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