ZMP
gsna
Ensembl ID:
ZFIN ID:
Description:
gelsolin [Source:RefSeq peptide;Acc:NP_001012312]
Human Orthologue:
GSN
Human Description:
gelsolin [Source:HGNC Symbol;Acc:4620]
Mouse Orthologue:
Gsn
Mouse Description:
gelsolin Gene [Source:MGI Symbol;Acc:MGI:95851]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa4941 | Nonsense | F2 line generated | Not yet available |
| sa37268 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa4941
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000020048 | None | 341 | 729 | 8 | 16 |
| ENSDART00000044078 | None | 341 | 728 | 8 | 17 |
| ENSDART00000109961 | Nonsense | 370 | 373 | 9 | 9 |
| ENSDART00000129979 | Nonsense | 370 | 373 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 16099233)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 17551012 |
| GRCz11 | 21 | 17587648 |
KASP Assay ID:
554-3512.1 (used for ordering genotyping assays)
KASP Sequence:
GTTCAGATTCTCCCAGAAATGGGCGAAACACCCCTTTTCAAGCAGTTCTT[C/T]AAAAACTGGCRTGATGTGGACCAGACAGAGGGCATGGGTGTAGCATATGT
Long Flanking Sequence:
ATTGTTTGTGAATAATGTCTTGTGTATTTACTACCATTATATGGATGATCAAGCAGGACTTTTTGGTATAAGAATTAGTGAAGGGCATATAACATTTAAGAAACTATGAAGCAGGTTTAATTATTGTTGTGAAATGTACTTTTAAGGTCTCTGATGCCAGTGGAGACATGGCGATTGCCCTGGTGGCCGCTGAAAATCCTTTTACCCAGAGTGCACTAGAATCAAGTGACTGTTTTATCCTGGATCATGGCTCAGATGGCAAGATCTTTGTTTGGAAAGGTAAATTCCATTGACCAATACAAACATAAACCTTTTAAAAAAATTTTTTGATTTTTTTTGAAACTCCATTGTTTATCTACAGGCAAAGATGCCAATATGGAAGAGAGAAAGGCCGCCATGAAGGCAGCAGATGAGTTCATCAAAAAAATGGGCTACCCCAAACACACACAGGTTCAGATTCTCCCAGAAATGGGCGAAACACCCCTTTTCAAGCAGTTCTT[C/T]AAAAACTGGCGTGATGTGGACCAGACAGAGGGCATGGGTGTAGCATATGTCTCAAACAGCATCGCTAAGATCGAGAAGGTGCCGTTTGATGCTTCAACTCTGCACGATTCACCAGCAATGGCCGCCCAACATGGAATGATAGACAGCGGCAATGGAGAAAAACAGGTTAGCAAGTAAAGCACACACACACTGCATGTGACTGCAAAGTTATGTATACACATGCAATGAGGGTATTAATTTGTCACCCGACACTTTAGATCTGGCGTATTGAAGGATCAGACAAAGTTCCAGTTGACCCATCTACTTACGGCCAGTTTTATGGTGGAGACAGTTACATTATCCTGTACAGTTACCGCCATGGTGGCAGACAGGGTCACATTATCTACATCTGGTACATCTTAGCTACATCTTCCATTTAACTATTTAGTTGTTCTTTGGTTGTTTTTTTACTGTTGACATACGGTATCTCTCACAGGCAGGGGGCAGACTCTACACAGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37268
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020048 | Essential Splice Site | 471 | 729 | 10 | 16 |
| ENSDART00000044078 | Essential Splice Site | 470 | 728 | 11 | 17 |
| ENSDART00000109961 | None | None | 373 | None | 9 |
| ENSDART00000129979 | Essential Splice Site | None | 373 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 16098666)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 17550445 |
| GRCz11 | 21 | 17587081 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTATCTTGGGTGCCCAGCTGGATGATGAGCTTGGAGGTGGACCTGTGCAG[G/A]TAATGCATATGAACAAACCGCTTGATCCACTTATTACGTACACATTCGTA
Long Flanking Sequence:
AAGATCGAGAAGGTGCCGTTTGATGCTTCAACTCTGCACGATTCACCAGCAATGGCCGCCCAACATGGAATGATAGACAGCGGCAATGGAGAAAAACAGGTTAGCAAGTAAAGCACACACACACTGCATGTGACTGCAAAGTTATGTATACACATGCAATGAGGGTATTAATTTGTCACCCGACACTTTAGATCTGGCGTATTGAAGGATCAGACAAAGTTCCAGTTGACCCATCTACTTACGGCCAGTTTTATGGTGGAGACAGTTACATTATCCTGTACAGTTACCGCCATGGTGGCAGACAGGGTCACATTATCTACATCTGGTACATCTTAGCTACATCTTCCATTTAACTATTTAGTTGTTCTTTGGTTGTTTTTTTACTGTTGACATACGGTATCTCTCACAGGCAGGGGGCAGACTCTACACAGGATGAGATCGGGGCATCTGCTATCTTGGGTGCCCAGCTGGATGATGAGCTTGGAGGTGGACCTGTGCAG[G/A]TAATGCATATGAACAAACCGCTTGATCCACTTATTACGTACACATTCGTATATATGTTACGTCATGCTGAATTTGTTATTGAGAGCTCATTACATTTAGAGTAGTCTTGCAAATCTTTTATTTAAAGGTGCAGTAGGTGATTTTCCACAATGCGGTGTTCAGTAGTTTTAGGACAGGTTTGATAAAAGGTTTGGCAGCACTTAAAATGTTGACTACTGTATTCACAGTCTGTTTTAGACTTTACATAAGTAAAGTGTAAATAAATGCAGGGCAATACTACACTAGATACATTGTGTACTACATTATATAGCTTGATTTGTGCCATCACTTAACATTCACTTAATCCAGGGGTTCCCAAACTTTTCAGCCCGCGACCCCCAAAAATAAAAACCTCAGTGAGTTGCGACCCCAATATTCGCTGAAGTGATTATAAATGTACACACAACACTCAACAGCGCACACACATACCAATAGGCCCAAGTGTATTCATCTTTTAATTT
Associated Phenotype:
Not determined