ZMP
si:ch211-121a2.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC564515 [Source:RefSeq peptide;Acc:NP_001098581]
Human Orthologues:
DUPD1, DUSP13
Human Descriptions:
dual specificity phosphatase 13 [Source:HGNC Symbol;Acc:19681]
dual specificity phosphatase and pro isomerase domain containing 1 [Source:HGNC Symbol;Acc:23481]
dual specificity phosphatase and pro isomerase domain containing 1 [Source:HGNC Symbol;Acc:23481]
Mouse Orthologues:
Dupd1, Dusp13
Mouse Descriptions:
dual specificity phosphatase 13 Gene [Source:MGI Symbol;Acc:MGI:1351599]
dual specificity phosphatase and pro isomerase domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:3
dual specificity phosphatase and pro isomerase domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:3
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43382 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39270 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43382
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023677 | Nonsense | 437 | 449 | 6 | 6 |
ENSDART00000140166 | None | None | 148 | None | 3 |
ENSDART00000145954 | Nonsense | 146 | 158 | 3 | 3 |
The following transcripts of ENSDARG00000039682 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 7245466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7080859 |
GRCz11 | 20 | 7070738 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCACGTTTTAAAAGTGAGATGCATCTGGCCCAACTTGGGCTTCTTGAAA[C/T]AGCTGGCAGTTCTCAACTCAAAGCTTGCATGTCAGCAATAAACTATCCAG
Long Flanking Sequence:
AGCAGAGGGGCATTACACACATCCTGAATGCTGCAGCTATTAAACACAATTTAATGGCGTCTTTGGGAATGCCACGCAAGGAAGATCTGCTACGTAAGGTCAAAACTGGGGCGCAATATTACAAAGGCATGAACATCACGTACTACGGTGTACCTGTAGTAGATGACCCCTTGTTTGACATCAGCAAGTACTTTTACCCCTCTGCAGCATTCATCCACCAGGCCCTCAGTGAGCCTGAAAGTAAGCTGAGACTCACACAACAGCACTTCTCAATGACAGGTGTTGTATTTTGACCAACTGTATTAGAATGAGTTTGCTTTGAGTGTTTTTGTGCTTCTATCTTCTCAGATAAGATGTTGGTGCACTGCTCGGATGGAGTAAGTCGATCTCCCACACTATTTTTGGCGTATCTGATGATTCACCGTAAAATGTCAGTGGAAGATGCCATGGGCCACGTTTTAAAAGTGAGATGCATCTGGCCCAACTTGGGCTTCTTGAAA[C/T]AGCTGGCAGTTCTCAACTCAAAGCTTGCATGTCAGCAATAAACTATCCAGACAGGCATAACTGTAAAAAGCACAGGAAAATAAAGCACATGAGTAAAATGAAAATTATGTGTGTGTGTTAGAATATTGTAAATACGTAATTAATTTTACGTCATTATTATAATTTTTATAATGATGGTGATTATTATTATTATTGTTATTATACATTAATATAATGTACTGTATTACATTCAATTTTTTAATATTATTACTGTAATGGGGGGCCTCACAGTGGCGCAATGTGTAGCACAATCGCCTCACAACAAGAAGGTCGCTGGTTCAAGTCTCGGCTGGGTCAGTTGGTGTTTCTGCATGGAGTTTGCATGTTCTCCCCATGTTGGCGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAAGCTAAAATTGTCCGTTGTGTTTGAGTGTGAATGAGTGTGTGGATGTTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39270
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023677 | Nonsense | 448 | 449 | 6 | 6 |
ENSDART00000140166 | None | None | 148 | None | 3 |
ENSDART00000145954 | Nonsense | 157 | 158 | 3 | 3 |
The following transcripts of ENSDARG00000039682 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 7245433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 7080826 |
GRCz11 | 20 | 7070705 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGGGCTTCTTGAAACAGCTGGCAGTTCTCAACTCAAAGCTTGCATGT[C/T]AGCAATAAACTATCCAGACAGGCATAACTGTAAAAAGCACAGGAAAATAA
Long Flanking Sequence:
CAGCTATTAAACACAATTTAATGGCGTCTTTGGGAATGCCACGCAAGGAAGATCTGCTACGTAAGGTCAAAACTGGGGCGCAATATTACAAAGGCATGAACATCACGTACTACGGTGTACCTGTAGTAGATGACCCCTTGTTTGACATCAGCAAGTACTTTTACCCCTCTGCAGCATTCATCCACCAGGCCCTCAGTGAGCCTGAAAGTAAGCTGAGACTCACACAACAGCACTTCTCAATGACAGGTGTTGTATTTTGACCAACTGTATTAGAATGAGTTTGCTTTGAGTGTTTTTGTGCTTCTATCTTCTCAGATAAGATGTTGGTGCACTGCTCGGATGGAGTAAGTCGATCTCCCACACTATTTTTGGCGTATCTGATGATTCACCGTAAAATGTCAGTGGAAGATGCCATGGGCCACGTTTTAAAAGTGAGATGCATCTGGCCCAACTTGGGCTTCTTGAAACAGCTGGCAGTTCTCAACTCAAAGCTTGCATGT[C/T]AGCAATAAACTATCCAGACAGGCATAACTGTAAAAAGCACAGGAAAATAAAGCACATGAGTAAAATGAAAATTATGTGTGTGTGTTAGAATATTGTAAATACGTAATTAATTTTACGTCATTATTATAATTTTTATAATGATGGTGATTATTATTATTATTGTTATTATACATTAATATAATGTACTGTATTACATTCAATTTTTTAATATTATTACTGTAATGGGGGGCCTCACAGTGGCGCAATGTGTAGCACAATCGCCTCACAACAAGAAGGTCGCTGGTTCAAGTCTCGGCTGGGTCAGTTGGTGTTTCTGCATGGAGTTTGCATGTTCTCCCCATGTTGGCGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAAGTCCAAAGACATGCGGTACAGGTGAATTGGGTAAGCTAAAATTGTCCGTTGTGTTTGAGTGTGAATGAGTGTGTGGATGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATCCGCT
Associated Phenotype:
Not determined