ZMP
mfng
Ensembl ID:
ZFIN ID:
Description:
Beta-1,3-N-acetylglucosaminyltransferase manic fringe [Source:UniProtKB/Swiss-Prot;Acc:Q5YB40]
Human Orthologue:
MFNG
Human Description:
MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Source:HGNC Symbol;Acc:7038]
Mouse Orthologue:
Mfng
Mouse Description:
MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase Gene [Source:MGI Symbol;Acc:MGI:1095404
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24114 | Nonsense | Available for shipment | Available now |
sa10647 | Essential Splice Site | Available for shipment | Available now |
sa37469 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24114
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 |
---|---|---|---|---|---|
ENSDART00000063008 | Nonsense | 139 | 360 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 15409909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15237918 |
GRCz11 | 22 | 15264301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCATGTGTGTTTTTGTCAACAGGTTTTAACGTTGTCGTCACTAATTG[T/A]TCACCTGAGCACAGTCATCAAGCATTATCCTGCAAGATGGCTGCTGAGTA
Long Flanking Sequence:
GGTCTGCTACAATTATGCTAGCAATATAAAGTTTGTTGAAGTTTTATTATATGTACTGATACTGTATACTTCTTTAGTGTCAACCCCATTATCTCAGCGTTTTTAGACAGAAACTCTTGAGAGCTGAACCACCTTGAGACAAGTTTAGTAATTACAGTACAGCTTCTCTGCAAAGGTAAATGCAGAGCACAGTTGCTCTGAGGCCTTCTTGAGCACCAGCTGTTGTCTCACAGTGGTGCATGATGGGAATTTGGATGTTACTTACCCTCGTAAGAGCATCAAATTTTCATTTCAGATTGAACATGCAGGTTTTGCCTCATTAATTTGTGGTTTTCCTCTTTCAGACGTACATCTTTACAGATAGTCCAGACGCAGACATTTCTTCAGAAGGTAGATATTTGTTCTTCTAAAGAACTAGTCTGAAACTCATGATTCTTGAGTGCTTTACACTCACCATGTGTGTTTTTGTCAACAGGTTTTAACGTTGTCGTCACTAATTG[T/A]TCACCTGAGCACAGTCATCAAGCATTATCCTGCAAGATGGCTGCTGAGTATGACTACTTCATGGCCTCCTACAAAAAGTGAGTAAGCTAATGGTGCTATTAATTTTCTCAAGATTTTGAATGTTCGGCAACACTGGTTTAAGAAGCAATCCCTACTATTAACTACTGGCTTATTACCTGCTTATTAATATTGGCCCATTTCCACTAAGTGGTAACCTATGGTACATGTCACCTTGATCAGGCTTGCATTTCCACTACCAAAAGCATACGCAGACACACGCTGCCACTTCAATAATCACACGCATGTTATTATCATCAGCTCAAGAAGTTTGTTATTTCAAATATAAACTCACACGCAAGCTCTCTCTCAAGAAAGTGTAACCGCTCACGGTTTGTAAACAACTACTGGGCACACGGTAGATTCTGCTCTTCTTCATGGCTTTGTGGCTGTTTATCAAGAAGACAAGGTTTGTTTAAGCTCGGGTCGACCATTGATCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10647
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063008 | Essential Splice Site | 165 | 360 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 15409831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15237840 |
GRCz11 | 22 | 15264223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTGCAAGATGGCTGCTGAGTATGACTACTTCATGGCCTCCTACAAAAA[G/A]TGAGTAAGCTAATGGTGCTAWWAWTTTTCTCAAGATTTTGAATGTTCGGC
Long Flanking Sequence:
GTCAACCCCATTATCTCAGCGTTTTTAGACAGAAACTCTTGAGAGCTGAACCACCTTGAGACAAGTTTAGTAATTACAGTACAGCTTCTCTGCAAAGGTAAATGCAGAGCACAGTTGCTCTGAGGCCTTCTTGAGCACCAGCTGTTGTCTCACAGTGGTGCATGATGGGAATTTGGATGTTACTTACCCTCGTAAGAGCATCAAATTTTCATTTCAGATTGAACATGCAGGTTTTGCCTCATTAATTTGTGGTTTTCCTCTTTCAGACGTACATCTTTACAGATAGTCCAGACGCAGACATTTCTTCAGAAGGTAGATATTTGTTCTTCTAAAGAACTAGTCTGAAACTCATGATTCTTGAGTGCTTTACACTCACCATGTGTGTTTTTGTCAACAGGTTTTAACGTTGTCGTCACTAATTGTTCACCTGAGCACAGTCATCAAGCATTATCCTGCAAGATGGCTGCTGAGTATGACTACTTCATGGCCTCCTACAAAAA[G/A]TGAGTAAGCTAATGGTGCTATTAATTTTCTCAAGATTTTGAATGTTCGGCAACACTGGTTTAAGAAGCAATCCCTACTATTAACTACTGGCTTATTACCTGCTTATTAATATTGGCCCATTTCCACTAAGTGGTAACCTATGGTACATGTCACCTTGATCAGGCTTGCATTTCCACTACCAAAAGCATACGCAGACACACGCTGCCACTTCAATAATCACACGCATGTTATTATCATCAGCTCAAGAAGTTTGTTATTTCAAATATAAACTCACACGCAAGCTCTCTCTCAAGAAAGTGTAACCGCTCACGGTTTGTAAACAACTACTGGGCACACGGTAGATTCTGCTCTTCTTCATGGCTTTGTGGCTGTTTATCAAGAAGACAAGGTTTGTTTAAGCTCGGGTCGACCATTGATCTTTATTATATGTATACATAATTTTGATACAATGTCACGGCCCTGTATTTAAAATGGCACTTTCTTTGTTTTCATTCTCCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37469
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 |
---|---|---|---|---|---|
ENSDART00000063008 | Nonsense | 262 | 360 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 22 (position 15402721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 15230730 |
GRCz11 | 22 | 15257113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCCCAGGTTTGAACAAACATCTGCTGTGATAATGTTGCCTGATGACTG[T/A]ACCGTGGGTTTTATAGTTGAGAGGCGACTGGGCATCTCGATGATCCATAG
Long Flanking Sequence:
TCTTGCTTTAGGCGAGGGTTTTACTCACAATGTCAGCGAGTCTACACATGTACCACTATTGCACTCTGACCGACTGAACTTCAGATCGGCCATTAATCACTCTGCACATAATTGTTTTAGGACTTGATACTTATAATTTGAATAACTATATAAAATGTATATTCAGAGCCACTGCATGACTGCCACTCAATATGCTAAGGTTAAAGTACGCTTTCTTTTGTTCTGTTGCAGAGGGATGTCCATTTCTGGTTTGCTACAGGAGGGGCTGGTTTCTGCCTGAGCAGGAACCTGGCAGAAAGGATGGCACCCTGGGCAAGGTGAGGTCCTGATTCAGCATTTGATTCTGAAGCAATTTCACGCATATGTTAGTACATGTGCCCTCATCACGAAAGGCATTTTGGTGGTTTCTACAAGTCATAAATTCAGAATATGTTTACCTCTATTTGCAGTGGTCCCAGGTTTGAACAAACATCTGCTGTGATAATGTTGCCTGATGACTG[T/A]ACCGTGGGTTTTATAGTTGAGAGGCGACTGGGCATCTCGATGATCCATAGCAATATGTTTCACTCTCATTTAGAAAACCTACTCCTTCTGTCCCCCAGCGATATTCCAAAACAGGTGAGATGGTTGCAATTTTTACCTTATTTTTTGTTGGTTATTAGTATTAGTGCTTATATTCAAGTTAGTTAGATAGTTTAGACCAATCTAATTGTTAAAAAAGAGATTTGAATTATAATTCCCAAGGTATTTTTTGACTTAAGCTAATAAGCAACCAGCTAGAAATGCCATATCAACCACCTAGGATACCTTCAACAACCCAGCTAGCAACCAATAGTAAAATACTTCGCCAAACACCTAGCAAAGTGCTAGCAATCAGTTGATCAGGCAAGAAATGTCTTTTAGCATACTGTAACTAGCACAACTGTTGAGAAGAATAATGTTTTTTTATTAATAAGCAGTCACTTTAATTACTTTAGTTACCATTTAAAGCACATATCTTGAAA
Associated Phenotype:
Not determined