ZMP

dolk

Ensembl ID:

ENSDARG00000076991

ZFIN ID:

ZDB-GENE-070410-59

Description:

dolichol kinase [Source:RefSeq peptide;Acc:NP_001103954]

Human Orthologue:

DOLK

Human Description:

dolichol kinase [Source:HGNC Symbol;Acc:23406]

Mouse Orthologue:

Dolk

Mouse Description:

dolichol kinase Gene [Source:MGI Symbol;Acc:MGI:2677836]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa12253	Essential Splice Site	Available for shipment	Available now
sa43570	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa12253

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:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112460	Essential Splice Site	None	524	1	2

Genomic Location (Zv9):

Chromosome 21 (position 4797805)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	4375217
GRCz11	21	4539782

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GAATATTTCCCTTTGTTCGAGAATTAAGCGACAAATAAGAGAGAAAYAGG[T/A]AAGAATAATYGTTATWTTGTGCAATGTGACGTTTYAGCGTTTGTTTACTG

Long Flanking Sequence:

TCAAAAGTATATTTCCCAAATATCCCAAGGCTAAATACGATATTTATAAAACTGACACATTATCCAACTACAAATATCAGCGTAGCTCTTTGAGAAGAGCCAAAGTAAGTTTCTCTTTCTTCCATTTTACCTGACACACATCTCCGAGTCCGCCATCTTCACCCGGATCACGTGACCAACACTCTAGAGCACTTTGAGTCACATGACTTGATTAAATCCTAAACACAAACATACTTATATTCTTATGTGAACATATGTGTATATTTAAAATATTAAGTACAAAAAAATATATAGATAATAAAAATACTTACTAAAAACATTTTTGATTTTGGTCACGTGATTATTCTGGCACCACGTGTCCCGGTTGGTTGTCCTACATGGCCGCTCCCACCGTCAGTCAGTCAGAGAGCAGCTGATCGTAAAAAAGCACGAGTCACAGCAAAATATTAGGAATATTTCCCTTTGTTCGAGAATTAAGCGACAAATAAGAGAGAAACAGG[T/A]AAGAATAATCGTTATATTGTGCAATGTGACGTTTCAGCGTTTGTTTACTGTACAGCTTGTTTAATAAAGAGAATGAGCTGTCATTTCAGTTGTGCTGTAAAGCCCATCATCCTCCTTAACAGCAGTAAAAACCCTTTAAAATGACAGAAATCATCAGTATTGCTGTTGGATTAGGATTCTGATTTAATGTTAAGGCTGACATGTAATTCAAATAAACATATAACATCTATGCGATTGTTTATTCATGCATTGTTAAGCTAATGTGCTTGTAAATGATGCATGGTTCCTTTCTAATATAATCTTTTATGTCTAATAATACAACTGTTCGTTAAACCTTCGTATTTTGGTGTAAAATAATTAGTATAAATGTGTAGGTAATTTGAAATGATTTTATAAATAGATTTATTCTGAAAACAAATGTTTTAAATATGGTTTCGTTAAATGTAATATTTTTCTGGGCACTTATTATATAATTTATTAGAGATAATTGTATATTAAAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43570

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:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112460	Nonsense	505	524	2	2

Genomic Location (Zv9):

Chromosome 21 (position 4792292)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	4369704
GRCz11	21	4534269

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACTCGTGGGTGGTGGGATCCATCTCTATGGTGGCCATGTTGGAGGCCTA[T/G]ACGTCGCAGATTGACAACCTTCTGCTTCCTCTGTATCTCTACATCCTCCT

Long Flanking Sequence:

GCTCTGGATCGTCCTTTGCTGCATTTGTCTGCGGTTGTTTGCCTCTCTGCATTTTTGTTTCTCGAATATGTCCGCTATTTTCGCATTCGACCATTCGGGGCTCCGCTTCGACGTCTTCTCACCTTATTCCTTGATGAGAGAGATTCAGGACCACTTATTCTCACTCATATTTATCTTCTTCTTGGCGTTTCTCTTCCACTGTGGTTGACACCTGGGATGTGCACCCCAAAAGGAGGCCTAGGGGGCGCTAGTGGGCTAGTACCCTATGCTGGAGTCCTTGCTGTAGGGGTCGGGGACACAGTGGCATCCGTTTTCGGCAGCAACGTGGGTGAAATCCGCTGGCCTGGGACTAAGAAGACATTTGAGGGCACGGCGTCCTCTGTGTTCGCTCAGATTATCGCTGTGGTGGTTTTCCTCATCGCCGACAGCAGTATTAACCTGAACGCCAGCTACTCGTGGGTGGTGGGATCCATCTCTATGGTGGCCATGTTGGAGGCCTA[T/G]ACGTCGCAGATTGACAACCTTCTGCTTCCTCTGTATCTCTACATCCTCCTGCTGCTATGAGGTCAAAACCACACTCATGCCAATGCACAGACATATTAAATTCATAAACTACGGTACCGCGCTAGTTTTGGACTTCTTTTGGATTTTGAACGAAATATGGGTACTTTATAATAAGGTCCCTGTTTTTAATGTTAGCCGCTACATTACAGAGATTGTTCACCCAAAAATGATAAATGTTTCATCATTAACTCATCCTCCACTTTGAATTTCTTTCTTCTGTTGAACACTGTTCTGTTCCATTGACTTCCATAGTATTTTTTGTTCCTACTATGGATGTTAGATGGCTGCGTATTATCAATGTTTCAGAATATTTATGTTCAACAGGGGCGCAGTAGGTAGTGCTGTCACCTCAAAGCAAGAAGGTCGCTGGATCCCTGGTTCGATCCTCGGCTCAGTTGGCGTTTCTTTGCAGAGTTGGCATGTTCTCCCTGCGTTCGCGT

Associated Phenotype:

Not determined