ZMP
si:ch73-193m8.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
MGAT4C
Human Description:
mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme C (putative) [S
Mouse Orthologue:
Mgat4c
Mouse Description:
mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme C (putative) Ge
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15529 | Essential Splice Site | Available for shipment | Available now |
sa14085 | Essential Splice Site | Available for shipment | Available now |
sa23268 | Nonsense | Available for shipment | Available now |
sa43072 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15529
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113715 | Essential Splice Site | 6 | 478 | None | 4 |
ENSDART00000143744 | None | None | 477 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 16050984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16402750 |
GRCz11 | 18 | 16391816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGTATTTTTTTANNTNCTGTTTTCTGCCAGATYACACCAGAATTGTTTCC[A/T]TCATGAGACTGGTGTTAAAGTACCTGGAWAAGATGAGGTGTTTCCGAAAA
Long Flanking Sequence:
AATCCAAACAATTTTGACACTTTTTGTTCTGCTTTTTACTTGAAGTTTTAGTTCAGATCAGTTGATCTATCCATCTACCCATCCTAGCTTTTTAAACTGTATTTTCAGCTTAATTTTCTGCTTATAAACAGTCAATTCCTGCATCTATCCATAAACTGTTTTTTCACTTGCCTTTCCATTGTATAATGATAGTTACAGCATGCTTATTTCTTCCCTGTCTTCATCTTCAAATTGCAGCTCTGCATCAAATCAAATTGAGGAACTTGGCTAGTTTCTCATTTCAGCTGTAAAACTTTGACTTCACTTCTTCTACCGCAGTAATTTTCTGTCTCAGGTCACACTTTTGTTTTTTTATTTTGAATGTCACAATTATATCGAGCTCAAAAAAGCATAGCGGGGTCCGTGCTCAGACCATCATCTGTCAAACTTAACACTAATGATACATCCTGATGCAGTATTTTTTTATCTGTTTTCTGCCAGATCACACCAGAATTGTTTCC[A/T]TCATGAGACTGGTGTTAAAGTACCTGGATAAGATGAGGTGTTTCCGAAAACGGTCCACCATTCCTTTCCTGGTGGCTCTCATTACCTTCCTGCTCTTCATAAACCTCTACATCGAGGACGGCTACGTGCTGGTGAGTGTGTTTACCTGTTGCGATCCAGCAGGTAAATTACAAAGGTCAATTTATTTACAACATCACTGGAGCAGATAACAAGACAATAGTGGGCTTCACAACAACTTGACTACTGCTGTTTGTGTGTGAGTTAGCATTAATTATCTCTGTGCTGAAAAGTTATTTTGTTTATATGCTTTAATTACCAAATGTTGCGTGTAAGGCTGCCGGTGATGTGTTGCGCATGTATAATTATCGGAGCTCACGATGCAGCCTATTTAAAATTGCATGATGTAGAGGCAGTCCAAATGCAAGAGACTCATTTATTATTCATGAGGCCAACTTTATGATCAAAACTTTGTGATCATAACATGTCGCGTGTGTTTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14085
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113715 | Essential Splice Site | 50 | 478 | 3 | 4 |
ENSDART00000143744 | Essential Splice Site | 44 | 477 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 16050068)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16401834 |
GRCz11 | 18 | 16390900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCTCAAAGCTTATGCTGCGATCTGTCTGWCTTGAATGTCATGTGTTTC[A/C]GGARGAAGATAAACGTCAGCTGCGAGAAACCTCAATGCATCCKCTGAACT
Long Flanking Sequence:
CAAATGCAAGAGACTCATTTATTATTCATGAGGCCAACTTTATGATCAAAACTTTGTGATCATAACATGTCGCGTGTGTTTGTCTGTTGAATTATTCAAAAGTTGTACCCGTTTTGACTGAGTCCCTTTTCTAAATAACCCCCATTTAATTGAAATACAAACACCATCACAGACAGAAAAAGTGTGAACAGTTCATGTGTGGTTAAAAAGACATTGAGGTATATTAACGATGCTATCATTTAATACTAGATAAGTTGTGTGAGTAATATTGTGTGTACAATTAATTATTCAAAGGCCGTCATTTAGATTTAATGAGATTATACAAGAGTGTGCAGGAAAATTGGCAAATCTAAAAATAATGACCTGCAGCGCTTACACTTAAAGATGCAAGAGGAGTCTTAGCATCTCATGTACATATAATCCTGTATTAGAAAACTCTTTCTAGCTTTGAGGCTCAAAGCTTATGCTGCGATCTGTCTGTCTTGAATGTCATGTGTTTC[A/C]GGAGGAAGATAAACGTCAGCTGCGAGAAACCTCAATGCATCCGCTGAACTCAGAGCGATATGTTCACACCTTTAAAGACATCACCAATTTTTCTGGAACAATCAATGTGACTTATCGGTACCTCGCAGGAACACCTTTACCCAGAAAGAGTAAGACTGCATTTGCTTTTTTATTTTGATATTTGCCACATACACATGCTGTCAACGATTTCTAAACAAGCAGTAGAAAATACAGCTGCAAAAAACATGTTTTATGATCTAGCATTTAAATAGATCCCAGTGTTTTTCATCACTAATTATTTTTAGATATTTTGATAAGCACAGGTTAGAATAAGTTGTGGCTGAAAGCTGATTTTTTTTTACAAATCCTATTTGAAACATTACGGTAGCCACTACATGTGATGTGCATGTGTTCACAAAAATAAAATGTTTTAAATATAATCTGATGCAGACACCAAAATGGTATTTTTTACCTACACTCACCGGCTACTTTATTAGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23268
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113715 | Nonsense | 159 | 478 | 4 | 4 |
ENSDART00000143744 | Nonsense | 153 | 477 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 16047890)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16399656 |
GRCz11 | 18 | 16388722 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATTTCGACCTTGCGTGGTGTGAAAGCCTAGTTCAAGAAATCTCCAGA[A/T]AGTTCGGCCACCATATCATTGCGGGACGGCTGCTTGTAATCCATGCACCT
Long Flanking Sequence:
AGGCATCTTGTTGTTAGAATATTTATATATAATTTTCACTGGGAAAATATGTTTAAAGGGAAGTATAAATTAAGAATGTACAATTAAAAGCAAAAAAATAGATAAATCTTCCTCCGTATTTGTTTTATTTTCTGGTACATTAAACATTCGTAAATCAAAATACTGGCACCTGTGAAGCTCATGTGTATTTTCTGTAAGGGCTTGCTTTTCAAACAGATTTAAAGATTTTTCTGTGTTTGTACTGGATTGTATTCACCTTATAGACAATGTGTCAAATCAATAGCATTCGCTTGCTCAATGATTTCCTGTGCTCTTTTGCAGAGTATCTCACCATTGGATTGTCATCTGTGAAAAGAAAGCGAGGAAATTACCTGTTGGAGACCATTAAGTCTATTTTTGACCAGTCAAGCTATGAGGAGCTCAAAGAGATCATTGTTGTTGTCCACCTGGCAGATTTCGACCTTGCGTGGTGTGAAAGCCTAGTTCAAGAAATCTCCAGA[A/T]AGTTCGGCCACCATATCATTGCGGGACGGCTGCTTGTAATCCATGCACCTGAGGAGTACTACCCATCCCTGGATGGTTTGAAGAGAAATTACAATGATCCTGAGGATAGAGTTCGCTTCAGGTCCAAACAAAACGTAGATTATGCCTTTCTGCTCAACTTCTGCACCAATCTATCAGACTTCTACATGATGCTGGAGGACGATGTGCGCTGCTCCCGAAACTTCCTCACCGCCCTAAAGAAAGTTGTGGCGTCCCGGGAGGGTTCATACTGGGTGATGCTGGAGTTCTCCAAACTGGGCTACATAGGAAAGCTGTACCACTCACGAGACCTTCCCAGACTTGCTCATTTTCTGCTCATGTTCTATCAGGAGATGCCTTGCGATTGGCTTCTTATCCATTTCAGAGGCCTCCTGGCCCAGAAGGATGCCATTCGCTTCAAGCCTTCGCTTTTCCAACACATGGGCTACTATTCCTCGTATAAGGGGGCAGAGAACAAACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43072
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113715 | Nonsense | 249 | 478 | 4 | 4 |
ENSDART00000143744 | Nonsense | 243 | 477 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 18 (position 16047618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 16399384 |
GRCz11 | 18 | 16388450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTCACCGCCCTAAAGAAAGTTGTGGCGTCCCGGGAGGGTTCATACTG[G/A]GTGATGCTGGAGTTCTCCAAACTGGGCTACATAGGAAAGCTGTACCACTC
Long Flanking Sequence:
CAAATCAATAGCATTCGCTTGCTCAATGATTTCCTGTGCTCTTTTGCAGAGTATCTCACCATTGGATTGTCATCTGTGAAAAGAAAGCGAGGAAATTACCTGTTGGAGACCATTAAGTCTATTTTTGACCAGTCAAGCTATGAGGAGCTCAAAGAGATCATTGTTGTTGTCCACCTGGCAGATTTCGACCTTGCGTGGTGTGAAAGCCTAGTTCAAGAAATCTCCAGAAAGTTCGGCCACCATATCATTGCGGGACGGCTGCTTGTAATCCATGCACCTGAGGAGTACTACCCATCCCTGGATGGTTTGAAGAGAAATTACAATGATCCTGAGGATAGAGTTCGCTTCAGGTCCAAACAAAACGTAGATTATGCCTTTCTGCTCAACTTCTGCACCAATCTATCAGACTTCTACATGATGCTGGAGGACGATGTGCGCTGCTCCCGAAACTTCCTCACCGCCCTAAAGAAAGTTGTGGCGTCCCGGGAGGGTTCATACTG[G/A]GTGATGCTGGAGTTCTCCAAACTGGGCTACATAGGAAAGCTGTACCACTCACGAGACCTTCCCAGACTTGCTCATTTTCTGCTCATGTTCTATCAGGAGATGCCTTGCGATTGGCTTCTTATCCATTTCAGAGGCCTCCTGGCCCAGAAGGATGCCATTCGCTTCAAGCCTTCGCTTTTCCAACACATGGGCTACTATTCCTCGTATAAGGGGGCAGAGAACAAACTCAAGGACGATGACTTCGAGGAAGACTCCCTCGATATCCCAGACAACCCACCTGCTAGTTTGTACACAAACATAAATGTATTTGAGAGCTATGATGCTGCCAAAGCATACAGTAGCGTGGACGAGTACTTTTGGGGCAAGGCACCGTCCACCGGGGACTTTTATGTTATAGTATTCAACAAGGCGACAAAAATCAGTAAAATCAAGATCATCACGGGAACCGATGATCGCCAGAATGATATTCTGCATCATGGAGCTTTGGAAGTTGGAGAGAA
Associated Phenotype:
Not determined