ZMP
si:ch211-215c3.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens ZNF827, zinc finger protein 827 (ZNF827) [Source:UniProtKB/TrEMBL
Human Orthologue:
ZNF827
Human Description:
zinc finger protein 827 [Source:HGNC Symbol;Acc:27193]
Mouse Orthologue:
Zfp827
Mouse Description:
zinc finger protein 827 Gene [Source:MGI Symbol;Acc:MGI:2444807]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18170 | Nonsense | Available for shipment | Available now |
sa19530 | Nonsense | Available for shipment | Available now |
sa4854 | Nonsense | F2 line generated | Not yet available |
sa9707 | Nonsense | Available for shipment | Available now |
sa12453 | Essential Splice Site | Available for shipment | Available now |
sa14020 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18170
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037516 | Nonsense | 267 | 1150 | 2 | 14 |
ENSDART00000139883 | None | None | 138 | None | 2 |
ENSDART00000141562 | None | None | 196 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 35826973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35386831 |
GRCz11 | 1 | 36118858 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCGCCAACGCCGTGCTCCAAGACAAGAACGCGGTGGCCTCCTCCACCT[C/A]GGCATCTTCATCCTCCTCGTCCTCCTCCTCATCCTCTTCAGTCACCTCCT
Long Flanking Sequence:
GCTTTCCTCTGTGGTGTCCTCTCTTTATGGAGACTCTAGCCAGGCTCTGGGTAAGCCACTCAGCAGTAATCTGCGCCGCCTCCTGGAGGCTGGCTCACTGAAGCTTGAGGGAGGGGAGCTGGCTGGACGTGGAACGGGTAGAGGACAAGAGTCACCCCCGGTCAGCCTGGTACTATCTCCGTCTTCACATCACGCACAGCAGCTGAGTGCCCTGGCGAGGAGGTTGGCAAATAGCAGCAACAACAGCGGAAATTCAAACTCTGCGTCACCTGCATCTGTAGCAACTGTCAAGCAGGAGCCCTGTGACCCATACGGCCCCAGCAACGGCCCTAACTCAGGCAGCAGTGGCTTTGTATGGGTAGGCGTCGCAGATAAATGGCCATCGACAAGTTGCTCAGCACCCAGTGGCAGTAGCCTCTCACCAGACTCAGCAATTCAGAAGTTAAAGGCAGCCGCCAACGCCGTGCTCCAAGACAAGAACGCGGTGGCCTCCTCCACCT[C/A]GGCATCTTCATCCTCCTCGTCCTCCTCCTCATCCTCTTCAGTCACCTCCTCCTCAATGGCAGCCCTGGGCACTCGCTCTGATGACGCAGTGCGCTTTGAACCATTCGCTTCACCCTTTAGCCCGCAGTCAGCCAGCTCTACGCTTGCTGCCCTCTCAAAGAAAGTGTCTGAAAGAAGTCAGCAGCAGGTGGGCTCATCTGAGCATCAACCCTCAGCTGGCTCCTTTCTCTCTCTGGTTTCCATGACCTCCTCAGCAGCTCTGCTAAAGGAGGTGGCCGCACGAGCAGCAGGGAATCTTCTTGCTGATAAGAAAGAGCCGGCGTTAGTACTGGGAGCCTCCGAAGATGTCAAGCCCCTGTTAGACAGGAACCAGAAGGTGCCCACCCCAACCCAGGCAATGGATCTTCTGCTGCCAACAGTCCCCAAGGGAAGGGCCAAGCCCAGCAGTCAAGCAGGTAACTTGCAGTTTATTCTTAAAATAGATGCATGACATTTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19530
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 |
---|---|---|---|---|---|
ENSDART00000037516 | Nonsense | 703 | 1150 | 5 | 14 |
ENSDART00000139883 | None | None | 138 | None | 2 |
ENSDART00000141562 | None | None | 196 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 35786565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35346423 |
GRCz11 | 1 | 36078450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCAAGAGAGGAGGGGAGCCCGATGTTGGGCAAGAGCAGCCTTCTCAGC[C/T]AGGACATCAACGTCAAAGTGGCCTCTGAATTGCTTATGAAGCTCTCAGGT
Long Flanking Sequence:
GAATCGTGATTCAGGTGAATTGTTACATCCCTAGTTAGTGGTTCTTTCCACAATAGCAACCGCTGTTAAATCAGCTGCTACTCCGAAGGAAAATGAATGAACAGTTGTAGATTTTTTTGTAGGAAAATAATGAGTTTAATCCATTTTGGACAAAGGGTGTAACATAAATTGCGGGAAAGTAAAGTTCTGGGAATTATTTCCATATGTACCCTACTGTTACATATCATTTAACTTCTCGCATTCGACATTGCTGTCAACAAAAAGCATGCGCACCAGAACATTGTTCTCAAAAGCCTCACTTCTCTTTTTCTTGCCCCACAGCAGCGAACCAGAAGGAGGCCCTAAAGGGTCCATACTGTGTCAAGGAAGAGCCCCAGGCGGAGGAGCCCCTGAACTCTCAGAGGGGACCCAGCTACAGCTTCTGCCAAGAAGGACCTCCAGGAGCCACCAAACCAAGAGAGGAGGGGAGCCCGATGTTGGGCAAGAGCAGCCTTCTCAGC[C/T]AGGACATCAACGTCAAAGTGGCCTCTGAATTGCTTATGAAGCTCTCAGGTCAGCAGGTGTATTTTGGTGCAAGCACTCATATGCGTGTTTATTTTCAGGCGTGCTTTCTGAGTGCTTGAATGCTGTTGAGGAAACCCAAAGGCCAAAGGATTGAGTGAGTGGGTGCATGTGTGTGTGTGAGAGAAGTGTGAGCTGTGCATTCTCTTTGGTGCTCAGGTCATATTTAGAATAACCTTATTTCGACAGTACAACTAAGGTTACAGAATAATATAAGTATTGTATATTTAAATCAAAAATAGGTCTATACGTTATGTAAAATTGTGCAAAACAATGTCAGGTCATCATAAACTCTAGCACTTGCGTATATTAGCTTGTCTTTACGTTTTGTTCTTTGTCTAGTCTTTCTTTCATTCTATCACTCCCTTTTGCTCTTTTTCTCGCTCTGACCTGCTGCTGTCCATTCCACTCACTCATGTGTTCTGGGCAGGAGGAAGAGGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4854
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000037516 | Nonsense | 773 | 1150 | 6 | 14 |
ENSDART00000139883 | None | None | 138 | None | 2 |
ENSDART00000141562 | None | None | 196 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 35765317)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35325175 |
GRCz11 | 1 | 36057202 |
KASP Assay ID:
554-3542.1 (used for ordering genotyping assays)
KASP Sequence:
TTCAGGACCATGTGAAAAGAAGGAACCAATGGTCAACCTCCMAGATCATT[T/A]GCCCCGCCCCCAGAATGACCTCTTCTCGCAGGACATATCGGTCAAAATGG
Long Flanking Sequence:
TAGAGGCAGGCCAGTGCAGAAATTCAATTGAAAATACTGATGTAACAATAATTTTTATATTTTAAAGACATAGTGTGGAACAATATCATTTAATGCAGTGCTTCTTGTTTGGTCTGAGACTCACTTTATATCGTATGCCAGCCAGGGAGTGAAGATCGCTGTTTTTTTTAAAGAAATCAGATCTTAAATGTATCAATTTTGTATGGGATGACAATTAACCGGAAGCCCTGGGGCTGGCGGACTGAATTTGAAAGTTTTGGTGCATATACCCAATTAGAATCAGTGCTATGATGGCTACTTGTAAATAAATTAACATATATTTTAATTTGTTTTTTCAGAGAACAACAAAGACGCTTGCGTCCAGAATGTTATTGTGAAGGCGGAGCCTATGGAAGTGGATCCACCCCTTGATCTGGCCTCACCCTCCTCCCATCTACTGGGCTTTAGCACTTCAGGACCATGTGAAAAGAAGGAACCAATGGTCAACCTCCCAGATCATT[T/A]GCCCCGCCCCCAGAATGACCTCTTCTCGCAGGACATATCGGTCAAAATGGCCTCCGAGCTGCTTTTCAAACTCTCTGGTAAGCAATAAGAAACAGCAGATTATTTGTTTGAAAGAAAAATATCTCTCTGTGAAGAGAGTCTTTAGGTTGTCATGTTTTCTGAGCGCTGCACTGACACACTAGAGAGTGGAGGGATATTTGTGGTGTTAAATGATGGCAGGATTGAGCTTTTCTTCCAAGAGCATTCTGAGGATTAGCAGAGACAAACCTGCCCCCAGCACTCCTCGCTGCCAACCACGGCTCTCTTTAAATGCCATCTAGCACCTCGGAAGCTGATCATAAAAAACCTGCACCCCCACATAATTTGTTGTATGTTTGTGTATGTGTGTATATATATATATATATATATAAACTATTTATATATATGTGTGTGTGTGTGTGTGTGTGTTTACATGTATACTACATACATACATACACACACATACCCAAACCACACACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9707
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037516 | Nonsense | 908 | 1150 | 10 | 14 |
ENSDART00000139883 | Nonsense | 37 | 138 | 2 | 2 |
ENSDART00000141562 | None | None | 196 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 35745049)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35304907 |
GRCz11 | 1 | 36036934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTTTGTCTCTACAGAAGAGAGGAAATACAAGTGTCATTTGTGTCCATA[T/A]GCAGCTAAGTGCCGAGCMAACCTCAACCAGCACCTCACCATCCACTCAGT
Long Flanking Sequence:
CTGAAAATGTTTCTACATATGTGCCCAACAACATTGTATGTTGTCATTAGGACAACTAATGCCACAGGTAAGTAAATAAGGTTCACCGGACTAGATTTCCCTTCCTTTAAAGAGATTAGGCTCCTGATTAGTCCTGGAGGGAAAAGTACCCAAGTAATTACTAAGCTGTAAAGATGTCTCCCCGAGCGCTAAGCTCCCCTGGAGTACTGCACAACCATGACCAGCCTCGCCTGATCCTTGAACAATCACATCCCGCAGGTCCCTGAGGAGCATCAATGAGCCGTCTGATCACCATCCACCCAAATACATCTCTGTCTAGAGTACAGAACAAATAAATGTATAAGTCATGTGAGGACGGTGGGCCTCAAGAGACCTGATGTTAGAATGGCCACCTTATAAACATCATCTATCCACAAAAGCGTCTTCTTTTGGTTGTTTATAAGTGCTCTTTGCTTTGTCTCTACAGAAGAGAGGAAATACAAGTGTCATTTGTGTCCATA[T/A]GCAGCTAAGTGCCGAGCCAACCTCAACCAGCACCTCACCATCCACTCAGTCAAACTGGTGAACACAGATGTCGAGCAGATTGTTACCGCTGTTACCAACGATGGCCCAGAGCTCAAAAACTGCCCCTACTACTACAGCTGCCATGTCTGCGGCTTCCAGACAGAGTTCAATGCTCAGTTTGTCAGTCATATGTCTCTTCATGTGGACAAAGAGCAGTGGATGTTTTCTCTCTGCTGTAGCACCTGTGAGTATGTGGGTGTGGACGAGGCCGAGATGAAAGCTCACATCAGTGCAGGGCACGCAGGTAAGATCTCACCATTTTAACATTGTAGACTTTCTTGATACTTCTGTATGTTTTACTCTGTGTCCTTACTACATACGTCCTGATACTGCGGCACGCAATTAATGTATTTGCATGTAAAAGTAGTTTTTTGTCCTAACCATCCACGACAGCAACATTCAAAATTTCTGCAAAGTACTGTCTGACCAACTGCATGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12453
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037516 | Essential Splice Site | 1076 | 1150 | 11 | 14 |
ENSDART00000139883 | None | None | 138 | None | 2 |
ENSDART00000141562 | None | None | 196 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 35740349)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35300207 |
GRCz11 | 1 | 36032234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAGCCAATCAAGCTTAGGCCCAGGAGCAGAGGAAAAAGCAGAGAAAGG[T/C]GAGACTTTTAGCAGATACACCTAGCGCATTTTATCCCTGATTAAGAGTGA
Long Flanking Sequence:
AAGAAAGCCCGCCTCCCGACTTTTAAGGCTTAATACCGCACTGCTCTAGGCATACATATTCCAGCCCGGCTCACTGGGCGGATTTCGATCAATTGCAGGATTTTTCTGCCTTTTGCTTTACTCATTACAGAATTCATTATCAAACCTTGAGCGCTGAAAGACGCTCCTGTCTAATTCTCTCATGGCTTAAGCTAAGCCGAGTCTTTGATACCATCATGTCATTCAAAAACCAAGTTTGTCTTATATTCAGGAAGTGACCCTCGATATCTCTTTGCTTCTTTTTTTTTTTAATCCCACACAGGTCTCAATTCTAGAAGCCCTCTCAGTGAGACCAAGAGCACTTCCTCCTCTCTGTCAGCCCTCAGCGACTCCCTCAACAGCTCTGAAGGTGGAGATGTTGCCCAAGGTAACGAAGAACTAAAAAGCCTTTTGGCTCCGCCTTCATCTGTGGGAAGCCAATCAAGCTTAGGCCCAGGAGCAGAGGAAAAAGCAGAGAAAGG[T/C]GAGACTTTTAGCAGATACACCTAGCGCATTTTATCCCTGATTAAGAGTGAACTAAAGCATGTTTGAAAAAGTTTTACATTTCAAAACCATGAACAGCTCTAAAAAAGGAGCTTATTTAATTCATTTATTTAGGTGGCTTTATAAAAGATGGCTGCCATATTTAGATTACATAACCAGTGCAAAAAACAGAATTCAGTCATTAAAATGGAATTAGATGTATGATGCAGAAGGTGTTTGAAGTCTTTAAATGGGTGGTCCACTACAATATCATATTTTAAACTTTAGTTGATGTGTAATGTAATTGTGTGAACATAAATAGCATTTCTGAATGTAAGGGTGACATTGGCTTAAACAGAGTCAGCTTAGTAATGCCTACAGCGAACAAAGTTTGGGGTCTACAAAAAAATACATCTGGGCTAGTGAGATTACAATGCTTTAGGTTACACGCATTTACCACGCGCATATACCCAGTGCAGCAGAGGGGTGTGGCCAGAGGCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14020
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037516 | Nonsense | 1092 | 1150 | 12 | 14 |
ENSDART00000139883 | None | None | 138 | None | 2 |
ENSDART00000141562 | None | None | 196 | None | 2 |
Genomic Location (Zv9):
Chromosome 1 (position 35737849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 35297707 |
GRCz11 | 1 | 36029734 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTTTGAATGCGTCTTCTGCAACTTTGTGTGTAAAACCCGACCCATGTA[C/A]GAGCGGCACCTAMAGATCCACCTGATCAYGYGCATGTTTGAGTGTGACGT
Long Flanking Sequence:
AATATTATATTTGAAATAAATGCATATCATTAGAACTTCCTGTTCATCAGAAAAATCATTAGAAAAAAAATCTCACAACCCCTTACAACATTGATAACAATAAAATCTTATCAAATTAGCATATTGCAGTAACTTTATTAGCATATTATTAAAAATATTAACAGAATATTGAGTTGAGTAATGTTGCATCAAAATTCAGCTAATTTCAGACTCAATATATGTGCGTAGTAAATATTAAATTATAATAATTCACAGTAACAATCGTTTAATGTCATTTTTGTTAAATAAACGCAGGTTTGGGGAACAGTTTTAACACAAGAAATCATACCGATCCCACATTTTTAATGCAACAATGCAGAAAATAGAAAATACTAAGTAATATAATTATATAATGTATATGAAAGATAATGAGATTAATTTCTTCTTCTCTCATCCTGACCTAATCTCCCAGGCTTTGAATGCGTCTTCTGCAACTTTGTGTGTAAAACCCGACCCATGTA[C/A]GAGCGGCACCTACAGATCCACCTGATCACGCGCATGTTTGAGTGTGACGTCTGCCACAAGTTCATGAAGACGCCCGAGCAGCTCCTGGAGCACAAGAAGTGCCACACCGTCCCCGCTGGAGGGCTCAAGTAAGGAAAGCAAGTACAGCACGTGCCTCCCTGCAACCTCACAAAATCCCCAAAAACCCACCCCCCAGCCCCTACCCCCCTCAGGCAGGACACATCCCAGATTTAAACACAGTCTATCCAGGTGCACTGGTCGAGGATCAGGCTGGATTCCAAACAGAAGGTATTCCAGAAAATGAGCTTCATTGAGCAGTGCTTTAGGGTAAACCCTTCTGTGGATCCACATATACAGTAGCATGCTATAAACAGAGAACGTTCCTGAATGTGCCTAAAAATAGATCAGTACTATGCTACTTTGTCAGATTTAAACTCTATTTAAATTCTAAATCTGTTTAAAAGTATATAAAATGTATTTAGTTAAGATACAAAAAAACT
Associated Phenotype:
Not determined