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
sa20978	Nonsense	Available for shipment	Available now
sa20977	Essential Splice Site	Available for shipment	Available now

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
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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:

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