Busch Lab

ZMP

eno3

Ensembl ID:
ENSDARG00000039007
ZFIN ID:
ZDB-GENE-031006-5
Description:
beta-enolase [Source:RefSeq peptide;Acc:NP_999888]
Human Orthologue:
ENO3
Human Description:
enolase 3 (beta, muscle) [Source:HGNC Symbol;Acc:3354]
Mouse Orthologue:
Eno3
Mouse Description:
enolase 3, beta muscle Gene [Source:MGI Symbol;Acc:MGI:95395]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa14478 Nonsense Available for shipment Available now
sa37797 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14478
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013194 Nonsense 15 433 2 12
ENSDART00000076595 Nonsense 44 410 2 11
ENSDART00000132361 Nonsense 15 277 2 8
ENSDART00000136667 Nonsense 44 96 2 7
ENSDART00000145905 Nonsense 49 467 2 12
ENSDART00000147587 Nonsense 28 168 2 9

The following transcripts of ENSDARG00000039007 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 44730129)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 44797578
GRCz11 23 44614098
KASP Assay ID:
2261-8259.1 (used for ordering genotyping assays)
KASP Sequence:
CTTTCAGGATGTCCATYAGTAAGATTCAYGCTCGTGAGWTCCTCGACTCC[A/T]GAGGAAACCCCACCGTTGAGGTCGACCTTTACACCACTAAAGGTAAAYGC
Long Flanking Sequence:
TACTGTATCTGGATCAGACAGCTGAAGTCTGTATATACAGTATGTAGGTGTCTGTGCAGATTTATTGTGACCTTTTTAAATAAATAAATAAATAATGTATGTATGTATTTGTTTTGATTAACTCTATTTGATAATCTTTCTTCCTCAACATTTGTCCTTAGATATGTTCAAACCTGTTCACTGTCTGTTTATGCTTTATTTTTTTTCTATTTCTCTCTTTCTTCTTTATCTTTCTATATTCGTCTTTCTATATTTCTCATGTGTTTATTACTGCTCTGGGGTTTAGCGTCATATAGTTCACATCACACCTTTTGGACCGAATGCATGAATTCATAGTCTCTTAAGTGAAATTGCTTTTTATATCATTTCAATAATAAAAACCCCCACTATTTCTGATCAGAGTGACCTCAAACAGCTGATGCACGTTTCACGTTTTAATCCTGTTTCTGTCTTTCAGGATGTCCATTAGTAAGATTCACGCTCGTGAGATCCTCGACTCC[A/T]GAGGAAACCCCACCGTTGAGGTCGACCTTTACACCACTAAAGGTAAACGCACACATCAATACCAGTGATTTAATGAATCTGTCCATCTAATAATCTCCTGATGAAGACTCCGTAAGGGAAGACATCAGCCACTGCTCGACACCTCGCTCGTCAGTAAATCAGAGTTTTTGTTTGAATATTTTTCTGCTGTGTTCAGGACGTTTCCGGGCTGCTGTTCCCAGCGGTGCTTCCACTGGAGTTCATGAGGCTCTGGAGCTCCGTGATGGAGACAAAACGCGCTACCTGGGAAAAGGTACACGAGGACACACACAAGTTCAAATTGCCTTATTGACTATAGTAAAAGCCACACATAAATGTGTTTAATAATTAGGTCAGAGTTTGGATTGGGCTGATAGACAATACCATCGCTGATGGCCAATAGACAACATGATGCTAAGCCGGCGTTACGATCCATCGCCCCACCCCCATCGCAAACCTGCTTGCGAAAAATACACACTAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37797
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:
C > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000013194 None None 433 None 12
ENSDART00000076595 None None 410 None 11
ENSDART00000132361 None None 277 None 8
ENSDART00000136667 Essential Splice Site 93 96 3 7
ENSDART00000145905 None None 467 None 12
ENSDART00000147587 None None 168 None 9

The following transcripts of ENSDARG00000039007 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 44730433)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 44797882
GRCz11 23 44614402
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCCGTGATGGAGACAAAACGCGCTACCTGGGAAAAGGTACACGAGGA[C/T]ACACACAAGTTCAAATTGCCTTATTGACTATAGTAAAAGCCACACATAAA
Long Flanking Sequence:
ACACCTTTTGGACCGAATGCATGAATTCATAGTCTCTTAAGTGAAATTGCTTTTTATATCATTTCAATAATAAAAACCCCCACTATTTCTGATCAGAGTGACCTCAAACAGCTGATGCACGTTTCACGTTTTAATCCTGTTTCTGTCTTTCAGGATGTCCATTAGTAAGATTCACGCTCGTGAGATCCTCGACTCCAGAGGAAACCCCACCGTTGAGGTCGACCTTTACACCACTAAAGGTAAACGCACACATCAATACCAGTGATTTAATGAATCTGTCCATCTAATAATCTCCTGATGAAGACTCCGTAAGGGAAGACATCAGCCACTGCTCGACACCTCGCTCGTCAGTAAATCAGAGTTTTTGTTTGAATATTTTTCTGCTGTGTTCAGGACGTTTCCGGGCTGCTGTTCCCAGCGGTGCTTCCACTGGAGTTCATGAGGCTCTGGAGCTCCGTGATGGAGACAAAACGCGCTACCTGGGAAAAGGTACACGAGGA[C/T]ACACACAAGTTCAAATTGCCTTATTGACTATAGTAAAAGCCACACATAAATGTGTTTAATAATTAGGTCAGAGTTTGGATTGGGCTGATAGACAATACCATCGCTGATGGCCAATAGACAACATGATGCTAAGCCGGCGTTACGATCCATCGCCCCACCCCCATCGCAAACCTGCTTGCGAAAAATACACACTAAGGACACGTTTACACTAATACGTCTTAGTGTTAAAATGGCATTTTAGAACGAAAATGATCCCCATCCACACCGTGTTTTACCTAGCATTTCTGAACAGCCCTGCTGAAAACGCACATCACGTGACCACACACACACACACACACACACACACACACACACACACACACACACACACAGAGCCACACGCTGTCATGCGCTCCTCTGAGCTCCAGGCAGAGAGTAGTGCACATCGGAGAGTTTATGAAGGATGTTTCGCTGGATTGCGTCTTACTACAGTTGTTAAAAGTGATGTTCAGACATCCCAA
Associated Phenotype:
Not determined