAAAGCAAAGTAATCAAAATGGGCACAGGCTTGTTCATCTTTCTCTGTGCTCTTGTGTTACAGTATCGACTGGCAGTCTTTGCGATGTATGGTTTGATCTCAGCTGGTTGGATTCTCGGGGTGAGGGGTGTGATTGTTTTGATGCTGCATCTGAGCATCTCATTGGTGGTTGCTCAGCTACGTAGCCCCGTCCTCTCGTGGTTTTGCTCCCTCTTGCTGCTCTCCACTCTTAATGTCAGTGCCCTTCAAGATTTACAGG[T/A]GTGTGTATGGGTTTGTCTGTCTGTCTGTAACTGCATGTATGTGAGACCAAGAAGTAGCTCTTTCTCTGAGAAGAAATTGCACAAAAGTGTCCAATTTAATGGGTTGTTCTCCCAAAAATGAAAGTCTGGCCTCATTTACTTACTTTCATATCATTTCAAGTTCTTGCTTTTTTCTACCCTTTGCAACACAAAAGAAAAATCTGAATGATGTGCTAGTTGCTTTCTTCCCTAGCAATTACCATGAATAACAGCTAGATATTTCAAGCTTCAAAAAGGACACTAAACCACTATAAAAGTATAGTGAATATGGTCCTGTGCCTTACTTCACATTCATGAAGGAAGTAGCAGAACCTGACTAGAACAAATAGTTTTTTTTTTTGTTTTTTTTTGAGTCAAATTGTTTGTGAGATTTATGTGCATTCAACATATTTTAACACCAAATAGCTTCTCAAAGAGAGTCTAAATAATTTGTTTCATGATGTGTTGTTTTAAACTCCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36421
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 |
|---|---|---|---|---|---|
| ENSDART00000113846 | Nonsense | 356 | 494 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 17 (position 25630243)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 25770162 |
| GRCz11 | 17 | 25788553 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATATGTGTGCGTTCTCAAAGCATGTGTTTATTCATTTCAGGTACATATA[T/A]GTGCCTCTGGGTGGTTCACGTCATGGTGCTTTCCGGAAGCTTCTCTCCAC
Long Flanking Sequence:
ATAAAAAAACAAAATAAAACAAACAAACAACAAAAGACCATTCCATGTGAGCTCCTGACAACCCTCAGGGACTATGCTAATTGGCTCTGTATTTAACCAATTTTACATTAAGTGATATCTCAGACCACACATCAGCTTAATATTAAAACCATGTCATTTGTATCTGTCAACATACACCCTTAAACATGAAGGTGCTTTATCATCATCAATAGTTACATTAAGAACCTGGAAACTTTTTATTCCAAAAATTTTATTGATCTATACAATGAAAAAAAGGTTCTTTAGTTTATGCAAACATTCATCACACTTTTAAAAAAAGGTTCTTTAACTAAAAGGTTTTCCGGGTTACCAAAAAAAAAAGCTGCTTCTATAACATCACTGATAACAAAAAAAAAAACATTTTGGTTCTTCCTGGCACCTTTGTGAACTTTAAAAAATCTCAGCTTTTTTCATATGTGTGCGTTCTCAAAGCATGTGTTTATTCATTTCAGGTACATATA[T/A]GTGCCTCTGGGTGGTTCACGTCATGGTGCTTTCCGGAAGCTTCTCTCCACTGCGCTGGCGTTTGGGTTTGTGTGTTTCTGGCATGGTTGCCATGACTACCTGCTGTACTGGGCACTGCTAAACTGGGTAGGGGTGTTAGTGGAGAACGCATTTGCACTCCTCTTCTCGTCTCCCCCTCTTCGTCATGCTATTGTGAGTTCACACAAAGCTTTATCTGTTAATAAATGATTACTTAATAAATATGAAATAACACAGCTTGATTGGTATTATCTGATATTTCTTGATCTAGGTCTACTGTCTGACACCTCGGATGCAGAGACGGGGCTTGGCTCTAATATCTGCCTTCTCCACTGCATTTCTTATTTTGTCCAATCTCTTCTTTCTGGGTGGGACCCATGTAGGTAGAATCTTCTGGAAGAAATTATTTGTCCAAGGTGGGTCATTTCAATGTATTCAATCTCCTACCTATGCTTTTAGAAAAGAAGAACACTTTTTAAACT
Associated Phenotype:
Not determined