Busch Lab

ZMP

ENSDARG00000016579

Ensembl ID:
ENSDARG00000016579
Human Orthologues:
PTPRK, PTPRM, PTPRT, PTPRU
Human Descriptions:
protein tyrosine phosphatase, receptor type, K [Source:HGNC Symbol;Acc:9674]
protein tyrosine phosphatase, receptor type, M [Source:HGNC Symbol;Acc:9675]
protein tyrosine phosphatase, receptor type, T [Source:HGNC Symbol;Acc:9682]
protein tyrosine phosphatase, receptor type, U [Source:HGNC Symbol;Acc:9683]
Mouse Orthologues:
Ptprk, Ptprm, Ptprt, Ptpru
Mouse Descriptions:
protein tyrosine phosphatase, receptor type, K Gene [Source:MGI Symbol;Acc:MGI:103310]
protein tyrosine phosphatase, receptor type, M Gene [Source:MGI Symbol;Acc:MGI:102694]
protein tyrosine phosphatase, receptor type, T Gene [Source:MGI Symbol;Acc:MGI:1321152]
protein tyrosine phosphatase, receptor type, U Gene [Source:MGI Symbol;Acc:MGI:1321151]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa44368 Nonsense Mutation detected in F1 DNA Not yet available
sa6819 Nonsense Mutation detected in F1 DNA Not yet available
sa11271 Nonsense Available for shipment Available now
sa16068 Splice Site, Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa44368
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
ENSDART00000079875 Nonsense 364 775 7 13
ENSDART00000111665 Nonsense 364 893 7 14
ENSDART00000115246 None None 724 None 10
Genomic Location (Zv9):
Chromosome 25 (position 38479462)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150168.1 8372
GRCz11 KN150168.1 8372
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATGGCGGCAGTGACTCTCTGAGGGCCGCATGGGTTCCTGCAGTTGGA[C/T]GAGTCGACTCATACCTGCTGTCTCTGCGGCCGGCTGGCACAGCTCTGACT
Long Flanking Sequence:
TTTCCCTGCTAAAGGCCGTCAGCGTTATCGCTATTTCCAGGATATTTTGAGCCTGCCTCTCCCTTCCTGCCTCAGCAGACGACACGCCTGCGTATCCTGTCTGTTACTGAACATGACCATGATGCTCCACACACTCACACGCTCTGGATATACACCTTTAGTTCCATAGGCGTGAAGAGTTTCATATTCAGATAATGATATTTTAAACCCCTCTCTCTCTCTCTACTGTACAGACTGTACTCTCTCCCCCTACCCCAACCCTTACCCTACACCCTACACCCTAACCCTAATCATAACCCTTACCCTACACCCTAACTCTACCCTTACCCTTGCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTGACTGATGGTCTTTCTGCAGCTCCAGCTCCTGTCTCCTCATTGGTCCTGCGCAGTGATGGCGGCAGTGACTCTCTGAGGGCCGCATGGGTTCCTGCAGTTGGA[C/T]GAGTCGACTCATACCTGCTGTCTCTGCGGCCGGCTGGCACAGCTCTGACTCTTCCTGCAAACGCGTCTCGGTGTGTTTTCACTGGTCTGACTCCTGGACAACAGTATGAGCTGTCAGTGAAGACCAGGAGTGGAGCTCGATCAGCTGAGCGGACGACCGCGGCCAGAACAGGTGAGAACTCGGATATCAGCCAGTGACACACAAGCTGGATTCATATGAACACACAGACTGAATGTGAGTGTGTGATGTCTGTTTGCTGGTCAGCTCCGGGACGGGCGGCTCGTCTGAAGCTGGAGGCTCTCCGTCTAAACACTCTGCGTTTGTCCTGGTCTCCTCCTGATGGGGTCTGGGATTTCTACCGTATTCTGCTGTTCAACGGCTCCTCTGTGCTGGAGAACCGGACGGTGGAGCGGCAGCGGCTGGAGATCAGCTTCACCAACTGCACTCTGATTCCTGGACGGAGATACAGAGCTGCTGTCAGTGTGCAGAGCGGAGATCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6819
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079875 Nonsense 399 775 7 13
ENSDART00000111665 Nonsense 399 893 7 14
ENSDART00000115246 None None 724 None 10
Genomic Location (Zv9):
Chromosome 25 (position 38479355)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150168.1 8265
GRCz11 KN150168.1 8265
KASP Assay ID:
554-4721.1 (used for ordering genotyping assays)
KASP Sequence:
GCAAACGCGTCTCGGTGTGTTTTYACTGGTCTGAYTCCTGGACAACAGTA[T/G]GAGCTGTCRGTGAAGACCASGAGTGGAGCTCGATCAGCTGAGCGGACGAC
Long Flanking Sequence:
TGAACATGACCATGATGCTCCACACACTCACACGCTCTGGATATACACCTTTAGTTCCATAGGCGTGAAGAGTTTCATATTCAGATAATGATATTTTAAACCCCTCTCTCTCTCTCTACTGTACAGACTGTACTCTCTCCCCCTACCCCAACCCTTACCCTACACCCTACACCCTAACCCTAATCATAACCCTTACCCTACACCCTAACTCTACCCTTACCCTTGCAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTGACTGATGGTCTTTCTGCAGCTCCAGCTCCTGTCTCCTCATTGGTCCTGCGCAGTGATGGCGGCAGTGACTCTCTGAGGGCCGCATGGGTTCCTGCAGTTGGACGAGTCGACTCATACCTGCTGTCTCTGCGGCCGGCTGGCACAGCTCTGACTCTTCCTGCAAACGCGTCTCGGTGTGTTTTCACTGGTCTGACTCCTGGACAACAGTA[T/G]GAGCTGTCAGTGAAGACCAGGAGTGGAGCTCGATCAGCTGAGCGGACGACCGCGGCCAGAACAGGTGAGAACTCGGATATCAGCCAGTGACACACAAGCTGGATTCATATGAACACACAGACTGAATGTGAGTGTGTGATGTCTGTTTGCTGGTCAGCTCCGGGACGGGCGGCTCGTCTGAAGCTGGAGGCTCTCCGTCTAAACACTCTGCGTTTGTCCTGGTCTCCTCCTGATGGGGTCTGGGATTTCTACCGTATTCTGCTGTTCAACGGCTCCTCTGTGCTGGAGAACCGGACGGTGGAGCGGCAGCGGCTGGAGATCAGCTTCACCAACTGCACTCTGATTCCTGGACGGAGATACAGAGCTGCTGTCAGTGTGCAGAGCGGAGATCTGAGCACAACCGCAGACTGCCATGGGGGAGCCGGTGGGTGATGGAGCAGCCACAGCAGTTAAACCCCACTAGTCAACTCATGTACCCCAATAATGAAGTCCTCCACGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11271
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000079875 None None 775 None 13
ENSDART00000111665 None None 893 None 14
ENSDART00000115246 Nonsense 402 724 5 10
Genomic Location (Zv9):
Chromosome 25 (position 38479069)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150168.1 7979
GRCz11 KN150168.1 7979
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGTCTGGGATTTCTACCGTATYCTGCTGTTCAACGGCTCCTCTGTGCTG[G/T]AGAACCGGACGGTGGAGCGGCAGCGGCTGGAGATCAKCTTYACCAACTGS
Long Flanking Sequence:
TGCTGACTGATGGTCTTTCTGCAGCTCCAGCTCCTGTCTCCTCATTGGTCCTGCGCAGTGATGGCGGCAGTGACTCTCTGAGGGCCGCATGGGTTCCTGCAGTTGGACGAGTCGACTCATACCTGCTGTCTCTGCGGCCGGCTGGCACAGCTCTGACTCTTCCTGCAAACGCGTCTCGGTGTGTTTTCACTGGTCTGACTCCTGGACAACAGTATGAGCTGTCAGTGAAGACCAGGAGTGGAGCTCGATCAGCTGAGCGGACGACCGCGGCCAGAACAGGTGAGAACTCGGATATCAGCCAGTGACACACAAGCTGGATTCATATGAACACACAGACTGAATGTGAGTGTGTGATGTCTGTTTGCTGGTCAGCTCCGGGACGGGCGGCTCGTCTGAAGCTGGAGGCTCTCCGTCTAAACACTCTGCGTTTGTCCTGGTCTCCTCCTGATGGGGTCTGGGATTTCTACCGTATTCTGCTGTTCAACGGCTCCTCTGTGCTG[G/T]AGAACCGGACGGTGGAGCGGCAGCGGCTGGAGATCAGCTTCACCAACTGCACTCTGATTCCTGGACGGAGATACAGAGCTGCTGTCAGTGTGCAGAGCGGAGATCTGAGCACAACCGCAGACTGCCATGGGGGAGCCGGTGGGTGATGGAGCAGCCACAGCAGTTAAACCCCACTAGTCAACTCATGTACCCCAATAATGAAGTCCTCCACGCTAATCACTGCAGCTAAACTACACTAATCAGCTCAATGAACTGAGCTAACTGCATTACTGTGGTGTTTCAGCTCCGCGGGCCGTGCAGATGTTGACTGTCCGCCACGCCGATGAGTCGAGTCTGCGGGCCGCCTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCAGAGAGTGTTATTGTGCAGAGCGGATGTTGATCATCTGAGAGAACAATCACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16068
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
ENSDART00000079875 Splice Site None 775 None 13
ENSDART00000111665 Nonsense 738 893 12 14
ENSDART00000115246 Splice Site None 724 None 10
Genomic Location (Zv9):
Chromosome 25 (position 38475996)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150168.1 4906
GRCz11 KN150168.1 4906
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCGGGCCAGGAGAGATTCGTCCCCAAACACRTCAACGAGGTCAGCTTC[C/T]AGCATCTGCAGCCCGGACAGCAGTACAACATCACTRTTACGTCAATCAGC
Long Flanking Sequence:
TGAAGTCCAGCTGCTGTTTAATGACATGAAGGTGTTTCCGCCCATCACTCTGACCAGCAGCACCACGCAGTACCTGCTGTCCTCACTCACTCCTGGCCGACTCTACAAGATCCTGGTGTCCACCTTCAGCGGGCCCAANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTTCCTCAGGGGCAGAACCGGTGTGTGTGTGTGTCCATGTGCTGAAGGAACTCTGCAGTATCTCGCCGAGTCTAATGTCGTGTTTATTTCTGTGTTTTGTAGTTCCCAGTACAGTGAAGAACATCCACATCAGTAACGAAGGTCAGAGCAGCAGTCTGCGGGTCAGCTGGACACCGGGGCAGGGTGATGTGGACCGATACACTGTGTCTCTGTCTCCGGGCCAGGAGAGATTCGTCCCCAAACACGTCAACGAGGTCAGCTTC[C/T]AGCATCTGCAGCCCGGACAGCAGTACAACATCACTGTTACGTCAATCAGCGGATCTCTGATCAACAACAGCACAGCAACAGGACGAACAGGTCAGATGAGGCATTTTATTAAACCCAGAGTCAGTCAGGTAACCCAGAAATGAAGGTCATTAATTCCTCTCTCTTATGTCGTTCTCCTGTGAGTTTCGTTCTTCTCCATCTAACCCTGTGCAGGTGTTTATCTCCAAACTCAGGCGTGTTATAATAATCAGAAGTTTCCCCTGTTGATTCTGCAGTTCCCTCTCCCGTGTCGGCTCTACAGCTGGAGGAGCAGCGCAGCACCTCCACCCTCTCGGTGTTTTGGCAGGCGGGTCAAGGAGTGTTCGACAGCTTTCGTCTGCAGCTGCTGGATGAGAGAGGAACACTGGTGTCCAACATCTCCACAGCGGCACAGGCCATTCAGCACACCTTCACACACCTCACACCAGGGAAACCCTACCGCGTCCTGATCCGGGCCCTCA
Associated Phenotype:
Not determined