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
sa16235	Essential Splice Site	Available for shipment	Available now
sa18081	Essential Splice Site	Available for shipment	Available now

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
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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