Busch Lab

ZMP

PRTG (1 of 2)

Ensembl ID:
ENSDARG00000059269
Description:
protogenin [Source:HGNC Symbol;Acc:26373]
Human Orthologue:
PRTG
Human Description:
protogenin [Source:HGNC Symbol;Acc:26373]
Mouse Orthologue:
Prtg
Mouse Description:
protogenin homolog (Gallus gallus) Gene [Source:MGI Symbol;Acc:MGI:2444710]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa28211 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa42311 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35610 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa28211
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082348 Essential Splice Site 20 1134 1 24
Genomic Location (Zv9):
Chromosome 13 (position 52216922)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 730517
GRCz11 18 619735
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAAAAGGGATTTATACCTGTTTCTTGCTGTATTTCTGTCAATCTCAGG[T/A]AAGAACGGCTATTTCAATTAAGTTGTGTGTGAACTTTTAGCCGGTTTGTG
Long Flanking Sequence:
GAAAGTATTTATGAGGCAACAACCAAGCTTTTCTGGAGTCTATATCATTAAATAATGCAACCAAATGGAACAAGGGAGAAAATAATAATAACAGAAAAAATATATATATAAAGGTTTACTTTATGCAATATTAACTTTCAAAGGGGTTGTGAAAGGGCACTAAATTCGTTGAAAATCTATAATCATCTGTTTTGATACGAGGGGGATTCCTCCGACGTCACGCTCCACGTGTAGTGCAGATCTGCAGGCGGATTAATCTCCACTCACCGCTGATTGGACGCGTCACACAACTTGCACTCTCTCGGACTGGTGCTCGTCCGAGAAAGTAGTGCGCTCACAGAGCGGTCAGCAGCAGCAGCATCGCGTGCGCGCTTCAGTCAGATAGTGTGGAGCTCGAGTCCGCGACCCACGGGCTCAGGCATGCTCGGAGTAACAGAGTAAATGGCGTCTTTTAAAAGGGATTTATACCTGTTTCTTGCTGTATTTCTGTCAATCTCAGG[T/A]AAGAACGGCTATTTCAATTAAGTTGTGTGTGAACTTTTAGCCGGTTTGTGGTCACGTTAGGATGCTTCATCATTTAAAGGGCTAGTTCAACCGAAAAATAACATTGTGCCATTATTTAATCACTCTCAGCTTGCTTTATTAGTTTCTTCTGTCAAACACTAAATAGGATATTTTGAATAAAGCCTAAAACCATTGACTTTCGCAATGGGAGACACAAATACTATGGAAGTCAATGTATGTCGTATTTCTTCAGAATATTTTAGCTTGTGTTCAACAGTAGAAAGACACTTATAAAGGTTTGAAAACACTTTGTGGTGAGTAAATAGAGAGTACATTTACATTTCTGTTTAAATTATACTCTATAAATGTGCTTAAAATACATTTAAATTCAGTATCGGGATCAAAATCAAGATTTAATGTGCTTAAAACTCCAAACTTTAACCTATAAACAGTGTTAAATGTGAAATAAGTGATTTATTAACGTTGAACTGATGTTATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42311
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082348 Essential Splice Site 605 1134 9 24
Genomic Location (Zv9):
Chromosome 13 (position 52239902)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150056.1 12337
GRCz11 KN150056.1 12337
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCCGCCTGGAGCTCTCACAGGACACCCAAAGCCTCCAGTACTAAAGG[T/C]GGAGCATCTGCCTGTCTCTCTGTCTGCCCATGTATCTCAAATGGCACACT
Long Flanking Sequence:
GAAATCATTCAGTGTAGTGATATGGAGCGGTAATGCGTACGAAACCTGCTGGAACTACTTTAGCTGTGTGTTTATCTGCAAATAACAGCACACCTTAGAATGCTCATCAGCCAATCAGAATCAAGCATTCAACAGCCACATAGTATTAATATTCTTCAGGAAGTTTTATTGTTGTTTTCTGTCTCTGTTTCAGTGCCCCTGCGTGCCCCTGAGCTGAGCCTGACGAGCCGCAGTCCCTCTGATATTCAGGTGTCGTGGCAGCCTTTGTCTCATAAGCTGAGCCGTGGCCGTGTGTCTGCGTATCGCCTCTCCTACAGGACCAGCTCAGACGGGACGCTGACACAGCTGGAGCTCTCGGCACACAAAACCCATCAGCTGCTGGAGGGTCTGCAGCCTGACACCACATACCTGCTCCGCATCGCTGCCGCCACCGCTGTGGGCTGGGGAGAACCGTCCGCCTGGAGCTCTCACAGGACACCCAAAGCCTCCAGTACTAAAGG[T/C]GGAGCATCTGCCTGTCTCTCTGTCTGCCCATGTATCTCAAATGGCACACTAGCAACAGCTCCTCTCCTTCTCCATTAGTTCCTCCCCTTCATTATTAGCTCCACCCTTTCATAATTAGCCACTCCCCTTCAGCATCAGCCCCTCCACATCATTATAAGCTCCTCTTCTTCATCATAAGCCCCTCCCTATCACAATCAGCTTTTTCTTTTCTTCATCAGCCCCTCTTCATAATTAGCTCCTCCCCCTTCTCCATTAGCCCCTTCCCTTCATCGGCAGCTCCTCCCCTTTGCAGTCAGCTCATCCTCTTTGTCATAAGCCCCATGTCTTCTCCATCATCTCCTCCCTTTCATAAGCAGCCCCTCTCCTTCACCACCATACCTCCCCTTCATCATTAGCTCCTCCCCCTTCTCAATTTGCTCCTCCCCTTAATTAGCAGGTCCTTCCTTCACTATCAGCTTCTCCTCTTTGTCATAAGCCTCTCCCCTTCTCCATCAGCTCCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35610
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
ENSDART00000082348 Nonsense 959 1134 22 24
Genomic Location (Zv9):
Chromosome 13 (position 52254977)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 2853306
GRCz11 18 2139429
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATGACAGGAAATCCTGCACTACCAAATCCATCAGGCAGGCAGGAGGA[C/T]AGACTCCGCCCACTGCAGTCCGTCTGGCCAATGAGAGTGCAGCTGAGAGT
Long Flanking Sequence:
TGAAAGCAAATAAAAGCTGAAATAAAATAAATAATAAAACCTAAATATCAATTAACATAAATGAAAAAATTATTAATTAATTATAATAATAATAATATAGTTGTTTTATATTCAGATCATACTACACAAAACTATTATAATTTAAATAGAAATAAATTATAAGTATTATAAATAATTAAATATTAGTTGAAAATCTTAGAACCTAATGATCTAAGCCTAAGTAGTAATAAAAGCAGAAAACAATCCCCAATAAAAATCACAAAAACATAATTAATAAATACATAAAAATTTTATTATTTTTAAAGAAATGATGTTTACACAACCATAAAGTACCCCTGTCTCCAAGCAATGCACTATCTTTATCTAATTATTGCTTATTATTGAGTTATAGGAAAAGACTTTCTCAGAAGTCAGATAATTGATTGTATTCATAATGATGTCCATGCATTATTCATGACAGGAAATCCTGCACTACCAAATCCATCAGGCAGGCAGGAGGA[C/T]AGACTCCGCCCACTGCAGTCCGTCTGGCCAATGAGAGTGCAGCTGAGAGTGTAGAGGTGATGATGCCCATGATGAGAGATCATTTCATCGATGCAAAGGTGCGTTCACAATCACATGACTTTATGCCTGTAAATATGCTTTGTGTGTACAATTTTCTGACAAATACTGTATATTACATTATTTCAGGGTGGAACAAATCTGATCATTAACAGTTATGGGCCCGTGAAGCCTACCATTGAGAAGAAGAGAAGAAAGAGATGGAGTTTCTTTAAGAAAAATGAAAAGGTACGAAACTGCAAGCTTTACAATGAGCTTTATTAAAGTAACTATCATTATTAACACATTTATTAGCATGAATCTGTTATTAAGATCAACAGAAATGTAAACTGTCTAATGAAACACTGCAAATGGGGCCTAATTTTTTAAACCATACAGTGAAATATATTATGTTCAGAACATTATTATTGTAAAAAAAATCTTTATTATTATTCATTTTAATA
Associated Phenotype:
Not determined