tm9sf3

Ensembl ID:
ENSDARG00000028748
ZFIN ID:
ZDB-GENE-040426-2714
Description:
transmembrane 9 superfamily member 3 [Source:RefSeq peptide;Acc:NP_998554]
Human Orthologue:
TM9SF3
Human Description:
transmembrane 9 superfamily member 3 [Source:HGNC Symbol;Acc:21529]
Mouse Orthologue:
Tm9sf3
Mouse Description:
transmembrane 9 superfamily member 3 Gene [Source:MGI Symbol;Acc:MGI:1914262]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa22233 Nonsense Available for shipment Available now
sa18308 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa22233
Current 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
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041609 Nonsense 48 586 2 15
Genomic Location (Zv9):
Chromosome 13 (position 9236078)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 9538698
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TACACAGATAAAGAAGAGGTGGTTTTATGGATGAATACAGTGGGCCCTTA[T/A]CACAACCGACAGGAGACCTATAAGTACTTCTCCCTACCGTTCTGTGTGGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18308
Current 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:
A > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041609 Nonsense 204 586 5 15
Genomic Location (Zv9):
Chromosome 13 (position 9231960)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 9534580
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GATCATCYCYACAGGTCAAGTGGAAGAAATCTGATGTGAAATTTGAGGAT[A/T]GAKTTGACAAATACCTTGATCCATCTKTYTTTCAACACAGAGTAAGTCTT
Associated Phenotype:
Not determined

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