ZMP
enpp1
Ensembl ID:
ZFIN ID:
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 |
sa11561 | Essential Splice Site | Available for shipment | Available now |
sa23648 | Essential Splice Site | Available for shipment | Available now |
sa16086 | Essential Splice Site | Available for shipment | Available now |
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa11561
Status:
Available for shipment
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:
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:
sa23648
Status:
Available for shipment
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:
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:
sa16086
Status:
Available for shipment
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:
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