ZMP

fgfr1op

Ensembl ID:

ENSDARG00000003058

ZFIN ID:

ZDB-GENE-090417-1

Description:

FGFR1 oncogene partner [Source:RefSeq peptide;Acc:NP_001002125]

Human Orthologue:

FGFR1OP

Human Description:

FGFR1 oncogene partner [Source:HGNC Symbol;Acc:17012]

Mouse Orthologue:

Fgfr1op

Mouse Description:

Fgfr1 oncogene partner Gene [Source:MGI Symbol;Acc:MGI:1922546]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43468	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa23732	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa43468

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
ENSDART00000010494	Essential Splice Site	140	511	5	19

The following transcripts of ENSDARG00000003058 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 20 (position 30609028)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	30680241
GRCz11	20	30583120

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCTGGTGAAAAGGGGACGACACAGGGAAAAGACCTCCATTTTCACAGAG[G/A]TGACCTTTAATGAGCTGCATTTCAGCCAGTCAGATCAGTCCCCTGCCTTT

Long Flanking Sequence:

GCAAGATCTTACAAGATATGGACTTTTAAATGTTTTTTTTTTGTAATGATTTATTTTGCTTGCATTTAATGAATTCTTGCATTTCTTGATCTTCTTCCAGGGCGTTTGGTAGCAGGTCTTATTACTGACTTTCTCCAAGTCTTCAATTTAGACTTCACCCTTGCTGTGTTTCAACCTGAGATTAGCACGGTACGTCAGTGTTAAATATCATGCTGTAATGCATACGTAGTAAGGTTTGAAGTTGTCACTCAGGATTGCGTGTGTGTTTAGCTATATTTGTCTGATTGATTGATTTGAATATGATATACTGCATCCTCTGTGACCTCAATCTTAACCAATGTATCGTACTATGTGTTTTTCAGCTGAATGGACTTGACAGTCGTGAAGTGCTATCTAAAGAGCTTGGCATCTCGGAATCGGAGGTCAATAAAAACTCCCCTCTCCTGCTAGAGCTGGTGAAAAGGGGACGACACAGGGAAAAGACCTCCATTTTCACAGAG[G/A]TGACCTTTAATGAGCTGCATTTCAGCCAGTCAGATCAGTCCCCTGCCTTTTTGGGGGTTTATGCAGGAAATTCCTAAAAATGCTCGAATTATAAGGTTTTAAAAGTGCAAAAGTTGAAAAATATTTTGATTAAAGTGCTTTAAACGGCTTGAAAGTAATTGTGTTGTTTTCATTATAATTGACGTGCACATGTGACTTGTTTGATCTGCCTGTGATCTTCCTGCCTTTAATAATGCAGTGGCAGAAGACAAAATGAGAGGAAAATGTTTCATGAGCAAAAAATGCATGAAATTACATTTAAATACGAATTTAAGATTAAAATGACACATTTAGGAAAATAAATGACAGTAAGTGCCATGCTTTGGGCTCATATGCAGTCAAAGTTTTCCCAATTCGTTTGTAAAGTGGCTCTGTGCAGGACTGGATGACAGAAAAGAAAGGGAGTTTCTGATGGTTTCGCTCACCTAAATCTGTTTGCATGATTTGGTTAATATCATCGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23732

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000010494	Nonsense	452	511	17	19

The following transcripts of ENSDARG00000003058 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 20 (position 30631756)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	30702969
GRCz11	20	30605848

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCACTCTTTTCATTTCCAAACAAATGCTTTGCAGATGATGATCTTGACTA[T/A]GATGACGACTTCAACAGGTAAATACATTGTCCGACTAGTGTTTTGCAGTT

Long Flanking Sequence:

TGAGCAGCAACAGTGGTTAAAGATACTGAAAGAATTTGCACTGAAATTAGGTCAGTCTGAACTGTTTCCGTTACTGCGATTCCGCAGATAATGGTTTATGCACTATTGCTAAACTATTTGTGGGCAGAGCTGACATATTCAAGTACCCAATTCATGTGTAGTCATTACACCGAATTTAACCTACCTGAGGTTTAAAAAAAATCTAAATGCATCATCAAAGTTTAATCTCTGACCAAATTAACTCATAATATGCCCAAAGATTATCACCATACTGATTTTTTCTTTTTGATTAACCTCTTAGGAACGTCTCTTTCTATAGATAAGGGTGGCAAAGATTTTTCTACACCAAATGAAAAAACTGGATCTCCGTTGCTAGGTAAGAACTTCTTGACAATCTTTTTTTTATTTGTTTGTTTTTTCAATGACTTGAACCCTCAACCCTTTAAAATTTCACTCTTTTCATTTCCAAACAAATGCTTTGCAGATGATGATCTTGACTA[T/A]GATGACGACTTCAACAGGTAAATACATTGTCCGACTAGTGTTTTGCAGTTATTTAGGTTAATCTGCGTCTCGATGAAGGTTTCTCATCTCTCCTTACTCTTCAGCCATCGTTCAGAAAACTCTAAAAGTGAAGTGAGCATTGACGAGGAGATCGAGGAAGTCTCAATAGAGGGGCCTGACATTAGTGATAAGGTATTGTTCTCTCCATCCACAAAAGAGTCACATTGTTTGTGTCGCCAATGACTAAGGGGAACTGTTCCATGAATAAGCTTGTAAAGAAATAATTGACCTTGTAATACTGATGTGGTTGTTTCTCATGTTGGTTAATTATGGTATTGGTTTTCGCAGTTCTTTATGAGAGTAAGTCAACAGAGTGGCCTCATGGATAGGATTGTATTGTTTAAAAGTTAAGAAGTGAGAAGGGGATGTTTTGTTAATGGCAAAGATAGTTGCCTAAAGAGGCCCAATGAGGCAACAAGAGGAAACCACTTGAAGAGTTT

Associated Phenotype:

Not determined