ZMP
mfn2
Ensembl ID:
ZFIN ID:
Description:
mitofusin-2 [Source:RefSeq peptide;Acc:NP_001121726]
Human Orthologue:
MFN2
Human Description:
mitofusin 2 [Source:HGNC Symbol;Acc:16877]
Mouse Orthologue:
Mfn2
Mouse Description:
mitofusin 2 Gene [Source:MGI Symbol;Acc:MGI:2442230]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13351 | Essential Splice Site | Available for shipment | Available now |
hu3528 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa21386 | Nonsense | Available for shipment | Available now |
sa34491 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13351
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108662 | Essential Splice Site | 104 | 757 | 2 | 17 |
ENSDART00000140266 | Essential Splice Site | 104 | 757 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 50073442)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 47925419 |
GRCz11 | 8 | 47914411 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGKGAAGTCCTGTCCCGAAGACACATGAARGTGGTCTTCTTTGGCAGG[T/C]ACRGTGCATAGATTTTGCCCCTCACAGAATAAACGCAAACATATGTCAAA
Long Flanking Sequence:
TATAAATTATAGAAAAACTACACACAGCACACATTTAGTCCTTTTTTGGGTTCAAAAACAACACGCAACATATAGCCCACAGTCAGAGCAAACTTCTCATCCGTATCTTTAATCTTCACCAGCACATGTAACCTCTGTTAGAGAGTCATTTCATCATTCTGAGTTCATAATAGTCCAAAAGGCGATGATAAACATGGCAGTTTGTTCATGATTCAGGTTCAAAGGAGCAACAATTTGCTCCTTTGTTTTGTCGGGCTTCTCCTAAGTTATTCCGCGCTTCTAGAATAGACTTTAAACAATGAATTGAAACATTATTAGCTGTATGTGTGAGAAGAAATTCAATGCCCGTTTTCCCTTTAACAGAAACCTACAGCAATGAAGAGCTGGATCCTGTTACCACAGAGGAGCAGGTGGCGGAGGTGCGGGGATACCTGTCCAAAGTGGCAGGGATTGGTGAAGTCCTGTCCCGAAGACACATGAAAGTGGTCTTCTTTGGCAGG[T/C]ACGGTGCATAGATTTTGCCCCTCACAGAATAAACGCAAACATATGTCAAAATCAGCACTAAATCATAAAGTCTATCTCAGTTTTTATGCAGACTCTAGGCTATGGACACTGTGCACCTGTGGTACATTTGACATCAGCAAATTATCTGCACAGACAGATTTTTCATTTCTTTTATGCTCAGCTAAAAGTACTGGAATAAATAAAATGTAGTGCTGTACACCTAATTGTGATGTTTACTAGTGCCTGTGAATAATAAACTGTAGAAGATGTCAGAGAAACATGTTAAAATCATATATGCACAGAACCATAAAGAAAAGTCAAATAAGTGGTTAAATTGAAATAAATTGAAAAACACTTTCACCGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTAGCTTTATTTTTGCTAGAATAAAAGCAGTTTTTAATTAAAAAAACATTTTAAGGTCAAAATTATTAGCCCCTTTATGCTATATTTTTTTTCTCGATTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu3528
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000108662 | Nonsense | 285 | 757 | 7 | 17 |
ENSDART00000140266 | Nonsense | 285 | 757 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 50087109)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 47939086 |
GRCz11 | 8 | 47928078 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGTTTTGTCAGGTGAGGCGGCAGCACATGGACCGCTGCACTAGTTTTT[T/A]AGTGGATGAGCTGCGGGTGGTGGATCGCTCTCATGCCGGGGATCGAATCT
Long Flanking Sequence:
GATTAAACAAAACACTATTGGCTGTTTTTTTAAAAGGGGAGGAGCTGTTCATTTTTCAGTTGAGATTACTTCAAACTTAGAATAAACAATGCACATTTCAATGCACTTCATGGGACTGTTGAGGTTGTTACAAATTTTAAAACGCGTTATCATCATGTGACTTTACTGGTGTCAGTCAACGTATTAAAACATGATTCTCCTCTTTTAAAGGAAAAATCTTTTTTTCACAAAGTAAACGAACGCCTCTCCAGCCCTAATATCTTCATCCTGAACAACCGCTGGGACGCATCGGCCAATGAGCCAGAGTACATGGAAGAGGTGAGGAATCACATGACACCACACACAACACCTTAAAGATGCATTTGAATCTGCAAAAACGAATAGTGGAAGCATAACTTTAAAGCAAACTAGTTGAACCTTTTAGATGATATGGAGTTTTTGCTCTCTTATGATGTTTTGTCAGGTGAGGCGGCAGCACATGGACCGCTGCACTAGTTTTT[T/A]AGTGGATGAGCTGCGGGTGGTGGATCGCTCTCATGCCGGGGATCGAATCTTCTTTGTCTCTGCTAAAGAAGTTCTTCAGGCGCGTGTACAGAAGGCCCAGGGAATGCCTGAAGCAGGTAGATTTAGTCTCAAATGATGTTTAAATGCTAAGATGTTATGTATTTTTAATTGTTTTATTTTGTTCATTTAATTGTCTATTTAATTGTTTAAAATTATTATTATTATTTTTTAATATTGTTGCAGAATGAATGTCACCAGGGCTTAACACTTGCCAATTGCGGGTAGATTTCAGCTTTGGCGGGTTAGAAAGTCACTCCCACTAGCCACTTTGGCAGGTTGAAAATATTTTTTTAATTGTGGTTTTCTTAAAAGCAGAATTCGACAATAAGGATGACCCAATATGCGTGCAAATGGGATAACAGAAATAATTGCTTTCGCACGAGCAATAGAAAGCAGGTGGATACCGAATGAGAGGATGATCAGTCGCGCAAACAGCTGAT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa21386
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108662 | Nonsense | 615 | 757 | 14 | 17 |
ENSDART00000140266 | Nonsense | 615 | 757 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 50099220)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 47951197 |
GRCz11 | 8 | 47940189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTATGGTTTCTATGGTGACAGGACTGGCATCACTCACCTCTCGGACAT[C/A]AATGGGCATCATAGTTGTTGGAGGAGTGGTAAGAACACACTGGATATCTC
Long Flanking Sequence:
ATGCACTACCCTAAAAAATCATCCCAGTCAATCTAAAATGATTAAGTTATCTTGTGAAATATAAACTGAAGAAAATCTAAATATCACAATGTAAGTTTTTTACCAATATGGTGCAACACTAAAATGCATGTAGTTATTTTTTATGGGATTAGATCAAATTTTTTATGATGCGATTTTATCTCATTTTCAACTTGAATATTAAGGAAATCTATTTTATTGTTTTTTTTTTTTTTTGCAAATTTTGTGGAGTTTGTTTTTTTCCCCCTATTATAATATAATATAGATATATTATAGAAAGCTTAAAGCATTAAGAAAGTAATTGTTTTGCTTTAGTGTGTTTTTGCAAACAAAAGTGTGTGTGGTGTGTGTGTAGGTTCCCAGATCCCTGGCCATTACTCCGGTCAGCACAAGTATGCCTCCATTCCCTCAAGGATCTATGACCCAGGAAGAGCTTATGGTTTCTATGGTGACAGGACTGGCATCACTCACCTCTCGGACAT[C/A]AATGGGCATCATAGTTGTTGGAGGAGTGGTAAGAACACACTGGATATCTCTGATTCACCAAATGCATCTGTTTCTATTTTTTATTTGCTAAGGGGCGGTTCACATAGAACACGTTTTTCCTTTTTCAGTTAGAGCTTAGCTCGTGCCCAAAAAAATTAACCCGACCCTACTCAAGCCTGAGCACTTTGGGCTCTATTTTGACGATCCATCGCAGAGCGCAAAACGCAGGGCGCAAACGCTTTCAGGGCGTGTCAGAACGCATTTTTGCTAATTTACTGATGGGAAAATGCGCTTTGCGCCAAGGCGCATGGGCTAAAAGGGTTGAGTTTATTTTCTTAATTACTTATAGGTGTGGAAGAAGACATAAAAGCAGTGATTTTTCATATTTATGTAGGCTAGAAAATAATATGTTTTGTAATATTTTAATCCTTTATATTTATATCCTATATCTATTCTTATTATATCCTATATATATCCTTAATATTACATTTTTTTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34491
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108662 | Nonsense | 752 | 757 | 17 | 17 |
ENSDART00000140266 | Nonsense | 752 | 757 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 8 (position 50104863)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 47956840 |
GRCz11 | 8 | 47945832 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATAAGGCGGGCTGGCTGGACAGTGAGCTCAACATGTTCATTCAGCAGTA[T/A]CTTCAACAGGGGCGATAAACTCCACAAGCCCTCAACAAGCTCCGTCGATC
Long Flanking Sequence:
TTGTAACGAGTGGTTATTTGAATTACTGTTACCTTTCTATTAGCTGGAACCAGTCTGGCCATTCTCCTCTGACCTCTGTGATCAACAAGGCATTTGCGCCCACAGAACTGTCGCTCACTTGATATTTTATCTTTTACACACCATTCTCTGTAAACCCTAGAGATGGTTGTGCGTGAAAATCCCAGTAGATCAGCAGTTTCTGAAATACTCAGACCAGCCCATCCGGCACCAACAACCATGCCACGAAAAAAGTCACTTAAATCACCTTCTTTCTCATTCTGATGCTCGATGTGAACATGCCTAAATGCATTGAGTTGCTGTCATGTGATTGGCTGATTAGAAATTTGCGTTAACGAGCACAGATGTACAGATGTACCTAATAAAGTGAGTGTGTGTGTGTGTGTGTGTGTGTATTTGGAATTGGATGTAATTTGACTTCTCTCCTACAGGAATAAGGCGGGCTGGCTGGACAGTGAGCTCAACATGTTCATTCAGCAGTA[T/A]CTTCAACAGGGGCGATAAACTCCACAAGCCCTCAACAAGCTCCGTCGATCTCTCTTGCAGATCATCTAACCCTTCAAACTTTTATTTCAGCGTACCAATCACATATTTTTCTATTCGTTGTTCTTTCCGCCATTGAGAGTACAGTGACACGTGCCACTTTAAAAAGAAGCTTTCTTTCGTTTGTTTGTTTTTTTTTGTACACAAGACACTGTTTCTTTTATATTTAATACAAGAGTAATTATTTATTCTTGACATAAGAGGTCATGTGACGTAGTGGCTCTCTTTGTTAGGTTGTGTTTATAGTCCATATCAGTTTTCTTAATACGCCACAGTCAATCAAAAAGTGAGACGATGTTTTAGACCAGTGTTTCCCAACCATGTTCCTAAAGGCACACCAACAGTACACATTTGCCACCTCTTCCGGTTTAAACACACCCGCATCCACTCATCAGAACATTAGAAGAGACTCCAAAACCTGATGTTAATGGGTCAGATAAGGG
Associated Phenotype:
Not determined