ZMP
si:dkey-26l17.1
Ensembl ID:
ZFIN IDs:
Human Orthologue:
ZNF385C
Human Description:
zinc finger protein 385C [Source:HGNC Symbol;Acc:33722]
Mouse Orthologue:
Zfp385c
Mouse Description:
zinc finger protein 385C Gene [Source:MGI Symbol;Acc:MGI:3608347]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13207 | Nonsense | Available for shipment | Available now |
sa33127 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26032 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13207
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 |
---|---|---|---|---|---|
ENSDART00000055890 | Nonsense | 119 | 460 | 4 | 9 |
ENSDART00000132622 | Nonsense | 119 | 458 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 17490247)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 17681123 |
GRCz11 | 3 | 17830863 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAAGCTGAAGGCATTGGAGGCTCAGAAGAACAAACAGCAGAGACGACAA[C/T]WGGACAACYCCCACCACAACCGAGAGCGAGAGAAGGACAGAGAGAGAGAT
Long Flanking Sequence:
ATAAAAGTTCGTAACATACAAAATCATAAAAAACTAAATCTTACCTATGAAATGTTAGGCCTATGTGCTTTGTTTTCTTTGTTTGCTTGTTACTACACCTGTACACAGCACTAAAGTCCAGCATCTTCACATTGACTTGGTCTTGTCTAGGTTGGTTGAATGACTTTTGTCCTGGGAGCACTGTACAAATGTGGCGGCAGTATTAACCCATACTCAGGGTCTGTATGCGATATCTAGTGTATATATATCTATGTGTTGTAGTTAGTAAATTCCCAAGTAGACACATAAAACAGAAACCTGCTGGACATCTGTTCGGTGAAACACTAGAATAGTGGTGTCTTGTGAATTGTGAAGCTTCATATAGTTTTGCAGATCTTTCACTCGCTCTGTTTCCACCTGTCGTTCTTTAGAATCAGGCCGAGGCTCATTATAAAGGCCATAAACATGCTCGCAAGCTGAAGGCATTGGAGGCTCAGAAGAACAAACAGCAGAGACGACAA[C/T]AGGACAACTCCCACCACAACCGAGAGCGAGAGAAGGACAGAGAGAGAGATAAAGAAAGAGAGAGAGTGAAGGCCAGCGCTCCAGATCCACCACCAGCCCTGCTGGACGACACCGCCATCGAAGGAAGTAAGTGGACTTTTTTAAAAATTAGCAAACTGTACAAAAACTGCCTTGATGCATGATTAAAATGTATTACAGGATCCATTTAATGCATTGGATTTCTGTAATCCTCTTGGAAAATATGCAAGCAACCCAGGCTCATTAGAGATATGTGCCCAGGGCTACATTTTTGAGAACCAAGAAATTTATACCCTGGAAACGTCGTCTTGCACATTTTGTTTTCACAAATTCACTAGAAGACGCCATGTACATTTTTGACAATCTCAAATATGTTATGGGGCCATGTTTTCTCATACGTGCCATTTCTCTTGTAAATCCATCAAAGGTCTCTGTGTACATTTTCTGGATTAACGTCCTTCTTGTAAGCATCCATGAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33127
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 |
---|---|---|---|---|---|
ENSDART00000055890 | Nonsense | 171 | 460 | 5 | 9 |
ENSDART00000132622 | Nonsense | 171 | 458 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 17474060)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 17697310 |
GRCz11 | 3 | 17847050 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGCTCTGTCTCTCTTCAGCTGCTGTCAGCGACCCGGAGTCTGCGCTA[C/T]GAGTGGACGACGCTCACTGCAGTTCAGTGGTGCTGACGCCCATATCAGAG
Long Flanking Sequence:
GTGCTCTTGAGTTGGGATAGAGGTTGGGTTATGGACAGGTTTGGTGGTATGGGTAGGTTTAAGGGTAGGTTAAGGTGTAAGGAATGGTCAACAGTGTATTTACAAATGTAATTACAAAAGTTAATTACAGATGTAATTACATACATGTATTTAATCAAGCATATGTACACAGTAAATACATGTATTTACATAATAAGTACATTGTAACAAACTATTAATTCCTATGTAAGTACATATTAGTTAGGGCCACTTAATATAAAGTGGGACCACAGATTTTTCTTACAATGTACATTTATGCATGCATTATTAGATGCTTTTATTCAAAGACATTTTTTGTAGTGTCATGTAATGTTTGAAGAATTCTAGAGGAAAATTTGGAGGAAAGTGTTAACAGTAAAAAAGTTAGGAATTGTTCAATTAATTGCATTATTTAAAAGTTTTTTTTAAATCAATGGCTCTGTCTCTCTTCAGCTGCTGTCAGCGACCCGGAGTCTGCGCTA[C/T]GAGTGGACGACGCTCACTGCAGTTCAGTGGTGCTGACGCCCATATCAGAGGTTTCGTCTGCTGACCTGTGCGCATCCTCTCCTCACTCGCAGCACCCCGACGCTCTCCTGGAACCCAGCGGAGACACAAGCCCTCCTCCACAGGACAGCCCTGCAGCAGACACACCGGCAGAGAAGGAGCCCAAAAAGTCCAAACAACACCTGCACTGCCCCATCTGCAAAGTCACGGTCAACTCCAGCATTCAGATGGAGGCTCACAATAGTGGTATGTAGCCTTTTTCTAGACCTGTTTAAAGACAAGATACTGCAGGCAAGTTTTTACTAGCACTAATACGTTTTTGGTTTGAGATTTTTTGGCTTGTCATCAAGTCTTTGTTTTTTCAGTCTAGCTTAAAACATGTACCACAGGTTTAAAATATAGTTGAGGTGGTAGCCGGATTGAAACCTTTTACAGCACATAAATGGTCAACTGCATGCGACAAACATATTGAGCCATGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26032
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:
A > C
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055890 | Missense | 355 | 460 | 8 | 9 |
ENSDART00000132622 | Essential Splice Site | 355 | 458 | None | 9 |
Genomic Location (Zv9):
Chromosome 3 (position 17462319)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 17709051 |
GRCz11 | 3 | 17858791 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAATTAAAAATGATTTTTATGCAGCTCAGTTCTCCCGATCTTTTGCAGC[A/C]GGGTGTCCGATGGAACGGTTATGCGGGCGGCGCAGTGTCTGCCATGAAGA
Long Flanking Sequence:
TGGTACTACAATTGGTGCATAGTTATTTTTCATATACTATTTGGGAAGGAAAATTTGAAAATTGGGGAGCGACAGTGAGATTGAAAAGAATTCATGAAATGTTCAAATGTAGTACATCTCAAATGCATTGTTTTGGATCAGTAATTTTGTAAAAAAAAAAAAATAAAAATAAATTGAGAAAAAAAAGTAAGTTTGCATCAGCTAGAACACTAAAAAGTCATATTCAACTAATCAGCACAGTGTAGTTAATAGTATTCAAATAAATCTGCCTCACATATTAAAATACCCAGAGTTGGTTTGAAACAATAGGACTGATGATGATTGACAGAACAAGATAATAAGCCGTGTCTGTTCTCAGCATGACAGAATGGGGAAATGTGAAGGGGAGGAAGTTATTGAAGGGAGGATGCCAGCAAAACATGCTCATTATGACACGAGGAGTAATTTTGCGTAATTAAAAATGATTTTTATGCAGCTCAGTTCTCCCGATCTTTTGCAGC[A/C]GGGTGTCCGATGGAACGGTTATGCGGGCGGCGCAGTGTCTGCCATGAAGAAAGTTATCAGCCAATGCAATCTCTCCTCTCTGTCCTCACAGGTGAGTACTTATGTTCATCGTTTGTTCATCGTTTAACCCAAAATATACTGTGATTCTATTAAGAGAATGCTTTACAAGCGCCTGCACATTGGTTAAAGGGATAGTTCACCCAAAAATTATTCATATATACTCAGTATTTCCTCTTTCAAGTGGTTACAAAACTATGAGTTTCTTTCTTCCACTGAACACAAGATATTTTAAAGAAAGCTGAAATCCTCACCATTTCCTTCCATAGTAAGAAAAACAAATACTATGAAAGTCAATGGTTACAGGTTTCCAGCTTTAAATGATCCTCTTTTGGGTTTAACAGTAGAAAGTCAAACTGCTTTGTGACAAGTGAAGGGTGTGTAAATAATGACAGAATTTTAATTGTGGGTGAACTATCCTTTTTAGGATAAACATTCTAGTG
Associated Phenotype:
Not determined