ZMP
gnptg
Ensembl ID:
ZFIN ID:
Description:
N-acetylglucosamine-1-phosphotransferase subunit gamma [Source:RefSeq peptide;Acc:NP_001002057]
Human Orthologue:
GNPTG
Human Description:
N-acetylglucosamine-1-phosphate transferase, gamma subunit [Source:HGNC Symbol;Acc:23026]
Mouse Orthologue:
Gnptg
Mouse Description:
N-acetylglucosamine-1-phosphotransferase, gamma subunit Gene [Source:MGI Symbol;Acc:MGI:2147006]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13050 | Nonsense | Available for shipment | Available now |
sa44180 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13050
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 |
---|---|---|---|---|---|
ENSDART00000056302 | Nonsense | 224 | 275 | 9 | 10 |
ENSDART00000141771 | Nonsense | 269 | 320 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 24 (position 38857374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37456592 |
GRCz11 | 24 | 37344312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATCCGTTGTAAACAAGCGTGTYTGTTTTAACAGGACTTTGAAAAGCAG[C/T]GAACAGAGATCGAACGGCTTCAGTCACTCCTAAMACAACACAACATCTCC
Long Flanking Sequence:
GCTGGCCTCACTAACACACTTCCAACAGCAACCTAGTCTGGACTCCCATCCGGGTACTGACCAGGCTCAGCCCTGCTTAGCTTCAGTGAGTAACCGGTCTTGGGCTGCAGGGTTATAGGGCTGTGGCCAATATGAGGGAATGATGTGCAAAACAAAGCCCCGCCCCTTACTTAATATTCAGTCTCAGTTAGAAGCCAATTAGCATATTAAAATAAAACACTCAGCAACTTCCAGTACACGCAAACCTTAAGAACATCAAATTAAAGGCATATGTGTGTGTTTAGGGTTATAATAAGCTGCTGAAGGAGCTGTTTGAAGAGGCTGGGTTTCTGAGAAAAGCTCAGCAGCAGAAGGCAGAGGAGAGCGTGACTTCTGTCTCACATCCCAGTCTGGAGCAGTGCACACAGGTCAGAGATGTAAATGCTGCACCCTTCACTCTGCTTAACTGCTGCATCCGTTGTAAACAAGCGTGTTTGTTTTAACAGGACTTTGAAAAGCAG[C/T]GAACAGAGATCGAACGGCTTCAGTCACTCCTAAAACAACACAACATCTCCTATGAGGCGACAGCAGGTGAGACGCATACAAAGCTTCACCTCATCTAATAGACTGTGGTAGATGTGAGTTATTTTAAGTGTGTAAAATTGAAATGTATTTTCTTGTGGTCAATCAGGTCAAAAGCAGAACTTAACTATAATAAGACTAACGCCATAGATTTCCCAGAATCAGTTTCTGTATAAATGTCTCTTGATACTCTTAAAATAATTAATAATTACCTAAATTAATAATTCGTTATATTTACATAGCGCTTTTCTGGGCGCTCAAAGCGCTTTACACATAGGGGGGAATCTCCTCACCCACCACCAGTGTGCGGCATCCACCTGGATGACGTGACGGCAGCCATTTTTGCGCCAGGCCGCACACATCACACAAGCTGATTGGTGGAGAGGAGACGTTGGAGTGATGAAGCCAATCATGATATGGGGAGGGTTAGTCTTTTTCGAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44180
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 |
---|---|---|---|---|---|
ENSDART00000056302 | Nonsense | 236 | 275 | 9 | 10 |
ENSDART00000141771 | Nonsense | 281 | 320 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 24 (position 38857410)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37456628 |
GRCz11 | 24 | 37344348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTTGAAAAGCAGCGAACAGAGATCGAACGGCTTCAGTCACTCCTAAAA[C/T]AACACAACATCTCCTATGAGGCGACAGCAGGTGAGACGCATACAAAGCTT
Long Flanking Sequence:
TCTGGACTCCCATCCGGGTACTGACCAGGCTCAGCCCTGCTTAGCTTCAGTGAGTAACCGGTCTTGGGCTGCAGGGTTATAGGGCTGTGGCCAATATGAGGGAATGATGTGCAAAACAAAGCCCCGCCCCTTACTTAATATTCAGTCTCAGTTAGAAGCCAATTAGCATATTAAAATAAAACACTCAGCAACTTCCAGTACACGCAAACCTTAAGAACATCAAATTAAAGGCATATGTGTGTGTTTAGGGTTATAATAAGCTGCTGAAGGAGCTGTTTGAAGAGGCTGGGTTTCTGAGAAAAGCTCAGCAGCAGAAGGCAGAGGAGAGCGTGACTTCTGTCTCACATCCCAGTCTGGAGCAGTGCACACAGGTCAGAGATGTAAATGCTGCACCCTTCACTCTGCTTAACTGCTGCATCCGTTGTAAACAAGCGTGTTTGTTTTAACAGGACTTTGAAAAGCAGCGAACAGAGATCGAACGGCTTCAGTCACTCCTAAAA[C/T]AACACAACATCTCCTATGAGGCGACAGCAGGTGAGACGCATACAAAGCTTCACCTCATCTAATAGACTGTGGTAGATGTGAGTTATTTTAAGTGTGTAAAATTGAAATGTATTTTCTTGTGGTCAATCAGGTCAAAAGCAGAACTTAACTATAATAAGACTAACGCCATAGATTTCCCAGAATCAGTTTCTGTATAAATGTCTCTTGATACTCTTAAAATAATTAATAATTACCTAAATTAATAATTCGTTATATTTACATAGCGCTTTTCTGGGCGCTCAAAGCGCTTTACACATAGGGGGGAATCTCCTCACCCACCACCAGTGTGCGGCATCCACCTGGATGACGTGACGGCAGCCATTTTTGCGCCAGGCCGCACACATCACACAAGCTGATTGGTGGAGAGGAGACGTTGGAGTGATGAAGCCAATCATGATATGGGGAGGGTTAGTCTTTTTCGAAGGACATCCTGGGATTTTTAACAACCACAGAGTGTCCTC
Associated Phenotype:
Not determined