si:dkey-189l3.1

Ensembl ID:
ENSDARG00000070467
ZFIN ID:
ZDB-GENE-061207-53
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2CF06]
Human Orthologue:
LACTBL1
Human Description:
lactamase, beta-like 1 [Source:HGNC Symbol;Acc:35445]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa13718 Essential Splice Site Available for shipment Available now
sa7351 Missense Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa13718
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103450 Essential Splice Site 48 653 None 8
ENSDART00000136061 Essential Splice Site None 71 None 3
Genomic Location (Zv9):
Chromosome 11 (position 29033778)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 27909764
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ACTCTTTCAACCATCAACGAAGAAAAGCGTTCCTAAACCAAACTAACAGG[T/A]AAGTTCATGWTAAAATAGATGYGTTTCTTGTGTTTTTGGTTCATGCGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7351
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 2017.
Mutation:
A > T
Consequence:
Missense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103450 Missense 310 653 7 8
ENSDART00000136061   None 71 None 3
Genomic Location (Zv9):
Chromosome 11 (position 29008947)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 27884933
KASP Assay ID:
554-4073.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TCTACCTCGAAGACTCCGTGGGACTAACTTACTGTGGAAAGGCAAGACCA[A/T]GACTGCAATCAACCTCCTACAAGATGATGTGCTCGTAGCAGATCCGGGGA
Associated Phenotype:
Not determined

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