ZMP

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 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39732	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa7418	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39732

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

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
GRCz11	1	59357247

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGTGTACGACAGCAGCTACCAGCGCATCATCCTGGACAAACTACAGCAG[G/A]TCTGAGATCAGTGTGTGTGTGTGTGTGCATGTGTGTGTGTGTGTGCGTGC

Long Flanking Sequence:

GTGTGTGTGTGTGTGTGTGTTGTGTCCAGTATGTGTGTGATAATCAGGATAAAGTTCATTCAGCCGGTTGTTTTCTCAGAATAACTCCTTCAGTCTCCTTCAGCAGTGCTGCGCTTCACACCGGCGGCTGATCCACCTGTCCGGCTCTACTCTGAGCTCTCCTGGCTCTGCTTTGTCTGTAATAGAGCAGTCTCGGTTATGCTGTGGGTCGGGCTCTGGGTTTGAGCATCAGCTGAACGAGTCTTTAATGATGGATCGACAGTGGTCAGGGATCCAGCATGTCTTTAATCCGGTGTAATCTTGTTCTGTCAGACGCGTCCTGCACCGCGGGCCAGATTCTGCAGCCTCAGGTGTTCAGTGACCTGTTCCCGTTCGCCTATGACCTGACGCAGTTTAACGCCTGTCTGAGCGCCAACACACTGGTGGGAAACCTGCAGGCGGTGACGGAGCGTGTGTACGACAGCAGCTACCAGCGCATCATCCTGGACAAACTACAGCAG[G/A]TCTGAGATCAGTGTGTGTGTGTGTGTGCATGTGTGTGTGTGTGTGCGTGCGTGCGTGCGTGCGTGCGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGCGTGCGTGCGCGTGCGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCATGTGTGTGTGCATGTGTGTGTGTGAGTCTGTGTGTGTGTGTGTGCATGTGTGTGTGTGTGTTTGTGGTCAGAAAAATGACGTGTGTGTATGTGTGTTCTGCAGGCGTACCCCAGCGGAGTACCTGACCTAGTACTGCAGGTGCTAGGTTCCTCCTCTCGTATCGCCACGGCCAATGACATCGCTGGGTGGAACATCACAAGGATCGACACGCTCTCAGCACTGATGGACCCAGCCAACGGAGACTGGGACCCGAGCATGGTACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7418

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > T

Consequence:

Missense

Transcripts:

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
GRCz11	1	59355752

KASP Assay ID:

554-4295.1 (used for ordering genotyping assays)

KASP Sequence:

GTGTGTGTTCCCGCAGGTCCAGCTGCTCGTCAGTAAGTAYCTGRGTGTGA[A/T]GGGAAACACTCTCGGCACCAATGAGCTGAACGYACTCGGGGGAACAAACC

Long Flanking Sequence:

CCTCATAAAACACCAATCCCAACATGTGTGACCGTCAGTGTGTGTGTGTGTGTGAGTGTGTGTGTGTGAGTGTGTGTGTGTTTCACATTCAGTCACTCTGTCACCAAAACACACTTTTGTTTGTGGAATACACACCCTCTAGTGGAGTAAATGAGGTACTGTGTCTTTAAAGGATGTGACCCAATGTTTGTTCTTAAACCGTCGCTGTGTATCGCCACCATCGCCCGCCAGTGTTCAGTTCTAATACTCACGGACGGCTGAACGACCCGAGTGTGTTCTCTGTGCTGATGACTGAGTCTGCTCCTGTGTCCTCCTGCTGATGATATCCAGCACCGCACTCTTCAGGAGAACCGACAGATGAGCCCTCATCAACCTGCTGGACCCAAATAATTGTGTTGATGTTGTGTTTAATATAGCGAAGAATGGGAAACATCAACAGTGTGTGTGTGTGTGTGTGTTCCCGCAGGTCCAGCTGCTCGTCAGTAAGTACCTGAGTGTGA[A/T]GGGAAACACTCTCGGCACCAATGAGCTGAACGCACTCGGGGGAACAAACCTGTGTGCCCTGAACACTAGTGTACTGAGCAACATCACCGCCAGCAGCCTGCAGTGAGTGCACACACACACACACACACACACACACACACACACACACACACACACACGTGTATATATATATATTGTGTTGCTTTTAAAACATTATTTAACTCCAAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTAAGGCGAGCGACGGCCCTCTCTTTGACCAACTGCAGCTCAGAGAAGGCTTCAGTTCTGTTCAGTATCGCCGTGAACGCTTTCAGCTCAGCAACACGCGCAAACACCATCAGCGTCAGCACATACCAGCTGCTGCAGAACTACCTCGGTAAACACACACACACACACACACATCCTCATATAGACACACACTCGTGAACACACACTGGTGCGGTGTTGCTGCAGGTGGAG

Associated Phenotype:

Not determined