ZMP

ptpn9

Ensembl ID:

ENSDARG00000077495

Human Orthologue:

PTPN9

Human Description:

protein tyrosine phosphatase, non-receptor type 9 [Source:HGNC Symbol;Acc:9661]

Mouse Orthologue:

Ptpn9

Mouse Description:

protein tyrosine phosphatase, non-receptor type 9 Gene [Source:MGI Symbol;Acc:MGI:1928376]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32512	Nonsense	Available for shipment	Available now
sa15211	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa32512

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110389	Nonsense	215	571	7	13

Genomic Location (Zv9):

Chromosome 25 (position 6765084)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	6284526
GRCz11	25	6411928

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTCATGATCTTCTTTTCAGGTTCAAATGGTGAAGATGGCCGATCTGCGA[C/T]AGCATCTGCCCAGAGATTGTTTACCCGAACACCTTGGCGGCTGTTTGCCT

Long Flanking Sequence:

TTAGCTGAAATAAAACAAATGAGACTTTCTCCAGAAGAAAAAATATTATACGAAATACTGTGAAACATTCCTTGCTCTGTTAAACATCATTTGTGGGAAAAAATCACTAGAGGGCTAATCGTTTTGTCTTCAACTGTATATCTATTATCATCACAGCTCATAGTTTGATCGTTCACTACTGTTTGTTATTCCTAGTCATTTCCCCATATTCAACAGTAGTTCTAATCGCCAAAAGCAGCTTACTTAACGTCAATAGGTGTCATCCAAAACAAAATCAGGCAAAAACAATATAGTAACAACCCTTTAACCAGCTGGTGTTTGCCTGTTATATCTTGGTTAGCCTGGTAGACCACTCTTGTTAAGCTGGTGGGGATTGATGACTGGTACGACCTACTTTTACACCTGTTCGCCCCACTTTTCTGACTCTAGTGTCAATTTGTGTGAGTTTTACTTCATGATCTTCTTTTCAGGTTCAAATGGTGAAGATGGCCGATCTGCGA[C/T]AGCATCTGCCCAGAGATTGTTTACCCGAACACCTTGGCGGCTGTTTGCCTCTTGACGTCCACAACTGGAACCTGCAGCTGCTGTCAGAGCAGAACGGACGTGTGGATCCTGTGGATGAGCTTGTTGGGATCCCGCTGGAGAACACGTCCATACACACTCCAGGAGCTGAAGCCATGAGTCTGGCTGAACTCATGGCACACCTGAACCGGGCTCAGCGCAGCGGGATCTACCTGGAGTACGAGGAGCTCCGGCGAGAGCAGCCGCCGGGAACGTTCACCTGCGCACTGTAAGTATTCACTTCAAGTTTATTTGTATAGCGCTTTTCACAATTATTATTGTTTCAAAGCAGCTTTACAAAAGGCCATAAATAGGTATAATTAAGGTTATTATTTGCTATAACTTTATTAATTAGTAGTAATCATCTACCCCAGCCCTACCTTCATCTATTTAGCCATGTCGCTTTTTTATTATCACTAGATGGTCGATTTTGATTTCACGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa15211

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110389	Nonsense	549	571	13	13

Genomic Location (Zv9):

Chromosome 25 (position 6757773)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	6277215
GRCz11	25	6404617

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CGGTCCGGCGAATGAGATCACAGCGTGCCTTCAGCATWCAAACACCCGAG[C/T]AGTACTACTTCTGCCACRCCGCCATCCTCGAGCACGCTCAGAGACAGGGC

Long Flanking Sequence:

TTTGGTTCCCATTGAATTGCACTATATAAATAAAAAATATCATTGAAAAAAATAGATAAAACCAAAACTGTTTGAATTTAACATTCTTCAAAGTATCTCTTTTTACATAAAATATTTTAAAATAAAAAACATGTCAACTGGAACCAAAATGTTACCAACATTTACCAGAATATCTATATGCAATCATTTTAGAAATACAGTAAATTCTTAGTTCATTTGAGACATAAAATGAAATGTGAATATTGCTGATAACATTCCCTTCTATTGTATTGAAAAATAACAATATATAATGGAGGTCAATGTGAACCATTTCTTCAAAATATCTAATGTTCCAACTGAAGTAAACAGTAACGCAATTTCAATATCTGTCCGTATTTTCAGGTACATTCTGTGCGCTGGACATCTGCCTGTCGCAGCTGCAGGACGTCGGGACGCTTAACATTTGCCAGACGGTCCGGCGAATGAGATCACAGCGTGCCTTCAGCATACAAACACCCGAG[C/T]AGTACTACTTCTGCCACGCCGCCATCCTCGAGCACGCTCAGAGACAGGGCCTGCTCTCAGCCAATCAGTGAGCAGCAGGGCCCACTCGTAGCCAATCAGAGACCGCACAGGACTGATTACGACCAATCAGTAAGAAGCAAGGCCTGCTGTCGTCCAATCATAAGACAGGGCTCGATCACGACTCTTAGACTGGATCGAAATTGCTGGGTTTTTGATTAAAACTCCACTAATAATAGAATGGAAGCAGAAATTGTTACCGTAAATGAAAATGGGGGTGTCTAAATGTTTAATGATCCAATTGTAGCGTACTGTATGCAATGTTGTGCCGCATTTCCTGCAGTTTATTCTGTGAATTTTGTCCAGAAATTCATGTGATGCTTCGCATTCGCAAAACAAAATTGGACATTTCTGAGGTTATTTTGTAATACTGTAAGGGTTTTAATTTCACGACATCTCCATACTCAAGTTTAAAATTTGTCCTAAAATACATATTACGTCTA

Associated Phenotype:

Not determined