Busch Lab

ZMP

ugt5g2

Ensembl ID:
ENSDARG00000043901
ZFIN ID:
ZDB-GENE-081028-66
Description:
UDP glucuronosyltransferase 5 family polypeptide g2 [Source:UniProtKB/TrEMBL;Acc:D3XDB4]
Human Orthologue:
UGT8
Human Description:
UDP glycosyltransferase 8 [Source:HGNC Symbol;Acc:12555]
Mouse Orthologue:
Ugt8a
Mouse Description:
UDP galactosyltransferase 8A Gene [Source:MGI Symbol;Acc:MGI:109522]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa41649 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34899 Nonsense Mutation detected in F1 DNA Not yet available
sa34898 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41649
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064471 Essential Splice Site 42 534 2 2
Genomic Location (Zv9):
Chromosome 10 (position 22285410)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 22115748
GRCz11 10 22085200
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATAGAAAACATACTTGGATTTAAAGCCTATGTGCACTCTGTTGCCCCCT[A/G]GGTGCTGGTGAAGAAGCTGCAGTCTCGTGGACACGAGCTGAGTGTGATTC
Long Flanking Sequence:
GACGTATCATGTCTTGCGTAATATCTGTATCAGTGTTTCAACCCTGGAAAGACTTGACATTTATGTACCCTACTGTGTTTACCCTAGGAAAGTTATCAGAGTCGAAAACTCATAAGTTAGCAAACTAAATATTTCATTTATTGAGTTTTTTTTTATGTTAGCAATGATTTAATGTTTACATTTTAATAGCGTATTAGTGTGATTAGAGGGGGATTTGCCCAACCTGCAATTTATCTGAAAAATCAGGTACCCCTAAAATCCTGCTCACACTGTACAGTTTTTAGTCCTGATTTGGTGGATGCAAATGATCAGAATTTATATAAAGTTTACCAACACATTTTTTACAGCTGATTAATTTGCACAGAATCGTTCACCTAAAGAATAACAATGTGCTCAAGCAAAATAAACATTGTGCATTTTGATTTCACATGGACTCAAGATTAAAACAATCATAGAAAACATACTTGGATTTAAAGCCTATGTGCACTCTGTTGCCCCCT[A/G]GGTGCTGGTGAAGAAGCTGCAGTCTCGTGGACACGAGCTGAGTGTGATTCGCCTGGAGGACAGCTGGTTCATCAAGGGCAATTCACCTTACTACTCCTCTATTACAGTGACGCTTAAGAAGAAATTTATAGACCTGGACCTATTTGAGACAGCAGTAAAAAAGATTCTTGATGCTCGTAGGGATGGCCCAATAATGGGAGTGCTGGCACAGATGTCTGAATTTATAGGCATCCTAAAGGTGGGTCATGGTGCAAACATTGCTATGCTCACCTCCATGCTAGAAAACAAAGCTCTGATGTCACAAATAAAGATGGCCAACTATGACTTGATGCTCACTGACCCTGCCATGCCTGGTGGGGTCATCTTGGCACATTACCTTCACCTTCCAATGGTCTATAATGTCCGTTGGATGAGTTTTGGAGAAGGCCACTTCTCCATAGCACCTTCTCCCATCTCCTTTGTTCCTGTGCCTGGTTCTGGTCTGACAGACCGAATGGGCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34899
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000064471 Nonsense 63 534 2 2
Genomic Location (Zv9):
Chromosome 10 (position 22285343)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 22115681
GRCz11 10 22085133
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCAGTCTCGTGGACACGAGCTGAGTGTGATTCGCCTGGAGGACAGCTG[G/A]TTCATCAAGGGCAATTCACCTTACTACTCCTCTATTACAGTGACGCTTAA
Long Flanking Sequence:
CCCTACTGTGTTTACCCTAGGAAAGTTATCAGAGTCGAAAACTCATAAGTTAGCAAACTAAATATTTCATTTATTGAGTTTTTTTTTATGTTAGCAATGATTTAATGTTTACATTTTAATAGCGTATTAGTGTGATTAGAGGGGGATTTGCCCAACCTGCAATTTATCTGAAAAATCAGGTACCCCTAAAATCCTGCTCACACTGTACAGTTTTTAGTCCTGATTTGGTGGATGCAAATGATCAGAATTTATATAAAGTTTACCAACACATTTTTTACAGCTGATTAATTTGCACAGAATCGTTCACCTAAAGAATAACAATGTGCTCAAGCAAAATAAACATTGTGCATTTTGATTTCACATGGACTCAAGATTAAAACAATCATAGAAAACATACTTGGATTTAAAGCCTATGTGCACTCTGTTGCCCCCTAGGTGCTGGTGAAGAAGCTGCAGTCTCGTGGACACGAGCTGAGTGTGATTCGCCTGGAGGACAGCTG[G/A]TTCATCAAGGGCAATTCACCTTACTACTCCTCTATTACAGTGACGCTTAAGAAGAAATTTATAGACCTGGACCTATTTGAGACAGCAGTAAAAAAGATTCTTGATGCTCGTAGGGATGGCCCAATAATGGGAGTGCTGGCACAGATGTCTGAATTTATAGGCATCCTAAAGGTGGGTCATGGTGCAAACATTGCTATGCTCACCTCCATGCTAGAAAACAAAGCTCTGATGTCACAAATAAAGATGGCCAACTATGACTTGATGCTCACTGACCCTGCCATGCCTGGTGGGGTCATCTTGGCACATTACCTTCACCTTCCAATGGTCTATAATGTCCGTTGGATGAGTTTTGGAGAAGGCCACTTCTCCATAGCACCTTCTCCCATCTCCTTTGTTCCTGTGCCTGGTTCTGGTCTGACAGACCGAATGGGCCTGTTAGAGCGATCCCGTAACTTTTTACATTATGGGCTGAACCTCATTCAAGAGCGCTGGATGGTGAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34898
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
ENSDART00000064471 Nonsense 356 534 2 2
Genomic Location (Zv9):
Chromosome 10 (position 22284466)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 22114804
GRCz11 10 22084256
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTTATTGGACAGAGACCTTCAACGTTGGGCAATAACACCCTACTTATT[C/T]AATGGCTTCCTCAGAATGACTTGCTGGGCCATCCGAAGACTCGTGCTTTT
Long Flanking Sequence:
CTTCTCCCATCTCCTTTGTTCCTGTGCCTGGTTCTGGTCTGACAGACCGAATGGGCCTGTTAGAGCGATCCCGTAACTTTTTACATTATGGGCTGAACCTCATTCAAGAGCGCTGGATGGTGATTCCAATGTATACCAGCTTGTTGCTCAACCACTTCCCTCCAGGCACTGACCTCCTTACCATGCAGCGATCAGCAGAACTTTGGTTAGTGCGTGCAGATTTTGTATTCGAGTTTCCACGACCTTCCATGCCAAACCTCGTCTACATTGGTGGCTTCCAGTGTCGTCCAGCCAAGCCTCTTCCTGCTGATCTGGAGGAGTTCATGCAGAGCTCAGGAGACCATGGGGTGGTCGTGATGTCTTTGGGAACTCTGATCGCAGGATTGCCCAAAGAAGTCATGGAGGCCATCGCCTCAGCGTTTGCTCAGATCCCGCAGAAGGTGATCTGGAGGTTTATTGGACAGAGACCTTCAACGTTGGGCAATAACACCCTACTTATT[C/T]AATGGCTTCCTCAGAATGACTTGCTGGGCCATCCGAAGACTCGTGCTTTTGTGGCTCATGGTGGCACCAATGGTCTATATGAAGCGATTTATCATGGAGTTCCAGTTTTGGGGCTCCCTTTGCTATTTGATCAGCTAGATAACATTGTACGTCTTCAGGCGAGAGGTGGAGCTCGGATGTTGGATGCAGCTACTTGTAGCACAAAAGAATTCCTCGTAGCTTTGACGGATATCTTAGAGAACCCAACTTATCGACAAAACATGCAAAAGCTCTCTAATTTACATCGAGACCGGCCTTTGCACCCTCTTGATAAAGCAGTGTATTGGATTGAGTTTGTCCTGCGTAATAAAGGTGCACCCCATCTGCGAGCAGAGGCCTACAACATGTCTGAGTTCTCCTACTACTGTCTGGATGTGGTCGCGCTGGTTCTCTTCATGCTTCTGGGGACTTTAGGAGGTGTTTATACAATATGTAAAAGAAGACCAAAAAGACAAGAAAAC
Associated Phenotype:
Not determined