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