ZMP

fshr

Ensembl ID:

ENSDARG00000071494

ZFIN ID:

ZDB-GENE-020423-5

Description:

follicle-stimulating hormone receptor [Source:RefSeq peptide;Acc:NP_001001812]

Human Orthologue:

FSHR

Human Description:

follicle stimulating hormone receptor [Source:HGNC Symbol;Acc:3969]

Mouse Orthologue:

Fshr

Mouse Description:

follicle stimulating hormone receptor Gene [Source:MGI Symbol;Acc:MGI:95583]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13419	Essential Splice Site	Available for shipment	Available now
sa42035	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13419

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105751	Essential Splice Site	206	668	7	10

Genomic Location (Zv9):

Chromosome 12 (position 26269769)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	24642210
GRCz11	12	24763429

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTCGTGAGATAGACAGCCATGCATTCAATGGTACCAAAATTGGAAAACWG[T/G]GAGTGGTTACATCTKTTATATATTTATAAATCACATAAAAYCTCTAATCT

Long Flanking Sequence:

ACGAATATGGTAGAATATACAGTATGAAGTCTTATAGTGATATCTAACACTTTTTCTTTTATTTTTATTTTCTTTTTTTATTATTTTAAATAATTTTTAGATTTGAGTGATTTTGGTTTTTTTATTTACATAAATTGCAGATCAGATTGACCATTAACACAAATGTATCTGGATATAATACCGCTGCTAAATTGTTTAAAAGTGACAGTAATGACACTTATTACTTGGAGAGAAGTTAAATTAAACGCTGTTCTTTTAAACTTTCCATTTATTAAAGAAACTTTTAAAAAAACCAAACACTGAATTGAAATAGTAACATTTGAAAGGTATTGCCAACTTTGCTGTAGTTTTGCTTTAATAAACAGCTTTGGTGAGCAGTATGTTTCCAAGCCCATTTTTTTAACTGATCTCACCTAATGTGCTCTTGCAGGAGATTAACGAAGAACGGGATTCGTGAGATAGACAGCCATGCATTCAATGGTACCAAAATTGGAAAACTG[T/G]GAGTGGTTACATCTTTTATATATTTATAAATCACATAAAACCTCTAATCTTTCATCTAATCCCTTTGGCTCTCTTTCTCACAGCTTTCTCATGGGAAACCAGCAGCTGAATCACATCCACAGTTACGCCTTTAAAGGAGCCGAAGGCCCCGTCGTTCTGTAAGCATGAACAGCTCTGACTTTCAACAACAATACAAACTCACCAGCTGGATCAACACACACACACTCACAGCAATTCCACTCACACTAACCTCTGCTACCTGAGGCCTGTACCATGAAGCTGGTTTAACTTAGTCGGGTAAATTTAAGTTTAGTTTGCTTCAACATAAAAGTGGTTTGGCTTTTAGCAGTGTTTATCTCTATAGCAAATTACACTCTGTGAGTAACTAACTAGGGCAACCCAATTGTGCACAACACATCAAAAATTTGAAAGAAAACATAAGTGTACAACACAATTGCCACAACAAGACAAAATCCAACCCAGGCTTATTTGAAATGCCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42035

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
ENSDART00000105751	Essential Splice Site	231	668	8	10

Genomic Location (Zv9):

Chromosome 12 (position 26269929)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	24642370
GRCz11	12	24763589

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCACATCCACAGTTACGCCTTTAAAGGAGCCGAAGGCCCCGTCGTTCTG[T/C]AAGCATGAACAGCTCTGACTTTCAACAACAATACAAACTCACCAGCTGGA

Long Flanking Sequence:

AAATGTATCTGGATATAATACCGCTGCTAAATTGTTTAAAAGTGACAGTAATGACACTTATTACTTGGAGAGAAGTTAAATTAAACGCTGTTCTTTTAAACTTTCCATTTATTAAAGAAACTTTTAAAAAAACCAAACACTGAATTGAAATAGTAACATTTGAAAGGTATTGCCAACTTTGCTGTAGTTTTGCTTTAATAAACAGCTTTGGTGAGCAGTATGTTTCCAAGCCCATTTTTTTAACTGATCTCACCTAATGTGCTCTTGCAGGAGATTAACGAAGAACGGGATTCGTGAGATAGACAGCCATGCATTCAATGGTACCAAAATTGGAAAACTGTGAGTGGTTACATCTTTTATATATTTATAAATCACATAAAACCTCTAATCTTTCATCTAATCCCTTTGGCTCTCTTTCTCACAGCTTTCTCATGGGAAACCAGCAGCTGAATCACATCCACAGTTACGCCTTTAAAGGAGCCGAAGGCCCCGTCGTTCTG[T/C]AAGCATGAACAGCTCTGACTTTCAACAACAATACAAACTCACCAGCTGGATCAACACACACACACTCACAGCAATTCCACTCACACTAACCTCTGCTACCTGAGGCCTGTACCATGAAGCTGGTTTAACTTAGTCGGGTAAATTTAAGTTTAGTTTGCTTCAACATAAAAGTGGTTTGGCTTTTAGCAGTGTTTATCTCTATAGCAAATTACACTCTGTGAGTAACTAACTAGGGCAACCCAATTGTGCACAACACATCAAAAATTTGAAAGAAAACATAAGTGTACAACACAATTGCCACAACAAGACAAAATCCAACCCAGGCTTATTTGAAATGCCTCAACGCACATTTTTACAAAATATGTCCAAAACTCAGACGTTTTGATATGAGTGTTTATTGCATGTTTCAAATGACTGGACAAAGCAGGTTCGGTCTAAATTTCAGTGAATTACTTAGGGTGCAATTTGTTATACGTTATATGGGAAGGCAATGCTTATCA

Associated Phenotype:

Not determined