ZMP
dync2li1
Ensembl ID:
ZFIN ID:
Description:
Cytoplasmic dynein 2 light intermediate chain 1 [Source:UniProtKB/Swiss-Prot;Acc:Q7SXY4]
Human Orthologue:
DYNC2LI1
Human Description:
dynein, cytoplasmic 2, light intermediate chain 1 [Source:HGNC Symbol;Acc:24595]
Mouse Orthologue:
Dync2li1
Mouse Description:
dynein cytoplasmic 2 light intermediate chain 1 Gene [Source:MGI Symbol;Acc:MGI:1913996]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22241 | Nonsense | Available for shipment | Available now |
sa35430 | Nonsense | Available for shipment | Available now |
sa31909 | Essential Splice Site | Available for shipment | Available now |
sa6287 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42151 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22241
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 |
---|---|---|---|---|---|
ENSDART00000058147 | Nonsense | 141 | 358 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10538941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10841270 |
GRCz11 | 13 | 10973745 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTCTAAACCCAATGCGCTCTGGGAGACCATGGAAAGTCTGCTAGGAT[C/A]AGCTCGAAATCAGGTGGAAAAAGTGTGTGCCGCGCTGCAGAAGACAGGAG
Long Flanking Sequence:
TTGGTGGTCTCCAAAATTAAACCAACAATAGACTTGTGCTGAATACATTGTGTCCACCAGTCTCATTGTCTGAGGTTAATAAATATTAAATTAAACAAAAATAAATAACTATAAAAATGATATGGTTGTTAGACTGTTGCATTTTTTGTGTTGTCAATATTCTTGTGTTTATATAGGCTTAAAGTTGTGTGCACAGCGTTTGTATATTTATAACCACCTCAGAGGAATTTGGGGGTCGCGATTCACTGTCAATGTGTTTTTTAGGGGTCGCGAACTGAAAAGTTTGGGAACCCCTGCTCTAGAGGGCTTTTAAAATGATTTACTTTTTCCTATTTCCTTCCTTTTTCCTATTCTATTTCCCTTCAAGTGAAATACATTTGACCTATAGAAGCAAACATTTTTACACTACAATTATTTCTGCAGTTTTTTGTCAGTTGTGCTTGTTTTGGATCTGTCTAAACCCAATGCGCTCTGGGAGACCATGGAAAGTCTGCTAGGAT[C/A]AGCTCGAAATCAGGTGGAAAAAGTGTGTGCCGCGCTGCAGAAGACAGGAGAATCCAGATCTGGCAAACAACGAGTCCCACGAGTCCTCCACAAGGACTATCCGGTACAGAGGATTACACCATTTCTTTAAATCAAGTGTGTTTGTGTTGCAGAGAATTACCTGAAACAATCTCTCTTCAACAGGACCGAGAGCTCATCAGCCCTTTCCCTGTTCCTCTGCTCATAGTTGGGAGCAAGTTTGACATTTTTCAGGTAAAACTTCACTGACATGTTCATAGTAGTATGTACAGTGTGGTGATGTCTGTGCTATGCTCCATTTTTAAACAGGCAATGTCAGAGCCTACATGCCTGCTACATTGTTACAGTGTAGAACAGGGGTCACCAACATGATGCCTGTGGGCACCAGGTAGCCCGCGAGGATCACATGTGTTGCCCACGGGCCTGTTCTAAAAATAGCTCACCATAGCGCCACTTACCAGTAAGCTTCATCTAATACAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35430
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058147 | Nonsense | 168 | 358 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10539021)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10841350 |
GRCz11 | 13 | 10973825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCGCTGCAGAAGACAGGAGAATCCAGATCTGGCAAACAACGAGTCCCA[C/T]GAGTCCTCCACAAGGACTATCCGGTACAGAGGATTACACCATTTCTTTAA
Long Flanking Sequence:
AAATATTAAATTAAACAAAAATAAATAACTATAAAAATGATATGGTTGTTAGACTGTTGCATTTTTTGTGTTGTCAATATTCTTGTGTTTATATAGGCTTAAAGTTGTGTGCACAGCGTTTGTATATTTATAACCACCTCAGAGGAATTTGGGGGTCGCGATTCACTGTCAATGTGTTTTTTAGGGGTCGCGAACTGAAAAGTTTGGGAACCCCTGCTCTAGAGGGCTTTTAAAATGATTTACTTTTTCCTATTTCCTTCCTTTTTCCTATTCTATTTCCCTTCAAGTGAAATACATTTGACCTATAGAAGCAAACATTTTTACACTACAATTATTTCTGCAGTTTTTTGTCAGTTGTGCTTGTTTTGGATCTGTCTAAACCCAATGCGCTCTGGGAGACCATGGAAAGTCTGCTAGGATCAGCTCGAAATCAGGTGGAAAAAGTGTGTGCCGCGCTGCAGAAGACAGGAGAATCCAGATCTGGCAAACAACGAGTCCCA[C/T]GAGTCCTCCACAAGGACTATCCGGTACAGAGGATTACACCATTTCTTTAAATCAAGTGTGTTTGTGTTGCAGAGAATTACCTGAAACAATCTCTCTTCAACAGGACCGAGAGCTCATCAGCCCTTTCCCTGTTCCTCTGCTCATAGTTGGGAGCAAGTTTGACATTTTTCAGGTAAAACTTCACTGACATGTTCATAGTAGTATGTACAGTGTGGTGATGTCTGTGCTATGCTCCATTTTTAAACAGGCAATGTCAGAGCCTACATGCCTGCTACATTGTTACAGTGTAGAACAGGGGTCACCAACATGATGCCTGTGGGCACCAGGTAGCCCGCGAGGATCACATGTGTTGCCCACGGGCCTGTTCTAAAAATAGCTCACCATAGCGCCACTTACCAGTAAGCTTCATCTAATACAGAAGTAATCATTTAAAAATGTAAATATTTGCAGAGATATTTAAAAATAAAGTGTTGCACATTGATACATTAAATGCAGGGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31909
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 |
---|---|---|---|---|---|
ENSDART00000058147 | Essential Splice Site | 198 | 358 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10539194)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10841523 |
GRCz11 | 13 | 10973998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCCCTGTTCCTCTGCTCATAGTTGGGAGCAAGTTTGACATTTTTCAG[G/A]TAAAACTTCACTGACATGTTCATAGTAGTATGTACAGTGTGGTGATGTCT
Long Flanking Sequence:
GTGTTTTTTAGGGGTCGCGAACTGAAAAGTTTGGGAACCCCTGCTCTAGAGGGCTTTTAAAATGATTTACTTTTTCCTATTTCCTTCCTTTTTCCTATTCTATTTCCCTTCAAGTGAAATACATTTGACCTATAGAAGCAAACATTTTTACACTACAATTATTTCTGCAGTTTTTTGTCAGTTGTGCTTGTTTTGGATCTGTCTAAACCCAATGCGCTCTGGGAGACCATGGAAAGTCTGCTAGGATCAGCTCGAAATCAGGTGGAAAAAGTGTGTGCCGCGCTGCAGAAGACAGGAGAATCCAGATCTGGCAAACAACGAGTCCCACGAGTCCTCCACAAGGACTATCCGGTACAGAGGATTACACCATTTCTTTAAATCAAGTGTGTTTGTGTTGCAGAGAATTACCTGAAACAATCTCTCTTCAACAGGACCGAGAGCTCATCAGCCCTTTCCCTGTTCCTCTGCTCATAGTTGGGAGCAAGTTTGACATTTTTCAG[G/A]TAAAACTTCACTGACATGTTCATAGTAGTATGTACAGTGTGGTGATGTCTGTGCTATGCTCCATTTTTAAACAGGCAATGTCAGAGCCTACATGCCTGCTACATTGTTACAGTGTAGAACAGGGGTCACCAACATGATGCCTGTGGGCACCAGGTAGCCCGCGAGGATCACATGTGTTGCCCACGGGCCTGTTCTAAAAATAGCTCACCATAGCGCCACTTACCAGTAAGCTTCATCTAATACAGAAGTAATCATTTAAAAATGTAAATATTTGCAGAGATATTTAAAAATAAAGTGTTGCACATTGATACATTAAATGCAGGGTATTTCCTACCCTGTTAAATCATTGTTGATAACTTTTGTGAGAATCATTAACATGATCAGTGTCTTCGCATGGATGAATATCATTATTTATTACCAAAAACATAAAGTATAATTAAAAGTAAATTGAGCAAATTTGTTATTTGAGAAGTGTTTATCAAACTGGTAGCCCTCCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6287
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058147 | Essential Splice Site | 275 | 358 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10541639)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10843968 |
GRCz11 | 13 | 10976443 |
KASP Assay ID:
554-4771.1 (used for ordering genotyping assays)
KASP Sequence:
AGTAAACCTCTGGCTAKTCCAGCAGGATCAGACTCYCTRAGTCAAATCGG[T/A]AAGATACGTATKTTTTTGTTAAAGACAAACTAACTTTTATGCTTTTCAAA
Long Flanking Sequence:
TAGGACTTTGATTCAGAGAAGAGGAAGGTGATTTGTAGGACTCTACGCTTCTTAGCCCACTTCTATGGAGCATCACTAATCGTAAGACTAAACTTATACTAAGAATTGTATACATTTTTTTTTTTAAAACAGTGATCACGGATTATAATTTTCAGATTTCTTTTCAGAAAAAAAAACAGGTGATCAGTTTTTTTATAGATGCTTTCTGTCTCTTCAAAGTTTACCAGCAGCAAGTCAGAAACCACAATGTCTAAAAGCAGGAGTTTTATTAATCAGCTGGCATTTGGGACTGAAAGACCGTAAGTCTAAATATACTTAATTTGTGAGGTTTTGTTATTATTTATTTTATATTAATTAGTTTCATTCAATTTCAGTTAATCTTCTAATCTTACAAAGACAGTAAAAGGCCTTCTCTTCTATTCTGTTAGAAAATCAATCTCTACAGACCCCAGTAAACCTCTGGCTATTCCAGCAGGATCAGACTCTCTAAGTCAAATCGG[T/A]AAGATACGTATGTTTTTGTTAAAGACAAACTAACTTTTATGCTTTTCAAAACAGTTTGATATTCAAGTTGTGGATCGATAAGATTTTGAATGCTCAACAAGAATACATTTATATTAAAAAAATGTATAATAACGGTATGTTTGAGAAATAGTATTACAGTTTATAACAGCTGGTTACAAATATCTTAAAATGTAATTTTTTCCTGGGTCAGCAAGAGCTGCATTTTACTCCAGTCTTGAGTGTCACATGATTCTTCAGATATTATGATAATATTAAAGTTTATTTTGATAAATGTTGTGTTGATTTGATTTAATTTTAATTGATTAATTTAAATTTAATTCATTTAAATTGTTTGATGAATAAAATATTAAAAAGATTGTTTAATTATATATTTAACATCAACAAGTGTTTTTACACTCAATTAATCAGTGCATCCTTGCTGAATATAAGAAAGAATTTTTACAGAATTTCTTTAAAAATGTGCTGATGCCAAACTCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42151
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058147 | Essential Splice Site | 308 | 358 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 13 (position 10543867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 10846196 |
GRCz11 | 13 | 10978671 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGACAACCTTATAATAAATGTTCATCTGACCCTCCTATTTATTTTTTC[A/T]GAGCACAAGGGAGCGTAAAGAGCTGAAAGACCCTGTCAAAGACCCTCAGT
Long Flanking Sequence:
CAGTATTTATAAACTGCTGATTAACGTCTATTAATTATTAAGAGTTAAATTCTTAACAAATGATGAATTAACTATTTGCTAATGCTTAATAAATGATTCATGTTCTGCATTTACTGTAGTATTACCCAATTTTATAATTTTACACTACCTTTTTCACATTAAAATGGTGAATTCAAATCTTTAATAACATTTTTAAAATCTAATAATCAATATAAGAATATAATCAATAAAACTCCTATACTGCAAGTGCATTAAACCTACAGTAGCTTAATTCACATCCATAATCACAATCTCATGCTGTAAATATTTCATTGGTTGATCCTCCAGGTCCTCCTGTTGCCACTGAGGTTGATATCGGGACTCTACATGCCAAAAACCCCTTTGACCTCTGGAAGAAGGTTTTTGAAAAAGTTTTCCCACATGAGGTACTTCTTGATATGTAAACAAAACACAGACAACCTTATAATAAATGTTCATCTGACCCTCCTATTTATTTTTTC[A/T]GAGCACAAGGGAGCGTAAAGAGCTGAAAGACCCTGTCAAAGACCCTCAGTTCAGCGAGCCGCTTATAGACTCTATCAGAGCACAGAAAGACCAGGTACGAGACACATTTACAGTCTGTCTTCACATTATTTGACTTCTAGTAACCTCTTGTCATAAGTGTTTATATTACCCTTCATTACAGCTGACTCAGAGTCATATACTTTACTGATCCTCCAGACTGATACATGTCCTGCTTTACTGTATGTGACTGCAAGTTACCCTGATCTCACAGCCAGTGCCCTTTAGTTACCTCTCACCCACACCGATTTTCCACTCATACTTCTTTAATTGCAATTATCAATCAGTATATTTATAAAACAAAATAATTTTAATCAGCATTTCCTAGTTTTTATCATCATAAACATGCTTCATCTGAAGTTTATAGCATGTGTATACTGTAGTTAGTAAGTATGCCAAATCTATTGAAATTTAAGATTGAGATTGTGTTTTTCTCTAGATTT
Associated Phenotype:
Not determined