ZMP
si:ch211-194p15.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
MYT1
Human Description:
myelin transcription factor 1 [Source:HGNC Symbol;Acc:7622]
Mouse Orthologue:
Myt1
Mouse Description:
myelin transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:1100535]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14230 | Nonsense | Available for shipment | Available now |
sa37614 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14230
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000123681 | Nonsense | 742 | 1142 | 10 | 20 |
ENSDART00000137003 | None | None | 91 | None | 5 |
The following transcripts of ENSDARG00000089464 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 7860749)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 7837622 |
GRCz11 | 23 | 7771594 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCATGGCAACAGCAGCATCTCGCCTCATTCTTTGCACACCTATAAACAA[G/T]AGGARTGGGAGGGGCCTCTGGACTACACTAAACCCAATCGGCAGAGAGAG
Long Flanking Sequence:
TGTCAGACTTTCAAAGTCCCTCATCACTTCAATTAAGATTATATTTATTACATTTTAAAGCACACCCACTAAAGAATCTGACTATAGCACCTCTTTCTACGTTAAATACAGATTAAGAAGTAGCAGCTATGATGCTGTTTTTTTAAACCAATTGTTTGCATTGCTATTCCAACATCCCAAACACCATGGTAACCACTCATAGCATACCATTTTTGGCTAAATGGTCATTTTGACACATTATTGTGATTATAAGCTTATTTATGAATTATAATTAAAACACATTTTGTTTTTTCTTGTTGAAGAGTATGGAAATTGAGGTTGATGAGAACGGCACTTTGGACTTAAGCATGAAGAAGCCCATAAAGAGGGAAGTGGGAATGTCATGCACCAGCCCTGAAGTGCGTTCCCCCGATCTGTCCTCATCATCTTCGTCATCATCCACATCTCTTCACCATGGCAACAGCAGCATCTCGCCTCATTCTTTGCACACCTATAAACAA[G/T]AGGAGTGGGAGGGGCCTCTGGACTACACTAAACCCAATCGGCAGAGAGAGGAGGAGCTAGAAGAGGTAGAATATTTGACATGTCCTGTTACATTAGGAAATGCAGATGCTGTGCCATCTGATTTAATATACTTTCCATCTTTGAACAGATGGACCACAGTGCTCCGTCTTTTGCCTCCTCTGACCCTGAAGACTGCGACATGATGCAAGATGGCCTGGAGGACAGGAAGTACCCTGGAGAGGTCACAACCCCCAGCTTTAAGGTCAGGTTCCAGCCCAAGGACAACAAAAAAGACCTCCTGATGTAAGTTCGGATGCACTTCTGTGCACATATTGATATTCAGCAAAATGCAATAGTTTCACTCAGTCAGGCTTTTGCTTTGTCCTATGCAGGTGTCCCACTCCGGGCTGTGACGGTAGCGGACACATTACCGGAAACTATGCATCCCATCGCAGGTACATGGTGTTCATGGGTCAGAGGGGAAGCATGGACTAAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37614
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 |
---|---|---|---|---|---|
ENSDART00000123681 | Nonsense | 988 | 1142 | 17 | 20 |
ENSDART00000137003 | None | None | 91 | None | 5 |
The following transcripts of ENSDARG00000089464 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 7855282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 7832155 |
GRCz11 | 23 | 7766127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTGATGATGAATCAATTGTGTTTGGCCCCAGTCTCTCCGGCTGCCCC[A/T]GAGCCTCCCTCAACAAGAAGAAAGCCAAGTTCCCTGGAGAAGAGTATCTC
Long Flanking Sequence:
ACCCCATTGACAAATTTTGGCCTCACTTGTCCCTCGCGCGAAACTGATGCATCCAGACAGTACATTTAGCATTTTACATTTTTAAGGATTGGTTTGGCCAAAAAAATTTAATTGCCATCATTTAATCCCTCCTGTGTTATTCCAAGGCATTTTAGATAACCTTCCAAGCACAAATTAAGATATTTCTATCATCATCAAGCACATCACATTTGATAAACACTAAAAAAAAAAAGCAAACACTGAAGCTTGAACATGCTAGCATGTGTTAATTCTGTGTTTGCATGAATCGCTGTAATAAAGTGATCTTACCTCTTCAAGAGACTTGTTTAGGTGAGCTATGCACTCAATAGCAAAAATATGACATACTTTACATCTAGGTTTAAGGTTATTTGCCAAGTCTGAGTCATTATGGGACTGCTCATGAAGCAAATGTGCTGTTGAGTTTTGTGATGATTGATGATGAATCAATTGTGTTTGGCCCCAGTCTCTCCGGCTGCCCC[A/T]GAGCCTCCCTCAACAAGAAGAAAGCCAAGTTCCCTGGAGAAGAGTATCTCAGCACTAAGTTCAGAGCCAGCGACGGTGAGACAATCGCACACTTTCCCTCCATAATTTTTTTCTAATCTCATGTTCTGTGAACATTAAAGATGACATCTTTCTCTTTACAGTGTTGGACAACGATGAAGATATCAAGCAACTCAACAAAGAAATAAATGAGCTCAATGAATCCAACAATGAGATGGAGGCTGATATGGTGAATCTTCAAACACAGGTTAGCCACACGTGCGTTCTAAAAATGTAGTGTTGTCATAAGAGCGCATTTTAAAATGTATAAAAATGTATTTTGAAGACACAGCCTTGAAAAGTATGAGATTTTGTTACTCCAGTTGTTTCTGACCCTAAATTGTTGCTCAGATGTTCCAAGTGATACCATAGTGCAACAAAATGTCTTTAGTGTATCAGTTCAATTAGCTGACTAGCTAGCAAATTTAAATCTACACTGGACA
Associated Phenotype:
Not determined