ZMP
entpd2a.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human ectonucleoside triphosphate diphosphohydrolase 2 (ENTPD2) [Source:Uni
Human Orthologue:
ENTPD2
Human Description:
ectonucleoside triphosphate diphosphohydrolase 2 [Source:HGNC Symbol;Acc:3364]
Mouse Orthologue:
Entpd2
Mouse Description:
ectonucleoside triphosphate diphosphohydrolase 2 Gene [Source:MGI Symbol;Acc:MGI:1096863]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38478 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa10744 | Nonsense | Available for shipment | Available now |
| sa38477 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa17661 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38478
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000043259 | Essential Splice Site | 37 | 454 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 31207298)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28968655 |
| GRCz11 | 5 | 29568808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATCCAAGACAAGTTTGTGGAAAATGTTAACAGATGTGTTTGTCTCCA[G/A]TATGGAATAGTTCTGGATGCTGGATCCTCTCATACGTCCATGTTTATCTA
Long Flanking Sequence:
CACCACTGAATATTTCAAATAAACATTCCATCCATCTGCATAAAATATAATAAACTAGATAAATACAAAACAAAGGATATAAAACAGAAAAACAAATTGTGCTTTATATATTTTTTCCAAGTCTTAAGTAGTTAGACATTGAATTATCCAATGTAAAGTAGCTCTTCACTATATATAAATTAAATGCAATTAATCTTTGTTAATGCTAAAATTATATAATTTCTTGCACCCTCATGCTTTAAACTCACTTATGTTAACATCATAACAGAAAAAAAGCTCATGAAAATTTTGAACTTTAACTATACAATGGCTAAACTTTGCAACTAAGTAAAAAAAAACCACATGCATTTTAAATTGTGGTCACCAATAATCCCCATCCTGAGATGTGACTATTGCGGATGTGCACATTTCAATTGTTTATGCTGAAGTGACATATGGTGCAGCCCTAAATGAATCCAAGACAAGTTTGTGGAAAATGTTAACAGATGTGTTTGTCTCCA[G/A]TATGGAATAGTTCTGGATGCTGGATCCTCTCATACGTCCATGTTTATCTACAAATGGCCAGCAGATAAGCAGAACGGCACTGGCATTGTCAGTCAGCACAGCGAGTGTCGTGTGAAGGGTGAGTAAATAGTATACATAATTTTTATTTTCTGATTGTAGAGGTAACAGAAAGAAAGAAGATACACAAGAAGTGTAAGATTGACACTTACCCTAATATCAAATACAGAGAAAACTCAAACATCAGATATTGCAGAACTCAGATGTAAAAAATTAATTATTGAAAGGGATTTGTCTTCATTTATTCTTCCTAAATATAGTTCTGAATTGGTCATGCTTTTTTATCTCATTGTTATTCTTCTGTTGTTCTCACATTGCTTCAGGTGAAAACATCTGCAGAAATGTAAATGAGACGAACAACACAGCGTTCCTAATTCATTTCCAGCATTGCATTAAATTGCATTGCATTAAATAATTGTCCCATGTTCTCTCTCTTATGATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10744
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000043259 | Nonsense | 353 | 454 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 31204582)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28965939 |
| GRCz11 | 5 | 29566092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNTATCTCTTTCTTTGGCACAGGCATTTTCTGCATTTTATTACATTCAT[C/T]AATTCTTGCAAAAAGCTGCAGGCATCACCATCACGTCTCCAGCGGATTTA
Long Flanking Sequence:
TAAGCCTTGCTACTGTGTAAAATATTATTCTTGAAATAAATTAGAAAAAACTTAGGAGTTGTTTCTTTTTAGTGAATCAGTGACATATAGTACATCACAATTAGCGTGATCTGACTCCTGAATAATTTATTCATAGAGTATGAGTTGTTCATTTTAGTGAATCAGTAAGATACAGTGAAGCTTTGACTCTTGAACAAATAGTTTTAAAATTGAGCAATAGTCTGATTGCCAACCAAATAACTATACATAGTCTGCTCCTTTTGGGGAATCAAAAAAATACCTTGTAAGCATTGTAGTCTGTTTCTCAAACCGTCTGGTTTGGAAATGTTGAACACCTTACAATCTGAATCTCTTGATGAGAGGGAAAAAAAGAACCCCTTAGATCCCAAAAGACTTTGTGATAAACTAAACTTTGAACAAACTATTATTCGCATATATATAGCTAATACAGTATATCTCTTTCTTTGGCACAGGCATTTTCTGCATTTTATTACATTCAT[C/T]AATTCTTGCAAAAAGCTGCAGGCATCACCATCACGTCTCCAGCGGATTTAGAGCACGCTGCCCAGTTTGTCTGCAACATGAGTTTTCAGCAGGTACCAGCCCATTGAGAGAATGTATTTATTTTAAAGGAACAGTTCACCAAAAGAATTATCTACACACTCTCAGAAATAAAGGTACAAAACCTGTCACTGAGGTGGTACCTTTTTAAAAGGTAGTTTTTTGTTTCTAACAGGTCCTTAAAGGCACATATTAATACCTAAAAAGTACAAATGTGTACCATAAAAGTACAAAAGTAAACCTTAAAGGCACAAAAAGTGTACCCTAAAGGTACTAATTGTCAAAACTGTACCTTTTGAAAAGGTACCACCCCATTGACAATTTGTGTACCTTTATTTCTGAGAGTGCATGTACACAAGGTCATCTGAGATGCAGGTGTTTTTTTAAATTCAATTAAATTTGCCTTTATTTGTATAGCGCTTTTACAATGTACATTGTGTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38477
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000043259 | Nonsense | 428 | 454 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 31202468)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28963825 |
| GRCz11 | 5 | 29563978 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGATATGGTTTCAGTGATCTCTCCTTTCCACACATCTCCTTTCAGGAA[A/T]AAGTAAGACACTCAGAAAGACCACTATGCAGTTTTAAGACATATCCTGTC
Long Flanking Sequence:
TAATGCAGTATTTCATCTTAGCTGTTTATGAAATTCAGTTCACTTAACCTTTATTTCTATAGCTCTTTTACAATGTAGACTGTTAAAGCAGCTCAACACAGAATTTGTTGTAAATTAATACTGTATCAGTCCAATTTTTAGAGTTGAAGTTCAGTTTGGTTCAGTTCAGTGTGGTTTAATTTTCACTGCTGAAAGTCCATCAATGCGCAGCTCCACAAGTCCCAAATTCAACCCAACACTACCAAGTGTATTACCAAGCTTGTCAGAGCTAAAAATTCTTTAGACCAGCCCTTAATTAAACTCAAATGTGATTAAACTTTAAATATTCCCTTTAGGCAATACCGTCTAACTCCCTCTTTCTTTCTCAGATGCAGAACAAGTTTCCCACTGAGGGGGATCATTTGAGAGACTACTGTGCAGACTCTGTGCTTATGCGGGTGCTCCTGATTAATGGATATGGTTTCAGTGATCTCTCCTTTCCACACATCTCCTTTCAGGAA[A/T]AAGTAAGACACTCAGAAAGACCACTATGCAGTTTTAAGACATATCCTGTCAGTAACGTCGACACATTGTGTTGGTTTGCAGGTTGAAGACACCTCTGTCGGCTGGTCTCTTGGCTACATGCTAAGCTTAAGTAACTTGCTGGATGCTGAAAATGCGATGGTGAGGAAAGCACTGCGTCCAGATGTGTGGCGTGCCGCCGTTCTTCTTTTCTCAGTCCTTGTTATTGCATCTTTATTTTTTCTGTTGCGAAGCTACCAAAAGAATGGCACTAAACTTTGTTGTTACATTTGATCATTGAGAACTGAAGAGTTTAACTGTGATTGTGAAATTATAAGCTTTATATGTAGAGGTGTAAAAGGTTTGTACTGACAAAACATTAATTATTTATGTGTGTTTGCGTCAGATCAGTGTGGTTCATCATGATAATTATTTTTTTAACACTTCAAAATATGAAATGCACTTAACATTTACAAGTATGTAAATGTGTAAAGACATGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17661
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 |
|---|---|---|---|---|---|
| ENSDART00000043259 | Essential Splice Site | 428 | 454 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 31202465)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 28963822 |
| GRCz11 | 5 | 29563975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATATGGTTTYAGTGATCTCTCCTTTCCACACATCTCCTTTCAGGAAAAA[G/A]TAAGACACTCAGAAAGACCACTATRCAGTTTTAAGACATATCCTGTCAGT
Long Flanking Sequence:
TGCAGTATTTCATCTTAGCTGTTTATGAAATTCAGTTCACTTAACCTTTATTTCTATAGCTCTTTTACAATGTAGACTGTTAAAGCAGCTCAACACAGAATTTGTTGTAAATTAATACTGTATCAGTCCAATTTTTAGAGTTGAAGTTCAGTTTGGTTCAGTTCAGTGTGGTTTAATTTTCACTGCTGAAAGTCCATCAATGCGCAGCTCCACAAGTCCCAAATTCAACCCAACACTACCAAGTGTATTACCAAGCTTGTCAGAGCTAAAAATTCTTTAGACCAGCCCTTAATTAAACTCAAATGTGATTAAACTTTAAATATTCCCTTTAGGCAATACCGTCTAACTCCCTCTTTCTTTCTCAGATGCAGAACAAGTTTCCCACTGAGGGGGATCATTTGAGAGACTACTGTGCAGACTCTGTGCTTATGCGGGTGCTCCTGATTAATGGATATGGTTTCAGTGATCTCTCCTTTCCACACATCTCCTTTCAGGAAAAA[G/A]TAAGACACTCAGAAAGACCACTATGCAGTTTTAAGACATATCCTGTCAGTAACGTCGACACATTGTGTTGGTTTGCAGGTTGAAGACACCTCTGTCGGCTGGTCTCTTGGCTACATGCTAAGCTTAAGTAACTTGCTGGATGCTGAAAATGCGATGGTGAGGAAAGCACTGCGTCCAGATGTGTGGCGTGCCGCCGTTCTTCTTTTCTCAGTCCTTGTTATTGCATCTTTATTTTTTCTGTTGCGAAGCTACCAAAAGAATGGCACTAAACTTTGTTGTTACATTTGATCATTGAGAACTGAAGAGTTTAACTGTGATTGTGAAATTATAAGCTTTATATGTAGAGGTGTAAAAGGTTTGTACTGACAAAACATTAATTATTTATGTGTGTTTGCGTCAGATCAGTGTGGTTCATCATGATAATTATTTTTTTAACACTTCAAAATATGAAATGCACTTAACATTTACAAGTATGTAAATGTGTAAAGACATGAAGTCAT
Associated Phenotype:
Not determined