ZMP
A0JMB2_DANRE
Ensembl ID:
Description:
Zgc:152720 [Source:UniProtKB/TrEMBL;Acc:A0JMB2]
Human Orthologue:
NEDD4
Human Description:
neural precursor cell expressed, developmentally down-regulated 4 [Source:HGNC Symbol;Acc:7727]
Mouse Orthologue:
Nedd4
Mouse Description:
neural precursor cell expressed, developmentally down-regulated 4 Gene [Source:MGI Symbol;Acc:MGI:97
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16624 | Nonsense | Available for shipment | Available now |
sa35609 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22392 | Nonsense | Available for shipment | Available now |
sa7381 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16624
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 |
---|---|---|---|---|---|
ENSDART00000058161 | Nonsense | 207 | 787 | 9 | 25 |
Genomic Location (Zv9):
Chromosome 13 (position 52174742)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 688337 |
GRCz11 | 18 | 577555 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGCCTGCRCTGCCCCCTGGCTGGGAGGAGAGGCAGGACAACCTGGGA[C/T]GAACTTACTACGTCAACCACGAGAGCAGGACCACACAGTGGCACAGACCC
Long Flanking Sequence:
CTGCATGTATGGATTTCTTTGGTTGTTACCAACATCTGGTGTCAACGGCACCTTTAGAAATCGGTTTTCTGTCGGTGCAATAGCCTAGTGGTTAGCGCGCCGACATATGGTGCAATAGCACGTCAGGGTGTTGCAAGTTCGAATCCTGGCTCGAGGACATTTCCCTACCCCCTTTCTCTCTCCAACTTCGCTTCCTGTCTCAATACTGTCCTATCTAATAAAGGCTAAAAGGCCAAAAAAAAAGAAAAAAAAAAAAGAAATCTGTTTTCTGAGAAAAATGGTGACGTGTTCAATACTCATTTCCCCCGCTGTAACACAGGATTTTCCCATAGAATTGCTTTTATGAGTAGTAAGCAATACTTGTAAGTAATATCCTGCTTGTTTCTGTGTCGTAGCCGGGTTGGGAGTTTTTGGAGCCTCATGAATTATGCAGTCCTCATCATCCGCATCAGCTGCCTGCGCTGCCCCCTGGCTGGGAGGAGAGGCAGGACAACCTGGGA[C/T]GAACTTACTACGTCAACCACGAGAGCAGGACCACACAGTGGCACAGACCCACCATCCAGTAATTATCACCCGCTTTAACCAAACACACAGCATGAACATGTGTACACAAGCCCAGGGGTCGTGTTTAAATACCATGCACAAGACTAGTACGCTATGTAGATATTTATATTTATGCTCTCAGTTTATTCTTTGGGTGTATGTTGTTATTCAAAATGACTCCCGGCCATGACCTTAGTGTTGCTAGTGTTTTTGGCCTGCTTGATTATTATATTTTGTTTAGATTAATATAATAACTTATGGTGGCTCAGTGGTTAGCACTGTGGCCTCACAGCTAGAAGGTCGCTGGTTCGAGTCCCGGCTGGGTCAGCTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCCATGTTGGCGTGGCGTTTTCCTCTGGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGCTATAGGGGAATTGATTAACTAAATTGGCAGTAGTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35609
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 |
---|---|---|---|---|---|
ENSDART00000058161 | Nonsense | 417 | 787 | 14 | 25 |
Genomic Location (Zv9):
Chromosome 13 (position 52182160)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 695755 |
GRCz11 | 18 | 584973 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTTTCCCAGAATGCCGCAGGCTACGCTCTGCCCCCAGACGTGTCCCCA[C/T]AGCACACACACACTCACACACACACTCACACGCCGGAGCACCCAGGACTG
Long Flanking Sequence:
GCAATATAATAATAATAATAATAATGATAACAACAATATTAATAATAATATAATAATAACAATAATAATGATAATAATAATAATAACAAAATAATAATGATAACAATAATAATAATAACAATATAATAATAATAATAATAACAATAATGATGATAATAATAATAATAATAATAATAATAACAATAATAATAACAACAACAATAATACTAATAACAATAATAATAATGATACAATAATAATAATAACAATAATAATGATAACAATAACAATAATAATAACAACAACAACAATAAAAATAATATTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTGTTATTACCCTGTGTGTTTCAGCTCATACAGCCGCCCTCAGAGTCTCCAGCATCCCCGATGGCCAGCGGATCAACGTCTCTTTCCCAGAATGCCGCAGGCTACGCTCTGCCCCCAGACGTGTCCCCA[C/T]AGCACACACACACTCACACACACACTCACACGCCGGAGCACCCAGGACTGATGCCGACTGGCTGGGAAGTGCGCAGCGCTCCAAGCGGACGGCCCTTCTTCATCGACCACAACACCAAGACCACCACATGGGTACAGCCAGCACACACTCAACACACAGCTTCATTTAGATATTAGGATGCCATATAGTCAAGAACAGTGATGTTATACAAGCAGATAATTACAGTTGAGGGCAAAAGTTTAACATTTTAAATATTTTTCACGTTTTTTCTAAGTGATTTTAAATGAATAAAAGATTATAGATATATTCTTAAACATTTTTATAACTAATAATATTACTTTTAGCTGTATACAGTTGATGTCAGAATTATTATTCACACTTCTACACATAACACAGCAAGAAGGTCGCCGGTTTGAGTCCCAGCTAGGCCAATTAGCATTTCTGTGTGGAGTTTGCATGTTCCCTCCGTGTTGGCGTGAGTTTCCTCCGGGTGCTCCGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22392
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 |
---|---|---|---|---|---|
ENSDART00000058161 | Nonsense | 554 | 787 | 19 | 25 |
Genomic Location (Zv9):
Chromosome 13 (position 52188809)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 702404 |
GRCz11 | 18 | 591622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCAAAAGCCTCTGTTGTGTGTCTGCAGGCAGAGATCCCGAATCGCTTC[G/T]AGCTGAGTGTGCGGCGTAACGCAGTGCTGGAGGACTCATACAGACGCATC
Long Flanking Sequence:
AAGGGATGAGAAAAATATATAATTTAATCACCTAACAAGCCTAATAAATAAATATGCAATCATATACAATTAAATAAAGCATACACACATAGGTATTTGTGATTTTTTTTAAATTTACTTTTTCAAATATTTTTAAAATGATTTTTAACATATTCAGGAATTTTTCACTGTATTTCCTATAAAAAAAATTCTTCTGGAGAAAGTCTTATTTGTTTTATTGCAGCTAGAACAAAAGCAGTTTTTATTTTTTTTAAACCATTTAAAGGTCAATATTATTAGGCCACTTAAACAATATTTGTTTTGAATTTTCCACAAAACAAACCACCGTTATACAATGACTTGCCTAATTACTGTAACTTTACCCTAATTGACCTAGTTAGGCCTTTAAGTGTCCTTTTAAGCTGAATACTAGTATCCTCAAAACTATATACGTTGACTTCAACTGTAAATAACCAAAAGCCTCTGTTGTGTGTCTGCAGGCAGAGATCCCGAATCGCTTC[G/T]AGCTGAGTGTGCGGCGTAACGCAGTGCTGGAGGACTCATACAGACGCATCCTGTCCGTCAAGCGCTCGGAGCTGCTGAAGGCCCGCCTCTGGGTGGAGTTTGAGGGAGAAAAGGGGCTGGACTATGGGGGCGTGGCCAGAGAGTGGTTCTTCTTGATCTCCAAGGAAATGTTCAATCCGTATTATGGGCTGTTTGAGTATTCAGCCACGTGAGTGAAGCAGCTTTCATTCTCTCAGAAAAATCAGACTCTTAGGAGTTGTGCTGTCAGATTGCATTATAGGCAAAACACTGCAGACAAAATTATTAAATGAGTGTGAATGGATGTTTCCCAGTGATGGGTTGCAGCTGGAAGGACATCCGCTGCGTAAAACATGTGCTGGATAAGTTGGCGGTTCATTCCACTGTGGCGACCCTTGATTTATAAAGGGACTAAGCCGAAAATAAATTGAATGATTTTTATAGACCTTTTTCTTGGAACGCAAAATTACCCATGATGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7381
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058161 | Missense | 760 | 787 | 24 | 25 |
Genomic Location (Zv9):
Chromosome 13 (position 52199184)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 712779 |
GRCz11 | 18 | 601997 |
KASP Assay ID:
554-4264.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTCTGGTGATGCAGTGGAGGTTTGTGGATCGCATACAAAGACAGATGA[C/T]GGCCTTTAAGGAGGTAAAGACAMMCATTCWGCCATTYGGGTCACTGTTRA
Long Flanking Sequence:
TTCTGTCAGGCTATTGAGACTCCTGTCGCTGTTCATTTGTGCTTCATCTAAAACTCCCCATCTATAGTCCTCTTAGTCTCTGCTGACATTATCTTCAGCAGCTCAAACACTCTAATGGCTAATGGACAGACGGCTGCTTCTCACTCATGGCTGCTGTTTATGCAAATGAGGGAGAGATGGGCACTAGTCGGCGGGGCTTTCCCCCTCTGATGACACGTACAAAGGGAGAATGTCAATCAAAGTGTTTCATTCATCAAGTCTGATTATAACAAACACAATTCATTCATGTTGACCATTAGAGGCTGAAGATATTCACACACTGCTCACACACAACTGTGTTTAAACCCATTATAAAAGTGATTTTTGCATGAAAGGTCTCCTTTAAAGTCATCAATGTTTGCCAGATCATGCTTCAGGATTGATTTCAGCGCTGTCTCTGGTGTTTGTTTGCAGTCTGGTGATGCAGTGGAGGTTTGTGGATCGCATACAAAGACAGATGA[C/T]GGCCTTTAAGGAGGTAAAGACAAACATTCTGCCATTTGGGTCACTGTTAAGAGTGAGAGTTTCTCTGTCTTATGTCACATTTAAAAGTCCCATGAGGTGCTTTGAGATGAGCATTTTGATGTTTGACATAATCTCAACTGAAACATGAAGACAGGGAGGGGCATAAATTAGCCACGCCCCTTTTTAAAAAACCGGCCAATAGTGTTTAGTTTTGATTACAGCTCTGCCAGTGAGAGTGGTTGAGCTCAAGCGCATCAAATAAAAAGTCAATGAGAAGAAGGGGGCGGGGCATGTCAGACACTAGAGAGCATTTGATTGGTCAGGAGATTTGATTAGAAACTGAAGTATGAGGTGATGTCAATAAATACGTTGATCCATTTAGGCTGAAGTGACAAAACTGCAAGCTTTACATGTTTATATCAGGTTTATATCTTCTAAACCTGGAGCACACTGGCTTATAGATATCCTTAACACTAACATACTGATACTGACAATGTTTA
Associated Phenotype:
Not determined