ZMP
si:dkey-75g22.6
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human H326 protein [Source:UniProtKB/TrEMBL;Acc:Q7T134]
Human Orthologues:
DCAF8, DCAF8L1
Human Descriptions:
DDB1 and CUL4 associated factor 8 [Source:HGNC Symbol;Acc:24891]
DDB1 and CUL4 associated factor 8-like 1 [Source:HGNC Symbol;Acc:31810]
DDB1 and CUL4 associated factor 8-like 1 [Source:HGNC Symbol;Acc:31810]
Mouse Orthologues:
Dcaf8, Pet2
Mouse Descriptions:
DDB1 and CUL4 associated factor 8 Gene [Source:MGI Symbol;Acc:MGI:91860]
plasmacytoma expressed transcript 2 Gene [Source:MGI Symbol;Acc:MGI:101758]
plasmacytoma expressed transcript 2 Gene [Source:MGI Symbol;Acc:MGI:101758]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11916 | Essential Splice Site | Available for shipment | Available now |
sa10596 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11916
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075913 | Essential Splice Site | 492 | 607 | 9 | 12 |
ENSDART00000139564 | Essential Splice Site | 492 | 571 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 37718536)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 38033450 |
GRCz11 | 2 | 38015778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACTCTGCTCGGGTGGTTCAGTTCATGGAGGGAGACCGAGGAGGAGTGG[T/A]AYGAYACTGTCATGTTACTAAGCTAATTATCAAAAGCCATATTTTATGAA
Long Flanking Sequence:
TACCTGTTTAGTGTACAGCCATGATGGCACAGGTAATATGCTAAGAATATGGCTCTTGTATTATTGCATGGCTTTTATTAAACTTTTCACATGTTGCAGCATTCAAAGTGTGTTGCACTGCATTTCAGAGCTGCTGGCGAGTTACAATGACGAGGACATCTACCTTTTCGACTCTAGCCACAGTGATGGAGCAGATTACCACCGGAAATACAAAGGCCACCGCAACAATGCTACAGGTTTCAAACCTGAACGCTTTTATTTGGTTCAATTGTGACATAATACTTGTATAACATTTTAGCATGCATGTTTTTACAGTCTTTAACCATTTCCTACTTTTCCTCTTTTCTCTGTGGAACGTGCTCCTCAAGTGAAGGGAGTTAACTTCTATGGTCCCTGTAGTGAGTTTGTTGTCAGCGGCAGTGACTGTGGACACATCTACCTGTGGGATAAGAACTCTGCTCGGGTGGTTCAGTTCATGGAGGGAGACCGAGGAGGAGTGG[T/A]ACGATACTGTCATGTTACTAAGCTAATTATCAAAAGCCATATTTTATGAAAAAATAAGTCACATGTGATTCAAAGTCATACCAGGTCACATTGTTGTAATAGAAATGTCTTAAAAGTCCCATGAAGGGTTTTAAATTGTGCATTTTTATTTGATGTATGAAGTAATCTTAACTAAAACACGAAGAAAGGGTGGGACATAGAGTAGCTCCACCCCTTTTTTTAAAAATGCAGATAGCGTTTAGTTTTTATCAAAGCTCAGTCAGTGAGATTGGTTGAGTTCAAGTGCATTAAATTAAAAGCAAATGAGAAGCATCTTGAAGGGGGCGGGGCATTTCAGATACTTGAGAGCATTTGATTGGTCAAAATGATAAGAAGCTAGAGTATGAGGTGTTGCATTTAAAATTTCGGCAGAAGTGAGAAACTGCAAGCTTTACATGTTTATATCAGTTTTATATCTACTAAACACAAATTTTGCACTGTTTTGAAGCACACCAGCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10596
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075913 | Nonsense | 558 | 607 | 11 | 12 |
ENSDART00000139564 | Nonsense | 558 | 571 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 37722296)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 38037210 |
GRCz11 | 2 | 38019538 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGAAGACAACGTTCGTCATGGTGACCAGTATGACACACAGCTCCTCTG[G/A]TTCCTGATGAGACACATGAGAAACCGAAGACCTCAACGGGTWAGAATTTG
Long Flanking Sequence:
CTCCACATAGAAACGCCAACTGAGTCTAGGTTCGACCCAGCGACCTTCTTGCTGTGAGGCGACAGCACTACCTCTTACGCCCGTTATAGAAAAATATTAAATACAAATTTTAAAATAGTGGACAAATCAAGAGAAGCAAAAAATAAATTTAAGGTTTGTTGGTTTAATTTTTTTGTAATAGTTTACTTGAATTTAAATGTATTATTTCTCAATTTCTAAATATGTTTGGTGACTAAAATATTATTTTAATAAATAAATCTGTGTAATAAATCTGTTTTGTTTAAATGCATCAAAATACAATGCTTAAATTCATTGACAAATGGATACAAATATTCATTTTTTAAAGTCATGCTGAGCACTGTATAATCAGTATTTTGTTAATAGTTTTACTAAAATGTTTTGCATTTTATCCTGGCTATTTAGGTAATGAAGAAGAACAAGCGAGAGCGTGATGAAGACAACGTTCGTCATGGTGACCAGTATGACACACAGCTCCTCTG[G/A]TTCCTGATGAGACACATGAGAAACCGAAGACCTCAACGGGTAAGAATTTGCTTTGCATTAGATTGCATTATCCTCAGCTTGATCATGTTTTCCATTTCAATGCAGTCCTATATAATCATTGTGTAAAATATTTTCTTATGTATAGAATCATTAAACATTAAAGTGATTCGACCCCCCCCCCCCCCCCCCCCACACACACACACACACACACACACAAACACACACACACACACACACACTCAACGGGTTAGAATTTGCTTTGCATTAGATTGCAATATCCTCAGCTTGATCATGTTTTCCATTTCAATGCAGTCCTATATAATCATTGTGTAAAATATTTTCTTATGTATAGAATCATTAAACATTAAAGTGATTCGACCCCCCCCCCCCCCCCACACACACACAAACACACACACACACACACTTAATCAGAAATTAATCAGAAAAGAACTAATGCTACACAAAATCAAAAAGTAAATGAACAAAAATTGTATTTTCTC
Associated Phenotype:
Not determined