Busch Lab

ZMP

NP_001165868.1

Ensembl ID:
ENSDARG00000061248
Description:
xylosyltransferase 1 [Source:RefSeq peptide;Acc:NP_001165868]
Human Orthologue:
XYLT1
Human Description:
xylosyltransferase I [Source:HGNC Symbol;Acc:15516]
Mouse Orthologue:
Xylt1
Mouse Description:
xylosyltransferase 1 Gene [Source:MGI Symbol;Acc:MGI:2451073]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa33177 Nonsense Mutation detected in F1 DNA Not yet available
sa6892 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa33177
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
ENSDART00000087118 Nonsense 190 919 2 11
Genomic Location (Zv9):
Chromosome 3 (position 26548508)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 26338464
GRCz11 3 26469335
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGATCTTCACCAGAGAGCCAATCCCACCCTCCGCCCACAGCAATCCCAG[C/T]AACACCGGCACCACTTCCAGCGACCCAAGCGATCGATCACACCCACTGCT
Long Flanking Sequence:
CTCCAGGTCTCTCTCATAATCTTTGTGCTTGATTCAGTGCATATCTATTAGATACTTTTCCTCCCATTATGTTGTTTTACCAAAAGTCTAATTGATGTATACCTTGCTTTTTACATACTTTCGTTGTATTTCGTTTGTTGTGACATTGACATTCTGGTCATAGCACCCACTAATTTCATCTTGTCTTGATTTTTTTTCAGGATGGCTACTATTCGCACCGGCCCAAGGAGAAAGTCCGTGTGGACAGCAACAATGAAAACTCTGTTCCCAAAGACTTTGAGAATATAGACAACAGTAACTTCGGTGCACGTTCCCAAACACAGAGACACGCACCTGGCAAGCACAAACAAGGCCTTCTGGAAAAGGCGCATGCACAGCAAAGCCTGAGCAAGAACTCCAATGAGGTCATTCAGTATGCACAGAACAAAGCTGGCCTCAATCAGACGCACACTGATCTTCACCAGAGAGCCAATCCCACCCTCCGCCCACAGCAATCCCAG[C/T]AACACCGGCACCACTTCCAGCGACCCAAGCGATCGATCACACCCACTGCTGACATCAAGTATGACCAACCACCCAAATGTGAGATCAGTGGAAAAGAGGCGATCTCTGCCTTGTCCCGTGCTAAAACCAAGGAGTGCCGGCAGCAGATAGTAGAGGTTTACTGCCGCCACAAAGAACACCAGCTCATGCCCGAGAAGGTCACCCGCTACTGTCCTGTAGAGGGTGAGCAGAATCTCATTACACTACGAATTTTTGAAATCAAAATGTTTGGCACATTTAATATATGCTTGAAGCTATTATGTGATGGAAACGTTATGATACGAAAAAATTCCCTACTTTCTAAATGATTGTTGTTGATCTTTGGAACAATTCTGATTAAAATGAAAGCATTTGACCAACATTTTTTAAAGATTTTATTTTTTAAGAATTTAATAATCTGTCAAGTTTGTAAAAAAAATGCTGCTTCTGTTTCACTGTGATTTTCATAGATATTAGGATCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6892
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
ENSDART00000087118 Nonsense 423 919 6 11
Genomic Location (Zv9):
Chromosome 3 (position 26571681)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 26315291
GRCz11 3 26446162
KASP Assay ID:
554-4705.1 (used for ordering genotyping assays)
KASP Sequence:
GTTATTTGCATTGTTRAAAATTGCCAACAGATTCATCAGAAAACAGGGTT[T/A]GGACCGGCTTTTCTTTGARTGCGACACCCATATGTGGCGGCTTGGAGACA
Long Flanking Sequence:
GCATGAAGTTGTTTCCCCTCTACCAGAAGCCTGCAGTGAAAGAAAATAAACATCAGAGCGGGATGTGTGTGGGGAAAAATGACTACAGACGTTCAGGCAGTGCACTGCGACAGGCAGTAAAACAGGGCAGCTTGCATTAGGGGCTGAATCTGGCTCTGAATGCGAGCTTGGACATTCCCAGAATCCCTGGTGCTCCGCGCTCATTTACACTGTGGCTCATTAGCCTGATTAGCAAACTCTCTGTTAGTCTCTTTTGCTTGTTTTTCCATTCTAACACCCTTTCGTTCTCTCCTCAGGACCAATGATCAGCTGGTGGCCTTCCTGTCCAAATACAGAAATATGAATTTCATCAAGTCTCATGGGAGAGACAACGCTCGGTGAGTGCTGACATGTGATGATGGCTGAAACGCACGCCAGCTGCACAGAATAATAACGGCTAAAAATACATTTGTTATTTGCATTGTTAAAAATTGCCAACAGATTCATCAGAAAACAGGGTT[T/A]GGACCGGCTTTTCTTTGAGTGCGACACCCATATGTGGCGGCTTGGAGACAGGAAAATTCCAGAAGGAATATCGGTGGATGGAGGCTCTGACTGGTTTCTGCTTAACCGGATGTTTGTGGAGTACGTCATTAACACTCAAGACGACCTTGTGACTAACATGAAGCGCTTCTATGCGTACACGCTGCTGCCAGCAGAGGTGAGATTCTGAAATCTAGTGCAAAATCACAAGCAAAGAAGTGTTGTTTTTCAGAAAAAAAATAAATAAATAAATCTGAAAATTCTTACAACAACATGAGTTTAGTCAATTAATAATTTCAGAATGTCTACATTTATGAGTCTTTAAACTAATTCTGATTCTAATTATTTATTCATTCATTAATGTTCTTGTCGACGTAGTCCCTTTATTAATCCGGGATCGCCACAGCGGAATGAACCGTCAACTTATCCAGCACATTTTTTACGCAGCGGATGTCTTTCCAGCAGCGACCCATCTCCGGGGT
Associated Phenotype:
Not determined