ZMP
glt25d2
Ensembl ID:
ZFIN ID:
Description:
procollagen galactosyltransferase 2 [Source:RefSeq peptide;Acc:NP_001123548]
Human Orthologue:
GLT25D2
Human Description:
glycosyltransferase 25 domain containing 2 [Source:HGNC Symbol;Acc:16790]
Mouse Orthologue:
Glt25d2
Mouse Description:
glycosyltransferase 25 domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2138232]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34369 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38683 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21257 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34369
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014183 | Nonsense | 385 | 613 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 19893746)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19338384 |
GRCz11 | 8 | 19368801 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAACACATCTCAGCTTCAAGCTCTTGGTATAGAAATGATGCCAGGGTA[T/G]AAAGATCCGTATTCTGGTCGAGTTTTGACACGTGGAGAGATCGGCTGTTT
Long Flanking Sequence:
ATTTCAAATGTCTTTTCTTGCAGTCGATCATAACATAAAACCCTCCGAGTTCCTCTTCACTCCAAGCAAACCTCAGGACAAGATGAGCTTTGATGAGGTGAGAGAGCAGAATCTCTGGAATGTCTTGCATGACTGGAGACTCATGATAGCAGAAACTCAAAGCTACTTCAAAGTGACATTTCGTCTCGATTTGTTCCTCCAATGCTCTTGTTCTTTTATTTCACCTCAGATCTTCTTGATTAATCTGAAGCGGAGGTTCGACCGAAGGGAACGGATGTTGAACACTATGGCAGTTCTGGGTCTTGAGGCGACGCTGGTTGATGCCGTCGATGGGAAGTAGGTCATCAAATGGACAATTTGTGGCATCCTGTTTATTTTGGGGTTTTTTGAAATGTGTCAGAACTGGTCATGTGAAAGCGCTTCAGACTTTGTTTGTTTACTCTCAGGACTTTGAACACATCTCAGCTTCAAGCTCTTGGTATAGAAATGATGCCAGGGTA[T/G]AAAGATCCGTATTCTGGTCGAGTTTTGACACGTGGAGAGATCGGCTGTTTCCTCAGTCACCACTTCACCTGGAAACAGGTACACACACACTCATGAATAGATATGCTGCACTTTACATTAAAAATGGCTGACTCTAAATAACTCTAAATATTTTAGAATCTCTGTGTAAAACTATTTAACACATCTAATGTATCTAATTATCACAACACAGTTTTAAATGTTTACAGATAATGGTTTAAAAAGTGGACTGAATAGTTTAAATTATCTTTACCTATTGGGTTTTACAGTGTAGCATCTGTTTTATTAAAGTTTTAGTAGTTTTACTAAAGATATAATTTATTAATTTAATTTAAATGTATCAAATGGAACTGACATTTCAAAACTCAAATTATGCTCAACATATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTAATTATATATTATTTTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38683
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014183 | Nonsense | 401 | 613 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 19893698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19338336 |
GRCz11 | 8 | 19368753 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATAAAGATCCGTATTCTGGTCGAGTTTTGACACGTGGAGAGATCGGCTG[T/A]TTCCTCAGTCACCACTTCACCTGGAAACAGGTACACACACACTCATGAAT
Long Flanking Sequence:
GTTCCTCTTCACTCCAAGCAAACCTCAGGACAAGATGAGCTTTGATGAGGTGAGAGAGCAGAATCTCTGGAATGTCTTGCATGACTGGAGACTCATGATAGCAGAAACTCAAAGCTACTTCAAAGTGACATTTCGTCTCGATTTGTTCCTCCAATGCTCTTGTTCTTTTATTTCACCTCAGATCTTCTTGATTAATCTGAAGCGGAGGTTCGACCGAAGGGAACGGATGTTGAACACTATGGCAGTTCTGGGTCTTGAGGCGACGCTGGTTGATGCCGTCGATGGGAAGTAGGTCATCAAATGGACAATTTGTGGCATCCTGTTTATTTTGGGGTTTTTTGAAATGTGTCAGAACTGGTCATGTGAAAGCGCTTCAGACTTTGTTTGTTTACTCTCAGGACTTTGAACACATCTCAGCTTCAAGCTCTTGGTATAGAAATGATGCCAGGGTATAAAGATCCGTATTCTGGTCGAGTTTTGACACGTGGAGAGATCGGCTG[T/A]TTCCTCAGTCACCACTTCACCTGGAAACAGGTACACACACACTCATGAATAGATATGCTGCACTTTACATTAAAAATGGCTGACTCTAAATAACTCTAAATATTTTAGAATCTCTGTGTAAAACTATTTAACACATCTAATGTATCTAATTATCACAACACAGTTTTAAATGTTTACAGATAATGGTTTAAAAAGTGGACTGAATAGTTTAAATTATCTTTACCTATTGGGTTTTACAGTGTAGCATCTGTTTTATTAAAGTTTTAGTAGTTTTACTAAAGATATAATTTATTAATTTAATTTAAATGTATCAAATGGAACTGACATTTCAAAACTCAAATTATGCTCAACATATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTAATTATATATTATTTTATATTAGTAAATTGGTTTCTTCAAATGGTTTTGAGTTTACTTTGGTTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21257
Status:
Available for shipment
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:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014183 | Essential Splice Site | 411 | 613 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 8 (position 19893666)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19338304 |
GRCz11 | 8 | 19368721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGTGGAGAGATCGGCTGTTTCCTCAGTCACCACTTCACCTGGAAACAGG[T/C]ACACACACACTCATGAATAGATATGCTGCACTTTACATTAAAAATGGCTG
Long Flanking Sequence:
AGATGAGCTTTGATGAGGTGAGAGAGCAGAATCTCTGGAATGTCTTGCATGACTGGAGACTCATGATAGCAGAAACTCAAAGCTACTTCAAAGTGACATTTCGTCTCGATTTGTTCCTCCAATGCTCTTGTTCTTTTATTTCACCTCAGATCTTCTTGATTAATCTGAAGCGGAGGTTCGACCGAAGGGAACGGATGTTGAACACTATGGCAGTTCTGGGTCTTGAGGCGACGCTGGTTGATGCCGTCGATGGGAAGTAGGTCATCAAATGGACAATTTGTGGCATCCTGTTTATTTTGGGGTTTTTTGAAATGTGTCAGAACTGGTCATGTGAAAGCGCTTCAGACTTTGTTTGTTTACTCTCAGGACTTTGAACACATCTCAGCTTCAAGCTCTTGGTATAGAAATGATGCCAGGGTATAAAGATCCGTATTCTGGTCGAGTTTTGACACGTGGAGAGATCGGCTGTTTCCTCAGTCACCACTTCACCTGGAAACAGG[T/C]ACACACACACTCATGAATAGATATGCTGCACTTTACATTAAAAATGGCTGACTCTAAATAACTCTAAATATTTTAGAATCTCTGTGTAAAACTATTTAACACATCTAATGTATCTAATTATCACAACACAGTTTTAAATGTTTACAGATAATGGTTTAAAAAGTGGACTGAATAGTTTAAATTATCTTTACCTATTGGGTTTTACAGTGTAGCATCTGTTTTATTAAAGTTTTAGTAGTTTTACTAAAGATATAATTTATTAATTTAATTTAAATGTATCAAATGGAACTGACATTTCAAAACTCAAATTATGCTCAACATATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTAATTATATATTATTTTATATTAGTAAATTGGTTTCTTCAAATGGTTTTGAGTTTACTTTGGTTTTGAAGTGTACTGACCACATTCTAATACATTTTATC
Associated Phenotype:
Not determined