Busch Lab

ZMP

zgc:195317

Ensembl ID:
ENSDARG00000074906
ZFIN ID:
ZDB-GENE-081022-210
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
sa14446 Nonsense Available for shipment Available now
sa14603 Nonsense Available for shipment Available now

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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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