ZMP

lipin2

Ensembl ID:

ENSDARG00000061214

ZFIN ID:

ZDB-GENE-060503-153

Description:

LOC558422 protein [Source:UniProtKB/TrEMBL;Acc:A8WGB6]

Human Orthologue:

LPIN2

Human Description:

lipin 2 [Source:HGNC Symbol;Acc:14450]

Mouse Orthologue:

Lpin2

Mouse Description:

lipin 2 Gene [Source:MGI Symbol;Acc:MGI:1891341]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18199	Nonsense	Available for shipment	Available now
sa44534	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18199

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000085242	Nonsense	116	904	3	19
ENSDART00000141575	Nonsense	116	905	4	20

Genomic Location (Zv9):

Chromosome 2 (position 30686423)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	30988058
GRCz11	2	30971591

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCAGCACACCTGGCCACCTCCCCCATTCCCACAGAGAGTCACTTATTTTG[G/A]ATCGGAGGCGAWCATAGGTCAAGKCAAAACCTGGACRATGAYCCACTTGA

Long Flanking Sequence:

ATAAAATTGAACATTTCAAAGGTCAGCCATTTGATTTAGAATCAAGGTGTCAGATAATTATACAAGCACAGGTCTGAAGTTAATACATTGGAGTGTAACATTAAAAAGTTTGAGGTGCCTTTCACATTACCACTGTGTTTTAAAATAATCCTCTTCAACTCCTTCAGATTGACATAGAGATCAACGGGGAGCCTGTGGATCTCCACATGAAGCTGGGAGATAATGGAGAAGCTTTCTTTGTACAGGAAACCGAGGAGCAGAATGTAAGTGACTTCTATTCCACATTTGCTGCTGGTTCTGTCACTCACATTAATGACTACTGATCATCCACAGTTTGCAATATGAAAATGACATTATGTTGGAAACTTATTTGCATTGCAAAGGCTGTCATGCTTTAATGGTCTTTTTAATGGTTTTTTATTCTCCTTCTCTTTTTTGTAGGAGATTGTACCAGCACACCTGGCCACCTCCCCCATTCCCACAGAGAGTCACTTATTTTG[G/A]ATCGGAGGCGATCATAGGTCAAGTCAAAACCTGGACGATGACCCACTTGATCCAGAGGACCCTCCTGATCGACCAGTTGCCAGCACAGGGGGAGCCAAGAAGAAGAAGAAACGGAGAAAGAAGCATAAAGGTGATCCCCGGCGAGAGGAGTTCACCCCCCCTGCCGTTATCAGCTCTACCCCTTCCACAGATGAAATATTTGAGATGGACCTGAGTTCTGATGAAGACGCTATTTCCAACACTAGGTAACCAATCCAACATATGAATGCATGTTAGACATACTGAAGGAGTGGACAATGTTTTTAGTGACTCGAAAAATCTGTCTTTCAGATCATCTTCAGTCAGTACAGTTAAAGAAAGTGAACCCAAATTACCAACAATTCGACATTCTTTGGACAGCTACCCTTACTCTGACGGAGACTGGTCTCCATCAGATAGGTTTGTTTATACTTGCAATCTCATACACACAGTTTAAAATATGCTTTTGGGCCATATCAGAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44534

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000085242	Essential Splice Site	276	904	5	19
ENSDART00000141575	Essential Splice Site	277	905	6	20

Genomic Location (Zv9):

Chromosome 2 (position 30687158)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	30988793
GRCz11	2	30972326

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGGAGTCACACATGCAATGGACATGGGGAGAGTTTCCAGAATCTACAAGG[G/A]TAAATTGTAGTTTTGGTTTTCTTTAAATTCGTTCTGCAGTTGTTTTCCCA

Long Flanking Sequence:

TCCAACACTAGGTAACCAATCCAACATATGAATGCATGTTAGACATACTGAAGGAGTGGACAATGTTTTTAGTGACTCGAAAAATCTGTCTTTCAGATCATCTTCAGTCAGTACAGTTAAAGAAAGTGAACCCAAATTACCAACAATTCGACATTCTTTGGACAGCTACCCTTACTCTGACGGAGACTGGTCTCCATCAGATAGGTTTGTTTATACTTGCAATCTCATACACACAGTTTAAAATATGCTTTTGGGCCATATCAGATTGAAAGGTTTGTAAAAGGTTCAAAGGCTTTGAGTGTACTTTACTTTCACTTTCTTTTATTTAATTTGAGTTAACGGGAGTTGCTGTTTGTTGTTCTATTTTGAGCAGTCATGCTATGTCAGAGGCCTTTTCTCCCAAGAGTGACTCTGAACTGGTTGTTCGGCCCTCAGAGAGCCTTCTCAAAATGGAGTCACACATGCAATGGACATGGGGAGAGTTTCCAGAATCTACAAGG[G/A]TAAATTGTAGTTTTGGTTTTCTTTAAATTCGTTCTGCAGTTGTTTTCCCAAACATAGGTTTCAACTTTAATTCCTGGAGGGACGCAGCTCCGCACAGTTTTGCTCTAACCCTAATTAAATACAGCTAATCTAGTAGTTTCTAGTAGTCTCGAACACCTTGATTAGTTGGATCAGCTGTGTTTACTTAGGGTTGGAGCAAAACTGTGCAGAGCTGTGGCCCTCCAGGAATTGAGTGTAAGACCTATGCTTTAAGGCAATTCAATTCACTCGGCCCCCATCTTGGACAATATGCTCGGGCATTCTGTCTGAATGGGGAAACAACAAATTCTACAAAATTGCTTTCCAAGCTTACTATTAAATTTCATGTTAGGAAGCACCAATAAAATAAAAAAATAACTGTCTTTTTAGTGTAATTTCTATTTTTTCCTAATTGGGGATGCTCCGATCAATCGGCCGATTATCACATTTCATTACTTGATTGGTACTCGTGAATCTGGGCG

Associated Phenotype:

Not determined