ZMP

ENSDARG00000087994

Ensembl ID:

ENSDARG00000087994

Human Orthologue:

PRPF39

Human Description:

PRP39 pre-mRNA processing factor 39 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:20314]

Mouse Orthologue:

Prpf39

Mouse Description:

PRP39 pre-mRNA processing factor 39 homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:104602]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22539	Nonsense	Available for shipment	Available now
sa35754	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22539

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000130291	Nonsense	591	616	14	16

Genomic Location (Zv9):

Chromosome 14 (position 48433012)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	46504330
GRCz11	14	45491622

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTTTGATGGGCGGAGACATGAGTGGGTCATATGGAAACTACAGCAGCTG[G/A]TACCAGGTAGATGACGGAGTTTGTGCAAATGTTTAAAATAGCATAATAGT

Long Flanking Sequence:

AGCATATGTTTCATGCAGCGGATGCCCAGTACTGAGAAACATCCATACACACTCTCGCATTCACATACATACACTACGGCCAATTTAGTTTACCAAATTCACCTATAGAGCATGTCTTTGGACTAAGGGGGAAACCAGAGCACCCGGAGGAAACCCACGCCAACACAGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGATGAGACTCAAACCAATGACCTTCTTGCTGTGAGGCCAGTGCGAACCACTGAGCCACCGTGCCGCCAGGAATCTCATCGCAACACTTAGATTTGCCAGACCTTTAAATGTTTTTCTGTATTCCTTCAGTGATGATGATGACCCAGAAAAGATGAGCAAAATGGACTATATATCTGCCATGACGGTGCCACAGACAGCTCCGCCCACAATGCCTCAGGTTCCCATGACGACACCGCCTCCCTCTTTGATGGGCGGAGACATGAGTGGGTCATATGGAAACTACAGCAGCTG[G/A]TACCAGGTAGATGACGGAGTTTGTGCAAATGTTTAAAATAGCATAATAGTCACATTAAAGGTGCGGTATGTACATTTGAAACCCAGTGGTTGAACTAGGTGTTACGTTCCTGGTTTAAAACACATGCAAGCGCAGGATACCAGATTGATGACACAAACAGAAGTGTGCCTAACTATCGAACCTAAACATTGATTTAAACTGTTCAAAATAAAAGCAACGGCACGCGATAGAAGGAATATTCTCCATATTAAAAGGAGTTTTTGTTCTAACTAACATCTCAAATGCAGCTTAACAGCAGGATAAACTGACAATGATCACCTCAGGTACACCTCATGTGCGTTATTCAGTGTTAAATGCTAATATTGTGAGTTTGAAGGCCATTTTACATGACATTTATTGCCATACTACTGAAAGCAGCAGCAGATAGTTCACCTCAGATCTTCACAATAAAATAAACTGTTTAATATTGAACTTTAGAACTGCGACTCAGCAAACCAACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35754

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
ENSDART00000130291	Nonsense	611	616	15	16

Genomic Location (Zv9):

Chromosome 14 (position 48430495)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	46501808
GRCz11	14	45489100

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGAGCTTATGGCAGCTACCAAAACCCATGGAGCCAGTACAGTCAGTACTA[T/A]CCTCCAAGCTAAAACCCTTCAGAGACGGAGATCTGGATCCGCTCTGGATC

Long Flanking Sequence:

GGCGGTACTTATCCCATCTTTTCTCAAAAACTACTGGTCCAAAAGACATAAATCAAGATTTGGATTGTGCAATAGGTATTCCCCCAGAGAATGAACACACAAGCATGCTTATCTGGCTTTCAATGACGGAGGAGTGGTCGTTTGAGTGCGCTGAATAGCGAAAAGTGTACGGAACATGGTTAGTCTACGTTAGTGCAGGGGTGACCAGCCCTGTTCCTGGAGATCGACCTTCCTGCAGATTTCAGTTGCAACCCATATTAAACACACCTGCCTGTAATTATCAAGTGCTGTTCAGGTCCTAATTAATTGATTCAGGTGTGTTTGATCAGGGTTTGAGCTGAACTCTTTAGGATGGTCGATCTCCAGGAGCAGGGTTGAGCACCCCTGATATAGTGGTTTTGAATTTGCTTTAAATCCAAATATTGTCCTGTGCCCTAACAGCTGCAGTATGGAGCTTATGGCAGCTACCAAAACCCATGGAGCCAGTACAGTCAGTACTA[T/A]CCTCCAAGCTAAAACCCTTCAGAGACGGAGATCTGGATCCGCTCTGGATCCTCCAGAAGCACAGCAGTGCGTGACCTGAGCCAGCGTCAAAAGAGTGAGGGATGAAATGCACAAACCTTATTATGCATTTTAAATGCTGTATACTCTCTTTATCGCAAATCTTTTGTACTTCATGCCAAAGTACTGTGTGCGCGTGTGTATTCAGTTGAAGTCAAAATGATTAGCTCTCCTGTGAATTTGTCTTTCTTTTACAAATATTTACTAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTGTTTGTTTTAATTCGGCTAGAATAAAAGCAGTTTTTTATTTTTTTAAAACCATTTTAAGATCAATATTATTAGCCACCTTAAGCTATATTTATTTCAATTGTTTACAGAACAAACCATCATTATACAATAGCCCCTTTCACACATACAAACCTTTCCGGAAAGGT

Associated Phenotype:

Not determined