ZMP
entpd1
Ensembl ID:
ZFIN ID:
Description:
ectonucleoside triphosphate diphosphohydrolase 1 [Source:RefSeq peptide;Acc:NP_001003545]
Human Orthologue:
ENTPD1
Human Description:
ectonucleoside triphosphate diphosphohydrolase 1 [Source:HGNC Symbol;Acc:3363]
Mouse Orthologue:
Entpd1
Mouse Description:
ectonucleoside triphosphate diphosphohydrolase 1 Gene [Source:MGI Symbol;Acc:MGI:102805]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17164 | Essential Splice Site | Available for shipment | Available now |
sa22131 | Nonsense | Available for shipment | Available now |
sa16712 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17164
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066257 | Essential Splice Site | 134 | 492 | 5 | 10 |
ENSDART00000126466 | Essential Splice Site | 138 | 496 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 32415246)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30636223 |
GRCz11 | 12 | 30751125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTGAATTAACTGTCAAAAGGTAAATTCCAAWACTWTTTATTTTCTCA[A/T]GGATGGAGRATGAAATGGCCTCAGAAAAAGTGCTTACCTCCGTTGCACAT
Long Flanking Sequence:
ACTCACTAATGAAGCATTTAGTTTTTCCACTTACAAATTCCAGCATGATGCAACTTAAAGGGGTGACTCTTAAAGGGAATGGGAGACAAGAGTCTAGTTGGTTTAATGCACATTAGGCTCAAAACATACCCATAACTCATTAAGAGAATAAGCACAGCCCGGTTAGACCATGCGCTGTGATGCAAACCTTATTTTTCCATCCTTAAAATAGTAAAAGTGGTCTCAGACACATCCCAAATGCTTTTGTGCCATGTGCTTTAGACTTTGCGCCTAGATCATTAAAAGAGCACAAACTAGCAAAAATCTACACACACAGCACATTTTTCCACAAGATTGTTTTATTCAATCACATTTTTAATAAAAAATAATATGCAAGTAAGCATAAGTAATTAGCAAACAAAATGTGCCTTATTCCCAACTTCATATAGTCTATATAATTCATCAAGTGTATTTTTGAATTAACTGTCAAAAGGTAAATTCCAAAACTTTTTATTTTCTCA[A/T]GGATGGAGGATGAAATGGCCTCAGAAAAAGTGCTTACCTCCGTTGCACATTCACTGAAGACGTACCCCTTCTCCTATCAGGGAGCTCGTATCCTTTCAGGCCAAGAGGAGGGAGCTTTTGGGTGGATTACAGTCAACTACCTTAGTGAAAACTTGAGAAAGGTACAGTTGTGTTTTCACTGCATCAAATATATATAGAGTAATAAATGTAATATGTAGAGAGTATAGAGGAAGGCAAATACTGTACAATAATCCCTGTATTTATCACGCAGCCCGCAGGCACTCTTGGAGCTCTGGACCTTGGTGGAGCCTCTACTCAAATAACCTTCGTACCTCAGCAGATTATTGAATCATCTGACAATTCGATTGACTTCAGACTGTATGGAAATGATTATCATCTATACACCCACAGCTTTCTCTGCTATGGGAAGGACCAAGCTCTCAAGCTTGCTATGGCTGAGAAATTGCGCTCAACACCTGACAAGGTATGCCATGCTCGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22131
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066257 | Nonsense | 280 | 492 | 7 | 10 |
ENSDART00000126466 | Nonsense | 284 | 496 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 32408229)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30629206 |
GRCz11 | 12 | 30744108 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTAAGGGATCCTTGTTTTCATCCTGGATATAACACCACCAAGACGCTT[G/T]AAAGTGTCAATACACCGTGTATGAAACCACTGAAAATGCCAAAGGAGCAG
Long Flanking Sequence:
TATATATATATATATATATATCCTTAATATTTTAATTCTAACATGCAAACTACACACAGAAATGCCAACTGACCCAGCCGAGGCTTGAACCAGTGACCTTCTTGCTGTGAGGCGAGAGCGCCACCCACTGCGCTACCGCGCTGCCTGATATTAGATATACTAATAGACATTTCATTTTGATATTTACTATAATCTTTTGACAGCTGACCAATTCATGGTATTTAGGCTTTTAGAAATGAGGAGCTTTGAGAAAGCAAATCTTACATTTAGCCATTTAGTAGTCACTCTTGTCTAAAGCGACTTAGTTTGAACTGTGCAAACTTTCAATTGGAAGTTGCATTTTGGCATATAACTTCTGTTAAATGTAACTACTGCATTTTATTGGCTACATGTGATTTTACTATATGTTTTTTAATCCGTTTTCTTTCCTCCGAAAGACAGATGCCATTTTGTTAAGGGATCCTTGTTTTCATCCTGGATATAACACCACCAAGACGCTT[G/T]AAAGTGTCAATACACCGTGTATGAAACCACTGAAAATGCCAAAGGAGCAGTTCTCCCACGTGGGGCTTGGAAATTGGTCTCAGTGCCAAGAATCAATCAGAAAGGTTTTTAATACTAGCCATTGTCCTTATTCAGGCTGCTCATTCAATGGTGTTTTCCAGCCTACTGTTGAAGGAAAATTTGGGGTAAGAAACAATGAAGATTGTTTGAATGAATTGGTTAAGTTTTAAGTCACAATCTGTGTTAACACTTGTGCCGTTTGACTTTCTAGGCTTTTTCTGCTTTCTTCTTTGTAATGGACTTTTTAAATCTGACAAACGATTCATTAGACAAAACAAAGCAGAGGCTGGCAATGTACTGCTCTACCCCATGGCAAAAGGTGAAATTGAGTTACTTCTGTGTAAAATGCTGGTATCTTGGTTGGGATTTAAATGTGAACATGTTTGGCTTTTTTCAGATTGTACAAGATCACCCAAAAGTAAAAGAGAAGTACCTTTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16712
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066257 | Nonsense | 305 | 492 | 7 | 10 |
ENSDART00000126466 | Nonsense | 309 | 496 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 12 (position 32408152)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 30629129 |
GRCz11 | 12 | 30744031 |
KASP Assay ID:
2260-5557.1 (used for ordering genotyping assays)
KASP Sequence:
CCACTGAAAATGCCAAAGGAGCAGTTCTCCCAYGTGGGGCTTGGAAATTG[G/A]TCTCAGTGCCAAGAATYAATCAGAAAGGTTTTTAATACTAGCCATTGTCC
Long Flanking Sequence:
CCGAGGCTTGAACCAGTGACCTTCTTGCTGTGAGGCGAGAGCGCCACCCACTGCGCTACCGCGCTGCCTGATATTAGATATACTAATAGACATTTCATTTTGATATTTACTATAATCTTTTGACAGCTGACCAATTCATGGTATTTAGGCTTTTAGAAATGAGGAGCTTTGAGAAAGCAAATCTTACATTTAGCCATTTAGTAGTCACTCTTGTCTAAAGCGACTTAGTTTGAACTGTGCAAACTTTCAATTGGAAGTTGCATTTTGGCATATAACTTCTGTTAAATGTAACTACTGCATTTTATTGGCTACATGTGATTTTACTATATGTTTTTTAATCCGTTTTCTTTCCTCCGAAAGACAGATGCCATTTTGTTAAGGGATCCTTGTTTTCATCCTGGATATAACACCACCAAGACGCTTGAAAGTGTCAATACACCGTGTATGAAACCACTGAAAATGCCAAAGGAGCAGTTCTCCCACGTGGGGCTTGGAAATTG[G/A]TCTCAGTGCCAAGAATCAATCAGAAAGGTTTTTAATACTAGCCATTGTCCTTATTCAGGCTGCTCATTCAATGGTGTTTTCCAGCCTACTGTTGAAGGAAAATTTGGGGTAAGAAACAATGAAGATTGTTTGAATGAATTGGTTAAGTTTTAAGTCACAATCTGTGTTAACACTTGTGCCGTTTGACTTTCTAGGCTTTTTCTGCTTTCTTCTTTGTAATGGACTTTTTAAATCTGACAAACGATTCATTAGACAAAACAAAGCAGAGGCTGGCAATGTACTGCTCTACCCCATGGCAAAAGGTGAAATTGAGTTACTTCTGTGTAAAATGCTGGTATCTTGGTTGGGATTTAAATGTGAACATGTTTGGCTTTTTTCAGATTGTACAAGATCACCCAAAAGTAAAAGAGAAGTACCTTTCTGAATACTGCTTCTCAGCAACATACATTCTCACTCTCCTGGAACATGGATACAATTTCACCTCAGACAACTGGAACGAC
Associated Phenotype:
Not determined