ZMP
znf865
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein 865 [Source:RefSeq peptide;Acc:NP_001076544]
Human Orthologue:
ZNF865
Human Description:
zinc finger protein 865 [Source:HGNC Symbol;Acc:38705]
Mouse Orthologue:
Zfp865
Mouse Description:
zinc finger protein 865 Gene [Source:MGI Symbol;Acc:MGI:2442656]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa43234 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43233 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23453 | Nonsense | Available for shipment | Available now |
| sa16969 | Nonsense | Available for shipment | Available now |
| sa36790 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43232 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23452 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43234
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 |
|---|---|---|---|---|---|
| ENSDART00000053300 | Nonsense | 686 | 1506 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 10827437)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10285976 |
| GRCz11 | 19 | 10204901 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCAATAGGTTCAGTGGATGGCAAAGTTGAAACCGATTTTCCTGGTGGA[C/T]AGATTACTGACACAAAAGATTTGGTATTTTGCAAGAATGAGGATAGCACA
Long Flanking Sequence:
GCCGACACATACGCTGCCATGAAGACGGCGGTGGTCAAAACAGCAGCACAAACACAAATCATCAACATCAGTCAGATCTCCCGCACTCAACACAAGATGGAATTTCTCAAAATGCACACCACCATGAGAATCCAGACCCCATGTCTTCCACTTGCTCAAGTCCAGATAAGTCATACTGTTGCAATGAATGTGGAAAGGGGTTCAAAAAGAGAGGACACCTCCTTCAGCATGGTGTCATCCACTCTGGAGATCGTCCGTATGCCTGCACTGTCTGTGAACGTTCATTCAACCGAAGAGAGTCTCTCACTCGACATGAGAAAATTCATGAAGAGAAACCCTACCGCTGCCCTGCTTGTGGCCGCTGCTTTAGAGAGAGCACTTCTTTGCTTAACCATGCTGCATCTGGTAACTGTGGAAAGCCTGGGAGGAGATCTAGAAGCAGTGATGGTAGCTCAATAGGTTCAGTGGATGGCAAAGTTGAAACCGATTTTCCTGGTGGA[C/T]AGATTACTGACACAAAAGATTTGGTATTTTGCAAGAATGAGGATAGCACAGCAGGGATGTCTTGTGACAGTCTATATTCGCAGGCAAGAAATGCTAATCAAAACCCTATTGGCAAACCTAAAGAAGAGTATAATCCTGAGTATTCAAGAGATCCTTACCAAACGTCATACAGGGTCGATGACTACCGTCGACAACAGGGCAACCCAGCATCCTACTCTGGAGATTCCTGTAGTAACAGCATGTCAAGTCCAGCCCTCAGAAAAGCTCCTTTAGCCCCAACACTTCACCCACACCCTCAAAATCAGACGCACCATCACCAACCGCAGTCTCATCTTCCTCTCTCCTCTCTTTTGGATGACTCTGAAGATGAAGTCACAAGTAGTGCCATGTCCGCAATTGCTGCAGCTGCTGCCGCCTCTGTCTTGCCTGCTGAAATGAACAATAATGGTGGACGAGAGGAACGGAGAGACATCATTGGAGGCCTGTTAGGAGGCCTTGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43233
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000053300 | Nonsense | 729 | 1506 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 10827306)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10285845 |
| GRCz11 | 19 | 10204770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGCAAGAAATGCTAATCAAAACCCTATTGGCAAACCTAAAGAAGAGTA[T/A]AATCCTGAGTATTCAAGAGATCCTTACCAAACGTCATACAGGGTCGATGA
Long Flanking Sequence:
CCAGACCCCATGTCTTCCACTTGCTCAAGTCCAGATAAGTCATACTGTTGCAATGAATGTGGAAAGGGGTTCAAAAAGAGAGGACACCTCCTTCAGCATGGTGTCATCCACTCTGGAGATCGTCCGTATGCCTGCACTGTCTGTGAACGTTCATTCAACCGAAGAGAGTCTCTCACTCGACATGAGAAAATTCATGAAGAGAAACCCTACCGCTGCCCTGCTTGTGGCCGCTGCTTTAGAGAGAGCACTTCTTTGCTTAACCATGCTGCATCTGGTAACTGTGGAAAGCCTGGGAGGAGATCTAGAAGCAGTGATGGTAGCTCAATAGGTTCAGTGGATGGCAAAGTTGAAACCGATTTTCCTGGTGGACAGATTACTGACACAAAAGATTTGGTATTTTGCAAGAATGAGGATAGCACAGCAGGGATGTCTTGTGACAGTCTATATTCGCAGGCAAGAAATGCTAATCAAAACCCTATTGGCAAACCTAAAGAAGAGTA[T/A]AATCCTGAGTATTCAAGAGATCCTTACCAAACGTCATACAGGGTCGATGACTACCGTCGACAACAGGGCAACCCAGCATCCTACTCTGGAGATTCCTGTAGTAACAGCATGTCAAGTCCAGCCCTCAGAAAAGCTCCTTTAGCCCCAACACTTCACCCACACCCTCAAAATCAGACGCACCATCACCAACCGCAGTCTCATCTTCCTCTCTCCTCTCTTTTGGATGACTCTGAAGATGAAGTCACAAGTAGTGCCATGTCCGCAATTGCTGCAGCTGCTGCCGCCTCTGTCTTGCCTGCTGAAATGAACAATAATGGTGGACGAGAGGAACGGAGAGACATCATTGGAGGCCTGTTAGGAGGCCTTGGCTTCGGCTCTATGGGTGCCTCTTCATCAACATCTGCAGGAAATGGTGGCAATGAAGAATGCCTGAGTGGTTCAATGATACCTTTATCTCACCCGACCCAACAGCAGCCTAATTCACAGAATGCCAACAATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23453
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000053300 | Nonsense | 1084 | 1506 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 10826241)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10284780 |
| GRCz11 | 19 | 10203705 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCAAGGATCTAATGCGAGCACAAGCAACCAACCCCCTCCAAAGCTATA[T/G]ACATGTGAGATTTGCTGGAAATCTTTCCGCCATCACTTCCATTTGACTGC
Long Flanking Sequence:
CCAGGAGAAGTAGTGAAACGTCGGAGAAGCAGTCAGGGTGGTGCTGCTGGAGATGGTTCCGACAGGCCTTATTTATGCACTGTTTGTGGAAGGGGCTTTAGCAGACGGGAGACATTACGTCGACATGAACGTGTGCATACAGGGGAAAAGCCATTTCATTGTGACATCTGTGGCAAAGACTTCCGAGAGCCGTTTCACCTTACCAAACATCAGACTGTTCACTCTGGGGAAAAGAATTACAAATGCACGCTCTGTGGAAAAGATTTTGGATATGCTCAGAGTCTGAAAAGGCATGAAAAATTGCATCTAAGGGGAGATTTCAAGCCAAGGCGGAGTAAAACCAAATCTGCTGCAAATCAAGGGGTGCCCGCTAATCAAGAACAAACTGATCAAACCAATCAAAATAATCAATCCAACCCTGGCGCTTATTACTCCTATTCTCAGGATAAAGTTCAAGGATCTAATGCGAGCACAAGCAACCAACCCCCTCCAAAGCTATA[T/G]ACATGTGAGATTTGCTGGAAATCTTTCCGCCATCACTTCCATTTGACTGCCCATCACCAAGCCATTCATGAACATGGTGGGGAGAAACTGTTTTCATGCGAAGTGTGTGGAAAAGCGTTTTCATACTCTAACAGCCTGACCAGACATAGATTATCTCAACATGGTTTGACTCGTGCTGGGCCAACAACACAACCAACAGGAAACGATTCTATTGGAACTGCCTCGTCTGTCTCGGAGAGCGAGGCTGCAACCAATGCACTCCTTCATATATCACCTGAAAGTGGAAGTCATGGAGTACAACAGCCCCATTCAACGATTGCTCACACGCAGCATCCTCAGCCTGCTGGATATTCACCACTCTTCTACACTCCAGAGTCAGGACATCACAGTTCAAATCAAGTCACTTCACACCCCCAACATCTGCACTACTCAAACCCCACGATGGGTCCCCTCCAGCTTCAGCAGCCAATCAGTGGGAAGCAGTTAATTTATTCAGGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16969
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 |
|---|---|---|---|---|---|
| ENSDART00000053300 | Nonsense | 1184 | 1506 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 10825943)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10284482 |
| GRCz11 | 19 | 10203407 |
KASP Assay ID:
2261-2990.2 (used for ordering genotyping assays)
KASP Sequence:
CAACCAATGCACTCCTTCATATATCACCTGAAAGTGGRAGTCATGGAGTA[C/T]AACAGCCCCATYCAACGATTGCTCACACGCAGCATCCTCAGCCTGCTGGA
Long Flanking Sequence:
AATTGCATCTAAGGGGAGATTTCAAGCCAAGGCGGAGTAAAACCAAATCTGCTGCAAATCAAGGGGTGCCCGCTAATCAAGAACAAACTGATCAAACCAATCAAAATAATCAATCCAACCCTGGCGCTTATTACTCCTATTCTCAGGATAAAGTTCAAGGATCTAATGCGAGCACAAGCAACCAACCCCCTCCAAAGCTATATACATGTGAGATTTGCTGGAAATCTTTCCGCCATCACTTCCATTTGACTGCCCATCACCAAGCCATTCATGAACATGGTGGGGAGAAACTGTTTTCATGCGAAGTGTGTGGAAAAGCGTTTTCATACTCTAACAGCCTGACCAGACATAGATTATCTCAACATGGTTTGACTCGTGCTGGGCCAACAACACAACCAACAGGAAACGATTCTATTGGAACTGCCTCGTCTGTCTCGGAGAGCGAGGCTGCAACCAATGCACTCCTTCATATATCACCTGAAAGTGGAAGTCATGGAGTA[C/T]AACAGCCCCATTCAACGATTGCTCACACGCAGCATCCTCAGCCTGCTGGATATTCACCACTCTTCTACACTCCAGAGTCAGGACATCACAGTTCAAATCAAGTCACTTCACACCCCCAACATCTGCACTACTCAAACCCCACGATGGGTCCCCTCCAGCTTCAGCAGCCAATCAGTGGGAAGCAGTTAATTTATTCAGGGGTTCCAAGTAACACACTTCATTCCACTCCACCTCATATCCACATCTCTCCACCCCAGCACTCGCAACACCACCAGCAACAGCATCCTTTTTTATTGCAGTCTCCACATCTACAGAGCCCGCAGCCCCAGGGGGATGCTACCCAAAGGAAGAAAAAAAAAAAAAAGAAAAAATATAAACTGCCGTTGATAACTGGATTCAGTGCTTATGAAATTGCCAGGAGGCAAATGTATTTAAAACGGAAGAAGTGCAGGCTTCAGCAGCAGCTAAAACGGAAGAAGTGGATGGCTCAGCTGAAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36790
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 |
|---|---|---|---|---|---|
| ENSDART00000053300 | Nonsense | 1315 | 1506 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 10825550)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10284089 |
| GRCz11 | 19 | 10203014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGAAGAAAAAAAAAAAAAAGAAAAAATATAAACTGCCGTTGATAACT[G/T]GATTCAGTGCTTATGAAATTGCCAGGAGGCAAATGTATTTAAAACGGAAG
Long Flanking Sequence:
AACCAACAGGAAACGATTCTATTGGAACTGCCTCGTCTGTCTCGGAGAGCGAGGCTGCAACCAATGCACTCCTTCATATATCACCTGAAAGTGGAAGTCATGGAGTACAACAGCCCCATTCAACGATTGCTCACACGCAGCATCCTCAGCCTGCTGGATATTCACCACTCTTCTACACTCCAGAGTCAGGACATCACAGTTCAAATCAAGTCACTTCACACCCCCAACATCTGCACTACTCAAACCCCACGATGGGTCCCCTCCAGCTTCAGCAGCCAATCAGTGGGAAGCAGTTAATTTATTCAGGGGTTCCAAGTAACACACTTCATTCCACTCCACCTCATATCCACATCTCTCCACCCCAGCACTCGCAACACCACCAGCAACAGCATCCTTTTTTATTGCAGTCTCCACATCTACAGAGCCCGCAGCCCCAGGGGGATGCTACCCAAAGGAAGAAAAAAAAAAAAAAGAAAAAATATAAACTGCCGTTGATAACT[G/T]GATTCAGTGCTTATGAAATTGCCAGGAGGCAAATGTATTTAAAACGGAAGAAGTGCAGGCTTCAGCAGCAGCTAAAACGGAAGAAGTGGATGGCTCAGCTGAAATGGGCCAAGTTTACTGGAGGAGGGCTTGGCTTAAATGTAGGCGGAGGCACATGGCGTGTGGGGAGGTTAAGGTTCAGAGGCCTTCGCTCTCTCATCGTGCCCTTGAAGTCATATACTTGCCCTGTTTGTCCCTTCACCACTTTTTCAAGCCGCATAAGTCTTTCGGTGCACCGAGTAACAAGGCACCCACCAAGAAAACATGGTCGCCATAATCGCCTCCGATGCACAGTCTGTGGAAAACGTTCTCGAAGGCTACTGACGGCTCTCTGTCATCGGGCCCAGCATCTCTCTCAAGGGGGGTTCTCTTGCTCACGATGTCCCTCACGATTCTGGAACGGCACTCTCCTACAGCGCCACAAATTTGCTTGTCGTCGTGTCAGTAGAGGAATCAGAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43232
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 |
|---|---|---|---|---|---|
| ENSDART00000053300 | Nonsense | 1454 | 1506 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 10825133)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10283672 |
| GRCz11 | 19 | 10202597 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTCTGTCATCGGGCCCAGCATCTCTCTCAAGGGGGGTTCTCTTGCTCA[C/T]GATGTCCCTCACGATTCTGGAACGGCACTCTCCTACAGCGCCACAAATTT
Long Flanking Sequence:
TACAGAGCCCGCAGCCCCAGGGGGATGCTACCCAAAGGAAGAAAAAAAAAAAAAAGAAAAAATATAAACTGCCGTTGATAACTGGATTCAGTGCTTATGAAATTGCCAGGAGGCAAATGTATTTAAAACGGAAGAAGTGCAGGCTTCAGCAGCAGCTAAAACGGAAGAAGTGGATGGCTCAGCTGAAATGGGCCAAGTTTACTGGAGGAGGGCTTGGCTTAAATGTAGGCGGAGGCACATGGCGTGTGGGGAGGTTAAGGTTCAGAGGCCTTCGCTCTCTCATCGTGCCCTTGAAGTCATATACTTGCCCTGTTTGTCCCTTCACCACTTTTTCAAGCCGCATAAGTCTTTCGGTGCACCGAGTAACAAGGCACCCACCAAGAAAACATGGTCGCCATAATCGCCTCCGATGCACAGTCTGTGGAAAACGTTCTCGAAGGCTACTGACGGCTCTCTGTCATCGGGCCCAGCATCTCTCTCAAGGGGGGTTCTCTTGCTCA[C/T]GATGTCCCTCACGATTCTGGAACGGCACTCTCCTACAGCGCCACAAATTTGCTTGTCGTCGTGTCAGTAGAGGAATCAGAATGTCAATAAAGGCGACGTATCTGGTGAAAACAGAGGGCCAGACTGAAAGATCAACAGTTGTGACAGGATACAGGCACTGAGCAAACTGACATCAAAACAGAAATTGTACAAGGCCTTAATAACTGAACTCTTCAAGGCAAGAGCAGGCACATAGGACTTTGATGGAAATCACCACAGATTCAACTCCTTGAACACGTGGTCAAACTATAAGCAAGGGAGTGCCTGGTTTCTCCAAAACAAGCCTGTACCTAAAGAACCATCCATTATAGACATGGATCTCTAACACGGTTTCTCCAAAGGGGAAGAATATTCTAGATTATGGAACTGTTTTTGGTAGCACCTTTGTTGTAATGGTAGCATCTCTATCCTCTAAAAAAAAATGCATTCATTATGTATTTTCGTAACTTTATTTGTGCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23452
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 |
|---|---|---|---|---|---|
| ENSDART00000053300 | Nonsense | 1466 | 1506 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 10825097)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 10283636 |
| GRCz11 | 19 | 10202561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTCTCTTGCTCACGATGTCCCTCACGATTCTGGAACGGCACTCTCCTA[C/T]AGCGCCACAAATTTGCTTGTCGTCGTGTCAGTAGAGGAATCAGAATGTCA
Long Flanking Sequence:
GGAAGAAAAAAAAAAAAAAGAAAAAATATAAACTGCCGTTGATAACTGGATTCAGTGCTTATGAAATTGCCAGGAGGCAAATGTATTTAAAACGGAAGAAGTGCAGGCTTCAGCAGCAGCTAAAACGGAAGAAGTGGATGGCTCAGCTGAAATGGGCCAAGTTTACTGGAGGAGGGCTTGGCTTAAATGTAGGCGGAGGCACATGGCGTGTGGGGAGGTTAAGGTTCAGAGGCCTTCGCTCTCTCATCGTGCCCTTGAAGTCATATACTTGCCCTGTTTGTCCCTTCACCACTTTTTCAAGCCGCATAAGTCTTTCGGTGCACCGAGTAACAAGGCACCCACCAAGAAAACATGGTCGCCATAATCGCCTCCGATGCACAGTCTGTGGAAAACGTTCTCGAAGGCTACTGACGGCTCTCTGTCATCGGGCCCAGCATCTCTCTCAAGGGGGGTTCTCTTGCTCACGATGTCCCTCACGATTCTGGAACGGCACTCTCCTA[C/T]AGCGCCACAAATTTGCTTGTCGTCGTGTCAGTAGAGGAATCAGAATGTCAATAAAGGCGACGTATCTGGTGAAAACAGAGGGCCAGACTGAAAGATCAACAGTTGTGACAGGATACAGGCACTGAGCAAACTGACATCAAAACAGAAATTGTACAAGGCCTTAATAACTGAACTCTTCAAGGCAAGAGCAGGCACATAGGACTTTGATGGAAATCACCACAGATTCAACTCCTTGAACACGTGGTCAAACTATAAGCAAGGGAGTGCCTGGTTTCTCCAAAACAAGCCTGTACCTAAAGAACCATCCATTATAGACATGGATCTCTAACACGGTTTCTCCAAAGGGGAAGAATATTCTAGATTATGGAACTGTTTTTGGTAGCACCTTTGTTGTAATGGTAGCATCTCTATCCTCTAAAAAAAAATGCATTCATTATGTATTTTCGTAACTTTATTTGTGCTGCAATGATGGATGCATACCAGTGAAAGTGGACTAATTT
Associated Phenotype:
Not determined