Busch Lab

ZMP

LOC556973

Ensembl ID:
ENSDARG00000032256
Human Orthologue:
TXNDC16
Human Description:
thioredoxin domain containing 16 [Source:HGNC Symbol;Acc:19965]
Mouse Orthologue:
Txndc16
Mouse Description:
thioredoxin domain containing 16 Gene [Source:MGI Symbol;Acc:MGI:1917811]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa42892 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa42891 Nonsense Mutation detected in F1 DNA Not yet available
sa16235 Essential Splice Site Available for shipment Available now
sa18081 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa42892
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105064 Essential Splice Site 196 804 7 19
Genomic Location (Zv9):
Chromosome 17 (position 14795293)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14946121
GRCz11 17 14954054
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTCCTCTCCTTCTTCAGTGTCTCTCTGATATTTTGTTTTTGTTTCAC[A/T]GGGTTGTCAACCCGTCGTCCTCACAAGCTCGACTGTGGTTTCTGCACTGT
Long Flanking Sequence:
AAATGGGAAAGTTATCGAAACTCTTTGGTCATTTTTGAGAGAGATGCTAATGATCTAATACAATTCAATGATCTATGCTAGGTGTCACCCTGCCAATCCTACATCACCCAACCCACTCAGAGCTGGGATCCAACCAGCGACTTTCCCCATGGGAGTCGGTTGCTCTACCAAGGAGGCTAAAGACCTTGGCCTCTAGCGTCTGTTGCTAGAGCACCTTTAGAGGTCAGAGGAGTGAGGTTTACCTGCACAGCACTGACTAGCTGGCCTCCGTTACACAGGCTATGCTAAAAGTGCCCCCGCCAAACATAGATATTGGTTAAATGGATTCAAAAATGGTAAAACTCAACTATCTAACTCTAAGGGGTTGTAAGATGAGCTTATTAATAAAAAAAAGTTTAGTGATCATTTAAAAACAGAAGTACCTTGCCATTTCTTTAATATTTTGTCTTCATTTTCCTCTCCTTCTTCAGTGTCTCTCTGATATTTTGTTTTTGTTTCAC[A/T]GGGTTGTCAACCCGTCGTCCTCACAAGCTCGACTGTGGTTTCTGCACTGTAAAAGTGTATCCCTGCAGTCTGATCCGTGTCCCAGCACTGCCATGAGCAAACCAATCAACACCATCAACATACACACATTCCTCCAGCTGATGGAAGCTCCTCTAGTGGTGAGTTATGATGGTAAAAGAGTTATGCTTAAGTTTCATGTGCATAATATTTTCTTTGGATGTAATTGTGGGCTTGTTTTCTGTTAGACCGAGGCAGTAACAGACCCATCTGAGGTCGATGTGGTTCATATCCACCTCAGTGTGCCGGTGCTGTATCTGTTCTCTCAGCCACAAACACAGCACCTGGATCGGGACACTGCTCAGACTGTCGCCCTGCAGCTCCGCGGGGAAGTCGGTGTAGTGCTCATTCACAGGTACTGATAAAACAATATGCAGCCATGCATATAATAAGACTGCAAGGGAAAGAGTGGAAAGGTCGTCTTTGCATATACAGTTGAAGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42891
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105064 Nonsense 201 804 7 19
Genomic Location (Zv9):
Chromosome 17 (position 14795277)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14946105
GRCz11 17 14954038
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTGTCTCTCTGATATTTTGTTTTTGTTTCACAGGGTTGTCAACCCGT[C/A]GTCCTCACAAGCTCGACTGTGGTTTCTGCACTGTAAAAGTGTATCCCTGC
Long Flanking Sequence:
GAAACTCTTTGGTCATTTTTGAGAGAGATGCTAATGATCTAATACAATTCAATGATCTATGCTAGGTGTCACCCTGCCAATCCTACATCACCCAACCCACTCAGAGCTGGGATCCAACCAGCGACTTTCCCCATGGGAGTCGGTTGCTCTACCAAGGAGGCTAAAGACCTTGGCCTCTAGCGTCTGTTGCTAGAGCACCTTTAGAGGTCAGAGGAGTGAGGTTTACCTGCACAGCACTGACTAGCTGGCCTCCGTTACACAGGCTATGCTAAAAGTGCCCCCGCCAAACATAGATATTGGTTAAATGGATTCAAAAATGGTAAAACTCAACTATCTAACTCTAAGGGGTTGTAAGATGAGCTTATTAATAAAAAAAAGTTTAGTGATCATTTAAAAACAGAAGTACCTTGCCATTTCTTTAATATTTTGTCTTCATTTTCCTCTCCTTCTTCAGTGTCTCTCTGATATTTTGTTTTTGTTTCACAGGGTTGTCAACCCGT[C/A]GTCCTCACAAGCTCGACTGTGGTTTCTGCACTGTAAAAGTGTATCCCTGCAGTCTGATCCGTGTCCCAGCACTGCCATGAGCAAACCAATCAACACCATCAACATACACACATTCCTCCAGCTGATGGAAGCTCCTCTAGTGGTGAGTTATGATGGTAAAAGAGTTATGCTTAAGTTTCATGTGCATAATATTTTCTTTGGATGTAATTGTGGGCTTGTTTTCTGTTAGACCGAGGCAGTAACAGACCCATCTGAGGTCGATGTGGTTCATATCCACCTCAGTGTGCCGGTGCTGTATCTGTTCTCTCAGCCACAAACACAGCACCTGGATCGGGACACTGCTCAGACTGTCGCCCTGCAGCTCCGCGGGGAAGTCGGTGTAGTGCTCATTCACAGGTACTGATAAAACAATATGCAGCCATGCATATAATAAGACTGCAAGGGAAAGAGTGGAAAGGTCGTCTTTGCATATACAGTTGAAGTCAAAATTATTCGCCCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16235
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
ENSDART00000105064 Essential Splice Site 434 804 12 19
Genomic Location (Zv9):
Chromosome 17 (position 14786677)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14937505
GRCz11 17 14945438
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTATGGCTTTCATTCAGTCGTATGTGGAGGTGGCAGAAGCAGTCGAAGG[T/C]AAAAGCACTTCTCTGAACAATATTGCAGAATGTTGAAGTGCTGTAAATCA
Long Flanking Sequence:
AATATGATTTAATTTTCCTTTTGCTAATAAATTTGATGATTTACTATTTTACTTTAGTTAGTTTTTTTATTTAGTAACTGTTGTTGTTTTTTTTAGGAGATAAAATGACAATTACCTTTAGTTTTTGTTTTCTAAAATAACCTTACTATACAACTTTTTAACTAGTATTAGTCCATTGGTTATTATCAACTTGTCCTTCTTAACTTCATCCAGATATCCTCGATGACGAAGTGTCTGAGTCTGTGTACAGAGATCGTGATCTTATGCTGGATCTGGAGCCTGTAACTGAACTCACGGCAGACACCTTTCAAACTGCAATCAAGCAAAATGAGATCACAGTGGTGCTGTTTTATTTTAAATGTGAGTTTAACTTTTTTCTCCCACTTGTTTTTGCCATCTGTGTGTACTCTACCCTGATATGTCCACTGTTGTCCTCTAGGGGATGCTGTCTGTATGGCTTTCATTCAGTCGTATGTGGAGGTGGCAGAAGCAGTCGAAGG[T/C]AAAAGCACTTCTCTGAACAATATTGCAGAATGTTGAAGTGCTGTAAATCAAATTAAGTTGTTTTGTTTCTTTTTTTTTTTAAATATTCATTTGATGGCATCTGTGTTCTGACAGTATAACAGAAAAAAATCAAGACTGATGTGCACAGAATAAATCGTTTTGCTTTTACAGCGTCCTCAAAATGTATTTGGAAATTTGAGTCATTGCATTAGATAATAAAATCAAACCAAGTGGAGTCAAATGATGTGTTTTTTCTCAGAACTAACATCGCTTTTCTGAGCATTTATTATTTCTGACTGGGTGTGGAGGGTTTTAGTTGATGTATGCAATAATTGACTGTCTCCTTTATTTCCTCATCTGCCTTTAATTAGATTGAATGCCTTTTTTAACGTAGCTTATTCACATTTATGTCATTTCTTATTTTTAAAAGGATAGCTCACCCCCCCAAAAAAGGGAAATTCTGTCATTTATTCATCCTCAACTTGTTCCAAACCCCTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18081
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
ENSDART00000105064 Essential Splice Site 565 804 15 19
Genomic Location (Zv9):
Chromosome 17 (position 14777889)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14928717
GRCz11 17 14936650
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGAGAGACCATTATTGGGCTGTTTRCCCATAAAGAGGCGGCAAAATGG[T/C]ATCWGSATGTTTCACCACAACTATTCTAATGACGTAATATGCTTAAGATT
Long Flanking Sequence:
CAAGGAGACTTGTGTGCTCTAGAAAACTGTAAATATGACTCTAGATGATATTTGCCAAAAGGCTCATTACATATGAATACAGTAAACAATTACTTAAGAAATAATATTGCTCTATATCACCTAAATTTCACTATCCCTTTTTAAGGTTTGTAGTTCATTCTGAGTAGCCAGGTTGACTTGCTACTGATGGCTTTTTTGTTTTTTTACAATACTTCAAACAATATGCATATAAAGTACACAATTTTTTAAAAAAGGGTTTTGATTGTGTTCCTAAAAAAATATAAAAAATAAAAAATAAAAATTAGTGCAATGTGGTTTGACAGCTAACGAGTGTATTTCACGGGTGTCAAATTATTGCAAAATTGATTCCATGTACAAAAGAATCTCTCAGTCATGTGCTTTGTATGTCTTCAGGCGTATCTTCATTTGAAGAAGCGGCAAGACTCCTCAGAGGAGAGACCATTATTGGGCTGTTTGCCCATAAAGAGGCGGCAAAATGG[T/C]ATCTGGATGTTTCACCACAACTATTCTAATGACGTAATATGCTTAAGATTATAACTTGCATTCAGAGGGGTTGTAAGGAACAAGATGTTACATGTGTGGAGGTTTCAGTGTGGCGTAAGACAGTGTTTTGTGTTTGATCAGGGTGGAGGGACTGTCAGTGAATCTGCCTGCTTTACTGGTGTCCCACGGTCCTGCACTTCCTCATCAGGTCTTTTCCCTCCCATCATCCTTGGCAACGGACCATGTCAAACTCATTCAACGAGTGGAGCTGGAGCGTTTTGTAAGTTATTTTGGTTGCAAATTCACCCCAGACTTCAAATATCGTGCTCCACAGTTGCACAATGAGACTTTATATTGGAATCACATGTGTTTTACTGGAAGTGTTCCTGCTGAAACATGAACCATCGCCCCATTCTGAGATCAACAGCACTCTGAAGCAGGTTTTCAATCAGGATGTCTTTGTACATTGCTGCATTCATCTTTCTCTCATCCTGACTAGT
Associated Phenotype:
Not determined