ZMP
desma
Ensembl ID:
ZFIN ID:
Description:
desmin a [Source:RefSeq peptide;Acc:NP_571038]
Human Orthologue:
DES
Human Description:
desmin [Source:HGNC Symbol;Acc:2770]
Mouse Orthologue:
Des
Mouse Description:
desmin Gene [Source:MGI Symbol;Acc:MGI:94885]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34555 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa5 | Nonsense | Available for shipment | Available now |
sa15298 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34555
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081550 | Nonsense | 206 | 473 | 2 | 9 |
ENSDART00000081553 | Nonsense | 206 | 488 | 2 | 10 |
The following transcripts of ENSDARG00000058656 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 7573966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7554059 |
GRCz11 | 9 | 7532450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGGAGATCCACCAGAAAGAGGAAGCTGAAAACAACCTTTCTGCTTTC[A/T]GAGCTGTATGTACTTTATGTCATCTTTACTTTTCAGTCGAATTTTGTTTA
Long Flanking Sequence:
TGAATGTGGAAACATCAAATTCTCCACAATTGCTTGCCAAGTTCATGATTACATTTCATTTAGCAATCAACAATAAGGTTAAACAACAACTGTGTCTTTAATTTCATTTCTAAATGTTAGAGTCACACAAAATCTGCAGAAACTCTCGTCTGGTCCGAGCCCCTCTCTCGTAGTTTCTTCAGTCTATAGCGATTGCGGATTGGCTCGTGTACTAGAAGGCGGGGCTTCATTCGCCATGTTGACCGTTACACTTTTCCCAATTTTAAACTACACAAGTGACACGTCTTGTGTATTCAACAGTCTTTGTGTTCAGCAGAAGAAAACAACTCAAATAGGTTTTAAAAACCTACTGTATGTAGGCATTTAATGGTATACTGTATGTTTTCTTAAAGTAATATGATTACGTATTATTCTATGAAGGCTTTAATGTCTCTTACTTCCACAGACTTCAAGAGGAGATCCACCAGAAAGAGGAAGCTGAAAACAACCTTTCTGCTTTC[A/T]GAGCTGTATGTACTTTATGTCATCTTTACTTTTCAGTCGAATTTTGTTTAAGAAAAAATTTCCTTGAAGAAAGTTAGGAAGAAAATTGAATGACAGATATAATATGGCCAAAATGTAAGCGTTCTATATTTGTTTAAATTATGGTTAGCATGATAGAAGTGCACAGGGCTTAACTCCAGAATTACTTCACAAAATTAATCCAAACATTCCTGATCAATGCGTAAAATGCAATGAAGAGACAGGAACTTTATATCATTGTTTATGGAAGTGTCCTTTGATTAAACAATTTTGGGAGAAAATTCTTAACTTTTTATCTATAGCAATAAAACAGGATATAACCAAATGCCCAAAACTGTGTATTCTAAATATATTTCCTTTTACAAGCACTTTTACTAGTTCAGATAAGAAACTGTTAACTTATTACAGGCAAAACTTATAATAGCAGTACAGAAATAGAGAAAGCCCGCATTTTGGACAATGGTTGCGGGAATTGTCTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5
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 |
---|---|---|---|---|---|
ENSDART00000081550 | Nonsense | 287 | 473 | 4 | 9 |
ENSDART00000081553 | Nonsense | 287 | 488 | 4 | 10 |
The following transcripts of ENSDARG00000058656 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 7567774)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7547867 |
GRCz11 | 9 | 7526258 |
KASP Assay ID:
554-0025.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTCGCCTGCAGTACGAGGCTATCGCTGCCAAGAATATCAGCGAGGCC[G/T]AGGACTGGTATAAGTCTAAGGTCTGTATCAGAGATAGATTCAGCTAGATC
Long Flanking Sequence:
GCTGTAAAATTAAAAATAAAAACAAATTGTAAAAACTCAAAATTGTAGATTTTTTTAACAAGATTTTTTTTTTTTTTTAAAAAGAAAAACATTTCTTTGGGTCTCAGGAGGATATTGAATTGACTGACAGGGACAACCTTTCACTATGGAGCATAAAATATGATGATGTGAACATGCATAGTGTGTCAATAGAATTGCTGTATGTCAGTCTAGCGTGTGTGTATACAAACATCAAACATTATAATGCCTCAATAAACTGTGCATGTCTAAATAAATAAGGTCAAAACACACACTCGCCAAACAAAACGCTAATTAGTGCCTTTTGAAGCTATGTATCTGTGTTTGCCTTTTTCCTTTAGGAGATCCGTGAGCTGCAGAACCAAATGCAGGAGAGTCAGGTGCAAATCCAAATGGACATGTCCAAACCAGACCTGACTGCGGCCCTCAGAGACATTCGCCTGCAGTACGAGGCTATCGCTGCCAAGAATATCAGCGAGGCC[G/T]AGGACTGGTATAAGTCTAAGGTCTGTATCAGAGATAGATTCAGCTAGATCACACATTTCAAAGGCTGTACGGCCAGTTAGAAACATGATAGTTACATTAGCATCCACATCAATGCACAATAGCATTCAATTTTACCATCTACCCCTTTAAATTCTTCATGAACCGGAAGTTGCTGAGACTTTTATTTCAGTATGTTGATGTACTTACAACTGAAACAGAATAATGAGTACGGGGTGAGGCTTTCTTATTGTGCATTCCCTCGTAGTAAAGTAAAGGGGGTCACACATCGAATGCGCTGCTTGGTGCCAGACCGAACTACGCAGCACCATGCATTTGATATTATAAAGATAGATTCCTATCAGTGTATGCACACCAGCGCCACAAGTCAGCGGCTGTCCATGGTGCCCAGCCATGACTTAGGTCACTTTTCATATTTTTGCCATGAATACTATCCTATTAAATAAAGTTCAAATGTGCTCGTCTGGTGTGAAATACTTCCA
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:
sa15298
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 |
---|---|---|---|---|---|
ENSDART00000081550 | Essential Splice Site | 460 | 473 | 8 | 9 |
ENSDART00000081553 | Essential Splice Site | 460 | 488 | 8 | 10 |
The following transcripts of ENSDARG00000058656 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 7561392)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 7541485 |
GRCz11 | 9 | 7519876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCAAGAAAACAGTCCTGATCAAGACCATCGAGACCCGCGATGGCGAGG[T/C]AACACACACAAACACAYACCTGCCAGGGCGATAGTCATATCTTGATGCTG
Long Flanking Sequence:
AAATGCACCAATTGATTTCCATAGTATTTTTTTCCTCCTATGGAAGTCAGTAAGTGGCAGCAAACAGGAATTTTTCAAAATATCTTATTTTGTGTCAAAAAGAAAGAAACTCATAAAGGTTTAAAGCAGCATGAGGGAAAATAAATGAGGTCATTTTCATTGTTTGGGTGAATTATACCTTTAATATTACAGATAGTTGCCCAAAGCTCTTCTCTTATTCCACCACTAGGAGGAGCAAAGCTTTTGTTTTTTTATTCAAACACTTCCTCTGTTTTTGTTTTCTTGTTTCTGAGCAGCTCCTACAAAGATGGCATCAATAATGCAGTGTTTATGTACTTACCATGTGGAGGCTGAGTTTAATGATGCATGTCTGCGAATTGTTTCCACAGAGAGCAGTCCAGAGCAGCACCACCACCAGCAGCAGCAACCACAACGCTCATCTGAAGTCCACTCCAAGAAAACAGTCCTGATCAAGACCATCGAGACCCGCGATGGCGAGG[T/C]AACACACACAAACACACACCTGCCAGGGCGATAGTCATATCTTGATGCTGTTATTGTCATTAAAGGATTGTTCGGCAAATCCTCAAAGAGATCCAAACCTTGAGTTTCTTTTTTTTTTCCGTCAAACACAAAAGAAGATATTTTGAAATAGGTATTGACATCCATAGTGGTAAACAAAAAATAACAGTATACAGAAATCAATAGCTACATATTTCCAATGTTTTCTGAAATGTTTTCTTTTGTGTTAAGCAGTAAACCTGTCTAGACAAAAGGTTTAGAACTCTAAACAATACTACATTTTTGTGCTTGCTCAAACTACTTATTTAAAATAAGTCGAAACAACTCATCTCTTAATGTTTTTTTATGTCTTAATTGTTTTATGTTTAATCTACCTAAATCTGTAAAAATGATTGAGTTTACTTAAAGAGGTGGTGCAGAATGTAATTTTAAGGCTTGGTTGTGTTAGTAAGATGCAAAGCAATGTGTGCTCATGTTTCACT
Associated Phenotype:
Not determined