ZMP

LOC100004729

Ensembl ID:

ENSDARG00000078132

Human Orthologue:

TEX2

Human Description:

testis expressed 2 [Source:HGNC Symbol;Acc:30884]

Mouse Orthologue:

Tex2

Mouse Description:

testis expressed gene 2 Gene [Source:MGI Symbol;Acc:MGI:102465]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14815	Essential Splice Site	Available for shipment	Available now
sa9607	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa14815

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
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Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112909	Essential Splice Site	584	997	3	11

Genomic Location (Zv9):

Chromosome 12 (position 19535551)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	18387712
GRCz11	12	18509586

KASP Assay ID:

2260-5250.1 (used for ordering genotyping assays)

KASP Sequence:

TTCTGTGTCCATCCAGAATGAAGAGGACCAYTATGAATCWACAWTTGGTG[G/A]YAAAGTTGCAATCAGTTTTGACTCAAAGTCAAAGACTTRTAAGGGTCCKT

Long Flanking Sequence:

GCTACCTTGGATGAGCCCTGCTACGAAAAGCATTTCATCCACTCACGGATATTTCGACTCACTGGAAGCAAGGTTGGCATACCATTGATTTCTGCCACTTAGTTAAAAGTGGTGCATTGCTCTTTAATGGCAGAACAAAACAGTTTTTTTTTTCTCTAAACCCAAATAGCTGTGTGGCAGAATGCTCTGTAGATGCCGTGTAATTCTAATGAAGCTGTTGCCTTGGTAACAGGTATTTCTTCTGCCACTGGCTTTGGCACACAAGAGAGTGTGGAACAGGAAGTATCCGATCTGCATAAGTTTGGCTGACGGAGAAAGAGCTTTGGAGGAAGGCGAGATGGTAGAGGTGCAGAAAGCTGAGAAACCTGCAACTAATGTTTCCCATCCTGTCACACTCTACTTGTTTGGTCGAACAGGACGAGAGAAGGAAGAATGGTTCCATCGACTGTTTTCTGTGTCCATCCAGAATGAAGAGGACCATTATGAATCTACATTTGGTG[G/A]TAAAGTTGCAATCAGTTTTGACTCAAAGTCAAAGACTTATAAGGGTCCTTGGTTATGATTTCACTTTATTTTTCACTTTCATATGTATGTAGAATTGTTTAAGCATTGACTACATCTGCAAAGTTACAGCTCTCAGGGTTCAAGTCAAAGGGAGATACTTCCTTTTATACAACAGCTCTTTCTGGTTCTCGAATCTGTTTGGCTGATAGCCGTGCAATATTCTGCAATATCAGAACCCGTACAGCCTCCTCACCCCTCTGTATTACTCCGCCCTCATAGAGTGACAGCAGATCAATGAACTCACTACAGTTTGACAAATATTGCAGCTGTTGGACAACATAATGTACTTTGAGGCTGTTTTAGGTGAAAATGTAGTTGTTTAGATTACAACTATGCAGTTTATTTATAATGTAGTGCCTATTTTATGTATTCATAATTTCTGAGATACAGCGGGTCGGCATCCATCAGCCTGTCATTGAGCAATTCATGGACAGTTAACG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9607

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112909	Essential Splice Site	585	997	3	11

Genomic Location (Zv9):

Chromosome 12 (position 19535550)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	18387711
GRCz11	12	18509585

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCTGTGTCCATCCAGAATGAAGAGGACCAYTATGAATCTACATTTGGTGG[T/C]AAAGTTGCAATCAGTTTTGACTCAAAGTCAAAGACTTATAAGGGTCCTTG

Long Flanking Sequence:

CTACCTTGGATGAGCCCTGCTACGAAAAGCATTTCATCCACTCACGGATATTTCGACTCACTGGAAGCAAGGTTGGCATACCATTGATTTCTGCCACTTAGTTAAAAGTGGTGCATTGCTCTTTAATGGCAGAACAAAACAGTTTTTTTTTTCTCTAAACCCAAATAGCTGTGTGGCAGAATGCTCTGTAGATGCCGTGTAATTCTAATGAAGCTGTTGCCTTGGTAACAGGTATTTCTTCTGCCACTGGCTTTGGCACACAAGAGAGTGTGGAACAGGAAGTATCCGATCTGCATAAGTTTGGCTGACGGAGAAAGAGCTTTGGAGGAAGGCGAGATGGTAGAGGTGCAGAAAGCTGAGAAACCTGCAACTAATGTTTCCCATCCTGTCACACTCTACTTGTTTGGTCGAACAGGACGAGAGAAGGAAGAATGGTTCCATCGACTGTTTTCTGTGTCCATCCAGAATGAAGAGGACCATTATGAATCTACATTTGGTGG[T/C]AAAGTTGCAATCAGTTTTGACTCAAAGTCAAAGACTTATAAGGGTCCTTGGTTATGATTTCACTTTATTTTTCACTTTCATATGTATGTAGAATTGTTTAAGCATTGACTACATCTGCAAAGTTACAGCTCTCAGGGTTCAAGTCAAAGGGAGATACTTCCTTTTATACAACAGCTCTTTCTGGTTCTCGAATCTGTTTGGCTGATAGCCGTGCAATATTCTGCAATATCAGAACCCGTACAGCCTCCTCACCCCTCTGTATTACTCCGCCCTCATAGAGTGACAGCAGATCAATGAACTCACTACAGTTTGACAAATATTGCAGCTGTTGGACAACATAATGTACTTTGAGGCTGTTTTAGGTGAAAATGTAGTTGTTTAGATTACAACTATGCAGTTTATTTATAATGTAGTGCCTATTTTATGTATTCATAATTTCTGAGATACAGCGGGTCGGCATCCATCAGCCTGTCATTGAGCAATTCATGGACAGTTAACGT

Associated Phenotype:

Not determined