ZMP

TXK

Ensembl ID:

ENSDARG00000015068

Description:

TXK tyrosine kinase [Source:HGNC Symbol;Acc:12434]

Human Orthologue:

TXK

Human Description:

TXK tyrosine kinase [Source:HGNC Symbol;Acc:12434]

Mouse Orthologue:

Txk

Mouse Description:

TXK tyrosine kinase Gene [Source:MGI Symbol;Acc:MGI:102960]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9793	Essential Splice Site	Available for shipment	Available now
sa44058	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9793

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:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000102003	Essential Splice Site	298	489	11	14

Genomic Location (Zv9):

Chromosome 23 (position 44236572)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	44304905

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTTGTGTKTKTGTGTGTGTNN[A/T]GGCGTCTCTGTCACCCTAAGCTGGTGCAGCTGTACGGTGTGTGTGTGACC

Long Flanking Sequence:

CTGCACATTTACTGATGGGTATGCGGCTTCAACTTCAACTTATATATATATATATATATATATATATTATTATTATTATTATTATTATTATTATTATTATTTGAAACTTTTAATATGAATAATTTCAAAAATAGTTGTGGCACAATGGCGCCCCCCCATGGGTGGCGCCCCTATGCCCCGCATATACTGCATACCCCCTTTTTGCGCCACTGTGTGTGTGTGTGTGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTAAACGTATGTGTGAATGTAAGCCTTTTTTACTGATGTCCCAGAGTGTTCAATAAATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTTGTGTTTTTGTGTGTGTGC[A/T]GGCGTCTCTGTCACCCTAAGCTGGTGCAGCTGTACGGTGTGTGTGTGACCCAACGCCCCATCTGCATCGTGACCGAGTTCATGGAGAACGGCTGCTTGCTTCACTTCCTGCGGCAGCACAGCAAGACTCTGGGACGCTCGCAGATGCTGTGCATGTGTCAGGATGTGTGTGAAGGGATGGAGTACCTGGAACACAACCAGTTCATACACCGAGACCTGGTCAGATATACACATTCACACACATATACACACACGGCTGTATGCATGACATCATATGTGACACCAAACCTGTATGTGTGTGTGTGTGTGTGTTTAGGCTGCACGGAACTGTCTGGTTAATGAGAGGAATGTGGTGAAGGTGTGTGACTTTGGCATGACCAGGTGAGTTTAACCCTTAATTTGATGACAAATTAAAAGGCAGCTATGATAAAAATAATCTTTTGTAAGCTGTTTGGACAGGACTGTGTGCAGGTATAGTGTGTCCACAGTCATATTGGGGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44058

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000102003	Nonsense	421	489	13	14

Genomic Location (Zv9):

Chromosome 23 (position 44231603)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	44299936
GRCz11	23	44060113

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCTCCAGGTTCCCTGTTAAATGGTCCCCGCCAGAAGTTCTGCACTTCAAC[A/T]AGTTCAGCAACAAGTCAGACGTGTGGTCATTCGGTGAGATCACCTGAAGG

Long Flanking Sequence:

CATCTTTCTGAATGAAACACCTACTTTACTACATCCAATCAGCTCGCAGTATATAAAAGAAGCCACGCCCACTTTTTTTCTTATTTAGTATTCTGTTTCTATAGGAACTGCATCACAAAACAGAAAAAAATGGTCAGAGCTTCCGGTTCATGTTGACTTTAAAGTTTGCAATATGTTTAAAAAATCTAATGCATTTTCTGTTGCGTGTATTTACACGCTTTTACCAGCAGGTGTCCTCATTCAATCAAAGACCAGAGAGTTGAACATGTCATTATGGAGATCATTTAGCATTTACAAAGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGTGTGTCTGGCAGGTATGTTTTGGATAATCAGTACACCAGCTCTATGGGCTCCAGGTTCCCTGTTAAATGGTCCCCGCCAGAAGTTCTGCACTTCAAC[A/T]AGTTCAGCAACAAGTCAGACGTGTGGTCATTCGGTGAGATCACCTGAAGGTCACTGCTCTATGTGTGTGTGCGTGTGCATGTTCGTGCTGGTGCTGATCTGTGTGTGTGTTAATAATAACATCACTTTATTATTAACATTACTTTATGTGTGTGCAGGTGTGCTGATGTGGGAGGTGTTCTCGGAGGGAAAGACGCCGTTTGATAACCGCACTAATGTGGAGGTGGTGGAGGAGGTGACGCAGGGCAGCCGACTGTACAGACCGCACCTTGCTACACCACACATCTACAACATCATGTACCGCTGCTGGCACGAGGTGACACACACTCACATACACCACTGACAGACACACAAACACTCACTGTCACACACGCACACACACACTCACAAATGCACACGCAGGCCACTTTATTAGGTACACCTTACTAGTTCCGGGTTGGACCCATTTTGCCCTTAGAAATGCCTTAATCTGTCGTAGCATAGACTCAACAAGATACTGGA

Associated Phenotype:

Not determined