ZMP
myt1la
Ensembl ID:
ZFIN ID:
Description:
myelin transcription factor 1-like protein [Source:RefSeq peptide;Acc:NP_001038364]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11068 | Essential Splice Site | Available for shipment | Available now |
sa10388 | Essential Splice Site | Available for shipment | Available now |
sa23731 | Nonsense | Available for shipment | Available now |
sa37064 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11068
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 |
---|---|---|---|---|---|
ENSDART00000044397 | Essential Splice Site | 1 | 1257 | None | 22 |
ENSDART00000129169 | None | 1 | 1257 | None | 21 |
ENSDART00000131032 | Essential Splice Site | 1 | 539 | None | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 30516588)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30587801 |
GRCz11 | 20 | 30490680 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAGCTCAGCTAGTAGACTGAGGTCAGGCTAATTGCTGCTTCTTTTCTCC[A/T]GATGGAGGTGGATGCGGCAGAGAAGCGTCATCGAACACGATCTAAAGGTG
Long Flanking Sequence:
CATCAAACTGACATCATCACTCTAAACGCAGAAGCAAATGGTCGAACTTTTAAGATTTTCTAAAAAAAAATTTTTCAGTAGATTAAATTGTTTGTGTTCTTGATTAACTAATTGTATTAATTTTTCACCTAAAGTATAATAACGTGTGCTAGCAAAATAAACATTGTACATTTAATTTCTAACAGACTTTAATGAATCAAAGCCCTCTCAAAACTAGTTAAAGCTATGGCACTGAATAAGAAGGAACACAGATCTTCATACAGGAAAAAAAAGTGAGGCATTATAGCTGCATGTACAGCATGACCAATGTAATTATCCACGCTTCACAGACTGTATTTTTCCTAATAAACATATTCTTTTCTCATCTCTGATCTGCCTCCCGTGCAGTTCAGTGCAGTTCATAACCGTCTTTGCTGCAGACATCATTGCCCTTTTACACTTGCTTTTCCAGTAGCTCAGCTAGTAGACTGAGGTCAGGCTAATTGCTGCTTCTTTTCTCC[A/T]GATGGAGGTGGATGCGGCAGAGAAGCGTCATCGAACACGATCTAAAGGTGCGTGAGGTACAACGCACTCACATGGTATTGGCTGTATGCAGTCTCAACCTACTGTTAAATCCATTTCCCCACTTCAATCCATAACCCAGGCTTTTTATTGCCTTTCACCAATTATTACTGACGTCAGTAGTGATGAACACGGACTATTGATAGGGCAGGTGAAGCGGAATCTATGAGCCTGGAAAATTACACTGCACATAATGATATGATTCCATTGTGTGATGAAGCTCATGCTGAGATGTTTCCTCACTAATTGTTTTTGATTTCATTGTTTTGCAGTTGCCGTAGAGGCTGCACAGGAGCTATTCAGGTCAGTCTGCCTTTAATATTAGAATCATATTTTTACTTCAAAATACAATGCAACCGTCATGTATTTTTTAGTGTAGAGGGATATTTGGCTTAAAGGAAAAGGGTAAACTTTACAATGATGTTCCATTATGTTAAATGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10388
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044397 | Essential Splice Site | 26 | 1257 | 3 | 22 |
ENSDART00000129169 | Essential Splice Site | 26 | 1257 | 2 | 21 |
ENSDART00000131032 | Essential Splice Site | 26 | 539 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 30516950)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30588163 |
GRCz11 | 20 | 30491042 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATTTCATTGTTTTGCAGTTGCCGTAGAGGCTGCACAGGAGCTATTCAGG[T/G]CAGTCTGCCTTTAATATTAGAATCATATTTTTACTKCAAAATACAATGCA
Long Flanking Sequence:
CATCTCTGATCTGCCTCCCGTGCAGTTCAGTGCAGTTCATAACCGTCTTTGCTGCAGACATCATTGCCCTTTTACACTTGCTTTTCCAGTAGCTCAGCTAGTAGACTGAGGTCAGGCTAATTGCTGCTTCTTTTCTCCAGATGGAGGTGGATGCGGCAGAGAAGCGTCATCGAACACGATCTAAAGGTGCGTGAGGTACAACGCACTCACATGGTATTGGCTGTATGCAGTCTCAACCTACTGTTAAATCCATTTCCCCACTTCAATCCATAACCCAGGCTTTTTATTGCCTTTCACCAATTATTACTGACGTCAGTAGTGATGAACACGGACTATTGATAGGGCAGGTGAAGCGGAATCTATGAGCCTGGAAAATTACACTGCACATAATGATATGATTCCATTGTGTGATGAAGCTCATGCTGAGATGTTTCCTCACTAATTGTTTTTGATTTCATTGTTTTGCAGTTGCCGTAGAGGCTGCACAGGAGCTATTCAGG[T/G]CAGTCTGCCTTTAATATTAGAATCATATTTTTACTTCAAAATACAATGCAACCGTCATGTATTTTTTAGTGTAGAGGGATATTTGGCTTAAAGGAAAAGGGTAAACTTTACAATGATGTTCCATTATGTTAAATGTTGAAGTGAATTTACTGGCATGAACAAACAATGGTCTTTACATTTATTGCAGTATTTATGCATCTTTTTATTTTACTTAATCAAAAAATATTATCTTTTTATAGTCCTTTTAGTTACTTAACTATTTGTTTTATTAACAAGCAAAACTATGGGTTGTAATCAGAGCTTAATTTGTGCCAGAACACGCCAGATCCAGATCCGGCACCTCATTTTACCAATCCCCTTCTCAACCACCCTCCTCTTCGACCGATGTTTACTTACACTTTTTTCCGTGACTTTTCAACCTTCTTCACTTTCGTGAGAGACACCTCTCCATCCTCGGGTAACATTCTGGATCTGTTACTCCGATCTGTTCCGGGAACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23731
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044397 | Nonsense | 741 | 1257 | 11 | 22 |
ENSDART00000129169 | Nonsense | 741 | 1257 | 10 | 21 |
ENSDART00000131032 | None | None | 539 | None | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 30579008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30650221 |
GRCz11 | 20 | 30553100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCGCTACTGTAAGACCTCGAGTCCGGCCAGCAGCACCACGAGCAGCTA[C/A]GCTCCCAGCAGCAGCAGCAGCCTGAGCTGTGGAGGAGGAGGAGGGGGAGG
Long Flanking Sequence:
ACATACCAATATATTTATATATATATAAGATGCTCTGTGTCATTCACAAAACTACTAATCACACAAAATACTAAAATAATCCATTAAACATTAATTATCTATATTAGATGTAACAAACTCAAATGTACAAAAAACTGAAAGCAATCGTATTAATATCAACAAAAAAGGCATAAAAAGTAAAGTGTCATGCAAGATATTTTGAGACAGTAAATGCATGGTTATTCAACTGTATATATTGAGAAAACTTACTGTTAAACTGATTTTTACTCTAACACTTTTACAGTATTTTACCATTAAAATCACATTTTTGGCCGTGAATCCTACAAATACCGTCAAATCATATCTCCTCCTCCTTTCTCTTTCTGTCCGTTCTGTCATTTTCTCTGTCCGTCCATCTATCTCCCCGTTCATTCATCCGAGTGTCTGTTATATATGTGCCTGTGTGCAGCGAAGCGCTACTGTAAGACCTCGAGTCCGGCCAGCAGCACCACGAGCAGCTA[C/A]GCTCCCAGCAGCAGCAGCAGCCTGAGCTGTGGAGGAGGAGGAGGGGGAGGAGGAGGAGGGGGAGGAGGAAGCAGCGCCAGCAGCACCTGCAGCAAGAGCAGCTTCGACTACACGCACGACATGGAAGCCGCCCACATGGCCGCCACTGCCATCCTCAACCTGTCCACGCGCTGCAGAGAGATGCCCCAGAGCCTCGCCGCAAAGGGCCCCGAGCTCCTGGCACAGGTGAGGGTCTGCCAGCTTCTCTCTCTCATGCTCACCCACTTCCACTGCTAATATTCTGTCTTCCATTCTCTCACTGGGCAATTCTGAGGTTTTCAGCAATGCCTTCTATGACTGTGTTTTATGGTTGGTAGAAGGCAGTGCACCAAAATGAGGGCATGCCACTTTGGAGTCATTTGGGGTAAACCCCTAGTCCCTCGTCAGGGTGCGATTTCACACATTTTTACCCTGCTAGAGCCTAATGGTCTGAGGGAGCCATGATTACTTTAATGACGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37064
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 |
---|---|---|---|---|---|
ENSDART00000044397 | Nonsense | 1004 | 1257 | 17 | 22 |
ENSDART00000129169 | Nonsense | 1004 | 1257 | 16 | 21 |
ENSDART00000131032 | None | None | 539 | None | 7 |
Genomic Location (Zv9):
Chromosome 20 (position 30591755)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30662968 |
GRCz11 | 20 | 30565847 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTCTTTCTTGCTGAACTGGTCTCCGCTGTGCCCAATGTCTCCAGGTG[T/A]CCAGTGCCAGGCTGTGATGGCCAGGGTCACGTGACAGGGAAGTATGCCTC
Long Flanking Sequence:
AAAAAAAGAGCCAAGGTCAAAATTGTTAGCCCCCTTAAGAAATGTGTCATCATGTACTGTCAACATGGCAAAGACAAAAGAAATAAATAATTTGAAATGAACTATTATGTTTAAAAATGTGTTGAAAAAAAAATCTATCCATTAACCTCACTTGGGAAACATAAAAAAAGACAAGAGGGCTAATGATTTTGTTTTCTTTATATTTGTGGAAAAAAAGAAACAACATACTTTTTCTGACTTGTACTTTATTGTAATATTGTTTAAATAATGGTTAATATATGATTAATTGTTATTATTCATATATCTTATGCTTTAAATGATTTTAAATTTGATGGATTTGGTCTTTTTGTTAATTAGGGAATTAGTTTTCCCCTTAATCCTGATTTTCTGTGAAAACTATGAAATTGTGGAAGAAACATTATAATGTATGAATGTGTGTAGAAAAGATGGTGACTCTTTCTTGCTGAACTGGTCTCCGCTGTGCCCAATGTCTCCAGGTG[T/A]CCAGTGCCAGGCTGTGATGGCCAGGGTCACGTGACAGGGAAGTATGCCTCCCACCGCAGTGCATCCGGCTGCCCGCTGGCCGCCAAGCGTCAGAAAGACGGTTATGTGAACGGAGCACCTTTCTCCTGGAAGTCGGGAAAGACAGACGGCATGACCTGCCCCACTCCAGGGTGCGACGGATCAGGCCACGTCAGCGGAAGTTTCCTCACCCACCGGAGGTACATGAGTATCTGAGCCTTTCTCTGCTAGGCTGTCAAATAGTAAGAAATCATTTTCTTAATCAGTGTGTTTGCATTGTTTTTCAATACACAAATCTGATCTCCTTAAAGGGTTAATTCACCCAAAGATTAAAAATCTGTTATTAATTACTCATCCTCATGACATCCTAATCTCTGCCATTCATTTTTAGAATATGAGGATGTTTTAGATATTTAGATATTGGTCACACTTTACAATAAGGTTCATTAGTTAATGTTAATTAATGCATTTACTTACATGAA
Associated Phenotype:
Not determined