ZMP
dyx1c1
Ensembl ID:
ZFIN ID:
Description:
dyslexia susceptibility 1 candidate 1 [Source:RefSeq peptide;Acc:NP_991251]
Human Orthologue:
DYX1C1
Human Description:
dyslexia susceptibility 1 candidate 1 [Source:HGNC Symbol;Acc:21493]
Mouse Orthologue:
Dyx1c1
Mouse Description:
dyslexia susceptibility 1 candidate 1 homolog (human) Gene [Source:MGI Symbol;Acc:MGI:1914935]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45503 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22393 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45503
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018411 | Essential Splice Site | 214 | 420 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 13 (position 52290041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2887346 |
GRCz11 | 18 | 2173469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCACCTGCAGACACAGCATTGGTGAAAACCGACAACACTATCACTGG[T/C]AAACAAACTTATACATCCTTGCCATTTGGAAATATCATTAAGAAGCAGTC
Long Flanking Sequence:
TGAACTGGGGCAGACACCACAACGCAACGTCTACAATCTTTAAATAAACTAGTTAAATATTAGATATTATGATTTGCATAAAAAATAAAGCTAATAAAACTTGACTCCATTTTTATGACACTTTATTAGCTATATATAAGGTGATATTTATAGTGAAGAGCGCTATACAAATAAACTTAAACTGAACTGATTATATAATTTGGCACAATCATCTTCTTCTTTGTTTAAATGTCATCTCAAGCAATTTCTGCCTGTGTTTAGCTTGAGAGCGAGGAGCGGGAGAGGATTCAGAAGAGGAAGGATGAAGAGTGTGCGAGAGCCACAGCAGAGCTGGATTTCTGGAGAGAAACACAGAGAACAACAGCCGAGGGAAACGAGAACCAGATAAAAGAGCAGAGAACCAGCACACATGACGACAAACCGGCTCCTCAGAAAATAAAGCATGCAAACACTTCACCTGCAGACACAGCATTGGTGAAAACCGACAACACTATCACTGG[T/C]AAACAAACTTATACATCCTTGCCATTTGGAAATATCATTAAGAAGCAGTCAATATACAGTTACAGTCAGAATTATGAGAATTAATTTGAATTCTTTTATATATTTATTCTCAATTTCTGCTTTATTTCAGCACATTTCTTAACATAATAGTTTTTAAGAGTTCACACTAAGCTCATGATTTATACATAGCTTGTTTGGCATGCTGTCCTGGGAGAGAGATCTGAGCTCAAGGGATCTTTGAGCCCAGGGCTTCTCCCTTTTGCAGGGCGAGGGGAGATTGAGCTCATGTCGATCTCAAACTCCCCCGCTGCTGAGGCCAAGGCGAACTTCCTGAGAGTAAGACATTATAAAAAAGGTTTAGGTTTATTTTATCTATAATATAGAGCACATTTGGATGGTGGGAGGAAACCGGGGAACCTGGGGGAAACCCAAGCGGACACGAGGAGAACTGAGATGCAAACTCCGCACAGAAATACCAGATGGCTCAGGGAGGATCCGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22393
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 |
---|---|---|---|---|---|
ENSDART00000018411 | Essential Splice Site | 294 | 420 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 13 (position 52292445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 2889750 |
GRCz11 | 18 | 2175873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCTGACAGAGGACGAGAGAAACCCAGACTGGCTGAAAGACAAGGGAGA[G/T]TCAGTGTCTTCATGCTGTTTTTCTCTCTTTTGTCTGACTTTTTGCAGTGT
Long Flanking Sequence:
AGATGCATATTTATATTATCTACTATTTTAATTATTAATGTTATTATTTACGTTACAGATCAGAGCAATAATTGGAATTAATTAGGGGGGTCAATCCCCCCAACCCCCCCTGTCATTTGCACCCAGCCTGTGAGTGTATGTCTGTGTTTGTGCATGTGTTTATGACATAATATAAGGACACAAACTTGAATAATGACATGGTTATAGGCAGAAGGTGTCTTATGAGGACATCTCCCATATTCCCATTTTTTTAAAAGGCTTATAAATCATGCAGAATTATTTTTTTCATGAAGTCAGAATGCACACAATTTTCTGTGAGGGTAAGGTTGGGGTGGAGCAATAGAAAACAGATTGTACAATGTAAAAACCATTATGCCTATGCTTAAACAGTGGTTGAAGAAGCAGGCGGAGGCCAGGAGAGCAATAGACACAGATCTGGCAGAACTGGACGACCTGACAGAGGACGAGAGAAACCCAGACTGGCTGAAAGACAAGGGAGA[G/T]TCAGTGTCTTCATGCTGTTTTTCTCTCTTTTGTCTGACTTTTTGCAGTGTGTTGCTGATCAAAGCTTTAGGTCTGTTTTTAATTTTTTTCATAGCTGCATTTATTTGGTTGAAACAGTAAAAATGCAAAACCTTTCAATAATATTTCATTCAAAACAATAACTGCTTTAATATAGTGTGAAATGTAATTTATTACTGTGATTCTATGCTGAATTTTCAGCATCATATCACCAGTCTTCAGTGTCACACGATCCTTCTGAACTCATTATAATATGAAGATTTAACTGTCAAGACACATTTTTCAAATATAACCAATGAATATTAATACATATATTTGATGAATATATGGAGTTATAAAATACTGTTATTACCTATTTATTTGAAATGTTTTATATTCCTTAATGCATCCTTGCTGAAAAAAAATTATAATCTAAAGAGTTTAGATGCCAAAACCTCAAAGTGCCGTCGGAGATTTTCATCTAAAATGAGCATTTTACACTG
Associated Phenotype:
Not determined