zgc:92242

Ensembl ID:
ENSDARG00000029443
ZFIN ID:
ZDB-GENE-040718-371
Description:
hypothetical protein LOC436899 [Source:RefSeq peptide;Acc:NP_001002626]
Human Orthologue:
SH2D2A
Human Description:
SH2 domain containing 2A [Source:HGNC Symbol;Acc:10821]
Mouse Orthologue:
Sh2d2a
Mouse Description:
SH2 domain protein 2A Gene [Source:MGI Symbol;Acc:MGI:1351596]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa8728 Essential Splice Site Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa8728
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
ENSDART00000045109 Essential Splice Site 60 280 2 6
Genomic Location (Zv9):
Chromosome 14 (position 8044680)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 7768307
GRCz11 14 8074421
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
RCAGGAGAGCAAGGGGGARATCAAAAAGGAAAAGCTCCGGAAAAAGAAAG[G/A]TATGAACGCGMTCACACCCTTTCTAAGAATACTGCCACGTMTGTCATTCT
Associated Phenotype:
Not determined

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