ZMP
edc4
Ensembl ID:
ZFIN ID:
Description:
Enhancer of mRNA-decapping protein 4 [Source:UniProtKB/Swiss-Prot;Acc:Q1LUT1]
Human Orthologue:
EDC4
Human Description:
enhancer of mRNA decapping 4 [Source:HGNC Symbol;Acc:17157]
Mouse Orthologue:
Edc4
Mouse Description:
enhancer of mRNA decapping 4 Gene [Source:MGI Symbol;Acc:MGI:2446249]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23299 | Nonsense | Available for shipment | Available now |
sa29034 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36647 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23298 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23299
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089787 | Nonsense | 765 | 1384 | 18 | 29 |
ENSDART00000132381 | Nonsense | 750 | 1361 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 18 (position 21677946)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21908169 |
GRCz11 | 18 | 21897235 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCCACCTGCTATCTCCAAGGGCCCGGAGCAGCGCTGAGCACAGTTTGT[T/A]GCCTCTTGAATTGGGTGCAGCGTCTGTGGATGGAGAGCAGAGACTCAGTA
Long Flanking Sequence:
CCTTCAAATTTGATTCCAAATCATTTACCAATTCTTCTGTTTATCTGGCATCCCTCTATCTCCACTTTTCCATTTAAAATCCCAATCTGGTTAGGCTTTCGCTCCCCCACTGGTTCTTTCTTCATCCCTCCTTCAAGAAGCCTCTCTGCTCTGCGAAGCTGCTCCTTATTCTCACCGACTCCCCCTCCCTTATTTCCCATCTCCTCCTCCGCAGGTTTCCCCTCCAAACCCTCCTCTCTCTCTGGATCTCCAGGCAATAGATCCCATGGTTGTCCCACAGGCGTCTCCAACAAGAGCTCGCTCACCGGATGTCATCTCATCTGCCTCTACTGCAATGTCCCAGGACATACCTGAGATTGCCTCCGAGACGCTGCAGAGGGGACTGTCCGGTGCCAATGCTGATTCGGGCCCCATCCTGCACTCTGACAGCATGGCATCAGCCGCATCAATTCTCCACCTGCTATCTCCAAGGGCCCGGAGCAGCGCTGAGCACAGTTTGT[T/A]GCCTCTTGAATTGGGTGCAGCGTCTGTGGATGGAGAGCAGAGACTCAGTAACACACCATCCCTGCTGGAGACTGCTCTCTCACAGGAAAACGCCGGAGCAGCCGGAGGATCCTGTTCTGACAGCAGTGTGAACCACGCATGGCCTGCTGCTCCTGATATCACGCGAGAGACGCGCAACAGCCTGCGAGACAACGGTTTAGGAGACTGGTGAGTACCTGTGCTTTACTATAATATATGTAATTTTATTTTTGTGTGGGTATGTTACAGTATATTTTGTCTTATTTATGCTTATGCATTTAACAATTAATGACATTTTTCATATTTAATACAATTTTAGTAATTTTAGCAGTTTTTCTAAAGTATTTTTTAGTACTTTTCAAAAGAGATGCCAATTTTTTTAGACATATGTTCATTTTAGACCACACGATACCACGGTTTAAACTTAACTGAAATAACAAACAGATGTTAGCATGGTTTTCACTACATTGGTTCTTCCATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29034
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089787 | Nonsense | 881 | 1384 | 20 | 29 |
ENSDART00000132381 | Nonsense | 858 | 1361 | 20 | 29 |
Genomic Location (Zv9):
Chromosome 18 (position 21671799)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21902022 |
GRCz11 | 18 | 21891088 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGATTGACAGTGATCATGACGATGAGGTTGCCAGTCTGGCCTCGTCCT[C/G]AGGGAACTGCGGCCCTCGCTCCTCTCACAGACTTCCTGTAAAGGACTGGA
Long Flanking Sequence:
TTCGAATTGACTGGTGAAAGTCTTATCTATCTGCTTACACTGCAGACATAAGGGCACAGATCCTATTAAAATCAAATGAATTTCCATAAATTATATATATATATATATATATATATATATATATATATATATATATATATATTTATTAAATTTTTTTAACATTTTGTTTTACATAGGCAATATCCAATCTGTGTCACATAGGAGAAAGAAAAAAAAATTGGGTCACTTGAATCATGCAGTGTAAATGAAGGCTTAGTTTCTCTACATTATGTGTGCATATCTGAACTTGTCCAAACCTGTCTGAGAAAGTCTGACTCATCAAATTGTGATAAAATGAATCTGAATATTCAAATAAGGAGGCATGTCTTGTTAATAAGACTTTTGTGGTGCCTTGATTAATACATTTGCTGCTGTTTAGCCTTTTTTAAATTATTTATTGTCTCTACCTGTTGTGATTGACAGTGATCATGACGATGAGGTTGCCAGTCTGGCCTCGTCCT[C/G]AGGGAACTGCGGCCCTCGCTCCTCTCACAGACTTCCTGTAAAGGACTGGAAAACATCACCCCGCAGCTCCCCTAAGCTCAAGCGGAAGAGCAAGAAAGATGAAGGGTGAGTGAGCTCCCCCATTTACTATGGAAATCTTCTTTATATTAATGTTTATATTCTTTAATGTGGGATCGGTGGAGTCTGTTCTGTCATATAATCTTATTAATCATCTTTGCTTTTCTTCCTTCCCAGAGAGTCCTCGCAATCTAGACAGATTGAAAGCCAGGTAAGTTCGTTGATCCTCTGCATCGCCATCTGAATGCATTTGTATGGCTATAAACCAATCAAAATGCATGAATGCTTGTTTTCTGTCTAGTCAGTGTGACTCATCATATAAATAAAACATTAATGCAGCGGCGACAGAAAACATAAGTAACATGACCAGCTCAGCAGTACGAGCGTTTATACTACTTGAACTGTTTTGCCGTCACTCAAGCATTCCTAGGAGTCCGGTGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36647
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 |
---|---|---|---|---|---|
ENSDART00000089787 | Nonsense | 923 | 1384 | 21 | 29 |
ENSDART00000132381 | Nonsense | 900 | 1361 | 21 | 29 |
Genomic Location (Zv9):
Chromosome 18 (position 21671545)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21901768 |
GRCz11 | 18 | 21890834 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTAATCATCTTTGCTTTTCTTCCTTCCCAGAGAGTCCTCGCAATCTAGA[C/T]AGATTGAAAGCCAGGTAAGTTCGTTGATCCTCTGCATCGCCATCTGAATG
Long Flanking Sequence:
AGTTTCTCTACATTATGTGTGCATATCTGAACTTGTCCAAACCTGTCTGAGAAAGTCTGACTCATCAAATTGTGATAAAATGAATCTGAATATTCAAATAAGGAGGCATGTCTTGTTAATAAGACTTTTGTGGTGCCTTGATTAATACATTTGCTGCTGTTTAGCCTTTTTTAAATTATTTATTGTCTCTACCTGTTGTGATTGACAGTGATCATGACGATGAGGTTGCCAGTCTGGCCTCGTCCTCAGGGAACTGCGGCCCTCGCTCCTCTCACAGACTTCCTGTAAAGGACTGGAAAACATCACCCCGCAGCTCCCCTAAGCTCAAGCGGAAGAGCAAGAAAGATGAAGGGTGAGTGAGCTCCCCCATTTACTATGGAAATCTTCTTTATATTAATGTTTATATTCTTTAATGTGGGATCGGTGGAGTCTGTTCTGTCATATAATCTTATTAATCATCTTTGCTTTTCTTCCTTCCCAGAGAGTCCTCGCAATCTAGA[C/T]AGATTGAAAGCCAGGTAAGTTCGTTGATCCTCTGCATCGCCATCTGAATGCATTTGTATGGCTATAAACCAATCAAAATGCATGAATGCTTGTTTTCTGTCTAGTCAGTGTGACTCATCATATAAATAAAACATTAATGCAGCGGCGACAGAAAACATAAGTAACATGACCAGCTCAGCAGTACGAGCGTTTATACTACTTGAACTGTTTTGCCGTCACTCAAGCATTCCTAGGAGTCCGGTGAGAACTGAATGTGCTATTGTGTCTTCAGATGAGCACAGAGGTGCAGGACGAGCTCCTGCAGATGCTGCGGAGCCAGCAGAGGGAGATCGCAGAGCTCCGACAGAATCAGCTTGATCTTCTGCAGAGAGTCACTAGCCACATGGACGCAGTGCAGAGCTCCATCATGGCTCACATCGAGCATGCCATGTTAGCTCAGCAAGAACAAGAACGTATCCTTCCACTAGAGGGAGACTCTGGCTGGCTTGAACACTATAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23298
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 |
---|---|---|---|---|---|
ENSDART00000089787 | Essential Splice Site | 1040 | 1384 | 23 | 29 |
ENSDART00000132381 | Essential Splice Site | 1017 | 1361 | 23 | 29 |
Genomic Location (Zv9):
Chromosome 18 (position 21668838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 21899061 |
GRCz11 | 18 | 21888127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCTTGAGAAAGTTTTGCGTGAAGAAATGAAGAAAACCGTCCCGCAGAG[T/C]AAGTGCTGATGTGATGAACTTTTTTAAGAGCTCAACTTAGCTTTTTTTTC
Long Flanking Sequence:
TTACATGTTCTCCCAATGTTCGTGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCTCACAAGTCGAAAGACATGCGCTATTGGTGAATTGGGTAAGCTAAAATTGTGTATATAGTGTGTGTTTAAATGACTTTGTATGGATGTTTCCGTTTCCCAGTGATGGGTTGCAGCTAGAAGGGCATCCGCTGCGTAAAACATAAGCTGAATAAGTTGGCGGTTCATTCTGCTGTCTGTGGCGACCCCAGGTTAATAAAGGCACTAGTCTGAAAAGAAAATGAATGAAGGATAACTTTGGATTGGTTAGGCTCATGCAATTTAGTGTTAACTTAACAAGCTGGTGATGCAGAGAGAAGAATGGAGCGAATTCTGGTCGAGGGTCAAAGTCGAAACCAACAGCTCCAGGACCAGCTAGTTCAGCAGCTCGTCCAAACTCTGAACAACAGTCTCTGCAACCGGCTTGAGAAAGTTTTGCGTGAAGAAATGAAGAAAACCGTCCCGCAGAG[T/C]AAGTGCTGATGTGATGAACTTTTTTAAGAGCTCAACTTAGCTTTTTTTTCTCACACAGTTCAATACAGCAAAGAACATTCTGTTCTTATTTTGTCTGTGAAATGGTTTAAATGAAGACTTTTATTGATTTGAGGCTTATGCAGAGCTTTGTGACATTATTTCTGTTTTTTGCAGCCATATCGAAGAGTCTCGAACCTGTGACCGGCCAGATGAACAGCACCATTGCTGCCAAGTTAACTGCAGTAGAAGGAGCACTCAAAGAAAACGTCACCAAAGTTGTTAAGTCCAAGGTCAGCGGCTTGTACGAAAATCAACAATTAAGTAGCGCTTTTTTATTGTTATCCAAACCTGATATTAATGCTACTATTTTCCACAAAAAAAAAAAAAAAACATTTCTAACTGGAAAGAATGTTTCTGTTAAAGAAATTTTAAAAACCTGGGCAGTCCAAAGAAGTGCAGCAACTTCTGTGCACCAGTGTAGCAGTAAATAATTCATCGCA
Associated Phenotype:
Not determined