ZMP
zgc:172323
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC564165 [Source:RefSeq peptide;Acc:NP_001107899]
Human Orthologues:
NES, SYNM
Human Descriptions:
nestin [Source:HGNC Symbol;Acc:7756]
synemin, intermediate filament protein [Source:HGNC Symbol;Acc:24466]
synemin, intermediate filament protein [Source:HGNC Symbol;Acc:24466]
Mouse Orthologues:
Nes, Synm
Mouse Descriptions:
nestin Gene [Source:MGI Symbol;Acc:MGI:101784]
synemin, intermediate filament protein Gene [Source:MGI Symbol;Acc:MGI:2661187]
synemin, intermediate filament protein Gene [Source:MGI Symbol;Acc:MGI:2661187]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18553 | Essential Splice Site | Available for shipment | Available now |
sa22891 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18553
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075191 | Essential Splice Site | 293 | 847 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 35054651)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32786151 |
GRCz11 | 16 | 32740181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAGCAGATCCAACACCAGTATGATGACATTGCCGCTAAAAACTTACAG[G/T]TATTTATTTTAACATGATAGCATTATCAGCAAYATGGGGAGCTTTTAATT
Long Flanking Sequence:
TTGCTGCAAAAGATGCTATGGCGGGTCAGCTGGAGATTATTAAGGTTAAATATGAAGAGGCCTTGGAAATGAGGAAGAAAGCTGAGCTTGACATTGAAGCTTTCCGCCCGGTATGATTCCAAACGAACGTTCTCATAATAAACATTATTTGATTGTCTCAGGACGTTTTTTTAAATAGCCTTTTTCATTAGGATGTGGACGCCGCCACTTCCGCACGCATTGCGCTGGAAAAGCAGCTGGAAAATCTGGAGGTGGAATTAGAATTCCTTCGAAGGGTTCACAAACAGGTAACTGAATCAGCAATTAATAAATGGTCGACTCCAATAAGTAAACAATATATAAAACCTGAATGTTTTATATTTCAGGAAATCGAGGAGCTTATGAAACAGATATATGCAGCGCACGCCTCAGCAATGGACGCATACAGCCTGCCAGACCTCTCAAACGCGCTCAAGCAGATCCAACACCAGTATGATGACATTGCCGCTAAAAACTTACAG[G/T]TATTTATTTTAACATGATAGCATTATCAGCAACATGGGGAGCTTTTAATTAGTCATTTTAAATGGCTAATTTTTCCGAGACCTGTATGATTCTAGATACAATGTGAAATATTTCTGTTAAAATATTTTCCTTTCAATTTTTAAGATGAAAAAGGGATGACAAAGAATGACAATTCTTTGTATAACTATCATGATTTTTTTCTAAACTAGTATTAAGAATTTTACTTAAACCCCAAATATGGGAATAATCCTCCAAAACTAAGTAATAAATTGGCAAATGTTTATGCAGGAAATGGATTCTTGGTACAAAAATAAATTTGATGACCTCAACAACAAAACATCAAAACATGTGGACCAGGTGCGGCATGTGAGAGAAGGAATTGCCTCTGCAAAGAAGGATGTAAGATTTAAGGATTTTCACTGTATATAACACATTTTTGTCATGTTACTTCTAGGGCAATTGCAAAATATTGTAAAAAAATAAAATAAATATGACATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22891
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075191 | Nonsense | 568 | 847 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 16 (position 35056142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 32787642 |
GRCz11 | 16 | 32741672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCCAAAGGGCTTCCGGGAGGTGTGGGTGGTGGTCCTGCCACAGGTCTT[G/T]GAGGAGGTGTAGGTGGTGATCCCGCCAAAGGGCTTCCGGGAGGTGTAGGT
Long Flanking Sequence:
TTTTCTCCTTATTTGTCATTCACAGGAAGCTCATTGAGGGTGAAGACTCTCGTCTGACTTCCATGGTGCAGAGCATGCAGACCATGACGCTTATGAGTGGCAGCACAAGCGTTCACACTGTAGCAGCAGGGGCTGCTAATAGAGGGGGCAGAGGTCTTGCTGGTGGTCTAGGAGGAGACGTTGGTCTTGAATTTGCTGGAGGCCTTGGTGGTCCTGCCACAGGTCTTGAAAGAGGTGTTGGCAGGGGTCTTGATGGTTCTGCCACAGTCCTTGGAGAAAGTGTAGGTGGTGATGCTGCCAGAGGTGTTGGTGGTGGTCCTACCACAGTTCTTGGAGGACATGTTGATGGTGGTCTTGGAGGAGGTATAGGTAGCGGACCTGCCATAGGTCTTGGAGGAGGTGTAGGTAGTGGTCCTGCCACAGGTTTTGCAGGAGGTGTAGGTGGTGATCCCGCCAAAGGGCTTCCGGGAGGTGTGGGTGGTGGTCCTGCCACAGGTCTT[G/T]GAGGAGGTGTAGGTGGTGATCCCGCCAAAGGGCTTCCGGGAGGTGTAGGTGGTGGTCCTGCCACAGGTCTTACAGGAGGTGTAGGTGGTGACCCTGGTAAAGGGCTTTCAGATGTGGGTGGTGTTCCTGCCACAAGTCTTGCAGGAGGTGTAGGTGGTGATCCCGCTAAAGGGCTTCCTGGGGGGGTAGGTGGTGGTCCTGCTACAGGTCTTGCAGGTGGCGTAGGTGTTGATCCCGCTAAAGGGCTTCCTGGAGGTGTAAGTGGTGGTCCTGCCTCAGGTCTTGCAGGAGGTGTAGGTGGTGACACTGCGAAAGGGCTTCCAGGGGGTGTAGGTGGTGGTCCTGCCACAGGTCTTGCGGGAGGTGTAGGTGGTGTTCCTGTCACAGGTCTTGCTGGAGGTGTAGGTGGTGACCCCTCTAAAGGGCTTCCAGGAGGTGTAGGTGGTGGTCCTGCCTCAGGTCTTGCAGGGGGTGTAGGTGGTGATTTTGCCAAAGGCTTT
Associated Phenotype:
Not determined