ZMP
MYT1L (2 of 2)
Ensembl ID:
Description:
myelin transcription factor 1-like [Source:HGNC Symbol;Acc:7623]
Human Orthologue:
MYT1L
Human Description:
myelin transcription factor 1-like [Source:HGNC Symbol;Acc:7623]
Mouse Orthologue:
Myt1l
Mouse Description:
myelin transcription factor 1-like Gene [Source:MGI Symbol;Acc:MGI:1100511]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1325 | Essential Splice Site | Available for shipment | Available now |
| sa43015 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa36540 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1325
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000047089 | Essential Splice Site | 49 | 721 | 1 | 29 |
| ENSDART00000047089 | Essential Splice Site | 49 | 721 | 1 | 29 |
Genomic Location (Zv9):
Chromosome 17 (position 51997429)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 51383175 |
| GRCz11 | 17 | 51472210 |
KASP Assay ID:
554-1239.1 (used for ordering genotyping assays)
KASP Sequence:
CCACCGCAGCCTGTCTGGATGTCCTCATAAAGAYAGAGTCCCRCCRGAAA[G/T]TAAGCCCTCGACACCGTCCCCGCAAACACCACATGAGCTGCTGCTGCCTT
Long Flanking Sequence:
GAGCCTCCAGTTGTCATTTTGTGTCCCCAAACAAATTCCCTGTGCAAAGGATCATGGGCGTCCGAAGTGTCCATCAGTTGTACCTTCAAAGTCAGTCATTCCGAAGAGCACTTTGAAGTGGCCAGTTCTGAGCACTTCAGTTTGGAACAACACTTCAATATGGCGGTCATGTTTGTTTCCAATCCAAAGTGCCCTACAGAGGGTGATAAATCCAGTTTAGAATGCGCCAATAGTCTGAAAGACTCTGAATAACTCATTCCTGAACAACTGAATCAGTGATAATCCAGTGTGTGTGCTCAGACTGAGGACCGTTTCTAAACAAATGGACTAGTGATAATCCTGTGTGTGTTTTTATATGCGTTTAGATTCGTCGCGGTCGGGGAAGAAGGAGAGCCGGTGTCCGACGCCAGGTTGTGACGGCACAGGTCATGTTACTGGTCTGTACCCGCACCACCGCAGCCTGTCTGGATGTCCTCATAAAGATAGAGTCCCGCCGGAAA[G/T]TAAGCCCTCGACACCGTCCCCGCAAACACCACATGAGCTGCTGCTGCCTTCACATCTGTGCTGTTATTCTGCTGAATGTGTGTGTTGTGTGTGTGATCACCTGTTCATTCTGCATGCAAACATCTGCACGCTGATACAGTATGCAAAAGCTTGGAACGGTTCGAATGGTTGATAATCCAAGACATTGGTCACTTTGTGGTGATGTACTGCAGTATGGGGGATGTGGATTGGTCCTTATATATGCATCCCATACTTCATATATACATAAATAAATAAATATATATTTATATATATATATATATATATATATATATATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa43015
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 |
|---|---|---|---|---|---|
| ENSDART00000047089 | Essential Splice Site | 49 | 721 | 1 | 29 |
| ENSDART00000047089 | Essential Splice Site | 49 | 721 | 1 | 29 |
Genomic Location (Zv9):
Chromosome 17 (position 51997429)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 51383175 |
| GRCz11 | 17 | 51472210 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACCGCAGCCTGTCTGGATGTCCTCATAAAGATAGAGTCCCGCCGGAAA[G/A]TAAGCCCTCGACACCGTCCCCGCAAACACCACATGAGCTGCTGCTGCCTT
Long Flanking Sequence:
GAGCCTCCAGTTGTCATTTTGTGTCCCCAAACAAATTCCCTGTGCAAAGGATCATGGGCGTCCGAAGTGTCCATCAGTTGTACCTTCAAAGTCAGTCATTCCGAAGAGCACTTTGAAGTGGCCAGTTCTGAGCACTTCAGTTTGGAACAACACTTCAATATGGCGGTCATGTTTGTTTCCAATCCAAAGTGCCCTACAGAGGGTGATAAATCCAGTTTAGAATGCGCCAATAGTCTGAAAGACTCTGAATAACTCATTCCTGAACAACTGAATCAGTGATAATCCAGTGTGTGTGCTCAGACTGAGGACCGTTTCTAAACAAATGGACTAGTGATAATCCTGTGTGTGTTTTTATATGCGTTTAGATTCGTCGCGGTCGGGGAAGAAGGAGAGCCGGTGTCCGACGCCAGGTTGTGACGGCACAGGTCATGTTACTGGTCTGTACCCGCACCACCGCAGCCTGTCTGGATGTCCTCATAAAGATAGAGTCCCGCCGGAAA[G/A]TAAGCCCTCGACACCGTCCCCGCAAACACCACATGAGCTGCTGCTGCCTTCACATCTGTGCTGTTATTCTGCTGAATGTGTGTGTTGTGTGTGTGATCACCTGTTCATTCTGCATGCAAACATCTGCACGCTGATACAGTATGCAAAAGCTTGGAACGGTTCGAATGGTTGATAATCCAAGACATTGGTCACTTTGTGGTGATGTACTGCAGTATGGGGGATGTGGATTGGTCCTTATATATGCATCCCATACTTCATATATACATAAATAAATAAATATATATTTATATATATATATATATATATATATATATATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36540
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000047089 | Nonsense | 615 | 721 | 25 | 29 |
Genomic Location (Zv9):
Chromosome 17 (position 52032621)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 51418367 |
| GRCz11 | 17 | 51507402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGCAGATATTAAACAGCTGGATGAAGATATTAAGGGTTTAAATGAAT[C/A]AAATTCACAGGTGGAAGCAGATATGATCAAACTCCGAACACAGGTAAGGG
Long Flanking Sequence:
ATAAATCTAATTTACATCTAATTTACATCTAATTACAACAAAAGACATCTAATTTACATCTAATTTACATCTAATTACAACAAAATACATCTAGTTAACATCTAATTTACATCTAATTACAACAAAAGACATTTAATTGACATCCAGTTGTAAAAAGACATCTAACTGACATCTAATTATAACAAAAGACATCTAATAAACACCTAACTGACATCTAATTGTAAAAAGACATCTGACAGACATATTAATGTAAATAGAAAGTTTGTGTAAAAAATATTTAGAAATAGAATTTATTGCAAACAGACATTGAATGGAGTGACGTCAAGGGTCGCTGAACTGTTTATACACAACTACCACTATTACTTTTGTGTCTTTTTGTGTCGCGGTTCAAGCTGGATGTGATTTACTATATGAATTATGTCTGTTTGTTCTCTTTTTAGGTTTAGACTGTGATGCAGATATTAAACAGCTGGATGAAGATATTAAGGGTTTAAATGAAT[C/A]AAATTCACAGGTGGAAGCAGATATGATCAAACTCCGAACACAGGTAAGGGGATTTACACAATCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATACTGATCATGTCAAAGCAGCTTCACAGAAATCTTTCTGTTGACCACAATGTCTTTCTGTCTCCCAGATCACCACAATGGAGTCTAATCTGAAGTCCTTAGAGGAAGAAAACAAGTGACTGAACAGCACTTTGACAACAGTGACCACATCCATTTACTTATTATATCCAGCAGTCACATGCTAAGAGCCAAACAGCACCCGCACAAACAGCATATGATGCTTTAGTTCATGTGGAATAATTAAAAAATAAAGCCTATTCTTGATGATACACTGGCAAACTGTTGAGCAATGTTGTCGGGCAACTTTTGGAAATTATGCCATCAGTGCATAACTAAGTGACACACAGTGCAACTTATTAGGGAAACCG
Associated Phenotype:
Not determined