ZMP
dpf3
Ensembl ID:
ZFIN ID:
Description:
Zinc finger protein DPF3 [Source:UniProtKB/Swiss-Prot;Acc:A9LMC0]
Human Orthologue:
DPF3
Human Description:
D4, zinc and double PHD fingers, family 3 [Source:HGNC Symbol;Acc:17427]
Mouse Orthologue:
Dpf3
Mouse Description:
D4, zinc and double PHD fingers, family 3 Gene [Source:MGI Symbol;Acc:MGI:1917377]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11991 | Splice Site, Nonsense | Available for shipment | Available now |
sa8788 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11991
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034245 | Splice Site, Nonsense | 253 | 381 | 8 | 11 |
ENSDART00000123387 | Splice Site, Nonsense | 263 | 391 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 28514967)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 28586180 |
GRCz11 | 20 | 28489059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTGTTGTTCTATGACCCTAATCCTTTAATTTGCCCTATTTTTACAGCA[C/T]AGAAAGCGCCTGATGGTTCGATCATCCCTAATGACTACTGTGACTTCTGT
Long Flanking Sequence:
TAGTTTTAAATACGTTCTTTCAGTTAGTTTTGTATGTACACAATACAGATTCAGGTAGTTCCAGTTTAAAAAAAAAAAAAAAACCTTTATTTTTTATTTCAGTTTACGAAAATTATTTTAAATTTTAGTTTTAGTTTTTTTTTCGTTTTTGTGAACTATAATAACCTTGATGTGGTGCATTCCCAAATCATAGATCTTTCCCAATCTCATCCACCACTCTTTCTCCGACTTTATTTCTCGTCACTACTTTCACTGTGCTATCATATTTTTTTAGAGGATTGAGACCAAATATTGTCATTAGATATGGCTAAAACAAAATATATTTCATGTTTAACCACTATAGAATCATACATCAAATACCATCTTAAGTGTCCGTGGTAAGGATGCTCTCCTTACTTAGACTACCTGGGAAGTGTAATAGCATTTACAATTTGTTCTTTTGTTCACCTCTGTTGTTGTTCTATGACCCTAATCCTTTAATTTGCCCTATTTTTACAGCA[C/T]AGAAAGCGCCTGATGGTTCGATCATCCCTAATGACTACTGTGACTTCTGTCTGGGAGACTCAGGCTCTAACAGGAAGACAGGCCAGGCCGAGGAGCTGGTTTCCTGTTCAGACTGCGGCCGCTCTGGTGAGTCCCTTCACTTCACCATCTTCTATGTTGCTCACAGTTACAGTATCTGCCCATGTTAGATCAAGATTCCACCTCCATTGTGCCCTTATTTCACTCTGAGGGAGATGATTAGTATGGCATAGTTGAATTTATAAAATAAAAGATTTTAAAATGCATTGCCAGATGTTTTAGTAGCAAATTACAAACATGCAAAAGCTGTCAAAATCAGCTTTCCGAGATTTCTCTCTCTCTGTCTCTGTCTGTAATCAGCATAACAATAGGGGTGTGCGATATTACTCCTCTATGTATAGTTAGGTAATTATAATATTAATAATGTATGGTATTATAATAATGTATGATAATAAAATAACCATATAATTGTAAAAGCAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8788
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 |
---|---|---|---|---|---|
ENSDART00000034245 | Nonsense | 379 | 381 | 11 | 11 |
ENSDART00000123387 | Nonsense | 389 | 391 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 20 (position 28527181)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 28598394 |
GRCz11 | 20 | 28501273 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGTTGTCATCTGTGCCAGAATCTGCTTAAGGATAAAGCGTCTGGTGTT[G/T]AAGATCCATAAGCATYGTGAGGAGGTTCTGCACACAGAGACGCACAGCAG
Long Flanking Sequence:
TATTTTACACCTGGCCTGTGATCACATGCAAATATGTATTGGATCATTTAAATTGACATGTTTTTTACAAGATACTTGCACTGCCAACACGACATACATTAATCGTGCTTAAAGCCATACATATTCATTTTACTAAACACACTTTAATGCATTTAAATGTAACAATCATTTTGCTTTACATTAGTTCATATTCATTATATTCATATTTTCAGTTGTATCATTAAAAAGACACAAAGAAGATAACGTATTACATGTACTTGTTTTTTTTTTTAATAACCTGTAATGACAGTTCTGTTCAGTACATTTATTTGTAATTTTGATGTCGACTGTACACTCATGCTTAAACGCAACCATACAACTAAACTTGTCCCTAACAGTAATGAAACTTATATGCAAGAACACACAGTATGATATGAATTACCTTATTATCTGTTTGGTTCACAGGAAGTTGGAGTTGTCATCTGTGCCAGAATCTGCTTAAGGATAAAGCGTCTGGTGTT[G/T]AAGATCCATAAGCATCGTGAGGAGGTTCTGCACACAGAGACGCACAGCAGACTCAGGATGGGTGTTAGCCTTGTAGTTTTTCCTCCTGTAGTGTGGAGTCTTCCTCTACCTCAGTGGTACAAACATTTTCCTCAAACACATCTGGGTAATCGGTAGTCTACTGTACCTCGCAAACATCCAGACTGTCCGATCACCTAGAAACACGAGTTGCATTTTGTAAAACACAAAAAAAGGTACTTTGTTAAATAGCATCATCAGCACAAGAACTACACTGAACGAAGTCAACCTCTTATACACACACAGAATCTCTTGATTCTAACACTGTTTCTAAAACAGTCACAAGCACAGAGATTCTACTCAAAGTAACACTCCACTTTTGTCTTTTGAATAAGACCCACTTTACATGTCCCCTACAGTTTTATCCTTTTTTTAATCCATTCAGCAAGTCTCCCAGTCTGTCAGGAGCACATTTAGCTTAGCTTAGCATAAATCGTTATAAC
Associated Phenotype:
Not determined