ZMP
entpd2b
Ensembl ID:
ZFIN ID:
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 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23867 | Nonsense | Available for shipment | Available now |
sa37247 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9390 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23867
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065838 | Nonsense | 296 | 504 | 6 | 9 |
ENSDART00000134620 | Nonsense | 305 | 377 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 9941204)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11424567 |
GRCz11 | 21 | 11517195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCCTTCAGACTGAAGGAAGTGTTTGACTCGCCTTGCACGGCGTCATGG[A/T]GACCCAAACCTTACAACCCTCATTCCCACATCACAGTGCAAGGCACCGGT
Long Flanking Sequence:
TTCTTAAAGGGACAATTCACTCGAAAAAATATAATAATCTGCCATTTATTTACCTTTCACTTGTTCAAAATGTATTTGAGTTTATTTTTTCAATTGAACACAAAAGATATTTTGAAAAATGTTGGTAACTGAAACTCATTGACTTCCATAGTAATGTTTTTAAACTATGAAAGTGAATGGGTCCCAGACACAAATATTCTTTAAAATATCTTATTTCGTATTCAACAAAAGAAAGAAACTCGAAGATTAAAAATGACATGAAGCAGAATAAATTATTCAGATTTTTTTTTTCTTTAATAAAGTGGCTGATAGGTCTTTATAGACTTTTTAAATATACATATTTTATTTATTATTGTCAAACAACTTAAGTCTAAAATGTTTCATTTTAGTCACAGGATTATACATCAACCAGTAAAATGTATCATCCCTGCTATCCATCTGACTTCATTAATGCCTTCAGACTGAAGGAAGTGTTTGACTCGCCTTGCACGGCGTCATGG[A/T]GACCCAAACCTTACAACCCTCATTCCCACATCACAGTGCAAGGCACCGGTGACTACCAAAGCTGCCTTGGCAACACTTCGAAAATATTTTCTTTCAAATCCTGCTCCTTTTCTCAGTGTGCCTTTAATGGAGTTTTCCAGCCAAACATCAGTGGAGGCTTCATGGTGAGGGGCATACAAACAGCCTTAATCGACTTGAACAGAACACAATGTAATGTGATTTCTCTTTCCATCAGGCCTTCTCTGCATATTACTTCACTCACAGTTTTCTCCAGCAAATCACAGAGATGAAGATCAGCACATATGCACAGCTAGAGGAGGCTACACAAGCTGTGTGCAATATGACCATAACAGAGGTTTAACTCGTTAATTATGACACTATATTGTTTATTGATATTTATTTATGTTGATTTTATGACATTGGCTATTGTAATACACCATCTAAAGTCCTGTAAGCTTATGCATTTGGTCACACTTTATTTTAAGGTACGATTTTTGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37247
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065838 | Nonsense | 315 | 504 | 6 | 9 |
ENSDART00000134620 | Nonsense | 324 | 377 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 9941261)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11424624 |
GRCz11 | 21 | 11517252 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTTACAACCCTCATTCCCACATCACAGTGCAAGGCACCGGTGACTAC[C/T]AAAGCTGCCTTGGCAACACTTCGAAAATATTTTCTTTCAAATCCTGCTCC
Long Flanking Sequence:
CACTTGTTCAAAATGTATTTGAGTTTATTTTTTCAATTGAACACAAAAGATATTTTGAAAAATGTTGGTAACTGAAACTCATTGACTTCCATAGTAATGTTTTTAAACTATGAAAGTGAATGGGTCCCAGACACAAATATTCTTTAAAATATCTTATTTCGTATTCAACAAAAGAAAGAAACTCGAAGATTAAAAATGACATGAAGCAGAATAAATTATTCAGATTTTTTTTTTCTTTAATAAAGTGGCTGATAGGTCTTTATAGACTTTTTAAATATACATATTTTATTTATTATTGTCAAACAACTTAAGTCTAAAATGTTTCATTTTAGTCACAGGATTATACATCAACCAGTAAAATGTATCATCCCTGCTATCCATCTGACTTCATTAATGCCTTCAGACTGAAGGAAGTGTTTGACTCGCCTTGCACGGCGTCATGGAGACCCAAACCTTACAACCCTCATTCCCACATCACAGTGCAAGGCACCGGTGACTAC[C/T]AAAGCTGCCTTGGCAACACTTCGAAAATATTTTCTTTCAAATCCTGCTCCTTTTCTCAGTGTGCCTTTAATGGAGTTTTCCAGCCAAACATCAGTGGAGGCTTCATGGTGAGGGGCATACAAACAGCCTTAATCGACTTGAACAGAACACAATGTAATGTGATTTCTCTTTCCATCAGGCCTTCTCTGCATATTACTTCACTCACAGTTTTCTCCAGCAAATCACAGAGATGAAGATCAGCACATATGCACAGCTAGAGGAGGCTACACAAGCTGTGTGCAATATGACCATAACAGAGGTTTAACTCGTTAATTATGACACTATATTGTTTATTGATATTTATTTATGTTGATTTTATGACATTGGCTATTGTAATACACCATCTAAAGTCCTGTAAGCTTATGCATTTGGTCACACTTTATTTTAAGGTACGATTTTTGCTATTAATTAGCACCACGGTGACTCGGTGGTTAGCACTGTTGCCTCACAGCAAGAAGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9390
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065838 | Essential Splice Site | 350 | 504 | 6 | 9 |
ENSDART00000134620 | Essential Splice Site | 359 | 377 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 9941370)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11424733 |
GRCz11 | 21 | 11517361 |
KASP Assay ID:
2261-5299.1 (used for ordering genotyping assays)
KASP Sequence:
GTGTGCYTTTAATGGAGTTTTCCAGCCAAACATCAGTGGAGGCTTCATGG[T/G]GAGGGGCATWCAAACAGCCTTAATCGACTTGAAYAGAACACAATGTAATG
Long Flanking Sequence:
ATGAAAGTGAATGGGTCCCAGACACAAATATTCTTTAAAATATCTTATTTCGTATTCAACAAAAGAAAGAAACTCGAAGATTAAAAATGACATGAAGCAGAATAAATTATTCAGATTTTTTTTTTCTTTAATAAAGTGGCTGATAGGTCTTTATAGACTTTTTAAATATACATATTTTATTTATTATTGTCAAACAACTTAAGTCTAAAATGTTTCATTTTAGTCACAGGATTATACATCAACCAGTAAAATGTATCATCCCTGCTATCCATCTGACTTCATTAATGCCTTCAGACTGAAGGAAGTGTTTGACTCGCCTTGCACGGCGTCATGGAGACCCAAACCTTACAACCCTCATTCCCACATCACAGTGCAAGGCACCGGTGACTACCAAAGCTGCCTTGGCAACACTTCGAAAATATTTTCTTTCAAATCCTGCTCCTTTTCTCAGTGTGCCTTTAATGGAGTTTTCCAGCCAAACATCAGTGGAGGCTTCATGG[T/G]GAGGGGCATACAAACAGCCTTAATCGACTTGAACAGAACACAATGTAATGTGATTTCTCTTTCCATCAGGCCTTCTCTGCATATTACTTCACTCACAGTTTTCTCCAGCAAATCACAGAGATGAAGATCAGCACATATGCACAGCTAGAGGAGGCTACACAAGCTGTGTGCAATATGACCATAACAGAGGTTTAACTCGTTAATTATGACACTATATTGTTTATTGATATTTATTTATGTTGATTTTATGACATTGGCTATTGTAATACACCATCTAAAGTCCTGTAAGCTTATGCATTTGGTCACACTTTATTTTAAGGTACGATTTTTGCTATTAATTAGCACCACGGTGACTCGGTGGTTAGCACTGTTGCCTCACAGCAAGAAGGTCGCTAGTTCAAGTCCCAGCTGGACCAGTTGGCATTTCTGTGTTAAGTTTGAATTTTCTCCCCATATTGGCATGGGTTTCCCCTACAGTCCAAAGACATTTAGTATAGGTG
Associated Phenotype:
Not determined