ZMP

LOC558876

Ensembl ID:

ENSDARG00000002794

Human Orthologue:

RNF14

Human Description:

ring finger protein 14 [Source:HGNC Symbol;Acc:10058]

Mouse Orthologue:

Rnf14

Mouse Description:

ring finger protein 14 Gene [Source:MGI Symbol;Acc:MGI:1929668]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39027	Nonsense	Mutation detected in F1 DNA	Not yet available
sa15812	Splice Site, Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa39027

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000042580	Nonsense	217	436	3	6

Genomic Location (Zv9):

Chromosome 15 (position 3660733)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	4065967
GRCz11	15	3811688

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTTGTTTTTCTGAGAACCTGGGCTCCAAATGTGTGCTCTTCAAAGAGTG[T/A]CAGCATGTGTACTGCAAGACCTGCGTGGAGGAGTACTTCAAGATCCTGAT

Long Flanking Sequence:

AAGCACAATGTCACATCTTATATAATTTTAACGATTATTCTGTCTTTTTGGACATTATATTGACATAATGATAATTACACAACCATTCAGATGACCTCTGCTCAGTTAATATATTGTTTATTGTATAAATAGATCGCAACACTTTGCAAGAGACTGGATGAACTTTGGGAAGAGAACAGGGGCAGTGTGGTTCTTTTTACCTGGATCCAGTTCCTAAAGGAAGAGACTCTGCAGTTTCTGAACATCCAGTCTCCACTTGAGATCCAAACCAATGGTGTCCAGCCTCAGTGTGAATCTGCTGAGAGCCAAGCAGCAGCTGCTGCTGTAGAAGAGCTGGACCAGCGAGCAGTTCAAGTAGCTGATCCTCACAGTGATATATTAACCCAGCTGCTGGATTTTAATGAAGCTCAGAAGAAGAAGGTGTTTGAGGCCACAGTTTTTAGCTGTAAAATTTGTTTTTCTGAGAACCTGGGCTCCAAATGTGTGCTCTTCAAAGAGTG[T/A]CAGCATGTGTACTGCAAGACCTGCGTGGAGGAGTACTTCAAGATCCTGATTAAAAATGGTGAAGTGCAGTTTCTTTCCTGTCCTGAGCCAGAGTGCACCTCCCTGGCTACTCCTGCACAGGTACTTTTTTGTTTGTGTTTGTGCCATTGTAAAACCTGGAGACCCGCCAGTGGCGTAGCGGACAGGCCCGCGGGGGGGCCCTGCGGTATTAGGGGGCCCTGCGTCGTTGCGATTTTCAATAATTGAAAATCTGGCAATCGCAATAATCAAACCCCTGGGAACAACTGTGGTCGGAACCAAAGTTCACAGGTCTGTGTTCTCTGAACTCCTTTCAAACGGTGGACTACTTCATTCTGATTGCTTGCTGCCAAACCGCGTCATAGCTCATTACCATAAAGTTGACTTGATTTCAAGTCCTCCTCGACGCCCACACCGGAAAAGACCCGCCACGCTGCTCATCGCCACCGGTTCTCATTGAAAATGAATGACTTCCGGCTACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15812

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000042580	Splice Site, Nonsense	257	436	3	6

Genomic Location (Zv9):

Chromosome 15 (position 3660851)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	4066085
GRCz11	15	3811806

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGTTTCTYTCCTGTCCTGAGCCAGAGTGCACCTCCCTGGCTACTCCTGCA[C/T]AGGTACTTTTTTGTTTGTGTTTGTGCCRTTGTAAAACCTGGAGMMCCRCC

Long Flanking Sequence:

TATTGTATAAATAGATCGCAACACTTTGCAAGAGACTGGATGAACTTTGGGAAGAGAACAGGGGCAGTGTGGTTCTTTTTACCTGGATCCAGTTCCTAAAGGAAGAGACTCTGCAGTTTCTGAACATCCAGTCTCCACTTGAGATCCAAACCAATGGTGTCCAGCCTCAGTGTGAATCTGCTGAGAGCCAAGCAGCAGCTGCTGCTGTAGAAGAGCTGGACCAGCGAGCAGTTCAAGTAGCTGATCCTCACAGTGATATATTAACCCAGCTGCTGGATTTTAATGAAGCTCAGAAGAAGAAGGTGTTTGAGGCCACAGTTTTTAGCTGTAAAATTTGTTTTTCTGAGAACCTGGGCTCCAAATGTGTGCTCTTCAAAGAGTGTCAGCATGTGTACTGCAAGACCTGCGTGGAGGAGTACTTCAAGATCCTGATTAAAAATGGTGAAGTGCAGTTTCTTTCCTGTCCTGAGCCAGAGTGCACCTCCCTGGCTACTCCTGCA[C/T]AGGTACTTTTTTGTTTGTGTTTGTGCCATTGTAAAACCTGGAGACCCGCCAGTGGCGTAGCGGACAGGCCCGCGGGGGGGCCCTGCGGTATTAGGGGGCCCTGCGTCGTTGCGATTTTCAATAATTGAAAATCTGGCAATCGCAATAATCAAACCCCTGGGAACAACTGTGGTCGGAACCAAAGTTCACAGGTCTGTGTTCTCTGAACTCCTTTCAAACGGTGGACTACTTCATTCTGATTGCTTGCTGCCAAACCGCGTCATAGCTCATTACCATAAAGTTGACTTGATTTCAAGTCCTCCTCGACGCCCACACCGGAAAAGACCCGCCACGCTGCTCATCGCCACCGGTTCTCATTGAAAATGAATGACTTCCGGCTACTTTGACGCTCTCGCCGCTTGTTTGTGAACGCTACCCCACGTCGTCGCTCCACCCCGCCCCCCTTTCCCGCTCCTTAGTTTGTGAAGGCTTCCCCGCAATGTCACTCCACTTCCCGCTCC

Associated Phenotype:

Not determined