ZMP

LOC100331354

Ensembl ID:

ENSDARG00000069995

Human Orthologues:

DPY19L1, DPY19L2

Human Descriptions:

dpy-19-like 1 (C. elegans) [Source:HGNC Symbol;Acc:22205]
dpy-19-like 2 (C. elegans) [Source:HGNC Symbol;Acc:19414]

Mouse Orthologues:

Dpy19l1, Dpy19l2

Mouse Descriptions:

dpy-19-like 1 (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:1915685]
dpy-19-like 2 (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2444662]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42798	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa36234	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42798

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000023452	Essential Splice Site	70	730	1	22

Genomic Location (Zv9):

Chromosome 16 (position 45505938)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	42764128
GRCz11	16	42667886

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGTTTGAGCCCCTCCGCTTTTGTAAGAGGAATAACAGTGCTGATTCTCGG[T/A]AAGAATGTCTGCTTTAGCTGCTAGGTAGCTAACGGTTATTTGGTTAGCAT

Long Flanking Sequence:

TTTTATGATTAGGGAATCTGATGATCAGTTTGGGGGGGATTTTATTTACAACGTTTACACCATAGGTTTACCCACTCCACCTTGCAGATTCCTGAAGAGGTTGCCATGGTAAGTGACGCTGCCAGTTGAGTGGCGCGTCCAGACGGGGGCGATGCGATGCCCGCTTCATTCAACAGATCAGCGGTGAAACTGAGCAGAGCCACAGATGAGAGGCGTCTGCGAGAGCCAAACTACTGATTTAACGCTCATCCGCGCCCCTGCTGCCGTCCTGCTACACAGAAATATGAAAACATGGTAGTAAAAACCAGAAAACCAAGTGCCAAGGAGCAGAGCAGCGAGAAAGACAGGAGTCAATCCGTGTCGGGGAAATGCAGGCGCGGAAAAGATGGGAAAGGCTCGGCTTTTCAGAGTAAAAACGGACTCTTTGCTGGGTTTATTAGAAACAGACTGGGTTTGAGCCCCTCCGCTTTTGTAAGAGGAATAACAGTGCTGATTCTCGG[T/A]AAGAATGTCTGCTTTAGCTGCTAGGTAGCTAACGGTTATTTGGTTAGCATCTAGCATGCTTTCAGTGTTTATAGGAGCTCGGATTGTAAACAAAGTTGTGCAAAACCCATATTTCATTTGTTTGGTATGAGATTAAATTGATAAATGTAATTAATGACCTGATTTAATTAATAAACAATAAATTAGAGGTTTAAAACTGTGGTTATTGGGCAATGCTCGGATGTTTATTGTAAGTTTGTTAGCAATCAGTCAAAATTACATCATTTCACTACAGGTATTTGCCATTCATATACTGACAGTTCCTAAGATTTTTTCTTGTCAACTACTTACAGTTTTAAGTATAAAAATTATTTATCAGAATCTTTCATCTGCTTTAAAAGTACAGCTTGTTCCTCTTCAATTGTTTTGGTTGGTCAGATAAAAGTCCCCCAAATGTGGCCACGTAGCAATCTGACTGACCTGCAAATAATTCTCTCAATATGATCTGTTTCTCTTTATAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36234

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000023452	Splice Site, Nonsense	492	730	16	22

Genomic Location (Zv9):

Chromosome 16 (position 45517023)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	42775213
GRCz11	16	42678971

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTTCCTCAGAAATGAGAAGCAAGAAAAGTCAGAGGATGATGAAACGGAG[C/T]AGTGAGTATGTTTTGTTCGGGCTGATCTGCAGCACTTTATTGTCGTGATC

Long Flanking Sequence:

TAGCAGTCTGATCAAATCCAAGTTCACAAGCTACAAAGACTTCGACACGATGATGTACACATGTGCGGCCGAATTTGACTTCATCGAAGCAGATGTGAGTAATGTTTTCCTGCAGCCTATCAACGGTTATTCTCTATTTTTTCATTGTACTTAATGTGTTTGCAGACTCCTATCCGGTACATCAAGACCATGCTGCTTCCAATTAATGTGCTGATAGTGGCTTTTATTGCTGGAAGGGTGAGTTGTTTTCACTTTGATAATGGATGGTTTCCGTCTCCTGTGTCTGGTGCCCTGGTTTTATCTATTTGCCCCCATAGTCAATGTTTACAGTTTTCTGACATTTTGGATAATCTGTTTATTGAAAGGCCACTAAGTAATCTACATATTAAAGTTCTCTTTGTATGCTTCCTCCTTTTGCTTCCTGAGTACAGACCATACAGGACGTCATTGTGTTCCTCAGAAATGAGAAGCAAGAAAAGTCAGAGGATGATGAAACGGAG[C/T]AGTGAGTATGTTTTGTTCGGGCTGATCTGCAGCACTTTATTGTCGTGATCAGGACAGATTCGTGAAATGGTGAAATCTGTGACAAAAGGAAAAATGTCAATATACTTTTTGTATTCTGTCTATATAGTATATAATTTGTCATATTATGTTTTGGGGGCAGTTTTGTTCTCCTAAGCTGCATTTATTTACTTAAAAATACATTACAAATTGTAACATTTAGAAATATTATTGCTTATATTTGTAAGACCCCTAAACATTGGTAGTGTATATCATGTTTCCATTAGACAGTTTGTTTAGATAATTAAGCCTACTGTCTAAACTTTGCCCTTCATTTTTTCAGGTCCCATCTTTTGGCGAAGGGAGTGGTAAGAGTAACTTTTCATGATTTCAACTAAAATGATAATATTTGAATTAAAATTAGTTTATCTATGACCGTGTTTCAATTGTGTGACTATATCTGAATATTTTAACAACTGATGGTTGGGTTTAGGGTTGGGGAG

Associated Phenotype:

Not determined