ENSDARG00000090320

Ensembl ID:
ENSDARG00000090320
Human Orthologues:
MSLN, MSLNL
Human Descriptions:
mesothelin [Source:HGNC Symbol;Acc:7371]
mesothelin-like [Source:HGNC Symbol;Acc:14170]
Mouse Orthologues:
Msln, Mslnl
Mouse Descriptions:
mesothelin Gene [Source:MGI Symbol;Acc:MGI:1888992]
mesothelin-like Gene [Source:MGI Symbol;Acc:MGI:3607710]

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa39732 Essential Splice Site Mutation detected in F1 DNA During 2016
sa7418 Missense Mutation detected in F1 DNA During 2016

Mutation Details

Allele Name:
sa39732
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 2016.
Mutation:
G > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122050 Essential Splice Site 184 378 4 8
Genomic Location (Zv9):
Chromosome 1 (position 60199505)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 58650802
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
GTGTGTACGACAGCAGCTACCAGCGCATCATCCTGGACAAACTACAGCAG[G/A]TCTGAGATCAGTGTGTGTGTGTGTGTGCATGTGTGTGTGTGTGTGCGTGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa7418
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 2016.
Mutation:
A > T
Consequence:
Missense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122050 Missense 248 378 6 8
Genomic Location (Zv9):
Chromosome 1 (position 60201000)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 58649307
KASP Assay ID:
554-4295.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
GTGTGTGTTCCCGCAGGTCCAGCTGCTCGTCAGTAAGTAYCTGRGTGTGA[A/T]GGGAAACACTCTCGGCACCAATGAGCTGAACGYACTCGGGGGAACAAACC
Associated Phenotype:
Not determined

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