Busch Lab

ZMP

LOC100151141

Ensembl ID:
ENSDARG00000078802
Human Orthologue:
RNF111
Human Description:
ring finger protein 111 [Source:HGNC Symbol;Acc:17384]
Mouse Orthologue:
Rnf111
Mouse Description:
ring finger 111 Gene [Source:MGI Symbol;Acc:MGI:1934919]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa26971 Nonsense Mutation detected in F1 DNA Not yet available
sa20978 Nonsense Available for shipment Available now
sa7068 Nonsense Mutation detected in F1 DNA Not yet available
sa20977 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa26971
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
ENSDART00000111626 Nonsense 14 958 1 16
Genomic Location (Zv9):
Chromosome 7 (position 31941517)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 30333859
GRCz11 7 30605009
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTGTGGGTGAAGTCGCCATGAAGAGTGAGATTTCGGCTGATGCACGA[C/T]AAAAGCAAGAGCCCCTGAAGGGGCCTCTGGCTAACCCCGAACCCATGGAG
Long Flanking Sequence:
TGTATGGTAGCATCAAGTGTTTATTTCTGACGATTCTGCTGTGGAGATAATTCTTTTTAGTTTCCTTAGATCAGCTGACTGCACTAATTACAACAGGTAAAGCCAGTCAATAAAGTAATAGTTTAATTATTGCTGTTATTAAGTCTAGTGTTCAATAACATTGCTGGTGCCACAGCACAACCGCTGCCCCCTAGCAAACTGAACCGAATAGTACCATGGGTCCGATATTGTAAACCGAATTGAACCATGGCATTCCATACCTAATACCTAAGGCATTACATACCTAATTTTTATAGAAATTTGCCTTGGTTTATTCTTCATGTAATCTGTTTCCTTCTTTTTGTCAACCATGTTCTCATTTTGTGCATGTTTTTCTGTGTCTTCCAGTTGTAGGATTGCTGATTCTCCAATGGAACCGTAGGATTCAGCATATTCAGCCTTAGTGGCACTTTGTTGTGGGTGAAGTCGCCATGAAGAGTGAGATTTCGGCTGATGCACGA[C/T]AAAAGCAAGAGCCCCTGAAGGGGCCTCTGGCTAACCCCGAACCCATGGAGACGGCTAAGAGCTTCCCTGCTGAGATGGAGGTGATCGGCAAGGCAGGAAGTGACTTCACTTCTCCATTGTGTGCTGAGACCAGGCATCGGCCCTCTCGAGATGCTGGAGGTCGTAGAGACTGTGAAAGGGGCTTGTCGGGGCGCAAAAAGCGCAAGAGCCAGCAGCCTGGACCCTCGTATTGTTCTTTGAAGGAAGCGCCAATGAGTGAGGCCACCCTTACTCCACCCCGACACAGGCCCATGCTTTTAGAGACACGTAGCGAGGATGAGAGGAACCCTGAGTCCTCGTTGAGTGACTGTGCGTCTTCGCCCTCCTCCAGCCTTCGATTTGGTGACTCGGACACTCTTAGTTCAGATGAGGATGGCATGCCAATGACCGTTAGACAGCAACTCAAAGCTCACGGTGCGGCCTCCACTGGCAGCACAGGGAGCAGCACAGGTACGGCAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20978
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
ENSDART00000111626 Nonsense 582 958 9 16
Genomic Location (Zv9):
Chromosome 7 (position 31910798)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 30303140
GRCz11 7 30574290
KASP Assay ID:
2259-8993.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGACCCCTGCTGTCCAGGCTCTGCCTCCCGGCCTCCCGTTTACGTTTCC[C/T]AGGCTGCACCTGGACCTAGCCAGCAAACTGTGGCCGACTCATTCAGTCCA
Long Flanking Sequence:
CCTTTTATTGTTTTTATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTTATTTATTTATATATATATATACATATATATATATATATATATTTATTTATTTATTTATTTATTTATTTATTTATATTTATTATTTATATTTATTGTTTATTATTTATATTTATATATATATATATATATATATCTTAGCTGCCCAAAGCAACACTCTGACAAACATTTGCACATATTTCAAGTATATGTGTTTGTTTGAATATATTATTTTTATCACTTTATTAACTGCTGGTGTCCTTCTTCCTGCTTCTTTCTTTGTCTCAGCAGACTCTGCCGGTGGATCTCAGTAGCAGTGCAGTGCGTAGCAGTGGATCCAGCAGCACAGGGTTTCACGGCACATCTGCCTTTGACCCCTGCTGTCCAGGCTCTGCCTCCCGGCCTCCCGTTTACGTTTCC[C/T]AGGCTGCACCTGGACCTAGCCAGCAAACTGTGGCCGACTCATTCAGTCCAACCATAGTGGCCCAGCCTCAGCCCCAACCTCCTCAGCTCTCTTCCTGCAGGCACTACATGCATCCCACATGTAAGAACTAATATTCACCCTAATGTTGATAATCCAATATTAATAATCAATGCCCCTAATGACCCTATAGGTTTTTTTATTCACAGTTTTTTTTTCTAACTGAACCTGTTCTAGACCTGTTTAATGACATGTTTGACTCACACTCAATCACATGCAGAAAGCATGTTAAAGTGCTTCAATAGTAATGTCATTGCTCTGTGTCTTGTGGCTATGGAAGTAGCATTTTATGTAAATATTTTATTTGAAAACCACATCTTAAATTTTTTACTTCATTTTTAATTACATTTTTATTCTGCAATATTCTAATAAACTTGTATTAAAATGTTCTTACTATTTTCAAAATAATAGTTTGTAAAATTCCTTTTTTATTAATTATTGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7068
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
ENSDART00000111626 Nonsense 772 958 11 16
Genomic Location (Zv9):
Chromosome 7 (position 31905844)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 30298186
GRCz11 7 30569336
KASP Assay ID:
554-4818.1 (used for ordering genotyping assays)
KASP Sequence:
CCCATAGAATGCACCCTAATTACGGTCACGGACATCACATTCACGTCCCA[C/T]AAACCATGTCATCCCTCCCTCGACAGTCTGACCAGAGGACAACATGGTAT
Long Flanking Sequence:
ATAAAACGTTATGATTTTTTTATTGATTATTATGAATATTATTTTTATATTTGAACATTATACATTTCACACACAGTTATAGTACACTGCTTCAAAGGTTATGGGTTGGTAAGAATTTATGAACATGACTAAAATTTTGCATTCTCAATTTATTTATGAGCAAATACATCACTGTATTCCAGTGATGGCAAAGCTGAATTTTCAGCACTCATTTAGTGGAATTTCATTATAATTTTTTTTTTTTCATGTTTTAAATTTGTACTTCATATGTTATGAATAAATGTTATGACCTCTCTTATTCTTAAAGCCTTCAGAACTTCTATAAAAAATTTATCAGTAAAATGTTTTGTGTTGATGCCTTTGCAAAAGCTGTTTTGCTTTAGTCTTTTTCTGTAACAAATTTTATTCTTTCTTCTTTAAGGCGAGCACACGAGAGACCCCCACCACACCCCCATAGAATGCACCCTAATTACGGTCACGGACATCACATTCACGTCCCA[C/T]AAACCATGTCATCCCTCCCTCGACAGTCTGACCAGAGGACAACATGGTATAGTGGATTTCTCTAAATTCGTTTTGAATACTGCACACTTGAACATGAGTTTAAGAATTTAAATGAACTTTTATAATAACAGTTTTGCATTTATGATATAAAGCACATATATTATAATGTATTATAAACTAATATTCAGTTATGAAATAAGGTTTTTGTTTTACACTACTTAACCTGCTCAAGCTGTGAATGTGTTGTTCTTAAGTTTGAAATGACAGAGTAGAGTCAACTTTGCTATCACATCAACTTTGCTATCACAGACTAATAATAATAGAAAACCGCTAATTTAAAACCCCATTAGATGTTCCTCAGGGAGCTTGTGGTAAATTAGCTTTCCTGTTTGGCCTACAGATTCACATCACCAATGAACATCTCAATATAATCGGGATCTGTTAGTCATGATGTTGCTGTTTCAAGCATTATGTTGTACAGTTGCTGTGTTTGAACATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20977
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
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111626 Essential Splice Site 827 958 13 16
Genomic Location (Zv9):
Chromosome 7 (position 31904817)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 30297159
GRCz11 7 30568309
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTAGCCCACTTTATACCATCACTGATTTTTATGTCTCTGTTTTTCTC[A/C]GCACACTGGCTCAATGCCTGAGGTGACATATCCACATATCCGCTATATCT
Long Flanking Sequence:
GGGAGCTGGGCATCGAGGCTGGCGTTACTGTTGCTCCCTACCCTTCAGGACACCTGCACCCGCATCTGCCTCATTATCACCCTCCACCCAGACTGCACCATTTCCCTATCCAGCTGATGGTGAGTCCCCCGCTCACCTCCATCAGCTCAAATATATGCATACATTAGCATGAATAAAAAAGCCCTGATATGCTCTCAGGTATGGCACAGATTAATGGCGTAAGCCCCGAGCCGTGTATCCGCAGCATCTGTTATTTCAGGGTGATTTGTACACGGCCATGAATTATGCATCACAAGTAATAATGGAAGCTCATTAGACATTTGAAGTGTGAAATCTGAATTTGATATATTTGAAAGTCTAAAATTATGTTTGAGTCGTATGGAGTGACATGCACACACAGGCATGTGAATGATTCGGGGTAAAATGATTGCAGTTTCTTTTCACTCTGATTCTCTAGCCCACTTTATACCATCACTGATTTTTATGTCTCTGTTTTTCTC[A/C]GCACACTGGCTCAATGCCTGAGGTGACATATCCACATATCCGCTATATCTCCTCCAGAATGACCTTTGGTCGCACATATGAGGTAAGAACTAGAATGTAGACCAAAATCTAAAGACGCATACAAGAACAGAACACTGTTTTCCCTTAAGAATGCATGCAAAAATGTTAATATATGGTGCATGTTTGCATGTGGTATAGCATATATATATATAGTGGATATATTTACTTAACAATAAAATGACACAATTATTAAAAAAAGTGATCATAATGAATTGATTTAAATCTATTTTAAATGAGAAAACACTTCTTATTGACAAATGAGTGAATTGTTAAACTATATTTAAGTAGTATTTTGCTGCTGCACTGTTATCTTTAAATAAAAATGGTAACACTTTTACACAATATGAATCGTTCGTTAAGCATTAGCAAATGTTAATTCATTATCTGTTAAGCATTAACTCTAGAGTAACAGATAAGTTAGTAAGCAGTTTATAACTGCA
Associated Phenotype:
Not determined