ZMP
LOC100004729
Ensembl ID:
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 |
---|---|---|---|
sa27938 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14815 | Essential Splice Site | Available for shipment | Available now |
sa9607 | Essential Splice Site | Available for shipment | Available now |
sa35256 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35255 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27938
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112909 | Nonsense | 437 | 997 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 19536154)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18388315 |
GRCz11 | 12 | 18510189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAGACTGTTTCTGCATTTCAGGGCTGGATGAATGAAATGTACACGTA[T/A]GATCCAGAGACCTACCAGCCGTCTCTCATGCATTCTGTACATGCCACTTT
Long Flanking Sequence:
GGCGTGGTGCCCTGCCATGGAAGAATGAATGTAGCGGAAACCATGCCTACTTTATCAAAACCAGCACTTTCTAGTAATAAAACATCCATTGAAATTTTAAAAATAAAGTTAAATCCCAAAACAGCATCAGCATCACAGGTAACAACAGCCTTGCAGACTGCTTTTAAGCTATTTCTTGGACTTTAATGTGTCAAAGCTAATGTCCTCTGGCAATCAGTTAAAAAAAGAAACACTGCAATAAATTTCACAAAATAAACATTAAACATCTTGCTTTTCTCTAAAGACCGAGCAAAGCCCTCATTGCCACTCTGTTCTTTGATTAATTCTGTGCTTCAGGAATAACATACACCCACTGCATGTCACATCCAGCTAGAGCTTTTATCCTGATGTCCCACTTTTTCAATTTTATGCCTGTGTGGTAAAACTTTATGGTGAAATACTGTGATTTAAGAGGAGACTGTTTCTGCATTTCAGGGCTGGATGAATGAAATGTACACGTA[T/A]GATCCAGAGACCTACCAGCCGTCTCTCATGCATTCTGTACATGCCACTTTGGACGGACCCTGTTTGCGACTTGACTACCCACGTAACAACATTCCCCGCTGGGCTACCTTGGATGAGCCCTGCTACGAAAAGCATTTCATCCACTCACGGATATTTCGACTCACTGGAAGCAAGGTTGGCATACCATTGATTTCTGCCACTTAGTTAAAAGTGGTGCATTGCTCTTTAATGGCAGAACAAAACAGTTTTTTTTTTCTCTAAACCCAAATAGCTGTGTGGCAGAATGCTCTGTAGATGCCGTGTAATTCTAATGAAGCTGTTGCCTTGGTAACAGGTATTTCTTCTGCCACTGGCTTTGGCACACAAGAGAGTGTGGAACAGGAAGTATCCGATCTGCATAAGTTTGGCTGACGGAGAAAGAGCTTTGGAGGAAGGCGAGATGGTAGAGGTGCAGAAAGCTGAGAAACCTGCAACTAATGTTTCCCATCCTGTCACACTCT
Associated Phenotype:
Not determined
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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
Mutation Details
Allele Name:
sa35256
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112909 | Essential Splice Site | 788 | 997 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 19509180)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18361341 |
GRCz11 | 12 | 18483215 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGATGGAATCCTTGAGGCAGAAACAGAACTGGAGGCCTTCAGTGTGTT[G/T]TAAGTTTCTTGAAAATAAAATAGCTTCTGAATTTAGACCACAAATTGTGT
Long Flanking Sequence:
CATGGCTTCAGGATCTCGACACTGTCGAAATGTCAGTTTTATGTCAGCTATCCCTATCTCATGGTTGTTTTTGTTACCTTTTATTTTATTTTCATAACAAAAACACGTAATGTTTAGTGCACTTAAGTCATTGCTCTCTTTCTGAAACTGATTGGATGGTTATTTCCCTGTTATAGATGCACTCTAAAAAATGAAGGTTCCAAGTAACAAAACTTTTTTAGCATGACATAATAAAACCATTCTGGGTTCCACAAAAAAACTTTCAGCAGAGAGCCATTATACTGACAAACCTTTATCTCCCAATATTCCCACTTTGTGTATGCTATCTTCTAATAACTGATGGCAAAAATGTATTTTTGTGTGACAGGTCTTTGGTTGCATTTGGAGATGGAGTACACAGGAGCGCTTCAGATGACTTTAGAGACCAAAATCAACCTTTCTAAACTTGGGAAAGATGGAATCCTTGAGGCAGAAACAGAACTGGAGGCCTTCAGTGTGTT[G/T]TAAGTTTCTTGAAAATAAAATAGCTTCTGAATTTAGACCACAAATTGTGTCATTATCTCGTATACATCTACTCACAGAATAGCCTATTCAATGTCTATAATCTACAGTTTATGTTATAGTACATAAATTACCATTTTGGGTAGCCAGACAGAAATCACAAGAAAATGTTAACAATACAATATCAGACAAAGGACTACACAAAACACAGGAGTATAAATACACAAGACCTAATGACCTGAATACAAGCAGGGAGTGAGAGACAGGTGAAACTAATGATTATCAAGAAAGGGTGGGAAACAGAACAAAGGAGTCACATGATATAAACAGAAAGCGCATGGAACATGGGAAAGATCACATGACATAAACATAGCACACCAGACTCGTGACACCGTGAGAGACATGTAAATATATAATACAAAATAACACCATCCTCAAACTTTACATAGTTTTTAACATTTTATACTGTAAAATAGTGTTTTTAGTTGTATGTGATTATGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35255
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112909 | Essential Splice Site | 945 | 997 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 12 (position 19494806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 18346967 |
GRCz11 | 12 | 18468841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGGAATTAGCCCCATAACAAATCTTCTCAAATATCCTGCTTTTTTTAT[A/G]GAATGTTTTTGTGTTGCCCAACATGGATGATATTTATCTGCCACTAATGC
Long Flanking Sequence:
AAATCTCATTCATTAACACAGAGAAGGTGGGCCGAGACCTTCACTCAAAAGCAGGCGTGCAGCCCATTTGCTTCTGTATCAGATCAGGGTGCAAGTTTACTACGGGCATATGAACTGCTGTCTATGGAAGATGAGAGAGCTCTCTGATTTCATCTAAAAAAAATTTAATGTGTTTGAAAAATGAATGAAGCTCTTGCAGGACAGAAATGACATGAGAGTGAGTAATCAACACAACTTATGTTTTTTAGGTGAACTAACCCTTTAAGTTTATATGTAAATTCAATTTTATAGATAAATGTATTCTTATTTCTTATTGATTTACTGTTTTGAAATATGGTAATCTAAAGTAGCACGTATATATTTTTTACACCAGTATATTTCTGTTATTATTATTATTTTTCATTTGGGTACACAATGAAATATATACTTCAATTGATTTAAATGAAAATTGCTGGAATTAGCCCCATAACAAATCTTCTCAAATATCCTGCTTTTTTTAT[A/G]GAATGTTTTTGTGTTGCCCAACATGGATGATATTTATCTGCCACTAATGCACTCTGGAATGGACAACCCACCACTTGCTCAACACCCTGCAAAGCTCTCTCAGAATTCCTCAATGGCCTCAACCGACAGGAGTGATCTGGAACATTCTGCAGAATTACAGTAGTGCCTCCCTGTGGACAGACATGACAGTGCAGAAGTATCAGAACTGGCTTATTTAACTTCAGCAAACTCAAAGCAGCATAACTTACCTTAAGCAAAGTGTGAGTAGCAAAGTGTATAATTTTCTCTCCCAATGCAACCAATACAAGGTATGATTTCCGTCATGTATTCCCATTTCCAAGACACTGAAGTTAGTTGTTGTCATCATACCGGTGGCTTAATTTGTGAATAATCCATTTTGCTACTTTATTGAATATATATGACAACTGATTTTGTGTTAGAACATCAGCAATATCTTAAAATAGACAAATAAGCATTAGTAATAAATAGTTTATTTATAT
Associated Phenotype:
Not determined