Busch Lab

ZMP

zgc:92542

Ensembl ID:
ENSDARG00000034042
ZFIN ID:
ZDB-GENE-040801-178
Description:
Dynein light chain 1, axonemal [Source:UniProtKB/Swiss-Prot;Acc:Q6DHB1]
Human Orthologue:
DNAL1
Human Description:
dynein, axonemal, light chain 1 [Source:HGNC Symbol;Acc:23247]
Mouse Orthologue:
Dnalc1
Mouse Description:
dynein, axonemal, light chain 1 Gene [Source:MGI Symbol;Acc:MGI:1921462]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa12375 Essential Splice Site Available for shipment Available now
sa39169 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12375
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000043651 Essential Splice Site 51 192 4 8
ENSDART00000125251 Essential Splice Site 74 215 4 8
Genomic Location (Zv9):
Chromosome 17 (position 33919100)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 33760831
GRCz11 17 33713342
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GWGTCAGAKATAATARCTCACTRTTACATCTTTMTTGTACTGWCCTTTCC[A/G]GGAGATTGTCCTTGTCTACAAACTGCATWGAAAAAATTGCCAACTTAAAT
Long Flanking Sequence:
CAAACTTCATTTTTGCCACGACTTGGGCAAAACATTGCTTCACTTTGTTGTGAGTGACTAGTCACATGTCTGTTGTTTGTGTTTTCAGGCAAAAGCAACAACTATTAAAGAGGCCCTGGTGAAATGGGTAAAACATTTTTTGCCAATTTAGTTTATTGATTAACTTTTCCAAATTTTAAACATTACTTGAGTAAAATGTATGATCTGATTTGTGTTAGTTTAGGAATTATATATAATGATTTTAAATATTTTACTTGTTTTTTTTTTTTTAAATACTAGGAGGAAAAAACTGGTGAAAAAGCAAATGATGCCACGGCAGTAAAGCTTTATGGTCAAATCCCTCCCATTGAAAAAATGGATGCATCTCTCTCTAATCTTGTCAACTGCGAGTAAGTCTAAATATTCATCTCTAATTTTTGTGTGTATTGTCTTATACACCAGCTACCATGTGAGTCAGATATAATAACTCACTGTTACATCTTTATTGTACTGTCCTTTCC[A/G]GGAGATTGTCCTTGTCTACAAACTGCATTGAAAAAATTGCCAACTTAAATGGTCTAAGTAAGTACACCTTTCAAGAGCATAACTTATGTGCATTTCTGATCCCTGAATATTATGTTTCTATTTTTCTCTTAGAAAACCTTAAGATATTGTCCTTGGGGCGGAATAACATCAAAAACCTCAATGGACTCGTAAGTAAAGTAAAAGAACATTAAAACATATGAGAGGCCTTTACACAACATATTTTCATCTATTTTTTTTTTCTTTTTGTTTTTGCGATTTGGCCAATAATTTACATGGCAGTAGGGCCTGAAAAAATAAACTTTTAAAAATAATACCACTATTATCTCCATGAAAGCTTCAAAAATATTTGTTTTGAAAACGTTGACATCTTATGCATGTGCATTACATGTTCTATGGCAAGGCAATAAAAAAGATGTCTCAATAAATTTTTTTGTTTGTGCTTTTGTGCACGTGTGTGTGCAAGTGGTCAATTGAATTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39169
Status:
Mutation detected in F1 DNA
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
ENSDART00000043651 Essential Splice Site 177 192 7 8
ENSDART00000125251 Essential Splice Site 200 215 7 8
Genomic Location (Zv9):
Chromosome 17 (position 33917272)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 33759003
GRCz11 17 33711514
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGATAGAGGAGGCTACAAAGAGACTTCCCAAACTCAAAAAGCTAGATG[G/T]TAAATAGCATATTTAACCCTCTATCTGCTCTTTGATTGTTTTACCTTTTT
Long Flanking Sequence:
AAATAGTGCTTTTTATTTTTTCACTTACTTTTCAAGGGATGTTTTATGATTTCATTGTTTATTAAGACAGTGCAATGTCAGATAATTCCATTATCATGCAGCCCTAACATACACTACCCTAAAAGCTAGAAATCAACTTCAGAATGTCTTCTGTTGTCATAGGAGGCAGTGGGTGATACTCTGGAGGAGCTGTGGATCTCTTATAACCTCATAGAAAAACTGAAGGGAATTCATGTCATGAAGAAACTTAAAGTCTTATACATGTCCAACAACTTGGTGAAGGAGTGGGGTGAGTCTAATAGCAGCTTTAATCACGTTGCTTTAGAGATGAACATTTATGAAGCTGTTTGTTTCTTTAGGGGAGTTTCTGAAACTGGCAGATCTTCCATCACTGGTTGACCTTGTCTTTGTGGGAAACCCATTAGAAGAAAAATATTCTGCAGATGGCAACTGGATAGAGGAGGCTACAAAGAGACTTCCCAAACTCAAAAAGCTAGATG[G/T]TAAATAGCATATTTAACCCTCTATCTGCTCTTTGATTGTTTTACCTTTTTTTACTTATCAAAAATCTTGCAAAATTTGGTTATGGCTATGTGAATATGGTGCATGTATATTTACAATATGGTAAGTAATACTGCAAAAACAATAATGTGTATGATTCAGAAAGATTAAATGTTTTATATGTGTTTACTTGTAGTCCAAAATGACCAAAAAAGTTAACCAATTGAATCTAGTGATTGTTTGGTACTGTGCCCAAACAGATTGCAACTTAATGGGCACATAGTTTAACTCTTTTTGTTATGATTTAATATTAATATTATGATTCTTCTGAGTGTGCCAGTTTAGGTTCAGGTCAAATCACATTTCAGATTTTTTTTATTATAATGTGTTAAAAAGTTTCATTTAGGGAGTGTGTACACAGCTCGCTGTTTTAGGGGCGTGTTGCGTCACATGAAAATCAGTTTCAAATTCCCGCCCAACGTAACAAGGCTCTGCCCTGCTCT
Associated Phenotype:
Not determined