ZMP
smyd3
Ensembl ID:
ZFIN ID:
Description:
SET and MYND domain-containing protein 3 [Source:RefSeq peptide;Acc:NP_001032477]
Human Orthologue:
SMYD3
Human Description:
SET and MYND domain containing 3 [Source:HGNC Symbol;Acc:15513]
Mouse Orthologue:
Smyd3
Mouse Description:
SET and MYND domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1916976]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36344 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42879 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36344
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 |
---|---|---|---|---|---|
ENSDART00000080847 | Nonsense | 212 | 380 | 7 | 11 |
ENSDART00000105236 | Nonsense | 213 | 429 | 7 | 12 |
ENSDART00000122178 | None | None | 151 | None | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 11652810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 11635332 |
GRCz11 | 17 | 11789398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTCTGCGCCAGCATGTCTCTGCTGAACCACGACTGCCAGCCCAACTG[T/A]ATCATGATGTTTGAGGGCAAGAGACTCACGCTGAGAGCTGTTCGGGTCAT
Long Flanking Sequence:
CACAGTTATGTAAAAACAGATCTGGATCTGGAATCTTCTCTATTACTATAGCTGATTATCCTTGTGAATTGAATGATAACAGCCTTCTGAGCCTACCAGTAGGCAGAAGGCCCCTACTGGCCCATATCTATCAGCTGATGACCACTTATAACTCCGAGTGATAACATTCAAATCTGGTAAATTTGCTCATTATTTACTCACCCCTAAGTGAACTTGTTTTAGTTTCTTTTGTAATCATTGACTTCCATAGTAGGATAAACAAATCATGTGGCAGTCAGTGGTTTTCAGCTTTCTTCAAAATATTTTCTTTTGTGTTTAACGGAAGAAGGAAAGTAAAACAGATTTGGAACAAGTGAAGGGTGAGTAAATGGTGACAGAATTTTCAGTTTTGGGTGAACTATCCCTTTAATCTGTGTCTCGGCGGTTTTCTAGATTAACTGATGTTTTGTGTTTGTCTGCGCCAGCATGTCTCTGCTGAACCACGACTGCCAGCCCAACTG[T/A]ATCATGATGTTTGAGGGCAAGAGACTCACGCTGAGAGCTGTTCGGGTCATCAGATCTGCTGAAGAGGTATACGTCCATACATACATACACTCAAAATATTATTTTAGCTGCTTGTTTAAACTACTTATTTAAAAATGTGCTCAGACAAAACCATTCCTGAGGTTTTTATTCTTTTGACAATTTAGTTGTTTTATGTTCAAATTACTTAAATTTGTAAAAACAATTAAGGTAATTTAATCAATCTGTGTTGGAACCACATGAAGGAATCGTGTGGAACCCAGCATTTTTTACAGTGTACATTCAAAAAATTACTTTGCTGCTTGTTCAAACTACTCATTTAAAATGAGTTGAAACAACACAAGTATTTTCAGTTTTTTGTGGGGGCACAACTTAATTGTTTTATGTTCAATCCACTTAAATTTGTAAAAACATTAAAAGTTAACTTAATCAATTTGTGTTGGAACAACATTATTACATGTTAACAAATAGTACTTCTGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42879
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 |
---|---|---|---|---|---|
ENSDART00000080847 | Nonsense | 258 | 380 | 9 | 11 |
ENSDART00000105236 | Nonsense | 307 | 429 | 10 | 12 |
ENSDART00000122178 | None | None | 151 | None | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 11629350)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 11611872 |
GRCz11 | 17 | 11765938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTTAGTCATGTCCTTAACTTTTTAATCAAAAGACTGGGATGAGCTGT[T/A]GAAGGAGAGCCAGGCCCTTCTGCACAGACATTCAGATGTCGTACCAGACA
Long Flanking Sequence:
GAGTTGTCAACTGGAGACTTGTTTAGAACAGATAATTTTAATCAGTTAGCTGTAAACTGGACTCTTGCTCTGAATGGATCATTTAATGCAGTGAGTTGCTGAATGGAAGCCTGATCTGGATTGATCCATTGAATCAGTGAGTTGACTTAAGAGCACATGCAATCAGATTTGTCAGTTCTCTAATGAATTGTTTAGTTTGATTTGCAAGCTGAACTCATCAAAATTCAGCTCACGTCTCCACTACATGGCTGAAATAAACTTTCATGTAACAGTTACAAACAGTTACAGAGATTCTCTCATAAAGATAATTTTTTTATTTTTTTTTTTAAAGATGAACACATTTCTGATTTTCTGTTTGGAATAACATATCTTTTTCATTATGGGGTGAACTAACCATGTAAACCAGCAAAGCTTCGTTGGCTGTTGTATTGTTATAATGAATTTCATCTTCATTTTAGTCATGTCCTTAACTTTTTAATCAAAAGACTGGGATGAGCTGT[T/A]GAAGGAGAGCCAGGCCCTTCTGCACAGACATTCAGATGTCGTACCAGACAGGAACATCTACATGCTCCGACTGCTGGATTTGGCCATGGATGCCTGCATTAGTCTGGATGACTATGAAACTGCTCTGGAATACGGCAACAGGGCTCTGGGTCCTTACAAGTGAGTGTGTGCATCTAAAACTTCTGTTCTGGCAGATTTTCTGCTAAATCTTAGTGGGATACACCTCCATCTCTCATTCAAATCTATAAAAGTCCCTTTATAACTGTGACTCACATAGACTCACTCACTTCTGAAGACCAAAAAGAAACAAGTGCAGCTCTAGTTCGCAGGAACTATTGCTATAAATGTATTGAAAAATTATCCTCTATTATAACATCTGTATATCTTAAAATGTATCTTATGTGTTGCATGTACAAATATCCCAAAAAGTGACATTACATAAATGAATTTAACAGCTTTTATTTCAATCAAACTAAAAGAAATAAGGAACAAAAATAAGG
Associated Phenotype:
Not determined