Busch Lab

ZMP

si:ch211-121a2.2

Ensembl ID:
ENSDARG00000039682
ZFIN ID:
ZDB-GENE-070705-21
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]
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

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.
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.
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