ZMP
zgc:195317
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100189616 [Source:RefSeq peptide;Acc:NP_001128615]
Human Orthologue:
ZNF831
Human Description:
zinc finger protein 831 [Source:HGNC Symbol;Acc:16167]
Mouse Orthologue:
Zfp831
Mouse Description:
zinc finger protein 831 Gene [Source:MGI Symbol;Acc:MGI:3641861]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa7353 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa8559 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14446 | Nonsense | Available for shipment | Available now |
| sa14603 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7353
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 > A
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000122253 | Missense | 30 | 1580 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 411684)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 398421 |
| GRCz11 | 11 | 424919 |
KASP Assay ID:
554-4023.1 (used for ordering genotyping assays)
KASP Sequence:
AGCCTCAGTGTTCAGAGTCTGCACAGAGAGAGGAAGAGGCGCATGTTCAG[G/A]CCCGTCTCACCRCTATGTATGTCCAGAACGTTCCTGCTTCTGGCCTGCAG
Long Flanking Sequence:
AAAGAGATTTCTATTTGGTTAAATATTCCTATTGATGAATCCTCAGCACTTTGTTTACATTTCCAGAGTCAATTAAACAAATGTTTGCGCAAGAGTTTACACATTTTGACACACGACTACACATTTTAAAAATAAATCATCTGCATGTTGACCAACATTTCTTTCTCTTGATATGGCATTTTCATCAGATGTACTGACACGATTGCAGTCACTCTAACCTCTAAAAAGATGGTGATTTGCTATATTATGGAAAAAAGCTTGTCTTCTTTAGCTTCCTGCATTTTAAATCAAATAAGGGTTTGAATGCTCTGATCCAGGGGAGTTCAGGTCGAATGAAGAAAAATAATAAAACTGTTTCTTTTTTTAGGTAATTAGCGAGCTCCGTCTCCCAGCATCACAAGGGTTGTGTTACCATGGCAACTAGAAAGCAGAGCTTTGTGCGAGCTACCGAGCCTCAGTGTTCAGAGTCTGCACAGAGAGAGGAAGAGGCGCATGTTCAG[G/A]CCCGTCTCACCACTATGTATGTCCAGAACGTTCCTGCTTCTGGCCTGCAGCCATACCCTCAGGCCCAACCTGGAGCCTTGCAGGACGCAACGGTTGTACCACTGTTCCTGCCCCGGATGTGTAGCAACTCGACTTTGCCCTCATTGACATTGCATATTGCCAGCACGGCTGCTTTGCAGCAACAAAGACTAGTGGCTCCAGCGTCCGCGGGCAGACCTAAGTCTCTTGGGAAGCATGTTTGCCCACATTGCGGGAAGGACTGCCTGAAGCCCAGCGTGCTGGAGAAACATCTTCGCTGCCACACAGGAGAGCGACCGTATCCCTGCACGACCTGTGGCATTTCTTTCAAGACACAGAGCAATCTTTACAAACACAAGCGCACCCAGGCTCATGCCCGTCATTCCAGCGAGTCTGAAAAAGGCACCTTCAGCAGTCAGGAGAGCATGGAGAGCTCGAAGGACAACTGTTTAAGTCCATCCTTAGAGACGAACTGTGTGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8559
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000122253 | Nonsense | 538 | 1580 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 410160)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 396897 |
| GRCz11 | 11 | 423395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTAGTCAGACAGGTGGCAGTGGATTGCCTGTRTAGTGCCGAGGCAGAA[A/T]GAGGCAGCATGAGCAGCCTGAGCTCAGACGGAGACAGCACCGATGTCGCA
Long Flanking Sequence:
AAGACCCAAAAAGCAAGGTGTCCGTTCAGGAGAAGCAGAAGCTGGAGGAGCGCATTTCAAAACTTATATATGAGAATAGTGTGTTGGTGGACAATAAGCTACTGGAAAACGTGCGACCAAGAAAGACAATATTGTCAAAGCAAGGAAGCATTGATCTTCCGGTGCCCTACACGTATAAAGACTCCTTTCATTTTGAGATAAGGAACTGCAAGCACGTCTTGAGCTCCCAAAATCCAGACCGAGGAGGTCAAGCCGTTCACAGGTCTTTGCCCACACAACTGTCCGCCAGTCTGGAGCACGCACCATTAACACGCAGCAGCTCTCTACCCTTCTCTATGGGAAGCAAACCAGCTGCCGATGGAGCAGTGAGTCTAAATCTCAGCAGACGATGCAGTGCAGGCCATGTTTACCCAATACGGCCATCAAATCAGAGGGCAGCAACACACCGCTCACTAGTCAGACAGGTGGCAGTGGATTGCCTGTATAGTGCCGAGGCAGAA[A/T]GAGGCAGCATGAGCAGCCTGAGCTCAGACGGAGACAGCACCGATGTCGCAACGGAGTCATGTGTGAAAGCAACCTACAGGAAGAAAGCACAGAAGTTCGACTACACAAAGTGGCACACCTACAAAGGAGGCACATTTAGGAAACTCTACAATACTCCGAAAGACTGTGCACTAAAGGCGAGGAAGACTGCGTCAAGCACTGAACCGACAGAGAGTCTGGACATCCAGAGACATAATGGATCAATGTTGACCTTGCCAAATGAGCTTAAAGTCTCACATACTGGCTTTGAACATGATAACGTGAAGGGATCAAGCGTGGAAGATATACAATTAACACAACACACCGTCTGCCATGTCCCATCAGAGCGGAAGAAACAGCGCACTGGGAATGATGTTCAAACGCTCAGTGTTTCAGATCCTAAAGATACTGGAAATCTGTGTACGTTAATGAGCCAGTCATTCTTGTCAAGTTGTGCAGAGAGCGGCTCCATCACTGTACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14446
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 |
|---|---|---|---|---|---|
| ENSDART00000122253 | Nonsense | 1086 | 1580 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 408516)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 395253 |
| GRCz11 | 11 | 421751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAYAAAGTTTCACATCTCGGCCTCAGYGGACTATCSTAAAAACACAACA[C/T]AMCCGCTGGAGTTACCAGAGCTGAWGAACTCTGGAAGTCTTSAGGTTGAG
Long Flanking Sequence:
ATCCTTCATTCTCTGTTATTGAATCAGGAGAACCCAATGCTTGTACAGACAACATCGCATCCACAGTGTGTGAGAGTCCTCAGAACAGCATGGCATCTAATATCCCCACGAGTGACTCAGAAGAGCTTCAGTCTGAAGGAAAAGTGATGCTGCTGAATGGCTCGGCTCAGGCTCAGAACACGTTCTATGTGCGCACGGCTGACCTCCAGATTGTCATGCAGCTCATTTCTGATGAACAGTTAGCACTGATCGAGCCTCATATTGAAGCCATGTCTTCAGCGCAGACGACACTGTTGCAGGAGGCGTACAGCAAAGATGTGCCGCAGGAACTCATCAATATTGGTGAGACGCAAATAAATAGCACTTTCAGGTGTTCAGCAAACAAAGCAGACACCTCTCAAAATGATGTTACCACCATGCCTCAGTGTGTCTCATCTTGGTCGCATCCACAGACAAAGTTTCACATCTCGGCCTCAGCGGACTATCGTAAAAACACAACA[C/T]AACCGCTGGAGTTACCAGAGCTGATGAACTCTGGAAGTCTTGAGGTTGAGTCAAGTCACAAACTAGTGGATGGAGACACTCTGACTGAGCCTAAATCAGTGGAGAGCAGTTGTTCTATAAGAAAATACGACAAGGAACCACAAAACTGTGTTCACAACAAAAACACAGTAAGCACTACTGAGGATCAAACATTCACAGAGGCAACCAGAGATCAACAAGTGGAATCAAATCACATTCCAACTATAAACACGAGTGAGCTAAAGGAAACAGGTCACTTCATGTCAGAGAGCGTTCACACAAACACAACTACACACCTCGCAACTTGTGTTTGTGAGAAAAAGACGACAAAAGAGATGCCAGAACAGCCCAGAGACAGCAAGACTAGCTTAGACACGAGAGAAATAAAGGCTTGTGACACAGATAAGGTGACTGAAACGTTGTGTCCTGAACAAACAGCTGCTCAGCAGGATTCCCAGCACGACTTTGCTCCCGGTGATTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14603
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000122253 | Nonsense | 1317 | 1580 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 11 (position 399906)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 386643 |
| GRCz11 | 11 | 413141 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGATGGYGTTMGGAAAAACCTGAGGTTTCAGAGGGACTCAAGGACAGAT[A/T]GAAGGGAATCARGAGCCAAAATACGGGAAGATGGAGATGAAGAGGGGAAA
Long Flanking Sequence:
ACTATAAGAAAAAATTTTAGCTTAAAGGGGCTAATAATATTGACCTTAAAATGGTGTTTAAAAAATTTATAACTGCTTTTATTCTAGCTGAAATAAAACAAATAAGAATTTCTTTAGAAGAAAAATATTATCAGACATTCTATGAACATTTCCTGAATATGTACATTATTATATATTATTATATATTATATATTCTTATTTATATATATATATATATATATATATTTACTATATATATTATAGTATTTAAAAAATATATATTATAGTATATAGTAATAGTAATATATATAGTATAATATAATATAGTATAATATACTATATATATTATAGTATTTAAAAATTTATATATATATATATATATATAGGGTTAGGGGTATATTTTTTATACTCAGACTCAAAAATAATAGAGCATTTATTAATTCAGCTCATGTTTTGCTTCAGAATCTGGGGAAGATGGTGTTAGGAAAAACCTGAGGTTTCAGAGGGACTCAAGGACAGAT[A/T]GAAGGGAATCAGGAGCCAAAATACGGGAAGATGGAGATGAAGAGGGGAAAAGATCAACCATGGAGATGACTGATGGAAACAACACATGCCGAAGCTCTGGAGACACTTACAAACAAGACAAAAGAAAGGTGAGAGAAAAGAAACAAAGCACTCACTGAGAACACACATCATACAGGACGTTTATTTATAAACTAATGTCGAGAGGATCACCATTGCTTGCGGCCGGTCCTGCATCATCCAATTTATAATTCACCAATCAGACGATTCCTAAGCCACTATAAATACCCTGAGCTCCATATCACAGCCATCTTCATTTTGAAGAATCCCCCTCCACCCCTACTTCTCCTCCTTTCCTAGATGGGTGGCACGGTGGGCCAATGGTTAGCACTGTTGCCTCACAGCAAGAATGTCTCTGGTTCTAGTCCTTACCAACCCAGCCGACATTTCTGTGTGGAGTTTAGACGTTCTCCCCGTGCTCACGTGGGTTTTCCCGGGTTCCC
Associated Phenotype:
Not determined