slc16a4

Ensembl ID:
ENSDARG00000042807
ZFIN ID:
ZDB-GENE-070112-602
Description:
solute carrier family 16, member 4 [Source:RefSeq peptide;Acc:NP_001074068]
Human Orthologue:
SLC16A4
Human Description:
solute carrier family 16, member 4 (monocarboxylic acid transporter 5) [Source:HGNC Symbol;Acc:10925
Mouse Orthologue:
Slc16a4
Mouse Description:
solute carrier family 16 (monocarboxylic acid transporters), member 4 Gene [Source:MGI Symbol;Acc:MG

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa9884 Essential Splice Site Available for shipment Available now
sa8810 Essential Splice Site Mutation detected in F1 DNA During 2018
sa21290 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa9884
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
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Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078656 Essential Splice Site 388 558 6 9
Genomic Location (Zv9):
Chromosome 8 (position 25613089)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 24741007
GRCz11 8 24760146
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GAATCTGGGAATCGACCCCATGGATGCTTCCTTCATCATCTCTGTGGCTG[G/A]TGAGTCTTATTATGGAACCCTAGAGTCATGTTTTTGCACCGTCATCCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8810
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078656 Essential Splice Site 459 558 7 9
Genomic Location (Zv9):
Chromosome 8 (position 25620010)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 24747928
GRCz11 8 24767067
KASP Assay ID:
2260-0584.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TTTTTGCCATCTTCTGTGGAGGGTACATGGCKCTCCTGCTTCCTGTACTG[G/A]TGAGTACTGAACATGAACCATTTTCACAATAAAGAAAATTSWTTCAGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21290
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:
G > T
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078656 Essential Splice Site 491 558 9 9
Genomic Location (Zv9):
Chromosome 8 (position 25631087)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 24759005
GRCz11 8 24778144
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TCAATTTGGCATCACTTTAATATGTCTAACGTTTTGCATTATGTCCCAAA[G/T]GCTTCCTATACGACTACACTCAGACGTACGACTGCTCCTTCTACCTGGCA
Associated Phenotype:
Not determined

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