ZMP

lhcgr

Ensembl ID:

ENSDARG00000026081

ZFIN ID:

ZDB-GENE-040806-3

Description:

lutropin-choriogonadotropic hormone receptor [Source:RefSeq peptide;Acc:NP_991188]

Human Orthologue:

LHCGR

Human Description:

luteinizing hormone/choriogonadotropin receptor [Source:HGNC Symbol;Acc:6585]

Mouse Orthologue:

Lhcgr

Mouse Description:

luteinizing hormone/choriogonadotropin receptor Gene [Source:MGI Symbol;Acc:MGI:96783]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22377	Nonsense	Available for shipment	Available now
sa35588	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22377

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
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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000097459	Nonsense	54	708	2	11

Genomic Location (Zv9):

Chromosome 13 (position 48049153)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	47300139
GRCz11	13	47589964

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTATGCAGCCTAATTATTAATATATCTTGTGATTTCAGAGTTTTGAACTA[C/A]ATCTCAGTGAAGACCATCAGCAGCCGGAGTTTCGACGGCCTGAAAGGAGT

Long Flanking Sequence:

TCACAAGGTTTTAAAGTGCTAAAGGAGTGGAGGTCAGCTGTCTGTTCCCTGAAAAAGTTAGTCCTTGCTGGACAAGCTTTTATCTGTTCCCTCTCTGTGTGACATTAAACTTCCTTGAGGCTTATCACACTTTTTTAAAAGCTTTATAAGATACACATCTGCTCACGTGCCTTATATTTAATACTAATTTCCCACTGAATAACAAAGATTTGGAGTTTCTTCTCTTTTTGTCCTAAATGCGTGACATATTTTTAAGCTTTGTTAAGAAATGTGGGGGTGACACGGTGGCTCAGTGGGTATTACTGTCGCCTTACATCAAGAAGGTCACTAGTTCGAGTCCCAGCTGGACCATTTGGCATTTCTGTGTGGAGCTTGCATATTCTCACTGTGTTTGTATGTTTGTGACTATTGCAGATGGGCACATTGCGATATCGATGCTGTAACCGTATATTATGCAGCCTAATTATTAATATATCTTGTGATTTCAGAGTTTTGAACTA[C/A]ATCTCAGTGAAGACCATCAGCAGCCGGAGTTTCGACGGCCTGAAAGGAGTAAGAAGAATGTGAGTAGTCATTGTTTTTTACAACATTACGCCATATAACCAGATGTTTAGCGAGTCCACTGAAGGGAACGCATCCATCCGTCCATCATCACTCCTCTCTGAGCCAGCAGGTTTACAGGGAAAAAGATTTGCAGAGAAAACTCTTTGATGTTCACTCCCTTTTTCAGGACGCACTGAGCTTTCAAATGCCAAGATTTCCCTGCCGCTCGCTCTATTGAAAAGCTCAGGACATCCAAGCTCAGGAGGAACAGTTTGAACGCTCGAACAGAATAGATTATTGTTTGGCGTGAACGAATTGAAAGAGCAGTATTTGAGCCAGTGATAGTTTAATATCACACTACAGCCGATCTTGTGAAGAATTCAAAGAGAAGCATCTCTTTCCTGAGGAATATACTGTTGTTTTTGAGGTTTTTTTTATGTGTGTGTGAATTTTCTATTATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35588

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000097459	Nonsense	684	708	11	11

Genomic Location (Zv9):

Chromosome 13 (position 48077361)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	47328347
GRCz11	13	47618172

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCGGAGAACATCAACCGAAGCAAAAGCAGCTCCGGCTCCAATGCGAACT[C/A]GAAAGGGCCTCGAGCCGTCATGTGGATGTCAAGCTTTCCTCAGTTAACAC

Long Flanking Sequence:

CTACAGTAAAGTCAGCATGTGTTTGCCGATGGACATCGAAACGCCTTTATCGCAAGCTTACGTTATACTCCTGTTGCTCTTTAACGTTGGTGCATTTCTCGTGATTTGCGGATGCTATGTGTGCATTTACAGTGCAGTACGTAATCCTGAATTCCCAGGACGCGCCGCTGATGCTAAAATCGCGAAGCGAATGGCGGTTTTGATATTTACCGACTTTCTGTGCATGGCGCCTATTTCGTTTTTCGCTATTTCGGCAGCCTTTAAAGTGCCTTTGATCACCGTGACCAACTCCAAAATACTGCTCGTGCTTTTCTACCCCATTAATTCCTGCGCCAATCCATTCCTCTACGCCATCTTCACCAGAGCCTTCAGGAAAGACGCTTGTATTCTCCTGAGCTCCATGGGCTGCTGTCAAAGCAAAGCTAACTTGTACCGGATGAAGACGTACTGCTCGGAGAACATCAACCGAAGCAAAAGCAGCTCCGGCTCCAATGCGAACT[C/A]GAAAGGGCCTCGAGCCGTCATGTGGATGTCAAGCTTTCCTCAGTTAACACCTCGACCGCACATACAGAGAGTCTAGCTGGGTTTCCATCACTCCATGTTAATGCGCATTTTGAAGTATCGCATGAGAAACGAGTGATACATTTCAAATAAAAATCCCTTAAAGGTGCTATAGGTGCATTTTGGACTCCTCCAGTGCATGAATATACCAAAATGGGCTGTATTTTATTGATCTAAGTGCATGGATTAAAACGCACGGTGCACTTAGAATGTGTCTGAATTCACTTATTTGAGGGGTGGAAAAACCGTTGTCGCACCAAGCGCATAGTCTAAAAAGGTTGTCCTTATTCCCTTGATGAAGTTATGGATGGCTTTGAAGTAACGCACCAGTAACAAGTGACGAATTTTGAATAAAAATGCCTTGAAGCTGCTGTAGGTACCTTTTTGGAATTCTCTAATGCATAAAATTACAATTTTGGGCTCTATTTTAATGATTTATGTGC

Associated Phenotype:

Not determined