ZMP
zgc:112079
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized glycosyltransferase AGO61 [Source:UniProtKB/Swiss-Prot;Acc:Q5NDE5]
Human Orthologue:
C3orf39
Human Description:
chromosome 3 open reading frame 39 [Source:HGNC Symbol;Acc:25902]
Mouse Orthologue:
C85492
Mouse Description:
expressed sequence C85492 Gene [Source:MGI Symbol;Acc:MGI:2143424]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36041 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25003 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa11424 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36041
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010739 | Essential Splice Site | 47 | 578 | 2 | 3 |
| ENSDART00000125642 | Essential Splice Site | 54 | 585 | 1 | 2 |
| ENSDART00000139432 | Essential Splice Site | 54 | 585 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 9459226)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 8245165 |
| GRCz11 | 16 | 8158894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGGAAGAGGAGCTACAGCTTACACGCCAGTCACAAGAATTTTCACAG[G/T]TGCACAGGGTTATGATAACTTTGCTTGTTGAGATTAATTGTGAAGGCTTT
Long Flanking Sequence:
CTTCAACTGTATGTGACAAAATGGGTCTGATTTTTCTTTTCATTTTAAATAAGAAGGTGGCATTGAAGATGAATCCAAAGAATTTTGATGAACCTTTGAGGGAGGCCATAATGCTTAAGTGGCCCTCTAAAAATTAAAAACCTTTACATGAAACTGTCTTATCAGAAGGATTCACATTAATTAATGCCCTTCTTGCTACTTCTTGCCCCCAGTGTTTATACTGTAATGTATGTTAATGATGAATTAGTGTTAGCAATGCAAACACAAACCTTCTTGTTGATCTTGGTTTTCTGACTGTTTCAGGTGGAGCATGAGTGTGGGGTCGGAGTTCTGCTGTGATGCGTGCTATCGGGTGTAGGATGAACCTGCCGGCAGTGCTGAATGGCCTGCTGGTGTCAGTGGTGGCAGCCTTGCTTTGGAAATACGTTCGTCTGGTTGAACACACATCACAGCTGGAAGAGGAGCTACAGCTTACACGCCAGTCACAAGAATTTTCACAG[G/T]TGCACAGGGTTATGATAACTTTGCTTGTTGAGATTAATTGTGAAGGCTTTTATCGCGATATAAAGTAAAATATAGCTGCAAAAAAGTCACTTTTGATAGGCATAATAAAAAAAGCTTGCTGTATTGTTCACATGCATAGAATAAACAAATGTTTTAACCTAATTAAATTATGAAATGATGATATAATGGGTATAATCGGTAACACTTTTCAATACAGTATCATTAGTAAATGTTAGGTAATTGATTAAAATCAATAGTAAGTAAAATCTAATTTATTACCATTACTATGTTAATAGTTTAATAAAAATAAAAAAAGTTTTTTGTTATTAACACATTTAATTAAATGATCAGATTATGACTGAAATTTTAATCCACTATCGTATTAATGTATTAAGGTTTAATAAAAGCTTTTGTACTTTTCATTGTGAGTTTTGTTAAATTTGCTAATGTTTAATATAGGAGCGTCATTACACAGTGTTAAATAGTCTTAAATTAGCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25003
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 |
|---|---|---|---|---|---|
| ENSDART00000010739 | Nonsense | 372 | 578 | 3 | 3 |
| ENSDART00000125642 | Nonsense | 379 | 585 | 2 | 2 |
| ENSDART00000139432 | Nonsense | 379 | 585 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 9461561)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 8247500 |
| GRCz11 | 16 | 8161229 |
KASP Assay ID:
554-7697.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCGTGGTGCAGCTGTGGTCGAACTCTTCCCTTATGGTGTGAACCCGGAA[C/T]AGTACACTCCCTACAAAACCTTGGCCTCCTTACCTGGCATGGACTTACAG
Long Flanking Sequence:
ATCGCTTGCTAAGCAGCAAGCAACCACTTCTCAAGGACCAGTTGAAGACCTTCGGCAAGCTCATGTGCTTCACCAAGTCCTACGTAGGACTGTCAAAGATGACCACATGGTACCAGTATGGCTTTGTGCAACCCCAAGGACCCAAAGCCAACATTCTGATATCAGGTAACGAGATCCGTCAGTTTGCTTCATTTCTGATGGAGAGGCTGAACATCACAAGAGAGGAGGAGGAGGAGGATGATGACTACATTGTAGTTTTTAAACGTACCACGAACAGGCTCATCCTGAACGAGGCCGAGCTGCTTCTGGCTTTAGCTCAAGAGTTTCAGATGAGGACGGTCACTGTGTCTTTGGAGGAGCAGTCGTTTGATAACATCATCCAAATTATTAGCAGAGCAGCCATGCTGGTCAGCATGCACGGAGCCCAGATGATCACCTCCATGTTTTTGCCCCGTGGTGCAGCTGTGGTCGAACTCTTCCCTTATGGTGTGAACCCGGAA[C/T]AGTACACTCCCTACAAAACCTTGGCCTCCTTACCTGGCATGGACTTACAGTATGTTGCCTGGAGAAATACCATGGAAGAGAACACTGTCACTTTCCCTGACCGCCCTTGGGATCAGGGTGGCATCGTTCATTTGGAGAAGGAGGAGCAAGAACGTATCCTTGCCAGCAAGGAGGTGCCAAGACATCTTTGTTGTCGTAATCCAGAATGGCTTTTTCGCATTTACCAGGACACCACTGTAGATCTTGCCTCTTTCCTGGACGTACTCAGAGATGGTCTGAAAAAGCTTAACCTCAAAAAGGCTAAGGTGGCTAGCACTGTACATCCCGGTCGAGTCCGAGAGCCCAAGTGCCAGACTTCAGTGCAGGCCACCAATGAAGCAAAGCTCTCGGTTTCATGGCAGATCCCTTGGAACCTGAAGTACCTGAAGGTCAAAGAGGTGAAATATGAGGTGTGGATCCAGGAACAGGGAGAGAACACGTATATGCCTTACATTCTGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11424
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000010739 | Nonsense | 532 | 578 | 3 | 3 |
| ENSDART00000125642 | Nonsense | 539 | 585 | 2 | 2 |
| ENSDART00000139432 | Nonsense | 539 | 585 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 16 (position 9462043)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 8247982 |
| GRCz11 | 16 | 8161711 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGAGGTGAAATATGAGGTGTGGATCCAGGAACAGGGAGAGAACACRTA[T/A]ATGCCTTACATTCTGCCCCACCARAACTACACCTTTTCAGAGAACATYAA
Long Flanking Sequence:
TATGGTGTGAACCCGGAACAGTACACTCCCTACAAAACCTTGGCCTCCTTACCTGGCATGGACTTACAGTATGTTGCCTGGAGAAATACCATGGAAGAGAACACTGTCACTTTCCCTGACCGCCCTTGGGATCAGGGTGGCATCGTTCATTTGGAGAAGGAGGAGCAAGAACGTATCCTTGCCAGCAAGGAGGTGCCAAGACATCTTTGTTGTCGTAATCCAGAATGGCTTTTTCGCATTTACCAGGACACCACTGTAGATCTTGCCTCTTTCCTGGACGTACTCAGAGATGGTCTGAAAAAGCTTAACCTCAAAAAGGCTAAGGTGGCTAGCACTGTACATCCCGGTCGAGTCCGAGAGCCCAAGTGCCAGACTTCAGTGCAGGCCACCAATGAAGCAAAGCTCTCGGTTTCATGGCAGATCCCTTGGAACCTGAAGTACCTGAAGGTCAAAGAGGTGAAATATGAGGTGTGGATCCAGGAACAGGGAGAGAACACGTA[T/A]ATGCCTTACATTCTGCCCCACCAGAACTACACCTTTTCAGAGAACATCAAACCATTCACCACGTATTTAGTGTGGGTGCGCTGCATCTTTAACAAGAACCTCTTGGGCCCATTTGCAGATGTTCTTATATGTAAAACTTGATTCAGCAATCCGGTTAAATGTACCACTACATTGTAGTCAGCTAGTGGAGAATTAATTGGAAGGTTCGTTCTCAGGAGCTGTCCTGAAATTGACATGATGTGACACGGGTGAATTGTTTCTTTGAACCTTGATTGTCGCTGATTGCTCTTCGTGGTACTTGTGGAGTGTCACGAACTAATTGAGAATCATGACCGCGGTGAAGGCTGGCCATGAATGCAGTTTTCAGAACTGCTAGACCTTTTAATACATCACAGTTCAAGCAAAGTTCTTAACTTTATTTATCAGAAATGTATTGCATAACTTAAATTCGTATTTATAAGTCCAAGACACTGGTTTTGTCGACACCTGTTTCTGTTAAC
Associated Phenotype:
Not determined