ZMP
entpd4
Ensembl ID:
ZFIN ID:
Description:
ectonucleoside triphosphate diphosphohydrolase 4 [Source:RefSeq peptide;Acc:NP_001002419]
Human Orthologue:
ENTPD4
Human Description:
ectonucleoside triphosphate diphosphohydrolase 4 [Source:HGNC Symbol;Acc:14573]
Mouse Orthologue:
Entpd4
Mouse Description:
ectonucleoside triphosphate diphosphohydrolase 4 Gene [Source:MGI Symbol;Acc:MGI:1914714]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34503 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa6105 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31685 | Essential Splice Site | Available for shipment | Available now |
sa34502 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34503
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056074 | Essential Splice Site | None | 611 | 1 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 52644181)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 50162383 |
GRCz11 | 8 | 50151029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGAGGATGGGTCTTAAATGAGGGCATCCGTCCCAGATGTAGCCGAACGG[T/C]GAGAGCATATGCCTGCGTTCACACACATATTCTAAATACTCAACCGATAA
Long Flanking Sequence:
ATCATAGCATCCTTGCATAAAATTATTATAAATAAAATTCCAAATTATCTCTTACATTTTTTAAATCCTTTCTGAAAGTCTTCATATCACCATTGCGTTTAGCTTTTCTTTTATTCTTTCAGGGAACAGGATTGTAAAAAAAAAAAAAGTATTTGTTGTACTCTCCCATTCACTGCGCAAGTTTACCCAACGATGACGACTTCTGCTACTGAGAAACCCGGAAATGCGAAAAGGGCACAATGACGTCAGAGCAGCAGTGTACACGCAGGCGCAAGTTTCCGGCATTAAGGCGCATGCGCACAAGCAGTCTGAACTGTTGCTCGGTAACTACCGGGAATTAGCGGCTTTTCTCCACCAAATTTGAACCACCGACGCTACCGGAGGAATTAAAAACCCGCATAGATGTGTTCACCGAGAGGATTTCAATTCTTGTCCTGAATTCACAAATCTCCGAGGATGGGTCTTAAATGAGGGCATCCGTCCCAGATGTAGCCGAACGG[T/C]GAGAGCATATGCCTGCGTTCACACACATATTCTAAATACTCAACCGATAAACACACCTGACAGCGTTTTAGTCAGGACAGTCTACCTCTACATAACCTTAAAAACATATGTCAGTGAAAACGTGATATTCGTTTATCAATGAAGCTGTTCTCGGCCTGGGAAGCGCACAGCTGATTATTAAACGTTAACAACGGTCGTGTTTCAAAAGCTAGCGAGCTTCCCTACCTAGACAGCATCTTAAGATCTCAAATTATGCGACTCAACGTGGTTTTAGAAGGACAAGAATGTAACCCATATAGGCTACAGACTGAGGTAAAGTTCGTTTTATTCATTCGGACTTTACTTTTTATGAATATAATTTCAGAAAAGTAACGTTATTGTTTGTAAATGCTACGTCAAATAGTGAGGTAATATTAGCAGTCATCGACTAGTAAAGTACATCGTTATTTACAGTTAAATAAGTTGTTTTAATGTTATTCTTAAATGTAATTTCAAACCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6105
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056074 | Nonsense | 281 | 611 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 52631767)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 50174797 |
GRCz11 | 8 | 50163443 |
KASP Assay ID:
554-3817.1 (used for ordering genotyping assays)
KASP Sequence:
CGTACRGCTGGTGTTTTGGACATGGGTGGCGTYTCCACTCAGATCGCATA[T/A]GAAGTGCCCAAAACTGTAAGCTTTGCTTCTCCACAACAGGTTATTATCTA
Long Flanking Sequence:
ACTTCTATACAGCTTAAAATGACATTTAAGTGCTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAATGATGGTTTGTTCTATAGACTGTCGAAAAAATAAATAGCTTAAAGGGGCTAATATTTTGTCCTTTAACATGGTTTTTAAAAAATTAATAACTGATTTTATTGTAGCCAAAATAAAACAAATAAGACTGTCTGCAGAAGAAAAAATATCATCAGACATACTGTGAACATTTCCGTAATCTGTTAAACATCATTTGGGAAATATTTTAAAAAGAAACAAAAATTCAAAGAGTGTATAATACTTCTGACCTCATCTGTATATAATAAATGCATCTTTTTTCTATTCTTTTCCTCTTCCCTTCAGAGCACGATGCAGTGGTGGAGGTGCAGGTTCCTGGCAGTGACCAGCAGGAGACGCTGTTGCGCAAGCGTACAGCTGGTGTTTTGGACATGGGTGGCGTTTCCACTCAGATCGCATA[T/A]GAAGTGCCCAAAACTGTAAGCTTTGCTTCTCCACAACAGGTTATTATCTATGACAATTTCCCGTATTTTCTTTTGAAAGCTGAAAGTCTGGCTTTGTCATTCTCTGCTTCTGGTTCTCCTGGTGCTCTGGTGTGCTTCTTCACCCGGTGCAGTTTCACGCCACGGTGAATCAGCTGAGTTAGCCTTGGACTGAGATAAGCCTGCTGCATGGTGCTATAGCTCTGAAAACAACACTCTCAGCTTTTAAAGGGGACTATTTTTTTAACACTTTTGCAATGCATTGGATTTTGTTTTGTCTGCTTTTAATATTAAGTTTCTCATGCTGAAAAGACCAGATTTTGTTCAGTTTGCATTTGCATTCATCTAAATTCTTATGTTCGCATTGGGAGTCGTTCGTATAGTCTCATTGTTGGGATGCACATATCTAGACTGGCAAAAAACGAAATAAGAAAAACAGACTATTGTTGTTATAAACTCACGATATACGTATTTTTGTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31685
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 |
---|---|---|---|---|---|
ENSDART00000056074 | Essential Splice Site | 286 | 611 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 52631750)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 50174814 |
GRCz11 | 8 | 50163460 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACATGGGTGGCGTTTCCACTCAGATCGCATATGAAGTGCCCAAAACTG[T/C]AAGCTTTGCTTCTCCACAACAGGTTATTATCTATGACAATTTCCCGTATT
Long Flanking Sequence:
AATGACATTTAAGTGCTTAATTAGGTTAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAATGATGGTTTGTTCTATAGACTGTCGAAAAAATAAATAGCTTAAAGGGGCTAATATTTTGTCCTTTAACATGGTTTTTAAAAAATTAATAACTGATTTTATTGTAGCCAAAATAAAACAAATAAGACTGTCTGCAGAAGAAAAAATATCATCAGACATACTGTGAACATTTCCGTAATCTGTTAAACATCATTTGGGAAATATTTTAAAAAGAAACAAAAATTCAAAGAGTGTATAATACTTCTGACCTCATCTGTATATAATAAATGCATCTTTTTTCTATTCTTTTCCTCTTCCCTTCAGAGCACGATGCAGTGGTGGAGGTGCAGGTTCCTGGCAGTGACCAGCAGGAGACGCTGTTGCGCAAGCGTACAGCTGGTGTTTTGGACATGGGTGGCGTTTCCACTCAGATCGCATATGAAGTGCCCAAAACTG[T/C]AAGCTTTGCTTCTCCACAACAGGTTATTATCTATGACAATTTCCCGTATTTTCTTTTGAAAGCTGAAAGTCTGGCTTTGTCATTCTCTGCTTCTGGTTCTCCTGGTGCTCTGGTGTGCTTCTTCACCCGGTGCAGTTTCACGCCACGGTGAATCAGCTGAGTTAGCCTTGGACTGAGATAAGCCTGCTGCATGGTGCTATAGCTCTGAAAACAACACTCTCAGCTTTTAAAGGGGACTATTTTTTTAACACTTTTGCAATGCATTGGATTTTGTTTTGTCTGCTTTTAATATTAAGTTTCTCATGCTGAAAAGACCAGATTTTGTTCAGTTTGCATTTGCATTCATCTAAATTCTTATGTTCGCATTGGGAGTCGTTCGTATAGTCTCATTGTTGGGATGCACATATCTAGACTGGCAAAAAACGAAATAAGAAAAACAGACTATTGTTGTTATAAACTCACGATATACGTATTTTTGTTTGTTTGTTTGTTGTTTTCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34502
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056074 | Nonsense | 350 | 611 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 52624560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 50182004 |
GRCz11 | 8 | 50170650 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTATGTGCTCCTGTTGTGTCCGTAGGCTGTTGAATCAGCATCAGGGA[G/T]AGAGCGCAGACTCGCCCATCCTGGACCCGTGTTTGCCTGTGGATCTTCAG
Long Flanking Sequence:
TCTCATTCTTTCAGAGAGAAAAAAAAAAGCTCAGAATGGCCTAGCCAATCACCTGACTTAAACCCAATAGGAAATACAAAAAAATGATTAGGATTGATAGACGAGACCCACAGAACCATTACGATTCTTACACTGTTGAAGTCTGTGAAAAAGTCACACCTGAGCAATGCATGTGACTACATTCTCCATATGAGAGGGGTCTTTAAGCTGCCATCACCAAAAAAACCTTTTATATAAAGTATTAAATACGCATTTCAGTACTTTCTCCTTGCCTTATTTCATTGTTATTACTCAACTAATTTTTCAGATTTGTTCCGTTTTATTTTTATGTCTGTATTGTTTGAGTTTTTACCAAAATCTGGTTCAATTGCATGTCAACGTCCATGTCAAGCTCCTTTTAAAAATATTATTTCCAGGAAAAAAACTTTGCGTTCAATACTTATTTCCCTCACTGTATGTGCTCCTGTTGTGTCCGTAGGCTGTTGAATCAGCATCAGGGA[G/T]AGAGCGCAGACTCGCCCATCCTGGACCCGTGTTTGCCTGTGGATCTTCAGGATGAGCTGGGACCTCCAGAGCAGCGGCTTCACCTGCGTGGTTCTGGAGACTTTGAGCGCTGCCGGCTACTGCTCCAGCCCTTCCTCAACCGCACAAATGACACCAACACGTCCCTCAACGGGGTCTACCAGCCGCCCATCGACTTCCACAACAGCCAGTTCTACGGCTTCTCTGAGTTCTACTACTGTACTGAAGATGTGCTGCGCATGGGAGGAGACTACAACTCCACCAAATACACCAACGCTGCTAAGGTAAACGAAGATTGCTCGCACTGCTCCTTTCTGGAGAATCAAAGCTTAAAGTACACATGAAATCAAAACTAACCATATTGACTTTGTTAGCTCACATTGCTAGTTTTGTGGTGAACAATTCATCAGTGCATGTCATAAAGAAAAAAACTATAGTTTGCCCTTGTAATGTTTTGTTTTCAGTTAAATTCTCAGATTAGG
Associated Phenotype:
Not determined