ZMP
PRR12 (2 of 2)
Ensembl ID:
Description:
proline rich 12 [Source:HGNC Symbol;Acc:29217]
Human Orthologue:
PRR12
Human Description:
proline rich 12 [Source:HGNC Symbol;Acc:29217]
Mouse Orthologue:
Prr12
Mouse Description:
proline rich 12 Gene [Source:MGI Symbol;Acc:MGI:2679002]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22012 | Nonsense | Available for shipment | Available now |
sa22013 | Nonsense | Available for shipment | Available now |
sa10141 | Nonsense | Available for shipment | Available now |
sa22014 | Nonsense | Available for shipment | Available now |
sa11454 | Nonsense | Available for shipment | Available now |
sa17820 | Essential Splice Site | Available for shipment | Available now |
sa17587 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22012
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110514 | Nonsense | 387 | 2532 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5357524)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4586740 |
GRCz11 | 12 | 4621752 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGACCGATAACACAGCCATCCTATGGGTCCTCCTCATCCTCATCCACT[G/T]GAGGGGCAGGAAAGGGGACAAAGAGCAGTTCCAGTAGTGGTTACTCATCC
Long Flanking Sequence:
GCCTGTTGTCATCACAGGGTGCAGCTGCAGCTTACCGTGGAAGTCATGATCCAACTGGGGCTGGAGTCACATCTGCTCAAGCTTCGTCTGCAGCATCAGTTTCTGCCCGCCATATACCATCTCATCAGTTTAATTTGTTGTCCTCCCAGCTTCAAGATCAGTCCTCCCAGCTGTACAGTGCCTCTGTATTTTCCTCCACCCCTGCACCACCTCAGCCAACATCCCAAGAGCGGACAGTACCAAGACAGGACAGTGTAATAAAACACTACCAGCGTCCCTCTCCAGCACAAGCCCCCTCATCCACACCTCACCCTCTCCAGCACTACCTTAGCTGTGGGGTGTCCGGATATCAACAAGCCACTCACACTCGCCATGCTGGTCTCTCTTGCAGTCCTCTAGGTGAACACAGTCCCTCCTCAGACCATAAACCCTCACCTAGGACTGAGCAGTACAGACCGATAACACAGCCATCCTATGGGTCCTCCTCATCCTCATCCACT[G/T]GAGGGGCAGGAAAGGGGACAAAGAGCAGTTCCAGTAGTGGTTACTCATCCTCTGGATCTGCATCCTCTTCCAGAACCCCTCACACACCACCCTCTGCCTCTTCTGCTTCATCCTCATCATCATCGTCTTCATCTTCCTCTGCATCTGCAAGTGCTCGTCAGTCTAATTCCATTCCAACCTCCACTTCTGCCTCTGCATCTTCTCGCCAACAGCCACCAACACAGTCTGTACCCCCACCACCACAGTCACATTCCCAGCCCCCACAAAGCTCCACTAATTCCTCCCAGCAAACCCTTCCCAAGTCGTGCCTCTCTGGTTATGGATCCCCAGTGGCTCCAGTTAAGTCATCAGGTGGTCTAACAGGCCAGACGCCTCCTCAACCACAACCGCAATCTTTCTCTCCAAGTCAACCTCCATCACACCTTTCCCAGTCATATGGGGGATTCAGTTCTCCACAGGCTCATGATCTGCCTTCAGCTAGGACCTCTGGAGTTGCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22013
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110514 | Nonsense | 457 | 2532 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5357734)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4586530 |
GRCz11 | 12 | 4621542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTAATTCCATTCCAACCTCCACTTCTGCCTCTGCATCTTCTCGCCAA[C/T]AGCCACCAACACAGTCTGTACCCCCACCACCACAGTCACATTCCCAGCCC
Long Flanking Sequence:
CTCAGCCAACATCCCAAGAGCGGACAGTACCAAGACAGGACAGTGTAATAAAACACTACCAGCGTCCCTCTCCAGCACAAGCCCCCTCATCCACACCTCACCCTCTCCAGCACTACCTTAGCTGTGGGGTGTCCGGATATCAACAAGCCACTCACACTCGCCATGCTGGTCTCTCTTGCAGTCCTCTAGGTGAACACAGTCCCTCCTCAGACCATAAACCCTCACCTAGGACTGAGCAGTACAGACCGATAACACAGCCATCCTATGGGTCCTCCTCATCCTCATCCACTGGAGGGGCAGGAAAGGGGACAAAGAGCAGTTCCAGTAGTGGTTACTCATCCTCTGGATCTGCATCCTCTTCCAGAACCCCTCACACACCACCCTCTGCCTCTTCTGCTTCATCCTCATCATCATCGTCTTCATCTTCCTCTGCATCTGCAAGTGCTCGTCAGTCTAATTCCATTCCAACCTCCACTTCTGCCTCTGCATCTTCTCGCCAA[C/T]AGCCACCAACACAGTCTGTACCCCCACCACCACAGTCACATTCCCAGCCCCCACAAAGCTCCACTAATTCCTCCCAGCAAACCCTTCCCAAGTCGTGCCTCTCTGGTTATGGATCCCCAGTGGCTCCAGTTAAGTCATCAGGTGGTCTAACAGGCCAGACGCCTCCTCAACCACAACCGCAATCTTTCTCTCCAAGTCAACCTCCATCACACCTTTCCCAGTCATATGGGGGATTCAGTTCTCCACAGGCTCATGATCTGCCTTCAGCTAGGACCTCTGGAGTTGCTAAAGGGTATGGGAATATGGGAAGTCAGTCATTTTCAACAGAATCAGTATATGGATCAGATTCAGGTTATGGGTCTCTGCCACCATCCTTAGGAGGGGCTGGAAGTCCATCAATGGGTTATGGTGCATCAGGACACTCTCCTGCCCTTCTCAGGTCAGGTGCAAGTGGTGGAACAACTGGTGGTAGTAGTAGTGGGGGCAGTACAGGAACTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10141
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110514 | Nonsense | 900 | 2532 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5359063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4585201 |
GRCz11 | 12 | 4620213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGATTCTCTGGGATCAGTAGTGCATTATGGGCGTGGTGACCCATATTCC[C/T]AWCACTCCATTCCTCAACACTCCACCTCCCACCATCAACACACTCCACAC
Long Flanking Sequence:
ATGATGATTTCCTCATTCAACACCTTCTTCAAGCCCAGAGTCCTGCTCCTCAAGTATCCCATCACCATCCTGCTCAAACCCATCATCCTTCCCAGCCCACCCAGCAGACTCCAGGCCTTCCAGCTCAGGATGGAAATAAGGGGCTTGCTTATGAGATGAGCAAAAGCTCAGAAGAGAGGTACCACCTTCAGAGTGTTATTCGAACCCATAGTGCAACCTCTAATGCTGCCGTCTCTGGCACAGGGAGTGGAGCTGGACTGGACAGTCAATTGGAGATGTCCCTAAAAAAACAGCAGCAGCAACACCAACAACAACAGCAACAACATCAGCAGCAGCAACAGCAGCATAAACAGCAACATCAACAACAATCACAGCAGAAGAGCAACAGAACTGTAAGCGATGGAGGACGAGGAAGTTCAGAGCAAACACATTCTCATCCTCATCATCATCACGATTCTCTGGGATCAGTAGTGCATTATGGGCGTGGTGACCCATATTCC[C/T]AACACTCCATTCCTCAACACTCCACCTCCCACCATCAACACACTCCACACACACCCACGCACTCACATCTACACTCTCACCCACACATGGATATTCAGAAAAAGACTCAAGATTCAGGAGATATGGCTTACATGCGTAAGACACCTGATGTGCAGCAACATCACCATCAGCATCAACAAACGCATCAACAGCAAACTCAGCATCATCAGACTCATCCCCAACAACATCAACAACAACCGCAGCAACAACAGCACCACTCTCAGTCACAGTCACTTATGGACTCTCCCACTGACCAGTCTCGCCAATCTTCTCATTTGCTGCAGTCTGTGCTTTCCCATACCCGCAGCAAAATAGACCCTCAGCAACAGCAGCATTCTGTAAGCCAGCAGTCTCTTATGGAAGCTACTGGGGGAGTTGTGTCTGCAGAGACCCATTCCCAGCCCCAGACATCACAACTCCAACTTCAGCTTCAGTCTCAAGCCTTGGAAGCAGCTGGTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22014
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110514 | Nonsense | 982 | 2532 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5359309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4584955 |
GRCz11 | 12 | 4619967 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGCATCATCAGACTCATCCCCAACAACATCAACAACAACCGCAGCAA[C/T]AACAGCACCACTCTCAGTCACAGTCACTTATGGACTCTCCCACTGACCAG
Long Flanking Sequence:
GTGGAGCTGGACTGGACAGTCAATTGGAGATGTCCCTAAAAAAACAGCAGCAGCAACACCAACAACAACAGCAACAACATCAGCAGCAGCAACAGCAGCATAAACAGCAACATCAACAACAATCACAGCAGAAGAGCAACAGAACTGTAAGCGATGGAGGACGAGGAAGTTCAGAGCAAACACATTCTCATCCTCATCATCATCACGATTCTCTGGGATCAGTAGTGCATTATGGGCGTGGTGACCCATATTCCCAACACTCCATTCCTCAACACTCCACCTCCCACCATCAACACACTCCACACACACCCACGCACTCACATCTACACTCTCACCCACACATGGATATTCAGAAAAAGACTCAAGATTCAGGAGATATGGCTTACATGCGTAAGACACCTGATGTGCAGCAACATCACCATCAGCATCAACAAACGCATCAACAGCAAACTCAGCATCATCAGACTCATCCCCAACAACATCAACAACAACCGCAGCAA[C/T]AACAGCACCACTCTCAGTCACAGTCACTTATGGACTCTCCCACTGACCAGTCTCGCCAATCTTCTCATTTGCTGCAGTCTGTGCTTTCCCATACCCGCAGCAAAATAGACCCTCAGCAACAGCAGCATTCTGTAAGCCAGCAGTCTCTTATGGAAGCTACTGGGGGAGTTGTGTCTGCAGAGACCCATTCCCAGCCCCAGACATCACAACTCCAACTTCAGCTTCAGTCTCAAGCCTTGGAAGCAGCTGGTCACTATGGTCATAGTTCCCAGCAGCAAGACCAGAGCCGCCCTAAGTCTAACACCGTGTCTTCACTTGACATGCTGGAGCATTCCCTCTCTCGGACATCAAGCCAAGAGGGTGCAATGGTTGATGAGAGGACAGGAGGTGAAGGAAACCGGGGGAATTCTGGAGCAGCAGCAGCAGGAAGTGTAGAAAGGCGCCAGTCACAGGAACAACAAAGACTTTCGTCTCACCACCAATCACAGCACCATGCCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11454
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110514 | Nonsense | 1539 | 2532 | 4 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5360980)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4583284 |
GRCz11 | 12 | 4618296 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCCCTTGGTCCCCCTCCTCAGCTATTGCCACAGGATGGACCGAAGAAA[C/T]GAGGCAGGAAGCCCACAAAGCCTAAACGAGAAGGACCTCCAAGGCCACGT
Long Flanking Sequence:
TGAAGACTCATGAGCTCCCATCAACAGTCAACACAGAGCAGCTTGGATTGATCCAATCTCAACCAGCCAGTCTTGGAATGGGTACAACTGGAACTGTTGGGGAAGGATCTGGTGCCAAAATAGGAGGTACTGGGGGATCTGGGTCTGGATCCGGGGGTCTTACCTCTCCAATCTTTTGTTCCTCTCGCCCAAAGAAGCTCCTGAAGTCCAGTTCCTTCCATCTGCTGAAGGAAAGACCTGATCCTAACTCCTTGCCCAAGAAAAGCTATGCACAGGAGTATGAATTTGAGGATGATGAGGATAAGGCTGATGTCCCGGCTGATATTCGCCTCAACAGCCGAAGCCGACTTCCTGATCTGATACCAGACCTTGTGTCGAGTTGTCGCAAATCAAGTGGAGTGGGAGGGGGAACTTTAAGCCCTTTAATGGGTGATCTAGATTTTGGATACCCATCCCTTGGTCCCCCTCCTCAGCTATTGCCACAGGATGGACCGAAGAAA[C/T]GAGGCAGGAAGCCCACAAAGCCTAAACGAGAAGGACCTCCAAGGCCACGTGGGCGACCACGTATACGCCCATTGCCAGAACCCAGGGCTATGATGGGAGAGTATGGAACAGGATTTGTTCCTGAAAGAGGTAGAGGCAGAGGAAGAGGCAGAGGCCGAGGTAGACGGGATGAATCTATGATGGACATGGAGATAGCCAATAAAGATCCAAATCAGATGTATCAGCAGCACATGCAGCAGCAAATGCATCACCAATCACAGCAGCAGCCACAGCACCAGGAGCCAATCAAACCCATCAAGGTAAATTCTTAATATACTTTTATTCATGTATTTAGTTTTTGTAATTTCTGACTAAAAACAAAAATTCTTCCATTTGAATCACTTTACAGGAATTTTTTCTAAAATGTCCTGTCTCTCCCTGTTAGATTAAACTTCCTGTTGGAACCTTGTCATCATCTGATGCCTTGTTACGGACAGACTCCTTGTCAGGCACTGACCCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17820
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110514 | Essential Splice Site | 2339 | 2532 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5368211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4576053 |
GRCz11 | 12 | 4611065 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGTGCCCTCGTCATCAGAGTCRGACTCTTCAGCAAGYGAGGATGAAAG[T/A]GAGTAGATGAGTCAGCGTGGCATGCAGCATGTAGGGCAGTTTCAGCATCA
Long Flanking Sequence:
TTGATTTTCAGAAGACAGTCTCAACCGGTCCCGAAATTAACTCCACCTCCCAACAACCAGATTCCCTTAGAGAAGGCTGAGAAAGACAGAGAGAAGATTAGAGAGCCGCGTGAAACCAGAGAGAGGAACAACATTCGGCTGAGAGAGCAGCGGGACAAAGAGAAGGTGCTCAGGACCAGGGAGAAGGAGGACAAGAAGGAGAAGGAGGACAAAAAGGAAAAGGAGGACAAGAAGGAGGAAAAGAAGGAGAAGAAAGCTCTGGCTCCTCCTCCTCCTCCGCCGCCGCCACCTCAGAAACCTGAGAAACGGCCAGTGGTGAGCGAACGAGGGAGGCTGAAGGAGGAGAAGAAGAGCAGCGCACAGGAGAAGAAGAGCGAGCGCTCGGCCAAACCTCAGCCAGCAAAGGTAAAGGCAGAACCTCCGCCCAAGAAGCGCAGGAAGTGGCTGAAGGAAGTGCCCTCGTCATCAGAGTCGGACTCTTCAGCAAGCGAGGATGAAAG[T/A]GAGTAGATGAGTCAGCGTGGCATGCAGCATGTAGGGCAGTTTCAGCATCAATATCTCAATGTGCGTGTCCCGAAAGGCCTGTGACTGTAAGCATTCAGGCACAAGTGGTCTGTTTCTTAAGTTGTTGGAGTGTTTTAGGGTGCTTTCACACCTGTGAATCGATTCAGTTGTTCCGAAACAGAGATTACAATTGTTACACTGTTGCTCTTTGCTCTTGGAGCGGTTCACTTTCACATTGCAAAGTTTCTAATCGGACCAAAAGAGCTAAAACAAGTCACGTGTGAGTAAACTCTCCTCACATTGGTCAGTGTCAGGGTTTATTTTGCAGCGTCCCGCTCAGCTGTCAGGAGTGGTGGTGGTTAAGTGATTGACAAGGTGCGCGCACGCGACGTGTCTGAGGAGAGACGCGGTAGGGAGGGGTGAAGGGTGCGCAACGATGCCTATTTGAGAACCGGGAGGGAGACGCAGGATTAGCGGGAGAACATCACTCGTTTACGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17587
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110514 | Essential Splice Site | 2380 | 2532 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5370061)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4574203 |
GRCz11 | 12 | 4609215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAAACACGRGCCCAAATTCACCCTTCCTCTTGTATTATYACCCATTTC[A/T]GATGAGTTGTATCTTCCTCCAATGCGSAAGATCGACAGCATTMTCAGCGA
Long Flanking Sequence:
GGGGGGGTGTTATTGGACGAAGATATTGAGATGAGAAAAGTCTGGTTATTAATAGTGAGTTAAGAATCGTCTGATAAGATAATCAGTTAAAAGTTGGAACAGATGTGAACAATCATAAGCACGTGATCCTCTCGAAATTTGTTTATAAATAAACTTCACTTACTGAACCGATACTGAATTGTTCGTGTCTGCATTGCGGTGCACCAAAGAAATACTAGATTTTGACACCCCTACTCTGTTACATGAAATAGCATGCAGTGCTAATGTGAGTGTGTCTTTTCCTGTGTGTCCAGCAGTGTCAGTAAAGGCTGGCCTGAACACGCGAGCGATGCGCGAGATGTACCGCAGCTATGTGGAGATGCTGGTCAGTACGGCGCTCGACCCGGACATGATTCAGGCTCTGGAGGACACAGAAGGTAATGCCAGAGTCATTGCTTACTGCTGCCATCATCAAAACACGAGCCCAAATTCACCCTTCCTCTTGTATTATTACCCATTTC[A/T]GATGAGTTGTATCTTCCTCCAATGCGCAAGATCGACAGCATTATCAGCGAGCAGAAGAGGAAGCTGTTGAAGAGAGTCAACATGAACTCCCAGCACCAGGTAGTGCAGATATTATTAGTGCCTGCTTGATTCTTTTCTTCAGTCACTGCTTTACTCTGCTTGTGCCTTAGCAACAATCACCACTGCATAAAAATCAAGGACATTCACAAGCACCAGTGTTTGGTAAGGAATTCATATAGGCTGCATTTACACTGGTTCATGGTTCAAGTGAGCCAATTCCGGCACAAATGGGATATGGCCTATGTACCTATTAGAGCTGCACAATTAATCGCTAAAAGATCGCGATCTCGATTCGACCCCCTAGACGATCTTAATCCAGCATTTCTACGATTCTGTCAATCATATTTTCAAGTTCAGGAGAGAAGAAAAGGCGGCTGCACGAGTCTTCGTCGTTTTACACACGTTGCTCAGTGACACTGACACCTCCAAATGATGAGTCA
Associated Phenotype:
Not determined