si:ch211-153o21.1

Ensembl ID:
ENSDARG00000069781
ZFIN ID:
ZDB-GENE-070912-113
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8BAB2]
Human Orthologue:
C15orf60
Human Description:
chromosome 15 open reading frame 60 [Source:HGNC Symbol;Acc:25065]
Mouse Orthologue:
2410076I21Rik
Mouse Description:
RIKEN cDNA 2410076I21 gene Gene [Source:MGI Symbol;Acc:MGI:1920923]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa23201 Essential Splice Site, Missense Available for shipment Available now

Mutation Details

Allele Name:
sa23201
Current Status:
Available for shipment
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Availability:
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Mutation:
G > T
Consequence:
Essential Splice Site, Missense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101825 Missense 171 242 7 8
ENSDART00000101826 Essential Splice Site 166 236 None 8
ENSDART00000135055   None 182 None 4

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 18 (position 956081)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 1264018
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
ATAAATGGATCTATTTCTGTCTCTTCTTCAGGCCCCTGAAGATGCTCCAC[G/T]GGCAGCCCCTGCTGTTGCTGAGGGGCCGCTGTCAATCAAACACCTTTCCC
Associated Phenotype:
Not determined

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