Busch Lab

ZMP

enpp1

Ensembl ID:
ENSDARG00000005789
ZFIN ID:
ZDB-GENE-040724-172
Description:
ectonucleotide pyrophosphatase/phosphodiesterase family member 1 [Source:RefSeq peptide;Acc:NP_0010
Human Orthologue:
ENPP1
Human Description:
ectonucleotide pyrophosphatase/phosphodiesterase 1 [Source:HGNC Symbol;Acc:3356]
Mouse Orthologue:
Enpp1
Mouse Description:
ectonucleotide pyrophosphatase/phosphodiesterase 1 Gene [Source:MGI Symbol;Acc:MGI:97370]

Alleles

There are 11 alleles of this gene:

Allele Name Consequence Status Availability
sa12823 Essential Splice Site Available for shipment Available now
sa17193 Essential Splice Site Available for shipment Available now
sa6620 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa11561 Essential Splice Site Available for shipment Available now
sa156 Nonsense F2 line generated Not yet available
sa23648 Essential Splice Site Available for shipment Available now
sa36987 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16086 Essential Splice Site Available for shipment Available now
sa43395 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12823
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045183 Essential Splice Site 43 878 1 25
ENSDART00000127350 Essential Splice Site 43 876 1 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13318235)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13507481
GRCz11 20 13403461
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACACAACACTGCAAAAGTCCAGTCAAGATACYTGAAAATCCTCTGTGCG[G/A]TAAGCGGACACTCNTCGGGGAAACAAAAGCCGGTTACTGAATCTARGTTAA
Long Flanking Sequence:
ATGTAATTGGTTTCAAACCGAATGTCTAATGAATGTCAAACAAACATTATACGATATGACGTGTTGTTGATCAAGAAGGCATCCTATTGTCCATTAGATAATGTCCGTAGATTATATATTACTGATATTTTACTGATATTGTTATTTTAGTGCAAACATGGTTTGCCTAAGTCCTGCCCTTTCCCAGGTTTAAATATAATTAGCCAGAAAGAGAGGGCATGTGCTGCCGATCATGTTACCTTTGGTTGACTAGACCGCAGCAGCTGGGCGGTCCTTCAGCTTCATGAACTACAAAGTCACTAGAGAACAAAGTTTGAAATGAGTCCGAGCTCAACAAACCTGTGCAAGGCAAAGCGAGCGCGCGGTCAATAATGGACTCAGCCAAGCGGGATGAACACATGAGCGAACACGCCGCCAACCTACTGGGCACAGGACAGCGGTACACACGGACACACAACACTGCAAAAGTCCAGTCAAGATACTTGAAAATCCTCTGTGCG[G/A]TAAGCGGACACTCTCGGGGAAACAAAAGCCGGTTACTGAATCTAGGTTAACCAAACATGACTGACTCGGGTTAAGTTACTCGTTTAAACTTTTTGCTTAAAAGTTTGTGCAGGGATTGATTGTTCTTTATTGTTATTTAAAATAAGTTTACAATAGAGTGTAGTGGACTGTTTTATAGTAAAAACTGAGTATACGGTGTATATTTAGATAAACAAACAGTAAAATACTGTGCTTGGCTGCTTTTCAGAAAAAAAAAAACACACAAATGTGTTAATGTTTTACATGCATTTTTAGGTAAATGATAATTTATTCACAGTTTTTTTTTTTTTTTTTTTTTGAAAATAACCTATTTAAAAAGTGGATTAAACAATTTATGTTTTTAAGGTATTGTCAGACCTTTTCACCCAGTGATAAACTATCTGGGAGATTAAAACCATATATATATATATATATATATATATATGAGCAATTCCATGAAAATGTCAACCTTGCCATGAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17193
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
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045183 Essential Splice Site 43 878 None 25
ENSDART00000127350 Essential Splice Site 43 876 None 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13318236)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13507482
GRCz11 20 13403462
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACAACACTGCAAAAGTCCAGTCAAGATACYTGAAAATCCTCTGTGCGR[T/C]AAGCGGACACTCNTCGGGGAAACAAAAGCCGGTTACTGAATCTARGTTAAC
Long Flanking Sequence:
TGTAATTGGTTTCAAACCGAATGTCTAATGAATGTCAAACAAACATTATACGATATGACGTGTTGTTGATCAAGAAGGCATCCTATTGTCCATTAGATAATGTCCGTAGATTATATATTACTGATATTTTACTGATATTGTTATTTTAGTGCAAACATGGTTTGCCTAAGTCCTGCCCTTTCCCAGGTTTAAATATAATTAGCCAGAAAGAGAGGGCATGTGCTGCCGATCATGTTACCTTTGGTTGACTAGACCGCAGCAGCTGGGCGGTCCTTCAGCTTCATGAACTACAAAGTCACTAGAGAACAAAGTTTGAAATGAGTCCGAGCTCAACAAACCTGTGCAAGGCAAAGCGAGCGCGCGGTCAATAATGGACTCAGCCAAGCGGGATGAACACATGAGCGAACACGCCGCCAACCTACTGGGCACAGGACAGCGGTACACACGGACACACAACACTGCAAAAGTCCAGTCAAGATACTTGAAAATCCTCTGTGCGG[T/C]AAGCGGACACTCTCGGGGAAACAAAAGCCGGTTACTGAATCTAGGTTAACCAAACATGACTGACTCGGGTTAAGTTACTCGTTTAAACTTTTTGCTTAAAAGTTTGTGCAGGGATTGATTGTTCTTTATTGTTATTTAAAATAAGTTTACAATAGAGTGTAGTGGACTGTTTTATAGTAAAAACTGAGTATACGGTGTATATTTAGATAAACAAACAGTAAAATACTGTGCTTGGCTGCTTTTCAGAAAAAAAAAAACACACAAATGTGTTAATGTTTTACATGCATTTTTAGGTAAATGATAATTTATTCACAGTTTTTTTTTTTTTTTTTTTTTGAAAATAACCTATTTAAAAAGTGGATTAAACAATTTATGTTTTTAAGGTATTGTCAGACCTTTTCACCCAGTGATAAACTATCTGGGAGATTAAAACCATATATATATATATATATATATATATATGAGCAATTCCATGAAAATGTCAACCTTGCCATGAAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6620
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045183 Essential Splice Site 355 878 11 25
ENSDART00000127350 Essential Splice Site 355 876 11 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13362098)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13551344
GRCz11 20 13447324
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAAGAGCCAGATGCATCAGGACWCAAATATGGACCAATGAGTACCCAGG[T/G]AAWCTAAAAAAGGAAAATAATTGTTAAACTTAAATATTTGCTTAGNTTAGG
Long Flanking Sequence:
CTACTTGTAATCTGAAACACTCTAATAAGAAATATTGTCTTTTTCTTTGATTAGGAACATTCTTTTCGAAAAGAGGATAGCACAGATCTTTCAATGGTTGCATTTGCCTGAAGGAGAAAGGTAATATTTATTTATTTATTTATTTATTTATTTATTTACTTGTTTATTTATTTATTTGTTTATATATTTATTTATGTATCGATATGTTTATTTATTTATTATTTGTTTTTTTTGTTTGTTTGTTCTCCCTCAACCTTTAAAAGTAGTAACCTTCAATTGTTGCCTTCAGTCTGTTTCAACATTTATGAATACATAAAATACTGCGTTATTATATAAATTCTTAGTGATGTTAAATAATATTTTTTTGACAGGAAGAAAAAAAAAAAAGATGTTGGCATTTTGAGATCAGTGTGTCTTTTGTTTCAGGCCAGACTTTTACACCTTGTACTTCGAAGAGCCAGATGCATCAGGACACAAATATGGACCAATGAGTACCCAGG[T/G]AAACTAAAAAAGGAAAATAATTGTTAAACTTAAATATTTGCTTAGTTAGGGGAAAATTTCTGATTTAGTACATAGAATATTAAATGAAGACACCATTATAATTATTACACTTCATTTTTTTTTCTGTTGGCTCAAACTAATAGATTTATCATGAGCTGAAACAATACAGTTCTTGAGTTGTTTTGGGGATAACCTAATTGTTTAATATGATCCACTTAAATTTGTAGAAACAATTAAGTTAACTTAATCGATTTGTGTTGTGTAGAAACAGCATGAATCATTTGTGTGGATATATATATATACAACTGAAAGCTGAATAAATCCACTGATGTGTGGTTAGTTCGAACAGGATAATATTTGACACAAAAAAATCAGGAATCTGAGGGGTGCAAAAAAATTGAAATATATTTTCAATGTAATGCATTCATGTTTATTCCTATAGTAGTTTGTTGTGAATTTCTCTTTCTGGCTCACGGCACCAAAACTGTTGTGAATTTTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11561
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045183 Essential Splice Site 392 878 12 25
ENSDART00000127350 Essential Splice Site 392 876 12 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13366101)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13555347
GRCz11 20 13451327
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGAAATCTGCACAAATGTGTCAAYGTGRTTCTTGTATCAGACCACGG[T/A]GAGTACAGCATTGCATTTTCAAGWKTAACTTTAATGGTAAATAATAAACA
Long Flanking Sequence:
AAGAAAGAATGCCACTTTGAAAGAGAAACTTTAGAGAAATTTTATGTTGGCATGGGATCTGAGTGATTACTTTAGATCACTTGCAAATTCTCAGTAGCCATATGTTGTTAGGACACAGTGTAAGGCTGGTTTTGTGGTCCAGGTTCACTTATGATTGGTATTTTAATAGTTTACTTTTTTCTTAGCTTTCTTTTTTCTTGTTTAACATTAATGCTAATACTCTTATGTTATATTGACTTTATTCTGCAATACAGAAGTGTGCTTATTGTTTTAGAACTTTTGATTCAGTTGCTTGTGAGAGAAATGAGGAATAATAATGGACAGAAAACAGGCAAACTTCTCACTCTATAAACAAAAGAATATACATGAACGATTGATTTTTTGTTGCAGGTTATTGAGGCATTAATTAATGTTGACAGGCTGATTGGGATGTTGATGGATGGTCTGAAGGAAAGAAATCTGCACAAATGTGTCAACGTGGTTCTTGTATCAGACCACGG[T/A]GAGTACAGCATTGCATTTTCAAGTGTAACTTTAATGGTAAATAATAAACAATAAAATAAACATTTCAAGATCTCACGTAAATTTAAGTTCTTATTGAGAGTTAACTGAGGTTTTTGATATTGTTTTAATTTTTTTATTTGAAGTCAGTATTGTGGTGATTAGTGTGACTTTTTTGGGGGTCGTTGCCTATTCACTTTGTAACATTAGTAAACATTTAAAAAAACTTTGACTGCATTGATTTGCGAAAAGAGATAGAAAGACAAAATATGATTAGGTGTTGGCTATGCGGTGATATTTGAATAGTGAGTTAAAAACGGTGGCGATCCTGCTTGAATGGTCCTGGTTTAAGCTAAGAGGAAAGCGTGTGTTTGTTAATGTTAGTCAATGGAAAGTGCTTAAAAATGTTTAAAATTGACTTAAAAATGTGTAAGAACACTGAACTTAAAATTAGAAAGCAATGTAAGTGTTTTAGTAGTTTAAAGATACAAAACAGCAGTATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa156
Status:
F2 line generated
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
ENSDART00000045183 Nonsense 427 878 13 25
ENSDART00000127350 Nonsense 427 876 13 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13377632)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13566878
GRCz11 20 13462858
KASP Assay ID:
554-0017.1 (used for ordering genotyping assays)
KASP Sequence:
ACATCAATGACATCACTGTGATCCAGGGTCCTGCCGCGAGAGTCCGACCR[C/T]GACACGTGCCTGAGGAGTTCTTCTCCTGTACGTGCACAGATTTAACTTGA
Long Flanking Sequence:
AGTATAAACATGTATACTTTTTCACACATAAACTGTAAATTCTAACAAAAAGCCAGGATGTACACTGTATTTTAAGGTACAGTTCTCTTGCTATAAAAACGTTTGCTTTGACTTAATAAGCTCAATACTTAATACCCAATATTATATAAACATTCAGGAATGTAAGAAGCATCAAGTAATATGCTGTGTATTAGTCATTAAGGTAGCAGTTTGGTTTTAAAAAAAAATTTTAAACATAGACTAAATATCCCAAGAAAAAGTTAGAAGTTCACAATCAAAATTTTGTAAACATAAACTCCCCTTTTTTAATGCTGTGGTAGAAAAAAGCGTGCATATCAAACACACAAGTGTCATTAAGTCGAACTCTGGTCTACTCTGTGTCTGTGAAACATTCAGGAATGGAAGAAGCGTCATGTAAGAAAGCTGCTTACGTCTCCAACTATCTGGACAACATCAATGACATCACTGTGATCCAGGGTCCTGCCGCGAGAGTCCGACCG[C/T]GACACGTGCCTGAGGAGTTCTTCTCCTGTACGTGCACAGATTTAACTTGACACACATCACTTCTTGATTCTCTTTCTATTTGAGTGTTTCTTCAGCTTTAAATATTATGAGTTATTAATTTGTGTAAGTGTTATGTCCATCAAATTTACTTTTTAATCTCTGTCTTTTGTCCTGTATTCATCTGGCAGTTGATTATGAAGGCCTGGTGAAGAATCTTTCGGTATGACCCTGTCTCAAAATCCCTCACCCAACTTAAAGGGACAGTTCATCGCAAAATTAGTTTTACCCACAGTCAAATGGTTGAAAACTTTTATGAATTTATTTCTTCTGTTGAATACAAAGGAAGATATTCTGAAGAATGTTGAAAAAAATCAGCTATTGACTTCTATAGTAGGAACAAACAATATTATGATAGTCAATGGCCTGCATTCTTCTGTTTATCTTACTACAAGTTTGGAACAAGTGAAAGATGAATAAATGATGACGGACTTTTCACTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23648
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
ENSDART00000045183 Essential Splice Site 489 878 None 25
ENSDART00000127350 Essential Splice Site 489 876 None 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13378347)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13567593
GRCz11 20 13463573
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATTGAGAGAGCACATCTGTACATGCAGCCGCAGTGGCAAGCAGCACTG[T/C]GAGTTTTATTATTCTTGTGTCAAAATATATGTTAAGTTCATTGATTTTCA
Long Flanking Sequence:
CTTTCGGTATGACCCTGTCTCAAAATCCCTCACCCAACTTAAAGGGACAGTTCATCGCAAAATTAGTTTTACCCACAGTCAAATGGTTGAAAACTTTTATGAATTTATTTCTTCTGTTGAATACAAAGGAAGATATTCTGAAGAATGTTGAAAAAAATCAGCTATTGACTTCTATAGTAGGAACAAACAATATTATGATAGTCAATGGCCTGCATTCTTCTGTTTATCTTACTACAAGTTTGGAACAAGTGAAAGATGAATAAATGATGACGGACTTTTCACTTTTGGGTGAACTGTTTCCTTAAAAACCATAGGTTCTGGTTAAACATTGTGACAACTGTATAATTTTTTTTGTCTTTCTGTATTTGAAGTGCAGAGAACCGAATCAGCCGATGAAACCGTATCTGAAGGAGCATCTGCCCAAACGGCTTCATTTTGCGAAGAACATCCGCATTGAGAGAGCACATCTGTACATGCAGCCGCAGTGGCAAGCAGCACTG[T/C]GAGTTTTATTATTCTTGTGTCAAAATATATGTTAAGTTCATTGATTTTCATTCAAAAACCTCACGTTTACCTCACCAATCACATTTAAACACTGCAGACACAGTCAATTTTTTTCTTTTCCAAATATTGAGAATATTCAATATTTTATTTTACTATTGTAAACAAAATATAAAACCACTTACAATAACATATTTTATACAATCAGATATATGGCCGTGAAATGACCATTATTTTGATTTATTTGTCATGTAATAATTACACTTGGTTTCAGAAAAATTGTACAAATATTGTAAAATTGTACAAAATTTTTATTTTTTTTTTACTTTATACACAGGCGGCAAGATGGCCCAGTGGTTAGCACTGTTGCCCCACAGTTAGAAGGTCGCTGGTTCAAGTCCCAGCTGGGCCAGTTGGCATTTCTGTGCGGAGTTGTTCTCCCAGTGTTGCCGTGGGTTTCCACTGGGTGCTCCAGTTTCCCCCACAGTCCAAAGACATGTGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36987
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045183 Essential Splice Site 603 878 18 25
ENSDART00000127350 Essential Splice Site 603 876 18 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13400807)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13590053
GRCz11 20 13486033
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTGAGAGACCCTCGTGGGTGCACCTGTGACTCCCTCACCGAGGCCGAG[G/A]TCAGAGTCAAACACCTCCATCACGCATTCATTATGTTCATCCACATCTGT
Long Flanking Sequence:
GTTAGCACTCAGGTGTCTTCTTGTCTACCATACCTTTACTTACCTGGAGCCTTGTCATTCCCGTGTTCCTTCCACCAGTTCTCTGGGCTATTTGTTATTTTTCTACCCTACCCAAGTTAAAACAGTTTTTTTCCGTCACTTACTGTACGCGTGTATCTTGATTTGTATTCACAGATATGGATGATTCTGTCCCTTGGAAATTCAAAAAACTGTTCATACTTTGTTTGCAAATGACAAGAATGATTATCTAAAGAATCTTTGAGGGCCAAAACTCTGCTAAATGAAATCAAAGTAATTGTGTTTATCTCTCTTTAGATTTGCTGGGGATTTCTCCTGCTGCCAATAATGGCACCCATGGCAGTTTGAACCACATACTGAAAAAGCCGCGATATCAGCCGGTGTTTCCAGCAGAGCGTTCGGCTCCATCTACATGCAGTGCTGTCAGCAGCAGCTTGAGAGACCCTCGTGGGTGCACCTGTGACTCCCTCACCGAGGCCGAG[G/A]TCAGAGTCAAACACCTCCATCACGCATTCATTATGTTCATCCACATCTGTTTTTACATGAAGCAATGCTAAACCACAATCTCTTATGATTGTTCATACTTATTGTAGCACAGTACATAATGCATTTCATTTCTATACTGTTGACCTCAAATTCTTGTATCCCATCAAACTATACAAGCTATAACACTAAATCAAATTACTTGGATGCTAACAGGGACACACGGACCATTGACACAAGGCATAGAGTTAGCATGGAAGGAGATGACATGTCCACAACAATATCCAACGATTATTAAAATGTCTCCACCAATAATTTAATCCACTCTAAATGAAGAGATATGAAATGAGTATTGTCAAGTATGATTACTAATTAATTACTAATTACTTATTAATTGGGCCTCTGGTTTTGATCCATTCAAATGCACAGATATGAGTGAGAAATGAGACAAACACATGCGTACACAAATACACAGTGATCACACAACCAGAGCAGTGGGCAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16086
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
Order Allele From EZRC
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045183 Essential Splice Site 780 878 24 25
ENSDART00000127350 Essential Splice Site 778 876 24 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13432613)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13621859
GRCz11 20 13517839
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGTACTTGGCAACAAATAAGCAGATGCAGATGRTTGTCCTCTACTTTC[A/G]GGAATGGAGCACCGATTCCTACACATTTCTTTATTATTCTTACAAGCTGT
Long Flanking Sequence:
ATTTTACAACAATATTTTATTGTTTTTGAATATTACCAACATTTTATTCAACCAATTTAATTCAAGCTCTTTAAAAAATGATTGTTTAAAACGGTTGATTTCTAAAGTTATAAGGCTAAGTAAAATATTAAAATCAGTTAGGACTTTCATGGCGCTGCATACTGTATACTAGGGTATAGTTACAAAGGTGCTTGATTTAAAAAGATTGATGGTTTAAAAAGTCAATGAATGTCCTTGAATCTGTTGTTGATGAAAGTGTAGGAACCCAATGTCAATGGCTTGTTTTTCTAACATTCTTCATCATTTATGAAGTTTTATGTTTAACAGAAGTTTAGAACCACTTGAAATGTTAATTTTTAAGTGAACTTTTTGTTTTATACATTAGGTTCTCTGTTACTATCTCATAAACTGTTCATACTGCCCACTGGTGGCCAAACTATGTAAAAAAAACAAGTACTTGGCAACAAATAAGCAGATGCAGATGATTGTCCTCTACTTTC[A/G]GGAATGGAGCACCGATTCCTACACATTTCTTTATTATTCTTACAAGCTGTAAGAACTCATCTCTATCAGTGCGCCAGTGTGAAGGTCCTTTAGACGCCGTGAGCTTCATTCTGCCTCATCGTCCTGATCATCTGGAAACATGTCATGTATGTAGTCAGCCATTTATAAACTACAACCGTTAATATAATATACACAGGAAGTATTGAGTAATTGGCTGCTTAGGTAACTTGTTAACTATTTTTTTAAACTCATGCCACACTTGTATTAGTTTAAAGGCATAGTTCACCCAAAATAAAAACCTTTTAAGTTATTTACTTACCACAAAATCACTAACAATCAAGGTTGTGAAGTGATACATTACATTTTGTTTTTCACAATACAATTGTAGAAATATAACAATTTATCAGTATTTCCAAACAAATAACATGTATTGTAGGTTTCAGACATGTAAATACACATAAAGAAGGCCCATACAGAATCTGCACCCACAGAAATCCACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43395
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
ENSDART00000045183 Nonsense 870 878 25 25
ENSDART00000127350 Nonsense 868 876 25 25

The following transcripts of ENSDARG00000005789 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 20 (position 13435050)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 13624296
GRCz11 20 13520276
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACAGGCTTGAGTTTTTACCATGACCGGATATCTGTAGCAGAAACGCTA[C/T]AACTCAAGACCAGACTCAAAACCTTCTAGAAAGATTAGTGAACTCAGACC
Long Flanking Sequence:
TGTGTTTGGACTGTGGGGGAAACCGGAGCAACCAACCAGAGGAAACCCTTGCAAACACAGGGAGAACATGCAAACTAGCCGGGGCTGATCCAGCAACAATTCTAGAACAGAAATTGTTATTTTAATGGAGCAGTGTATTTTGTTAATTGTTTACTGGAGTAACTTAAACACAAGCTGCAAATGCTACGCCTTCTTCTGGAAAGGGACAAGGGCAGTACCTCATTTGCAAATAAATAGTCACACAAAAACTGTTTTCGCTTTCAGTTTGATATTTTCCTCAAGAATGAATCTGACGTTTCTCTCACATTTATTTATATTTTTCTTATTGTGCATTTATTTTTTACACTTCCATTTTGTTTTCTCATTTCTTTTTCCAGAATGGCACCGACTACTCATGGTTTCAGGACTGGGTTCAGCTTCACGTGGCGCGAATCAGAGACATTGAACTTTTGACAGGCTTGAGTTTTTACCATGACCGGATATCTGTAGCAGAAACGCTA[C/T]AACTCAAGACCAGACTCAAAACCTTCTAGAAAGATTAGTGAACTCAGACCTCATTTCACTGCAGACCCATTCAGAAAAGCATCTTTCAACATCAGAAAGAAGCGGCACTTTTAGCATACTCTAAAACAAAGACACAAGTTCATTCAGAGACTCTTTGATCTGGGAGTATAAAAAATGGGAGTATAAAACTTCTCTTTAATAAAATCTTTATTCTCAGAGTGAATTTATTTATTACTTGGGAAGTACCGACTGGCACTGTGAGTCCCTAAAATTCTGTTTTTCAAAGAAAACTGTTTTCCAGCACACATATGTTAGCGATTTAACTGTGGTTGCATGTAATCCTTCATTGAGCATGTTCAAAAAAGAAAGTTTTAAGAGTTTTGTGCCACTTTTGCCACAGGAATCACTCTACATTTCAACATTTAGTGTGTGTCTGTGTGTTCTGTTCTATTTAAAATTAAATTTATTCCCTTCCTAGTAGTTTTAATGACGTATGTACA
Associated Phenotype:
Not determined