Busch Lab

ZMP

LOC100332780

Ensembl ID:
ENSDARG00000076477
Human Orthologue:
ZMIZ1
Human Description:
zinc finger, MIZ-type containing 1 [Source:HGNC Symbol;Acc:16493]
Mouse Orthologue:
Zmiz1
Mouse Description:
zinc finger, MIZ-type containing 1 Gene [Source:MGI Symbol;Acc:MGI:3040693]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa24926 Nonsense Mutation detected in F1 DNA Not yet available
sa35381 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa2634 Essential Splice Site F2 line generated Not yet available

Mutation Details

Allele Name:
sa24926
Status:
Mutation detected in F1 DNA
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
ENSDART00000113972 Nonsense 379 1054 7 20
Genomic Location (Zv9):
Chromosome 12 (position 50224088)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 48783288
GRCz10 12 48837458
GRCz11 12 48790781
KASP Assay ID:
554-7603.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCAGTTATGGGGGCGGTCCTAATTATGCAGGTGGGATGGGCTTATCA[C/T]AGACACGCCCCCCTTCTGACCTCAGCCAACCAGCTGCTGCTGCTGCCGCT
Long Flanking Sequence:
GTATTGTCGTCTTTCAGGTTATATCTCAGCTTCAATGCGCTTTTTAAATAAATAAATAAAATACAAAGCAGCCGATTGCCATCGTGACAGCAATAGGATCCAATGGACAGCCGATCGCTTTCACTCCTGAATCCGGGTCTGTTGCTGGGCGCTGCTGTTGCAATGGAGCGTTCTATTGAGTGTCGCCTTTCGGTGATTCTAAGCTCTTTGATCATAGTGACAGATTCAAAGCACAACTAACGTTATCTGTGTGAAAAAGTGAGCGTCAGTGTGGCAGAAGAAGTTGATATTGCATAATAAACTCCTCAGTCCTATACAACAGCTGCTGATAAACCTGTCACACTTTACTCTGTGATGAACTGCCTGTATTGCTATATTTAAATGGATTTTTTAAAAATAAATAAGTAAATAAAAACCTTGTACAGCATATAAGAAATGAAATCTCTCTCTTCTGCAGTTATGGGGGCGGTCCTAATTATGCAGGTGGGATGGGCTTATCA[C/T]AGACACGCCCCCCTTCTGACCTCAGCCAACCAGCTGCTGCTGCTGCCGCTGCTGCTGTTGCTGCCGCTGCTGCCACTGCAACAGCCACGGCCACGGCAACGGTTGCCGCGCTGCATGAGACACAACACAAGGACATGAACCAGTACAGTGCGGTACGACAGCACATATAATATTAATAATACTATCATTATTTATAATAATAATAATAAAATAATAATAATAATAATCTAGTATTTGTTTGTATTTTTTGTTGACGTGATGTTTTGGATTCGAATCATAGGCAGACTATTCCTAAACTTTCAGTCTGTTATTGTGCAAAAATTGATGGCAGTTTAATAACTGTACAGTCAAAAAATCATAATAAATTAAAACATATACTGAATTAAAATTGACACATTTAAATGTGATTAATCATGAATAATGAATAATAATAGAAAATATAGGTTGTGCAATATAAAACAATGGAAACTTTTGGAAAGTCTTCAGAATTCACAAAAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35381
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113972 Essential Splice Site 738 1054 14 20
Genomic Location (Zv9):
Chromosome 12 (position 50229088)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 48788288
GRCz10 12 48842458
GRCz11 12 48795781
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGTGTGTGTGTGTGTATGTGTGTGTATGTGTGTGTGTGTGTGTCCTCA[G/T]TGAAGAAGAGTTTCAGCAGTGTGTGTGTGTCTGGACTCTCTGATGAGCAT
Long Flanking Sequence:
TACACACACACACACACATGCTCTCATGCATACATGGACACTCACATATACAACCAAACACTCATGCACACACACACAAACACACAAACAGAAACACACACAGATAGACACACACATTCTCATGCATGCACAAGCATACGCTCAGGTTGACACACACACACACAGGTGGACGTTAAATGAGTGTGTGTGTGTGTGTGTGTTGTGTTTTCTCTGCAGTCGCACCTTTTTGTCCTGCAGCTGGTGCACCGGCCGTCTGTGCGCTCCGTCCTGCAGGGCTTACTGAGGAAGAGGCTGCTGACCGCTGAACACTGCATCAACAAAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAAGTACGTGGGTGTGTGGGTGTAGGTGTGTGTGTATGTCTTAGTGTGTGTGTAGGTGTTTATGCGTGTGTATGTTCTCAGTGAAGAAGCATTTCAGCTATGTGTGTGTGTGTGTATGTGTGTGTATGTGTGTGTGTGTGTGTCCTCA[G/T]TGAAGAAGAGTTTCAGCAGTGTGTGTGTGTCTGGACTCTCTGATGAGCATGTGGAGCAAACGGCCATCAGGGTTTCTCTAAAGTGTCCCGTCACGTTCAGACGCATCCGGCTGCCGGCCAGAGGACACGACTGCAAACACGTGCAGGTCACTCACACACACACACACATACACAATATCTAGTCTGAGAAAATATTACACAGACACACATATACACACTTTAATCTAGGAAAACACAGACGCACACACACACACACCATCATTGACATGTACACACTGACATATACACACTAATTTACACTGACACACACACACACACCAGACACACAGTGATGTGTGTTTTCTCATCAGTAAAGTGTGTGTGTGTCATGTGTTCTCCACAGTGTTTTGACCTGCAGTGGTACTTAGAGCTGAACTGTGAGCGCGACACGTGGAGGTGTCCCCTGTGCAAGTAAGAGTCTGAATGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2634
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113972 Essential Splice Site 832 1054 16 20
Genomic Location (Zv9):
Chromosome 12 (position 50229763)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 48788963
GRCz10 12 48843133
GRCz11 12 48796456
KASP Assay ID:
554-2702.1 (used for ordering genotyping assays)
KASP Sequence:
GTCTGGAGGTGGACCAGTACATGTGGKGGATYCTGAACGCTTCACAGAGG[T/C]ACATGTGCCTTCNTTTCCCACACACTCAGCACACACTCACACTGGTTAAAG
Long Flanking Sequence:
ATATCTAGTCTGAGAAAATATTACACAGACACACATATACACACTTTAATCTAGGAAAACACAGACGCACACACACACACACCATCATTGACATGTACACACTGACATATACACACTAATTTACACTGACACACACACACACACCAGACACACAGTGATGTGTGTTTTCTCATCAGTAAAGTGTGTGTGTGTCATGTGTTCTCCACAGTGTTTTGACCTGCAGTGGTACTTAGAGCTGAACTGTGAGCGCGACACGTGGAGGTGTCCCCTGTGCAAGTAAGAGTCTGAATGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACTGCTGCAGAGCTGATGTGTGTTTCTCTCCTGCAGTAAACCGGCTCTGCTGGAGGGTCTGGAGGTGGACCAGTACATGTGGGGGATCCTGAACGCTTCACAGAGG[T/C]ACATGTGCCTTCTTTCCCACACACTCAGCACACACTCACACTGGTTAAAGGGAGAGTGCAGTGCAGATGTTGAGCTGATTTATGGACAATACAGTTGATGAAGTCTGATTTCCTGTCTGTAAGTGGATCTTCAATATGAGAGAGCTGTTTTAGGTCTGTTCATTTAATCCGTGTTTCTAACTGTATTGTGTTAGCATTGCAAACCTTAAACACAGTCTCAGCTCCTTTACTCTCAGCATCTTCCCTATAACTGCTGCACAGTAATGGCGAAAGGCTGTCTGTTGATTCAGCTGAGCCTGCTGACTGATGCTGGACCTGTGTTTCAGCTCAGAGCTGGAGGAGGTGCTGATCGACCCGTCCTGCAGCTGGAGGCCCGTCCACATCAGATCTGAGCCGCATATAAAGCAGGATCCAGACGAGCTGCTGAGCAAACGCTGCAAAACCACCAGCGCCAGCCAGACCCTGCTGCCCGACGCGACGGAGATGATTGCACAGCTGGG
Associated Phenotype:
Not determined