ZMP
ogt.1
Ensembl ID:
ZFIN ID:
Description:
O-linked N-acetylglucosamine transferase isoform 1 [Source:RefSeq peptide;Acc:NP_001017359]
Human Orthologue:
OGT
Human Description:
O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylgluco
Mouse Orthologue:
Ogt
Mouse Description:
O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylgluco
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18601 | Nonsense | Available for shipment | Available now |
| sa42376 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18601
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 |
|---|---|---|---|---|---|
| ENSDART00000054556 | Nonsense | 227 | 1052 | 6 | 23 |
| ENSDART00000080383 | Nonsense | 237 | 1062 | 6 | 23 |
| ENSDART00000080496 | Nonsense | 237 | 1046 | 6 | 22 |
| ENSDART00000122502 | Nonsense | 227 | 1036 | 6 | 22 |
The following transcripts of ENSDARG00000057702 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 18638527)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 14432980 |
| GRCz11 | 14 | 14738543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGACCCAAACTTTTTGGATGCTTACAWCAACTTGGGTAATGTTCTGAAA[G/T]AGGCTCGTATCTTTGACAGGTAAAGGGTCACTTCTTCTATCATTATATTT
Long Flanking Sequence:
GCGTAGGAAAAAGTGTGCAGCTTAGCGCGGCAGAAATTTGCGCATGCGAGCCCATGCTGTAGGCTCACTTTTTGCTTTTGTGAGAGTAGATACTAACTTTTTTTTTCATCTGCCTTTTTTTTCTTCCTTTTTATTTGATATTTTGGTTTCTTTTTTTTTTTACAACCCCTCCTCTGTCTACTCCTATTTCTTTTTTCTACCTCTTTTTCTTCCTGTTTGTTTTAAACTCTAAACCTGTTAAAGGCTTGTTACCTGAAGGCAATCGAAACTCAGCCAAACTTCGCTGTTGCCTGGAGTAACCTGGGCTGTGTGTTCAATGCCCAGGGTGAGATCTGGCTGGCCATCCATCATTTTGAGAAGGTTGGTACATATAACAATCTCACTTTGAAAAATAATATGATTTAATGTAATGTTCATGGGGCTCTTCAATGGGTTTACAGGCAGTGACACTGGACCCAAACTTTTTGGATGCTTACATCAACTTGGGTAATGTTCTGAAA[G/T]AGGCTCGTATCTTTGACAGGTAAAGGGTCACTTCTTCTATCATTATATTTTAATATCATATTCATTTACAGTCAGTCTCATGCTTGTTATTGGTTTCCTCTGCAGAGCCGTTGCTGGGTATCTGCGAGCCCTTAGTCTGAGCCCAAACCACGCTGTTGTCCATGGAAACCTGGCTTGTGTTTATTATGAACAGGGTCTGATCGACCTAGCCATTGACACATACCGTCGTGCCATTGAGCTGCAGCCACACTTTCCTGATGCATACTGCAATCTTGCTAATGCTCTGAAAGAAAAAGGCAATGTAAGAAACTTTAGTACTCCATTATGTGCAATGACTGCTGTCATGTTTGGTGACATTATTGAAATTTTGCTAAAAAGAGATGCAGTGTTGAAACTGTTATGGTTTATGAAGATTGGCTTTTTACAGAAACCAATTTTAAACCCAAGCTAATTTTCCAGTTTGTTTTGTCAAAAGAACTGGTACTTTGGTACCAAGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42376
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 |
|---|---|---|---|---|---|
| ENSDART00000054556 | Essential Splice Site | 430 | 1052 | 10 | 23 |
| ENSDART00000080383 | Essential Splice Site | 440 | 1062 | 10 | 23 |
| ENSDART00000080496 | Essential Splice Site | 440 | 1046 | 10 | 22 |
| ENSDART00000122502 | Essential Splice Site | 430 | 1036 | 10 | 22 |
| ENSDART00000054556 | Essential Splice Site | 430 | 1052 | 10 | 23 |
| ENSDART00000080383 | Essential Splice Site | 440 | 1062 | 10 | 23 |
| ENSDART00000080496 | Essential Splice Site | 440 | 1046 | 10 | 22 |
| ENSDART00000122502 | Essential Splice Site | 430 | 1036 | 10 | 22 |
The following transcripts of ENSDARG00000057702 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 14 (position 18633514)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 14427967 |
| GRCz11 | 14 | 14733530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATCCTGCTTTTGCTGATGCTCACAGTAATTTGGCTTCCATACACAAAG[T/A]AAGAATCTGGAATAATACTCTTTGTTTAAAGTTGTTTTAGTGTTGTTTTG
Long Flanking Sequence:
AATTAGGATCATCAAAAATGGCTGCTTACATGGTAGACTCTTAATCAGAATATTAGTGCCTATGTAAAGGTACTTGGTGAGACCCTTGCTTATTCGATTAATTTAGCTAAATATGTTGTACATTTTGTTATTGTTTTTTTGTAAAGGTGTTCCCAGAATTTGCCGCTGCTCATTCAAACCTTGCCAGTGTCCTGCAGCAGCAAGGAAAGCTTCAAGAAGCCCTCATGCACTATAAGGAGGCCATCAGGCAGGATTCTGTTTTAGCTACAGTCTTGCATGCTTTGTTTTTTTATTGGTGTCTTTTAAAGATTTCTTACTGTCTGTTTGTACTCGAACCCCAAACAGAATCAGCCCTACATTTGCGGATGCTTACTCCAACATGGGCAACACTTTGAAAGAGATGCAGGATGTTCAGGGGGCGCTGCAATGCTACACTCGAGCCATTCAGATTAATCCTGCTTTTGCTGATGCTCACAGTAATTTGGCTTCCATACACAAAG[T/A]AAGAATCTGGAATAATACTCTTTGTTTAAAGTTGTTTTAGTGTTGTTTTGAATTTAAATGGCAACATTTGTCAATTAAAGGACTCTGGGAACATTCCTGAAGCAATTGCATCTTATCGCACTGCGCTGAAGCTCAAGCCAGATTTCCCAGATGCTTATTGTAACCTTGCTCATTGTCTACAGGTATGCAGGCTTACTAAATTTGTCTCTTTTTATTGCACATTGGGCATCCTTATATGCTTTTGCGTTGTTCTCTGGTGTTTAGATTGTATGTGATTGGACTGATTATGACGAGCGCATGAAGAAACTGGTGAGCATTGTTGCTGATCAGTTGGAGAAGAACCGCCTGCCATCTGTGCATCCGCATCACAGCATGCTTTATCCCCTCTCTCACGGTTTCCGCAAGGCCATTGCAGAGAGACATGGCAACTTGTGTCTTGACAAGGTGTGTTTATTACAAATATTGACATTTAGCTTTATTTTCTGTATGAGCTTCAGTGT
Associated Phenotype:
Not determined