Busch Lab

ZMP

si:ch211-242b18.1

Ensembl ID:
ENSDARG00000054723
ZFIN ID:
ZDB-GENE-030131-1518
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RIJ0]
Human Orthologue:
PDE4DIP
Human Description:
phosphodiesterase 4D interacting protein [Source:HGNC Symbol;Acc:15580]
Mouse Orthologue:
Pde4dip
Mouse Description:
phosphodiesterase 4D interacting protein (myomegalin) Gene [Source:MGI Symbol;Acc:MGI:1891434]

Alleles

There are 12 alleles of this gene:

Allele Name Consequence Status Availability
sa16686 Essential Splice Site Available for shipment Available now
sa15948 Nonsense Available for shipment Available now
sa18459 Nonsense Available for shipment Available now
sa12868 Nonsense Available for shipment Available now
sa32308 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa16686
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076946 Essential Splice Site 208 2016 7 42
ENSDART00000136651 None None 92 None 5
ENSDART00000138338 Essential Splice Site 170 2431 4 38

The following transcripts of ENSDARG00000054723 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 34617182)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34689695
GRCz11 20 34592574
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGTTTGCCTGTCATGGCACAGTATGAAGAGATGGCAAAGAAGGACAGG[T/G]AAAATATTACAGCAGTGCCATTCAAAACATCATTTTGTTATTCTATKGTT
Long Flanking Sequence:
ACTAAGATCCAGCTTCTGCAGGAGGTGCTTCATGCTTACTTACTCTTGAACACCCATGACCACAACTGTTTTTTGTATTTTTTTGTTGTGTTGGATAGCCTTTTAGAATGATTTCTGAAGCATCACGTGCCCTGTAAAAAATCAGTTTTGCAACCACAGGAATAAATTACATTTAAATATATTAATAATTATGCTTCATTACAATTAGCATAACAATTTTTACTGTAATTCTAATCCAATAAATGCAGCTTTTTATTTTTACTCATTGAATTGTACTGTATTTTTTTCATCATCGCATTTTACTTCATTGAGTTTTATTTTATTTTTTTCTTCAGGAGGCTCGATTGGCAAGAGATGAAGCAGAAAAAATGGCTTCTATGGCTGAATCTGAGTCCCAGCGCTGTTTGGACCTAGAAAATAGGATGATGACAGTAATGCAGGATGGAAATGAAAGTTTGCCTGTCATGGCACAGTATGAAGAGATGGCAAAGAAGGACAGG[T/G]AAAATATTACAGCAGTGCCATTCAAAACATCATTTTGTTATTCTATGGTTTCTATTATTGAATGAAATTTAATATACATCTTTTAACCCATTCCTCTTTATCTTTCAATTAGGTTGATTGAGGAACTGAACGAAACCGTATGCAGGAAAGAGCGAGAAGCAGCTGATCTGAGTTCACAACGGGACGTCCTTACTGTAAAACTAACTCAACTGGAAGAGCAAGTGCAAAGCCTCCAGCAGAAAGAGAAGCACACACAAGTAAGATCTACGACAGGACGCTCATGCACTAAAACAGATTTCATGCGCTCTGATAATTAATAACATGTCATCACATGATGCTTTTGGGCATATACATACACAACCTTGCACATGAGTCAATATGAGTTATATGTGATCATTCATGCGTGATCTGGATCTACTGTAAATCAACACTCACTATAATTCAGCATCTAAGTAGGTCACTTTGGCCTCTGGCCCCTCTTCAACCCTCATAGAGAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15948
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076946 Nonsense 280 2016 10 42
ENSDART00000136651 None None 92 None 5
ENSDART00000138338 Nonsense 611 2431 7 38

The following transcripts of ENSDARG00000054723 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 34624629)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34697142
GRCz11 20 34600021
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTAAATATTTGTGTGATCTGTCNNTGTTTCAGAGGTTGATTGAGGAG[C/T]AGCAATGTCATCTGGCGGAGTATGAAAACGCAGCGGGACAGTGTGTGAAT
Long Flanking Sequence:
CTTCAGTAACATGCTTTGAGAATCCACAAAAAAAAAGCTATATTAATGTAGCGAATAATTATTACTAATACAAAAATCGGTATATATAGACAGAGAAATGACTAAGTGAAAATGAAAAACAAGGAAATGAACGGCATGCCGCCATGGAAAAATAGGACTTCCTGAGGAAGTTGTAGAGTGCTGTAGAGTTATTGAGCTATAGTCATAACTGTTCGTTCAGCACTTTGTTCTCTCTTATTTACAGTACACTGCTGTATTTATTAGTGAATATAATCATTTAGTAATCACAGACTGCTATATTTTGCAGTTATATATTAAAACTAAAACACAAAACAATATTGCAGTATTTTTAACTTCAGTGCAATGAATATTCAGTCAGACATAATGAAGACTTATTTGAATTAGTAGCAGAAGCAGACAATTTGCATTGCTGTCTTTGAAACAATTGAGTTTTTAAATATTTGTGTGATCTGTCTGTGTTTCAGAGGTTGATTGAGGAG[C/T]AGCAATGTCATCTGGCGGAGTATGAAAACGCAGCGGGACAGTGTGTGAATGAGCTGCAGAAGGCCCAACAGCAGGTGCAGTCTCTCCAGACCAAGATCCGAGACAGTGAAGCCAGTAATAAGGTACTGATATTGAATGTATAAGCTTCAGTCATTTGTCTTTTGACTGTTGTGTTTGTATGAGGCACTGTAGCTGCAGATTCTGCTGAGGCTTTTTGTCTCAGCAGGCATGACAGTCATTAAATTGTTGTTGGACTGTGCTCTTTGTTTTGTGTGTGTGTGTAGAAGTTACAGCAGAAGCTTCGGGACATGGAAAATGAACTACGCTCTGTCAGAGAAGCAGCATGTGGTCAGGAGACAACAATACAGACCTTGGGTGACTCACTCAGTACTAAAGACTATGAGGTATGTCTGCAACTAAAGCAGTGATGAGAATTTCAATTAATCCTTACAGATGCATGCCTTGGGCTGCTATATAATGCATGAGGGGGGGAAAGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18459
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076946 Nonsense 359 2016 11 42
ENSDART00000136651 None None 92 None 5
ENSDART00000138338 Nonsense 690 2431 8 38

The following transcripts of ENSDARG00000054723 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 34625030)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34697543
GRCz11 20 34600422
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGAGACAACAATACAGACCTTGGGTGACTCACTCWGTACTAAAGAYTA[T/A]GAGGTATGTCTGCAAMTRAAGCAGTGATGAGAATTTCAATTAATCCTTAC
Long Flanking Sequence:
TTAGTAGCAGAAGCAGACAATTTGCATTGCTGTCTTTGAAACAATTGAGTTTTTAAATATTTGTGTGATCTGTCTGTGTTTCAGAGGTTGATTGAGGAGCAGCAATGTCATCTGGCGGAGTATGAAAACGCAGCGGGACAGTGTGTGAATGAGCTGCAGAAGGCCCAACAGCAGGTGCAGTCTCTCCAGACCAAGATCCGAGACAGTGAAGCCAGTAATAAGGTACTGATATTGAATGTATAAGCTTCAGTCATTTGTCTTTTGACTGTTGTGTTTGTATGAGGCACTGTAGCTGCAGATTCTGCTGAGGCTTTTTGTCTCAGCAGGCATGACAGTCATTAAATTGTTGTTGGACTGTGCTCTTTGTTTTGTGTGTGTGTGTAGAAGTTACAGCAGAAGCTTCGGGACATGGAAAATGAACTACGCTCTGTCAGAGAAGCAGCATGTGGTCAGGAGACAACAATACAGACCTTGGGTGACTCACTCAGTACTAAAGACTA[T/A]GAGGTATGTCTGCAACTAAAGCAGTGATGAGAATTTCAATTAATCCTTACAGATGCATGCCTTGGGCTGCTATATAATGCATGAGGGGGGGAAAGAAAAAAATAATTATAACGTAGTATGACCACTTAGTTTATCAATAACTATTCGTTGTGTTATATGTTGTGATTTTTATTTTACATTTTTTTATTTTTATATATATATATATATTTTATATAATTTATTTTTTCACTGTTACTTTTAATTTCTTTAGGTAATTAAATATATATTTTTTTGTATATTATTTGTATTAATAATATAAAGCAATGCTCCTTTATGTTAGATTACTGATCTCCAGCGGGTCATTGAGGAGCAGAAGGAGCTTCTGTGCTCTCTAAAGCAACAGAACAACCATTACCAGCTTCAGCAGCAGCAGGTTGGAGTCCTTTTTCAATAAAGCTCATTCACATCAGTTCTACTAAATGCATTGCACCTACAGCCACGAGAAAATGAAATAAACCTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12868
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
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Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076946 Nonsense 1076 2016 25 42
ENSDART00000136651 None None 92 None 5
ENSDART00000138338 Nonsense 1402 2431 22 38

The following transcripts of ENSDARG00000054723 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 34639575)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34712088
GRCz11 20 34614967
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTCTTGTCTTTYGTWTAGCGGAAACATCGGTACAGCAGGACAGTAAG[C/T]AGGTCCAGGTGGACATTCAGGATCTGGGCTATGAGACGTGTGGCCGCAGT
Long Flanking Sequence:
TTGCATAACTTAAATTTAGTTGAAACTAAATTGTTATTGTTATACAAATTACTGGCTGTTTTGACTTCTTGTAATTATTTTTTTTTTCAGTGTACTAATGATTTTGGCTTTTTTTTTTTACTCATACAATGTATATTTGGCTATTTCTACAAATATAAAGCTGTGCAATTTTAGACTGGTTTTGTGGTCCAGAGTCAATTATTAAATTAACATATTGTTTTGCTGTTTTTTAAATATTTTGGGTTTTTAAATGCAATTTGTTTTTGTTGATTGTTTGAATTTTAATGAATATATACAATTCTGTGTAATTTGACACTTTCTTGAACCATATATCTACAGAATATGAAGTGCATAAGTACAAATGTATTGTATATAATAAACAAAATTGTATTACAGTAGTGTACTATTATACTACACTTCAGTTTAATGTGCGAGTTTCTAAAACACTAGTTTGTCTTGTCTTTTGTATAGCGGAAACATCGGTACAGCAGGACAGTAAG[C/T]AGGTCCAGGTGGACATTCAGGATCTGGGCTATGAGACGTGTGGCCGCAGTGAGAACGAGGCCGAAAGAGAAGACACCAGCAGTCCAGGTGAACACATACACTGTAAACACTAGAGGGCAATACTGACTAAATCCATGCTGTTTAAAGGGATAGCTCATCTAAAAATGAAAAATTATATGGGGACAAAAGAAGTTATTTTGAAGAATGTTAAAACAGGTTTGAAACAAGGGGAGTAAATTATGACAATTTTCATTTTGGGTGAACTATCACTTAAATTTTATGGTTACACCTTAACTATACATGTACAGGGTTCCCACGCTTGAATTTCAGACATACGAATTCGAGGCCTGTATGGTACATAAAACAAACATACAGTGCTCGACATAATTGAGTACACCCCATCTTAAAAATGAATATCTTTATCTATTTCTCAGTGAATATAGGCAAAGTGCATTTAAACAAAACAGATTTATTAAACAGATATATTTATTCAAATAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32308
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000076946 Essential Splice Site 1756 2016 35 42
ENSDART00000136651 None None 92 None 5
ENSDART00000138338 Essential Splice Site 2189 2431 32 38

The following transcripts of ENSDARG00000054723 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 34657564)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 34730077
GRCz11 20 34632956
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACTTCAAGTGTACAAGAGAGTCTGTGGCACTGCTGAGAGCAATGCAGG[T/C]AAGAAACAAATGCACCTGTCCGAAACTCTTCATCAGACATTGCTAACTGC
Long Flanking Sequence:
TAAAATGAGATGAAACTAACCCTTATTTCAGTTTATAATAAAGTAACTATTGTAGCCAATCTGCCCTGAGTCCTGATACGTATTGCATTTGCATGCAGATGGCAGTAAAGAGATGGAGCGATTGAGAGAGGCGGTTCTTTCTGTACGTGGCCAGTTAAAGCAGGCGGAGCTTGAGGCAGACAAGTGGGCGGATCAGTGCAGGCGAATGCAGGCTCAGATTAGAGATCAAACTCAGACTGTACTGCAGCTTAAAGAAGAGAAACAGAACAGCCTGGACAACAGCACCAGGTACAGAGGCAATCTTGAGAAAAAACTGCATTCTGGAAAAAACTGTGACAGGGTGCATTGAATATTCATGTGTAATCTTCTGTGAACAGGCTACAGCAGGAGGTGAATGTTCTCCAGCAGCAGTTGAGTGAGTGTCAGTGTCTAGTACACACACTGCAGTGTGAACTTCAAGTGTACAAGAGAGTCTGTGGCACTGCTGAGAGCAATGCAGG[T/C]AAGAAACAAATGCACCTGTCCGAAACTCTTCATCAGACATTGCTAACTGCAATTTTTTTTTTAATTACTGGAATTTGTGTAGAATGTGCATCCAGCATTAGATTAAGAATAGGTCTACCAAACTAATGATTCTGTCAAAATGGTTGCATTAAAAACACTACTGCTGCGGCCCAATTCGCATATTATCTGTCCTAAGTAGTATTTCGAAAATAGAATTAGCATGTCCCAAACCGTGTTATGGTGAAGAGTATGTCAAAGGTTCCTGGATGGTGTATGATGCTTCCATTAGAAATTCAAAGTGTAGAACTGTACGTACTCTAACCACAAATATTGCCCATGTTACATTGCACAGTAGATGTTGATTCGATCAGTACTATAACTATAAAAATATCTACTAAAATGGCAGACATTTGAGACCAACCATTATGTAGAGAGGCTTCAGTAAAGTTATTTAAATGACTATTAATTGATATATAACCAGCTGGCAAATATTTAAATCA
Associated Phenotype:
Not determined