ZMP
gnpnat1
Ensembl ID:
ZFIN ID:
Description:
glucosamine 6-phosphate N-acetyltransferase [Source:RefSeq peptide;Acc:NP_001019545]
Human Orthologue:
GNPNAT1
Human Description:
glucosamine-phosphate N-acetyltransferase 1 [Source:HGNC Symbol;Acc:19980]
Mouse Orthologue:
Gnpnat1
Mouse Description:
glucosamine-phosphate N-acetyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:1858963]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32139 | Nonsense | Available for shipment | Available now |
| sa42894 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa36360 | Essential Splice Site | Available for shipment | Available now |
| sa36361 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25038 | Missense, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32139
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 |
|---|---|---|---|---|---|
| ENSDART00000058351 | Nonsense | 54 | 184 | 3 | 6 |
| ENSDART00000131663 | Nonsense | 54 | 77 | 3 | 4 |
| ENSDART00000138831 | Nonsense | 54 | 184 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 15057533)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15208361 |
| GRCz11 | 17 | 15216294 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTTACTACATCAAATCAAAATGTTTTAATGGATTTTTTTAGGTTTCTA[C/A]AAGGTCTTAGCACAACTCACAGAGGCTGGAGATGTCACAGAAGAACAGTT
Long Flanking Sequence:
TAAAAAGTCTTACATTTACTTTTAATAAAATCTAAAGCAACCATTATAACTATCATATTTTACAGTGTTTTGTAGTTTAAAAGGTCTGATCATTTCATTAGTAGACGCATCAAGCTGGACACAAGTTTGACTTTGAATTGTAAATGTTTGGTTGATCAAAGTCCGATTAAATAGTCGTCAGGAAGGTATTCATTGACAGGGATTCTTCAGTGATCATAAATTGGAATAACGTACTATTTTATTTCAGGGCTTCTGGAATGTTGCTCGACGAAACTCCGCTGTTTGATCCTTCTCTTCTCCAAGAGCTGGACTGGAGCAGCAACAGTGTCTCCTTCTTGCCAGCCATTTCTCCCTTTCAGCCCGGAGAAGGTCTGGTCCTCCGTCCTCTCTGCACTGCTGACCTGAACAGAGGTACTGCTCACCAATCAGTAGTCTGACTCTAAACACTTTGGTTTACTACATCAAATCAAAATGTTTTAATGGATTTTTTTAGGTTTCTA[C/A]AAGGTCTTAGCACAACTCACAGAGGCTGGAGATGTCACAGAAGAACAGTTTAAAGGTAATGCAAGATCATCATTTAGAAAAATACTCTCTCTCTCTCTCTCTCTCTCTCGCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATTTATATATATTTACACACACACACACACACACACACACACACACAGTTGATGTCAAAATATTATCCCTCCTATGTTTTTTTATATTTCTCAAACGGTGATTACCAGAACAAGGTGTTTTTCACAGTATTCTCTATAAAATATTTAAATATTAAAACATTTAAAATATATAAAATTATTCTTCTGGAGAAAGTCTTATTTTATTTTGGCTTAAATAAAAACAGCTTTTAATTTTTAAAAACAATGGTCCATATTATTCGCCCCCTTGAGCAATATATTTTTTTCTGATTCTGTACAGCAGTGGGGGTTGGGGGACAATAGGGGTCGTTTGGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42894
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 |
|---|---|---|---|---|---|
| ENSDART00000058351 | Nonsense | 70 | 184 | 3 | 6 |
| ENSDART00000131663 | Nonsense | 70 | 77 | 3 | 4 |
| ENSDART00000138831 | Nonsense | 70 | 184 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 15057579)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15208407 |
| GRCz11 | 17 | 15216340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTACAAGGTCTTAGCACAACTCACAGAGGCTGGAGATGTCACAGAAGAA[C/T]AGTTTAAAGGTAATGCAAGATCATCATTTAGAAAAATACTCTCTCTCTCT
Long Flanking Sequence:
TAACTATCATATTTTACAGTGTTTTGTAGTTTAAAAGGTCTGATCATTTCATTAGTAGACGCATCAAGCTGGACACAAGTTTGACTTTGAATTGTAAATGTTTGGTTGATCAAAGTCCGATTAAATAGTCGTCAGGAAGGTATTCATTGACAGGGATTCTTCAGTGATCATAAATTGGAATAACGTACTATTTTATTTCAGGGCTTCTGGAATGTTGCTCGACGAAACTCCGCTGTTTGATCCTTCTCTTCTCCAAGAGCTGGACTGGAGCAGCAACAGTGTCTCCTTCTTGCCAGCCATTTCTCCCTTTCAGCCCGGAGAAGGTCTGGTCCTCCGTCCTCTCTGCACTGCTGACCTGAACAGAGGTACTGCTCACCAATCAGTAGTCTGACTCTAAACACTTTGGTTTACTACATCAAATCAAAATGTTTTAATGGATTTTTTTAGGTTTCTACAAGGTCTTAGCACAACTCACAGAGGCTGGAGATGTCACAGAAGAA[C/T]AGTTTAAAGGTAATGCAAGATCATCATTTAGAAAAATACTCTCTCTCTCTCTCTCTCTCTCTCGCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATATATTTATATATATTTACACACACACACACACACACACACACACACACAGTTGATGTCAAAATATTATCCCTCCTATGTTTTTTTATATTTCTCAAACGGTGATTACCAGAACAAGGTGTTTTTCACAGTATTCTCTATAAAATATTTAAATATTAAAACATTTAAAATATATAAAATTATTCTTCTGGAGAAAGTCTTATTTTATTTTGGCTTAAATAAAAACAGCTTTTAATTTTTAAAAACAATGGTCCATATTATTCGCCCCCTTGAGCAATATATTTTTTTCTGATTCTGTACAGCAGTGGGGGTTGGGGGACAATAGGGGTCGTTTGGAGATTTCCAAATTTCAAATTCACTTTATTAAAATATTAGACCTAACATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36360
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058351 | Essential Splice Site | 73 | 184 | 4 | 6 |
| ENSDART00000131663 | None | None | 77 | None | 4 |
| ENSDART00000138831 | Essential Splice Site | 73 | 184 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 15058751)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15209579 |
| GRCz11 | 17 | 15217512 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAATAATAGTCTTTTATATAACCATCAAATGTTTATTTTTTATTAAA[G/A]CAAATTTTGAACATATGAAGAAATCTGGAGACTATTATGTGATAGTGGTG
Long Flanking Sequence:
CACCTTTAAAGCACCCACGCACATTAAAAATAAATAAAGGCCACAACTGAACATGGAGAATAGTCTAAATTATGGTGTGTTTGCGCTGTTGTGTGCAAGGTTTGTTTATTTATAACTACCTCAGATTTGCAAGTCACTGCCATTATTTTGGGGGTCGTGAGCTGAAAAAATTGGGAACCCCAGGTCTACAGAACAAAACAGTTCTACAACGACTTGCCTAATTTACCTAGTTAAGCCTTTAAATTGCACTTGAATAGTAGTATCTTGAAAAATATCTAGTAAAATAGTATTTACTGTCATGGTAATGATAAAAGAAATCAGGTATTAGAAATGAGTTATTAAAACTATTATAAGAACTAGAAATATGTAACGGAAAATTTTCTTTCCGTTAGACAACTATTGGCGAAAAACATGCGGGGGCTAATAATTCTGACTTCAATATATGCATTAAAAAAATAATAGTCTTTTATATAACCATCAAATGTTTATTTTTTATTAAA[G/A]CAAATTTTGAACATATGAAGAAATCTGGAGACTATTATGTGATAGTGGTGGAAGACACAAACCTTGGGCAAATTGTTGCTACAGCAACACTAATCATAGAGCACAAATTCATCCACGCTTGTGCAAAGGTACATTTTAAACATGTTTCAGCTTCATGTCAATGTTTTCATTGTGCAAAATTATACACTTTATTATATATATATATTTTTTTGTCATCCTGACAGAGAGGCCGTGTAGAAGAAGTGGTTGTGAGTGATGTTTGCAGGGGGAAACAGCTAGGAAAACTGTGAGTTTGGGTTTTAAAGTGCCCCTTTTCTGCTTTCAGATATTACCTTTCATGTAGGTGTTTGTGGAAGTAAAAAGGTCTGTAAAGTTTCAAAGGTTCTGTTCACACCTGGCATAAAGGCGCATTGTTGCCAATCTGATTAGAGGTGGATTACTGTACATACAAGTTTAAATCAGGTTAAAAAGTTCCACTTCTAGAGGTAATTAAAGACTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36361
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 |
|---|---|---|---|---|---|
| ENSDART00000058351 | Essential Splice Site | 115 | 184 | 4 | 6 |
| ENSDART00000131663 | None | None | 77 | None | 4 |
| ENSDART00000138831 | Essential Splice Site | 115 | 184 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 15058881)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15209709 |
| GRCz11 | 17 | 15217642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGCAACACTAATCATAGAGCACAAATTCATCCACGCTTGTGCAAAGG[T/A]ACATTTTAAACATGTTTCAGCTTCATGTCAATGTTTTCATTGTGCAAAAT
Long Flanking Sequence:
AAGTCACTGCCATTATTTTGGGGGTCGTGAGCTGAAAAAATTGGGAACCCCAGGTCTACAGAACAAAACAGTTCTACAACGACTTGCCTAATTTACCTAGTTAAGCCTTTAAATTGCACTTGAATAGTAGTATCTTGAAAAATATCTAGTAAAATAGTATTTACTGTCATGGTAATGATAAAAGAAATCAGGTATTAGAAATGAGTTATTAAAACTATTATAAGAACTAGAAATATGTAACGGAAAATTTTCTTTCCGTTAGACAACTATTGGCGAAAAACATGCGGGGGCTAATAATTCTGACTTCAATATATGCATTAAAAAAATAATAGTCTTTTATATAACCATCAAATGTTTATTTTTTATTAAAGCAAATTTTGAACATATGAAGAAATCTGGAGACTATTATGTGATAGTGGTGGAAGACACAAACCTTGGGCAAATTGTTGCTACAGCAACACTAATCATAGAGCACAAATTCATCCACGCTTGTGCAAAGG[T/A]ACATTTTAAACATGTTTCAGCTTCATGTCAATGTTTTCATTGTGCAAAATTATACACTTTATTATATATATATATTTTTTTGTCATCCTGACAGAGAGGCCGTGTAGAAGAAGTGGTTGTGAGTGATGTTTGCAGGGGGAAACAGCTAGGAAAACTGTGAGTTTGGGTTTTAAAGTGCCCCTTTTCTGCTTTCAGATATTACCTTTCATGTAGGTGTTTGTGGAAGTAAAAAGGTCTGTAAAGTTTCAAAGGTTCTGTTCACACCTGGCATAAAGGCGCATTGTTGCCAATCTGATTAGAGGTGGATTACTGTACATACAAGTTTAAATCAGGTTAAAAAGTTCCACTTCTAGAGGTAATTAAAGACTCAATCAGTCAGATTGCTTGATCGGATTGCTCAACTCCTTAGGTAATTTTCACACCTAAACATCACTTGCCTTCTTTCTTAAGTTTACTTTTGCAAGTCAGTAGGAGCATCCCAATTTATATACTTATAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25038
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:
Missense, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058351 | Missense | 138 | 184 | 6 | 6 |
| ENSDART00000131663 | Nonsense | 74 | 77 | 4 | 4 |
| ENSDART00000138831 | Missense | 138 | 184 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 17 (position 15060133)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 15210961 |
| GRCz11 | 17 | 15218894 |
KASP Assay ID:
554-7553.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAAAAGTAAAGGTTTAAACCATTGTTTTACTTTTGTTTTTTTAGGTTG[G/A]TATCAACACTGACCCTCCTCAGCAAAAAACTGCAGTGCTACAAGGTTACA
Long Flanking Sequence:
CTGTTGTGTGGCTTAAACTTTTTTTCTTTGTATATTTCTACATTTTTTTTTTAAATAATGTATTTTTATTCTTCTTTTATGTTGATTTACTATAGTATCTTATTTATGGGCACTTGCTGCAGGAAAGAGCAACAATAGTTTTGTTGCATCTCCATGTGCAATGACAAATGAAGTCTATTCTATACTATATTTCCAAGCAAACCAAAAATCACATTCAAGTAAACGATCGTCTCACTGGTCAAAGTGCACCTCCATCAGCTCAGCGTGCTTAACGTGGCTTTCTTTGTAGCTATCATTGTTATTATTTTGATCAAGGCTGTCTGTATTTTGGATTTGTTAATAGTAGACAAATCACAACACTGGGCCATCTGACTGTTCAAACCAGAGAGGCACTTTTATATTAATTGTCAAAAAAACAAAATAAAATGAATAAAAATCAATTTAATCTGAATCAAAAGTAAAGGTTTAAACCATTGTTTTACTTTTGTTTTTTTAGGTTG[G/A]TATCAACACTGACCCTCCTCAGCAAAAAACTGCAGTGCTACAAGGTTACACTGGAATGTGCGCCAAAAAATGTGGAATTTTACAGAAAGTTTGGCTATTCCGCTTCGGATGAGACTTACATGCAGTGCCGGTTCTTCAAATGAATCCAAACGAATGTTGAACATCACAGAATGTTTGCTTTAGGACTCTTGATCTGTTCTGGGAGAACCTCAGATCAGACTACCTCGAAGTTGCACATTTTCTAGCCAGTAAAAAAAAAGAGACAATAAAGCTTGGTAATGTGATGTCAATTAAGTATCAGTAACAAAATATTGTGACAGAAGCATTTTGAATTCACTAGAACACAGAACAATGTGCAGAAATGGCACTTCAGTTTGCAGAATGTGTGGTTTACAGTGACTGAAACTAAAAGTAACACTGTGGCCTGTAAAAAGAGAAAAGACAAACATTTTGTTGTATAGAGGGGGTTTATATACTTGAATATTTTCTTATGTCAATTT
Associated Phenotype:
Not determined