ZMP

ext2

Ensembl ID:

ENSDARG00000056648

ZFIN ID:

ZDB-GENE-041124-3

Description:

exostosin-2 [Source:RefSeq peptide;Acc:NP_001008400]

Human Orthologue:

EXT2

Human Description:

exostosin 2 [Source:HGNC Symbol;Acc:3513]

Mouse Orthologue:

Ext2

Mouse Description:

exostoses (multiple) 2 Gene [Source:MGI Symbol;Acc:MGI:108050]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38611	Nonsense	Mutation detected in F1 DNA	Not yet available
sa34076	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38611

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079165	Nonsense	94	719	2	15

The following transcripts of ENSDARG00000056648 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 7 (position 27973225)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	26576164
GRCz11	7	26847357

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTGGGAGGGGTGACCTGAGCTGCCGGATGCACACCTGCTTTGATGTTTA[T/A]CGCTGTGGATATAATCCTAAGAACAAAATCAAGGTAATGCACAAACAGAG

Long Flanking Sequence:

TCTGTCATCCTGAGGCCACCGGGGGCGGTGAGCCCGGGTGCGAGGTCCCTATCATCGCTGCTTGCAGCTTTAATTAATTTATTAAAATCATGTATGTCCTTGAGAACATTTAATGATATTCTCTGACATATGTTCATATACAGTACATCAGTGCTGTTAGTGTATTCTGAGGGGCTATTTTGTGTCCTTTCGCAGTGGTTTTGTCTGGACAGGCTCATCATGTGTGCATCAGGGAAGTACGGTTCACGGGGCCCTGCTCTCATACCCCGCATGAAGACTAAACACCGGATCTACTACATCACCCTCTTCTCTGTGGTCTTGCTGGGATTGATCGCAACAGGGATGTTCCAGTTCTGGCCTCACTCCATTGAGTCTTCAGCCGAATGGAGTCTGGACCGCCGCAGTGTGCACGATGCTCCTTTGGTCAGGATTCCTGTGAACAGTCCTATTCCTGGGAGGGGTGACCTGAGCTGCCGGATGCACACCTGCTTTGATGTTTA[T/A]CGCTGTGGATATAATCCTAAGAACAAAATCAAGGTAATGCACAAACAGAGAATGTCCTATCAAATTTTTTAAACTTGTTTGCTGGATGTCATCCCTGTGCATCTTTTAATTAAGAAAACTTGCAGTAGCATTTGCAAATTTGAAACATCATGTTAGTGAACATTCGGAATCAGCTCACGATGCACATTAAATAAACAAGCCACCTGTGAGAGACACAATCTTTCCTCTCCCTATGCATCAGACACTATAATAAACAATAAACACTCCATGTTTCTGAGCAATCCTGGGTGTGCTTCACACAGGTGAGTGGGCTTGGCAATCACTCATAAGGAAACATACTCTTTCCTCTATCAGGCTGTATTTACACTGCAGATCTTGTTGCTAAATTCAATTTTGTGACTGCATCCGTTTTTTTTTTTGTTTTTTTTTTGACGACCCACTTACATCATCTTTTGTCTGCATTTGCACTGCATATGCAAAGAAATAAAGAGCAGGCGCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34076

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
ENSDART00000079165	Essential Splice Site	674	719	15	15

The following transcripts of ENSDARG00000056648 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 7 (position 28017519)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	26620458
GRCz11	7	26891651

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGATTATCCACATTGCCCTATTCCTCAGCCTCTTTCTTTTTTCCTTCCA[G/A]GTCTGAGTGCATAAACAAGTTCGCCTCTGTGTTCGGCACCATGCCTCTGA

Long Flanking Sequence:

TTAGTTAATACTCCCAAAATGATTCCACATAAATTTGCAGTTTTTTTTTTTTTACAAAATTCTAAACAGAGATAGCAAAAAAAATGTCTGCAGATTCTGTCTGGCCCTAGAAATAACTTATTATGATATAGTATACCATAAAAAAAATCCTGTATAAGTTTGAAATTCCTTTTATTATGGTCTTAAAAAGGTCTTAAAAAGTCTTAAATTTGACTGTGAACTGCTTATGAACTGGCATCATGGCAAAGACAAAATAAATTAGTTATTAAAACAATTATGTTTAAAAATGTGTCAAAGTCTGTACGCCATTAAACGGCGCTTGGGGAAATATTTTTTAAATAACTAAAAGGAAAATTTTGCTTTTAACTGTGTCTCAGGATTCAGGCGACTGTATAGAAGTCTCGTTATCAATTCTTTTTTTCAACAGAAGGCAAATTTCCCGACATCAGCAGGATTATCCACATTGCCCTATTCCTCAGCCTCTTTCTTTTTTCCTTCCA[G/A]GTCTGAGTGCATAAACAAGTTCGCCTCTGTGTTCGGCACCATGCCTCTGAAGGTTGTCGAGCACCGTGCTGATCCTGTACTCTACAAAGACGACTTCCCAGAGAAACTCAAAAGTTTCCCCAACATTGGCAGTCTGTGACACTACCACAGCGACTCTTTCCCACCACTTATTTTTTTTCTCTCAGACAGGCTACGGGCACTCCGGGATTTCTCTTTATGTTCCTTATCTGACCTAATGACTCTGGAGGAGTGTTGTTCCACTGTTTTGTGATGGGAACTCACACACTGTATAACTTATTATGTTTTCACTCTTGAGGACAGTTGCTGAAACAACAGTTGCGACGCATCAAAGCAGTGGATGATTTCTATGAGGACTGGTCACAAGCCGAAACCTTCCTTGTGGCTGACACCTGTGTATCTGTGTGAGAAAAGTGAACACTTTGAGGTGTATCACAATCCACTGGTAAACAGTGGAGACTATGTATTAATGTAATTTTACA

Associated Phenotype:

Not determined