ZMP

selt2

Ensembl ID:

ENSDARG00000023220

ZFIN ID:

ZDB-GENE-030411-4

Description:

selenoprotein T2 precursor [Source:RefSeq peptide;Acc:NP_001091957]

Human Orthologue:

RP11-392O18.1

Human Description:

Selenoprotein T [Source:UniProtKB/Swiss-Prot;Acc:P62341]

Mouse Orthologue:

2810407C02Rik

Mouse Description:

RIKEN cDNA 2810407C02 gene Gene [Source:MGI Symbol;Acc:MGI:1916477]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa11371	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa11371

Status:

Available for shipment
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Availability:

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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
ENSDART00000006716	Essential Splice Site	171	210	None	7
ENSDART00000065002	Essential Splice Site	171	210	None	6
ENSDART00000143486	Essential Splice Site	171	210	None	6

The following transcripts of ENSDARG00000023220 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 14 (position 15417948)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	17279934
GRCz11	14	17585587

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTGGAGACCCATTTCCTCTCAACAGGAGCTTTTGAGATTACACTGAATGG[T/C]AATCTCATTAGGATCACCACTATTCTCTTTAGGAAAAATATCTACTTTTT

Long Flanking Sequence:

CAATTATAACCGTGTGATCATAATAGAGATTTGTGATTGTTCATTACGCAAATTTTATTTCAAGCTGTCAGTTTTCTTAAAGGTTTGTAGCTCTAAAAAACAATTATCAACAGAACATATTTTTACCAATTTTAAACATTTTTTTTAAGTTTTGTTCTTTTTTTCCCCACAATTTTTTTATATATAATTTTTTTTGTATTAAACTAAAGTCTACATTTTATTTAGATTTAATATACCTTCTATGTATAAAATCTCTCTTGTGAATTTTAGTTGATGCAAACACCAAAATGGGTCGTCACGTCTTTGACCCATATACATGTTTATCTGTCTATTCTTTGCACTGTGTTTCTAACCTGAAGCTATTTTAGCTTGAAAGAACGATTTCTCACAATTGCTTGCTCTGTTTTGCAGATTTTCTCCTGCCTCATGGCCTTTTTTATTAGTAATATGCTGGAGACCCATTTCCTCTCAACAGGAGCTTTTGAGATTACACTGAATGG[T/C]AATCTCATTAGGATCACCACTATTCTCTTTAGGAAAAATATCTACTTTTTACGCCATAATCACAGAAACATCATTATGCCTTTCTGTTTTAGATATCCCAATTTGGTCCAAGTTGCAATCGGGATATGTACCCAACATTCAGGAGCTGTTCCAGATCTTAGATAACCACCTTAAGATGAATCAGGCCGACAAGATGAACTTTCCTTCACCGTAGTGCTGTTGTTTTTGCCAAGAGACATGTGAGTGGTTAAACCTGTACAATTACATCAGCATGTATGTCACAGCAAGTACAAGCATAGCAGCTTTTAACAAAGACTTTTTTTGTTTACGTTGTTTTCGATAGATGTGTTTCCCTCTAGGCTTTTGAGTTATTTGCAAATCTCAGTTCTTGGCAAAACATTTTTTAAGCTGAAGTGTTTTTTTAATCATTTTTATTTTGATAGTCGTATGTTCTGCACTTATTTGATCAATGGCTTTTCAGTAATATTAAAATGAATTAT

Associated Phenotype:

Not determined