ZMP

LPHN2 (4 of 4)

Ensembl ID:

ENSDARG00000087965

Description:

latrophilin 2 [Source:HGNC Symbol;Acc:18582]

Human Orthologue:

LPHN2

Human Description:

latrophilin 2 [Source:HGNC Symbol;Acc:18582]

Mouse Orthologue:

Lphn2

Mouse Description:

latrophilin 2 Gene [Source:MGI Symbol;Acc:MGI:2139714]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa19648	Nonsense	Available for shipment	Available now
sa5119	Essential Splice Site	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa19648

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

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000129221	Nonsense	79	564	2	11

Genomic Location (Zv9):

Chromosome 2 (position 1644796)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	1503979
GRCz11	2	1846661

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTGGACACACTAGAGGAAGGAGCGTTTGTGCTGGCGGACAACCTGATC[G/T]AGCCGGCGGTGGTGCGCATGCCTGCAGAAAACATCAGTGAGTCTGAACTA

Long Flanking Sequence:

ACAAACCACCTGTGGAACACACCCTCTTTCATCTCTCTAACACTTTTTCAGACACTTGCATTTGACACTTTCTCAATGTCTCTGAAAATAAAACAGATGAGTGGGCTTGACAAACCACCTGTAGACAAAAGTATCTACTAAAAGACTGAATGTGATGTCATTTGAATCTAATTTGGACTAGAAACAAGACAAAAACTCAATCATATTTGCACCAATGACCGCGTGGTTCTCCATCATGGCTGTTTTCTCATTGACTTCTCCATGTGTTGCCTGCATTTCTACATGTTTTTTCTTGGGAAAGGAAAGGCAAAAATGGTCTCGTCGGTGATTGGAGTTTGTTTTCTTCATTTCAGGCCATCGTGGACACAGTTGACAACCTGCTAAGGCCAGAAGCGCTCAAATCCTGGGAAGACATGAACTCGACGGAGCAAACTCACGCTGCCACCATGCTGCTGGACACACTAGAGGAAGGAGCGTTTGTGCTGGCGGACAACCTGATC[G/T]AGCCGGCGGTGGTGCGCATGCCTGCAGAAAACATCAGTGAGTCTGAACTACATTATTTGGCCACAATCTTCTCTGTGTTTTTGCAAATGGAGGGATTTTTGGTGACAAGCCTTACACATATAATCTTATGACACATATTCTGGGAAAATGCTTTCAAAAACAATATACTCTGGGCAAATTGACTCCTCTTTGGTGTCTGTTTTTGACCCATTGACTTCCATTATAATCTCACATTTTTTCATTGCAAAGCCATGCCAGCATATAATCATGCATTCTTCATTGTTGCTGGTTTTCCCTGTTGGAGGGAAAGGGTAGCATTTGTAATGTTTACTGTTTAGTTTTAATGCCACCAAATAAAAATTGTGCTAAATATGCCTGACAATTTTTTTTCTGGTATTTACACTATTTTTGACTAAATGATATTTTAACGTCTAATAATAATAATAAATAATAATAACACTGACATTATTGTTAATAATAATGGCAAATATAATAATAAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa5119

Status:

F2 line generated
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
ENSDART00000129221	Essential Splice Site	403	564	7	11

Genomic Location (Zv9):

Chromosome 2 (position 1666425)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	1525608
GRCz11	2	1868290

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGGGCATTTCAGCTGCCATCGACTACAAGAGCTACGGGACCAAAAAAGCG[T/C]GAGTAATGTTTGTGTTCCCATCAACATATTGAGCTGCGGTTTAATATCTT

Long Flanking Sequence:

ATCGCCGTTTCTCTTGTCTGCCTAGCCATTAGCATCTTCACCTTCTGCTTCTTCCGTGGCCTTCAGAGTGACCGCAACACAATCCACAAAAACCTCTGCATCAACCTCTTCATAGCAGAGCTGCTCTTTCTGGTGGGCATCAACATGACCGAGCCTCCGGTGGGTACTCTTTTATTTTAATTAATTTTAGTTTTTTTTTTTTGGATCAATGAAGTTCTTCTAAAGAAAATCTGCACTTGTTTGGAAGGCTGAACTCCTCCGGTTTCTTTTGCGTTCAGATTGTGTGCTCGGTGATTGCTGGAGTCCTGCATTTCTTCTTCCTCGCTGCATTTTCCTGGATGTGTTTGGAGGGCGTTCAGCTGTTCCTCATGCTCGTGGAGGTCTTTGAGAGCGAATTCTCCAGACGCAAATACTATTACGCATCAGGCTACCTGTTCCCCTGTGTGGTGGTGGGCATTTCAGCTGCCATCGACTACAAGAGCTACGGGACCAAAAAAGCG[T/C]GAGTAATGTTTGTGTTCCCATCAACATATTGAGCTGCGGTTTAATATCTTGCACGGGTAGTTCATCCAAAAATGAAGTACACTCTCCATCGTGTGGATTATGAATTGAATTTCTTTCCTCTGTCCAGATGGTTAGGACACAAACATTCCTTTTAACATGGAAAAGATGGACATGGTGTTACTTTGTATGTTGAAAAAGAAATTGTATTCATTTTTGGAAATCCTTAGGGGGTAGTTCACCCAAAAGTGACTATTTACTCACGCTCAAGTGGTTCCGATTTGTTTAGAAGTTTCTTTTTTCTATTGAATACAAAAGAAGATATTTTGAAGAATGTTGGACACCTATAACCATTGACTTCTTTAGTGGAAAAAACTAATGCTATGGAAGTCAGGGGTTTTCGGCTAAACAGGAACTGTAATAAGTAATCAAAACAATAAGTTTAAGGAACAGTAAGTGCAAGATGACAGATTTTTTAATTTTGGGGGGGTTTATCGCATGTT

Associated Phenotype:

Not determined