Busch Lab

ZMP

ogt.2

Ensembl ID:
ENSDARG00000095552
ZFIN ID:
ZDB-GENE-051128-1
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 5 alleles of this gene:

Allele Name Consequence Status Availability
sa7388 Missense Mutation detected in F1 DNA Not yet available
sa38988 Nonsense Mutation detected in F1 DNA Not yet available
sa30674 Nonsense Mutation detected in F1 DNA Not yet available
sa35673 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35672 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa7388
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000143891 Missense 108 1102 3 23
ENSDART00000148252 Missense 52 1046 2 22

The following transcripts of ENSDARG00000095552 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 18603428)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 14397881
GRCz11 14 14703444
KASP Assay ID:
554-4229.1 (used for ordering genotyping assays)
KASP Sequence:
AGATTTTGAGGCAGCAGAGCACCACTGTATGCAGCTGTGGAGGCAAGAGC[C/T]GGATAATACTGGTGTGCTGCTGCTGCTCTCCTCTATCCACTTCCAGTGTC
Long Flanking Sequence:
TTCTTGTAATTTTCCTCTTGTTTTGACTCCCATGATTAGTGTTTGAATTTCAGCTCTGGGTTTACCTGCTCCAGCCAATAACAGAACTAGTTGGTTAGGTGGGGATAAAGATAGTAAGGCCCCATTTGTTTATAATTTAGATAAGCAATGCAAAAAATGCAATTTATCATGCATCTGCAATATGTTTATTGCATATACTATTGTCGTGATATTGATAATTTTTGTGACATATTATGCACCTATCATAACTGCATTAAATGGTTTTGCACTGAATAGTGTTTATATGAAGTTTTATTATTTATTTATTATTATTATTTTTTACATTATTTCCATTTCTTCTAACATGCCGTTTTCCCCTCCTCTGGGTTGTGTTGGTGCTTCAGAACCAACCAAACATGTTCTTTCCTTCCAAGGGTTGGCAGAGCTGGCGCACCGTGAATATCAGTCAGGAGATTTTGAGGCAGCAGAGCACCACTGTATGCAGCTGTGGAGGCAAGAGC[C/T]GGATAATACTGGTGTGCTGCTGCTGCTCTCCTCTATCCACTTCCAGTGTCGCAGGCTAGACATGTGAGATGAAAAACTTTATGATTCTTTTTTTTTTTTTTTGGGAAGATGGAGTGGTATGACATTTGTCATAATGGCGTTGCAGATTTTTCTTAGTATCGAAAATATAGGTTGCGACCTTTTTGCAAAACAAATACATGCTAGTTAACATGTAAAAATCCCTTTTTAGTTTTATAATTCATGCTCTTAGAATTCTGCATGTGATTCTTAATAAATTTTCATTTTAAAGTTTTTAAATTGTACATTTTAGTCACAATATAATTAAAACAACAAACATTTGTCTGATTTACTTGAAAATGCACGTAGGTCATTTCAATTTAGCACTCTGGCCACCAAGCAGAACCCCATGCTAGCTGAGGCCTACTCTAACCTGGGCAACGTTCACAAGGAACGAGGTCAACTGCAGGAGGCCATTGAACGTTATCGTCAAGCTCTTCGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38988
Status:
Mutation detected in F1 DNA
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
ENSDART00000143891 Nonsense 465 1102 11 23
ENSDART00000148252 Nonsense 409 1046 10 22

The following transcripts of ENSDARG00000095552 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 18595865)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 14390318
GRCz11 14 14695881
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACATTTGCGGATGCTTACTCCAACATGGGCAACACTCTGAAAGAGATG[C/T]AGGATATTCAGGGGGCACTGCGGTGCTACACTCGAGCCATTCAGATTAAC
Long Flanking Sequence:
TCTAGTTATTTTTATTTTTTCTGTTAGGTTTCTGAAGCTGAAGAGTGTTACAACACTGCTCTGCGTCTGTGCCCAACCCACGCTGATTCCCTTAACAATCTGGCCAATATCAAGCGTGAGCAGGGCAACATTGAGGAGGCCGTGCAGCTCTACAGGAAAGCACTGGAGGTGAGTGGACCAGAAAAGTCCATTTGAAAACCTCTGATTTGTTTTAAATAATATATATTTCATATTTTTTTTGTAAAGGTGTTCCCAGATTTTGCTGCTGCCCATTCAAACCTTGCCAGTGTCCTGCAGCAGCAAGGAAAACTTCAAGAAGCCCTCATGCATTATGAGGAGGCCATCAGGCAAGATTCTTTTTTAGCCACACTTTTATTTATTTTTTATTTATTGGTGTCTTTTAAAGATTTCTTACTGTCTGTTTGTACTCGAACCCTAACAGAATCAGCCCCACATTTGCGGATGCTTACTCCAACATGGGCAACACTCTGAAAGAGATG[C/T]AGGATATTCAGGGGGCACTGCGGTGCTACACTCGAGCCATTCAGATTAACCCTGCTTTTGCTGATGCTCACAGTAATTTGGCTTCCATACACAAAGTAGGAATCTTTAATTAATACGCTTTATTAAAGTTGTGTGTAGTTTTGTTGTTTTGATTTTAAATGGCAACATTTGTCAATTAAAGGACTCTGGGAACATTCCTGAAGCAATTGCATCTTATCGCACTGCGCTGAAGCTCAAGCCAGATTTCCCAGATGCTTATTGTAACCTTGCTCATTGTCTACAGGTATGCAGGCTTACTAAATTTGTCTCTTTTTATTGCACATTGGGCATTCTTGTATGATTTTTGCATTGTTCCCTGGTGTTTAGATTGTATGTGATTGGACTGATTATGACGAGCGCATGAAGAAACTGGTGAGCATTGTTGCTGATCAATTGGAGAAGAACCGCCTGCCGTCTGTGCATCCGCATCACAGCATGCTTTATCCTCTCTCACACGGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30674
Status:
Mutation detected in F1 DNA
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
ENSDART00000143891 Nonsense 698 1102 16 23
ENSDART00000148252 Nonsense 642 1046 15 22

The following transcripts of ENSDARG00000095552 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 18594095)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 14388548
GRCz11 14 14694111
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGGATCCATCAAGATGGAATCCACATCCTGGTCAACATGAACGGTTA[T/A]ACTAAAGGAGCACGCAATGAGCTGTTCGCATTGCGGCCAGCACCCATTCA
Long Flanking Sequence:
TTGAAGGAGCAGTATCGACAGATATTAACCAGACAGTCTACTAATACTCAAATGGACAATCAAAATAAAGTGTTACCATTTTAAGGTGCATAATTTGAATCATTGTAATTTAGGAACAATATAATGTAAGTGTTTCTTCTAGTTATATAATTTTTTTGCTATTATTGACCTGTGTGAAGTTTGCGAACCACAAAATTCAAAACATCGGCAGATGTCTCTACTGTCTGTCCTTACTTAATTTGTGCTGGTTTGTGCTGATTAAAGTTTTGTTGAAGCTGCTTCTGGTGTTAATGTAATGGATATTGAATTAATAGCAATGATGCCCCACCACTTTTTAAAACTGCTTTGAAAAACTGCCACAACACGCTTTAATCTTTTCTTTTTTTTTGTCTGTTTTAATTTCATGATTTTTTTTGTCTTTAAAAGATTCCCTGTAATGGAAAAGCTGCAGACAGGATCCATCAAGATGGAATCCACATCCTGGTCAACATGAACGGTTA[T/A]ACTAAAGGAGCACGCAATGAGCTGTTCGCATTGCGGCCAGCACCCATTCAGGTTGGCATCTGAAAGAACCATTTATTGAATGTAATTTACTTAAAGAAGTGTGTGTGTGTGTATCTGTGCTTGGAATTTATGCATTTTTAAATATGAGAGTTATGTAACATGCATTGAATAGGAAGTCTGGAGGGCTGATGTCCTGCAAAATTTAGTTCCAGCCCCAATCAGACACAACTTGGCTAGCTAATCAAGCACTACTAGGCTTTCTTGAAATATCCATGCAGATGTGATAAGGCAAGCTGGAGCTAAAATCTGCTGGACACCAGCCCTCCAATAATGTTTTAATTGCTACTCTTGATCAATTTAATTTGTTATTGTTGAGTAAATATTGTAAGATTGTGTTGTATTGGCATTGTATTGGTTCCTGATCATATAAAAAGGGCTGGCTTAATATTAATTGTTTCTCACAATATTTTTAGGTCATGTGGCTTGGATACCCAGGCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35673
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000143891 Essential Splice Site 716 1102 17 23
ENSDART00000148252 Essential Splice Site 660 1046 16 22

The following transcripts of ENSDARG00000095552 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 18593622)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 14388075
GRCz11 14 14693638
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATATAAAAAGGGCTGGCTTAATATTAATTGTTTCTCACAATATTTTTA[G/T]GTCATGTGGCTTGGATACCCAGGCACCAGTGGAGCTCCATTTATGGACTA
Long Flanking Sequence:
CCACATCCTGGTCAACATGAACGGTTATACTAAAGGAGCACGCAATGAGCTGTTCGCATTGCGGCCAGCACCCATTCAGGTTGGCATCTGAAAGAACCATTTATTGAATGTAATTTACTTAAAGAAGTGTGTGTGTGTGTATCTGTGCTTGGAATTTATGCATTTTTAAATATGAGAGTTATGTAACATGCATTGAATAGGAAGTCTGGAGGGCTGATGTCCTGCAAAATTTAGTTCCAGCCCCAATCAGACACAACTTGGCTAGCTAATCAAGCACTACTAGGCTTTCTTGAAATATCCATGCAGATGTGATAAGGCAAGCTGGAGCTAAAATCTGCTGGACACCAGCCCTCCAATAATGTTTTAATTGCTACTCTTGATCAATTTAATTTGTTATTGTTGAGTAAATATTGTAAGATTGTGTTGTATTGGCATTGTATTGGTTCCTGATCATATAAAAAGGGCTGGCTTAATATTAATTGTTTCTCACAATATTTTTA[G/T]GTCATGTGGCTTGGATACCCAGGCACCAGTGGAGCTCCATTTATGGACTACATAGTTGGGGATAAGGTGACTTCTCCCATTGAGGTTGCAAAGCAGTACTCAGAGACTCTGGTGTACATGCCAAATTCATTTTTCATTGGGGATCATGCTAACATGTTCCCACACCTTAAGGTACGATTCTTTTTTTTAAAATGTTTTTTTATTGTGTGTGCTCAAAAAGTAGCACTAAAATGTTTTTTTGGCATCTATGGAAAAAAATTAGCTGAAGATTTAGTGAAGATTTGTGTTTTTTTACCCAATAGAAAAAAGCAATTGTCGACATCAAGTCAAATGGGCACATTTTTGACAATCGCATTGTGCTGAATGGCATTGATCTAAAAGTGTTCCTGGAAAGCCTGCCGGATGTCAAAGTTTTGAAGGCTAGTAAAAACATCACTCCATTTCTATTATCATGTAAAACAGACATGCTTATGTTTTCTTATCAATTACCTTCTTTCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35672
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000143891 Nonsense 895 1102 20 23
ENSDART00000148252 Nonsense 839 1046 19 22

The following transcripts of ENSDARG00000095552 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 18591105)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 14385558
GRCz11 14 14691121
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAACAATTGTGGTGACCACCCGCTCACAATATGGGCTTCCTGATGATT[C/A]AATTGTCTATTGCAACTTCAACCAGCTCTATAAGATTGACCCTCCAACCC
Long Flanking Sequence:
GTAGAATAAAATGTGAAAGTGTCTTGAGTTTGTGTTAGCCACGAACCTTATTTAAGCGATTTAATCGTAATCCCATTCAAAAAACCTATTGACTTTGGGACAAGAGAACTGAAACTGCTATAATGCCAGCTCGTTTCCAGGTTTTTGCATACAAATTGACATCATAGTTCCGCCACTCTATTCAGCATCTTTTCACGTTCCTTAGCAATGTGTAGAATACCATTTTAAGATGTAAAGCATGTCCTGTGCATGACCCCCTAATTAATGGTGCGAGCTGAAGTCATCTAAAATCTCTCAATTGTTTTATATGTTAGACTAATACGAAGACGGGAAATTGGCAGGATCCCATCACTGCACCTCATGATTGTTTCAGAACCTAAACAAGTAACATCTGTGTTTTTACTTTTTTCTTTAGATTAACAATAAAGCAGCAACAGGAGAAGAAGTTCTTAAAACAATTGTGGTGACCACCCGCTCACAATATGGGCTTCCTGATGATT[C/A]AATTGTCTATTGCAACTTCAACCAGCTCTATAAGATTGACCCTCCAACCCTGCAGATGTGGGCCAATGTAAAATTCAACAATTTTTCTGTTATATATACATATTTTCCCTCTAATATAGTTATATTATTTGTGAGTATAGTTTTTTGTGTAAATCAAAATTGAGTAACATTTTACAGTGGATTAACTTAACTAAACAGCATGTGCTTATTGTAAAACTGATTCTGCAGCAGCTCTACTCACTGTGCTCATTGTTGATTACCAGATCCTGAAGCGTGTGCCCAACAGTGTGATCTGGCTGCTGCGCTTCCCAGCCGTGGGTGAGCCCAATATCCAGCAGTACGCTCAGAATCTGGGCCTGCCTGCCTCTCGCATCATCTTCTCTCCTGTGGCTCCCAAAGAGGAGCATGTACGACGTGGACAGTTGGCTGATGTGTGCCTGGACACCCCGCTTTGTAATGGCCACACCACAGGCATGGACGTGCTCTGGGCTGGAACCCCC
Associated Phenotype:
Not determined