ZMP
GLT25D1 (2 of 3)
Ensembl ID:
Description:
glycosyltransferase 25 domain containing 1 [Source:HGNC Symbol;Acc:26182]
Human Orthologue:
GLT25D1
Human Description:
glycosyltransferase 25 domain containing 1 [Source:HGNC Symbol;Acc:26182]
Mouse Orthologue:
Glt25d1
Mouse Description:
glycosyltransferase 25 domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1924348]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa8744 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39726 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8744
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113371 | Essential Splice Site | 21 | 479 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 58384610)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 57285187 |
| GRCz11 | 1 | 58020869 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGAACATTCAGTGATGAATNNGTTTAAATAAGCTGACTATSTGTGTTGTA[G/A]TTGGTGGACTGTGATAACCTGCTGACCAATCGTGATGTGYTGTGGAAATT
Long Flanking Sequence:
GGACATCTTTGGATGTAAACGCAGCTAGTGGTGACCCAAACTGACCTGCGTCAGCTCTCAGTGTACTGACCGATGCGGTGATCTTCAGTTATTTCTGTGAGTGTTTATTTCTGCTGGTCTGTGATCAGCTCAATCCTCTGTCCAGCGGCTCTCGACTGTGTGTTTAACTCAAATGTCCAGTTAAACACAGTTTCTGCTGAGCCACCGGTGAATCAAACCAAACTCTGGCCGTGTAAATCATGTTTAAAACCGATTTATAAATATCCACACTGTGTTTTTACTTTCATAGCACTCATTCATTACATTGGCCACGTTTTTTTCCTCTTTCTTAGTTCAAAACGATCAAGCTTGTTTAAATGAAGTGAATGCGATTGTAAATTAAGGATCTAACCATGTAAATGAGATGTTAAATTAGCCACAGAATTGTTTTACACTTATTGAATGAAATCCCATGAACATTCAGTGATGAATGTTTAAATAAGCTGACTATGTGTGTTGTA[G/A]TTGGTGGACTGTGATAACCTGCTGACCAATCGTGATGTGCTGTGGAAATTAATGCGGGAAAACAAGACGATCGTGGCGCCGATGCTGGAATCCAGAGCGGCGTACTCCAACTTCTGGTGCGGCATGACGTCTCAGGTACTGCCAACATTAGAGAATTCGATAATATTTGCAGTAATGTTTACTTTTTTACATTTGCATTTTTTAAATAAGAAATAAAAATGTTGATTTTTATTATTTAAGCTGCACTTTTTACTCTTTAAGCTGTGAAATATTGAATTCAAGCTTATTTGTATATCGCTTATCACAATAATTATTGTTCAAATATACATTTTATAGATCTGAAAGGGTGTACAAATGGTACACTGAATTGTTGTGTGCTTTAAAACATTAAATATGCATGTTAATAGTAACCATTTTTATTATGAATATTAACCATTGTTTGTTTCATCTCTATTTGCTTTCATAAATTGTACTTTGTTAATGCTAATGGCTACATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39726
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113371 | Nonsense | 449 | 479 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 58378621)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 57279244 |
| GRCz11 | 1 | 58014926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTCTGGGACAACGAGAGCGTGCTGACCGACTGGGACAGAGCGCGCTCA[C/T]GAAAGAGCCGCGAGCAGGAGGAGCTGAGCAGCGAAGCCCAGAACACTGAC
Long Flanking Sequence:
GTACAACAAACACCCCATGTAAGACACACAAACACTTCTGCTTGAGTTGACTGAAGTCAAAATTATTAGCCTTTTTTTTAAGCATTTCCCAAATGATATTTAACAGATAACATTTATTTTATTTTATTTTATTTTTATTTCACAGTAATATTTTGTCTTCTGCAGAAAGTCATATTTCGGCTAGAATAAAAGGTCAATATTATTAGCCTCCTTAAGCAATATTTGTGTTTGATTGTCTACAGAACAAACCACTACCACATCATGTAATATTGTACATTACTGCATGTTCAGCATCTCTATCTAATGTTGTGTGTTCTCCGTCTCGCAGTGAGGAGTACATGTCTCATTTCCCACAGCGGGACCTGCGGGCCTTCTCTGCGGAGCCACTGCTGATATACCCTACACACTACACAGGAGACCAGGGCTACATCAGCGACACAGAGACCTCCAGCGTCTGGGACAACGAGAGCGTGCTGACCGACTGGGACAGAGCGCGCTCA[C/T]GAAAGAGCCGCGAGCAGGAGGAGCTGAGCAGCGAAGCCCAGAACACTGACGTCCTGCAGTCACCGCTCGACAGCACAGCCAGAGACGAGCTCTAGAGCCATAGGATATATAGACACAGAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACCTCTAGAGCCCAGAAATACACAGACACGCAACTACAGAGACC
Associated Phenotype:
Not determined