ZMP
nsfa
Ensembl ID:
ZFIN ID:
Description:
vesicle-fusing ATPase [Source:RefSeq peptide;Acc:NP_001037793]
Human Orthologue:
NSF
Human Description:
N-ethylmaleimide-sensitive factor [Source:HGNC Symbol;Acc:8016]
Mouse Orthologue:
Nsf
Mouse Description:
N-ethylmaleimide sensitive fusion protein Gene [Source:MGI Symbol;Acc:MGI:104560]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33227 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44566 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33226 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33227
Status:
Mutation detected in F1 DNA
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103043 | Nonsense | 76 | 744 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 34869514)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34654710 |
GRCz11 | 3 | 34784218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTCTTAACCCTTCTTAAAGAGGAAATGGGCAGGCCTGTCCATTGGG[C/T]AAGAAATAGAAGGTGTGTATATTATTCCTGGAGAACATTTAGAACACAGT
Long Flanking Sequence:
TTGAAGGGGCGTCATGGTGGCTCAGTGGTTAGCACTGCAAGAAGGTCTCTGGTTTGAGCCCCAGCTGGGCCAGTTGGTGTTTCTGTGTTGAGTTTGCATGTTCTCCCCATGTTTGTATGGGTTTCCTCTGGGCGCTCCGGTTTCCCCCCACAGTCCAAAGACATGCACTATAGGTGAATTGAATAAGCTTAATTGGCCGTAGTCTATGTGTGTGAATGTGAGTGTTTGGGTGTTTCCCAGTGCGGGGATGCAACTGGAGGGGGATCCGCTGAGTAAAACATATGCTGGATAAGCTGGCAGTTCATTCCGCTGTTGCCACACTTGATAAATAATGGGAATAAGCTGAAAGAAAACAAATGAATGAACAAGTTTTGAATTATATAAGTGATGAACAAATATTCATTATTGTCTGAACATTATATTTTGATGGACCTTTTACATGTTATTCACTCTCTTCTTAACCCTTCTTAAAGAGGAAATGGGCAGGCCTGTCCATTGGG[C/T]AAGAAATAGAAGGTGTGTATATTATTCCTGGAGAACATTTAGAACACAGTTCAATTCAGCACACAATTCAAATCACTGATTTTATTCCCACCATTTCAGTGTCAAACTACAACTTTGACAAGTCCAGGCAGTGCATTGGTGCCATGACCATTGAGATTGACTTCCTGCAGAAGAAGAGCACAGACTCCAGCCCTTACGACTCAGACAAAATGGCTGCTGAGTTCATCCAGCATTTTAACAATCAGAGCTTCTCCGTGGGGCAGCAGGTCAGAAACACATCACCAAAACTAAATGATTTACAAAGAGCTGAAAATCAATAAATGTTTTGAAAAATAATTCCTGCATAAGTTTTGAGATTTTCATAATGAACCGCTCTTGCCTTTTGAGTCGATTCTGTTGTTAACAGCATATGACGCTGTATGCTTTACAAACTGCTGGACTCTGCTATTTCTGCTAAGTATGTTACCCACAGCCAATATCTCAGACCATAATCTTAGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44566
Status:
Mutation detected in F1 DNA
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103043 | Essential Splice Site | 248 | 744 | 8 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 34866616)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34651812 |
GRCz11 | 3 | 34781320 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGCCTTTGCCTCTCGAGTCTTTCCTCCAGACATTGTGGAGCAGATGG[G/A]TATGTGCTGTTTGTTCCTTTCATAATAAAAGTCATCCATGTTCCAGAACA
Long Flanking Sequence:
AGCTCTTCGGCCTACTTATCAAAGATATTGAGGCGATGGATTCCAGCATTCTGAAGGGTGAACCAGCATCTGGCAAAAAGCAAAAGGTGTCAGAAAGTGCATATTAAATTTGCACTTTAATATTACAGAAAGAAATGATCCATTAATTTGTATACATATCTAATCGTCCTGTGTAACATCACAGATTGAGGTCGGCCTGTTGGTTGGAAACAGTCAAGTGATTTTTGAAAAATCAGAGAGCTCATCTCTCACTCTAGTTGGTGAGTTTTATCAGACTTTAAATAATACATTTCCATTCACTGTCATATAAACAGCTTCTTAATCTTACTCTTTTTGCCCTCCAGGCAAGGCTAAAACTAAAGAAGCCCGTCAAACCATCATCAACCCTGACTGGAACTTTGAGAAAATGGGCATTGGTGGTTTAGACAAGGAGTTCTCTGATATCTTCCGCAGGGCCTTTGCCTCTCGAGTCTTTCCTCCAGACATTGTGGAGCAGATGG[G/A]TATGTGCTGTTTGTTCCTTTCATAATAAAAGTCATCCATGTTCCAGAACAGGAAAATGCAAACATCTTCATCTTCTACATTGATGTTTATAATCATATTGTGCTAATGTAGAAGTATATTTATCTAGTGTAAAAGTGAGATGTTGTTTGTTCTGCAGGTTGTAAGCATGTGAAAGGTATCCTGCTCTTTGGTCCTCCTGGCTGTGGTAAAACACTGATGGCCAGGCAGATCGGTAAAATGCTAAATGCCAGAGAGCCAAAGATAGTCAACGGACCAGAGATCCTCAACAAGTACGTGGGAGAGTCTGAGGCCAACATTAGGAAACTGTTCGCGGATGCTGAGGAGGAACAGAAAAGGGTGAAAAGTTTCTCCTCACAAATACACTGTCCTACTATATTATAATCTCTTCTGTGTCTTAATTGTAATGTTGTGTGTGTTTTTGTGCAGTTGGGTGCTAACAGCGGTCTGCACATCATCATCTTTGATGAACTGGATGCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33226
Status:
Mutation detected in F1 DNA
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000103043 | Essential Splice Site | 587 | 744 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 3 (position 34862182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 34647378 |
GRCz11 | 3 | 34776886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGATGATCGGCCACTCAGAGATCTCCAAATGCCAGGCAATCAAGAAG[G/T]TTAGTGGTTAACATACAGTATAGTATCTCACAAATACATTGAAGAATATA
Long Flanking Sequence:
GCTGGCAAACACATTAATGTACATATATATTTTAAATGAAAAGAAAAATCTAATATGGGGAAAATATTGTAGTTTTGGACAGAGTAGATTGCTTGCAAGGTTAATTGATAACAATCTTTATGTCAAATATTCATTGACTAAAACTAGACTAAAACGTCAGAACTTTTAGTGGTCTAAAACTAGACTGAACCTACAATGATTCAGAAGACTGTAATATGATTAAACTAAATCTAAAATATGCTGCCAAAATGAACACTGGCTCAAACACTGCTGTATTACAAATCCTCAGGCTTTCAAATGCCAATAACTGTGTTTATATACAGTATGTGTTTATATATTACATGAAGTTTTTGTTTTTCCCGTCAGGACCTCCTCACAGTGGAAAGACAGCTCTGGCTGCCAAAATCTCAGAGGACTCGCAGTTCCCATTCATTAAGATCTGCTCTCCAGACAAGATGATCGGCCACTCAGAGATCTCCAAATGCCAGGCAATCAAGAAG[G/T]TTAGTGGTTAACATACAGTATAGTATCTCACAAATACATTGAAGAATATAATGATTTAGAGTCTATTCACAGTTTTATCAGCCTTCTCATACACAAAGTAGTTGCATTGCATCATTTAAAATTTTAATTATTATTTACTTTTCAGATCTTCGATGATGCCTACAAGTCTCAGCTCAGCTGTGTCGTGGTTGATGACATTGAGCGCCTCTTAGGTTAGACATTTGCTATTTACAATTAAAAAATTATTATTATTATTGTCGATTAATTGTTTTTTTCAAGAATGGCTCTTAAATGGGAAAATTTGTTGAATTAATATAACAAATTACATTTTTAAAAAACATTAAAATAAAACTAAAGTTTTTTAAATATATATTAAAGTATATAATATAATATAATATATAATATAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCAAGTATAATAATATA
Associated Phenotype:
Not determined