ZMP

wu:fc07e02

Ensembl ID:

ENSDARG00000078473

ZFIN IDs:

ZDB-GENE-030131-2424, ZDB-GENE-040912-175

Description:

nuclear ubiquitous casein and cyclin-dependent kinases substrate [Source:RefSeq peptide;Acc:NP_0010

Human Orthologue:

NUCKS1

Human Description:

nuclear casein kinase and cyclin-dependent kinase substrate 1 [Source:HGNC Symbol;Acc:29923]

Mouse Orthologue:

Nucks1

Mouse Description:

nuclear casein kinase and cyclin-dependent kinase substrate 1 Gene [Source:MGI Symbol;Acc:MGI:193481

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41902	Nonsense	Mutation detected in F1 DNA	Not yet available
sa45440	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa41902

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000102858	Nonsense	173	305	6	8

Genomic Location (Zv9):

Chromosome 11 (position 39780319)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	38278575
GRCz11	11	38545780

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGGCAGTGAGGATGAGGAGAAGGATGAGGAAGAACAGGCCTTCCTGGAC[C/T]GTAAGTGTCATCATCATTATCTTTTATAAAATTCCTCATTGTTGAAGCTT

Long Flanking Sequence:

ATATAGGTCTTAAATTGAATACTTGATGGTCTTAAAACATCTTAAATTTGACATTACGATATCAGCAGAAACCCTGTATAGTGTGTTTAACCATACTGACAGTTGGCACCTCCAATAGAGATGGAGATGATGCACAATCAGCTAAAATGTTGCTTGAATTGCTTTTTGTGTATGGACTATATATATTGCAACATCATAAATGATTGAGGTCATGTCCATGTGTTGTGTGGTAAGTCCATATATTAATTATTCTCACAGGCCTATTTGGAATAGGTGTAGAAACGCACAACTAAATGAGAATAAATGATGTATTTGTGTGTGTTTTTGACAATTGTGTGTCCTCTGCAGATGATAGTGATGATGATAAAGAGGTGAGCAGGAAACCGAGGCAGGTGAGACAGGCTGCGTCAAAGGCTGTGTCCAAACAGAGAGAAATCCTGCTGGGAGACGGAGGCAGTGAGGATGAGGAGAAGGATGAGGAAGAACAGGCCTTCCTGGAC[C/T]GTAAGTGTCATCATCATTATCTTTTATAAAATTCCTCATTGTTGAAGCTTGTGGGGAAGAAAGTCTTTTTGTTTTTATGTAAATTAAATCTTGAGGCATTTAAGGGTGCACTAGTCTGTCCAAATTGTGCCCAGGTGCGTTTCCCGGTTTGACCAAGTGTAATGCTGTGTTCACACCATATGCGGAAGGTGCGTCAAGCACAAGTGATTTACTGTTAAGTCAATGCAAATTCAATGCGCGAATTGCACGTTTTGCGCAAATCACTCAAGTTTTAAAATCTGAACTTAAGCGGATATTCGCCCCGCCTTAACCAATCAGGAGTTTGCTCTTGTGGGAGCGTAATTGTGACGAGGGCCTGTTGTTGGTGTCCCAGGGGAAATCCTCAAGCTGACGCCTACAACAGTTCATCAAACTGGGCTCGGCTCAGTCAGAAGCACCGCTGAAAGCCTCCGTCATTCAGGTTAAGTTTCTGGAGGAGTTTGAGCTCACAGAGCTGGATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa45440

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000102858	Essential Splice Site	226	305	7	8

Genomic Location (Zv9):

Chromosome 11 (position 39777125)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	38275381
GRCz11	11	38542586

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGGAGAAGAAGGAGAAGAAATCCCCCAAACCCCGGCTAAAGGCTACAGG[T/C]AAGCAATAGCACTCTTGAATATTTAGGATTTGGGAAAATAAAGGGCAGAT

Long Flanking Sequence:

CAACTGTATTTTCATTAACTAACATTAACTTGCATGAACAAATATGTAATGTATTGTTCATGATAGTAATGCATTACTAATACAACCTTACTGTAAAGTGTTTCTCTAAATTGTATATGAGAGATGTGTGTGTGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCACTGCGTAAAAACCTGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGGGACCCTGGATTAATAAATTGACTAAGCCGACAAGAAAATGAATGAATGAATATGAGAGAAGCTGTGAATTTCCAAGTGGTCTCTCTTAAAATGTGAATCTTCAATTTTTTTTTGGTGCTGCAGAAGAGTCAGGCAGTGATGAAGACTTCATGGTTGATGATGATGATGACAGCGATTATGGCCACTCCAAAAAGAAGGGCAAAAAAGTGGTGCCAAGAGGTGGAGGACGGAGAGTGGAGAAGAAGGAGAAGAAATCCCCCAAACCCCGGCTAAAGGCTACAGG[T/C]AAGCAATAGCACTCTTGAATATTTAGGATTTGGGAAAATAAAGGGCAGATATGATAAATAGTATCTAATTCTTAATTAAATAATCAGTTAAAACAACATGTGTGCATGTTTTTCTGTTCTAAAATATAGCAAATATGAACGTAAAAGTTTTGAACAGTAGTGCTAACATGTCTGTTTGTCCCTCAGTGAACCCCAGCCCTATGAAAGGCAAAGGTAAAGGGCGCCCGAGCGCAGCTAAAGCGCTGGAGAAATCCTCGCCTAAAGATGAAGAGGAAGCCGAGAGTCCCGCTGAAGATGAAGAGGAAGACGAGGTGGAGAAGAAAGAGTCTCCTCCATCCAAAAAGACGAAGGATGAAGCCCCCGAAGACGAGGAAGAAGATGAAGAAGAGGACGGCTCAGAAGAGGAGGCTCCATCCGGGGAAGACTAGCCATGCTAATAACAGCGGCCCTTTCTTCTCTTTCCCTTTACACTCTCTTCTCCCCTTCTCTGCTTTTATTTC

Associated Phenotype:

Not determined