ZMP

GFRA1 (2 of 3)

Ensembl ID:

ENSDARG00000039936

Description:

GDNF family receptor alpha 1 [Source:HGNC Symbol;Acc:4243]

Human Orthologue:

GFRA1

Human Description:

GDNF family receptor alpha 1 [Source:HGNC Symbol;Acc:4243]

Mouse Orthologue:

Gfra1

Mouse Description:

glial cell line derived neurotrophic factor family receptor alpha 1 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22273	Nonsense	Available for shipment	Available now
sa8781	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22273

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:

C > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000058415	Nonsense	83	158	1	2

Genomic Location (Zv9):

Chromosome 13 (position 20624800)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	20326539
GRCz11	13	20425265

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAAACACAGCTATGGCATGCTGTACTGCTCCTGTCCTCTAGGGGACCAGT[C/G]AGCCTGTTCTGAGCGCAGGCGCCAAACCATCGTGCCAGCTTGTTCATATG

Long Flanking Sequence:

AGCAGTGGCATGTCACTTTCACTATCCACTTTCACAGTTGGAATTTTATATATAGCTGTGTAATGGATAACAAATGGTTTGTGCAAAGCATGCATACAGAGATCAATGTATTTTATTTCCACTGTAAAATATATACTAATATATATTTGTAAATTTGTAAAAATGTAAATGCTGAGCAACTATTAAATTTGAAAACAGACGCAGTGCCTGGTGATTAAAAAAACTCATATTGTTTCTTACACTATGTATCTTTATCTTTGCAGGTGAGCCAGCGCTTGCAAAGGAGAACAACTGTCTGAATGCAGCAAAGGCCTGCAACCTGAATGACACCTGTAAGAAATACCGCTCTGCGTACATCAGCCCATGCACGAGCAGAGTCTCAACAGCTGAAGTCTGCAACAAGCGGAAGTGCCACAAAGCCCTGCGGCAGTTCTTTGACAAGGTGCCACCCAAACACAGCTATGGCATGCTGTACTGCTCCTGTCCTCTAGGGGACCAGT[C/G]AGCCTGTTCTGAGCGCAGGCGCCAAACCATCGTGCCAGCTTGTTCATATGAGGACAAGGAGAGACCCAACTGCTTGACACTGCAAGCTTCATGCAAGACCAACTACATCTGCAGGTTTGAATGCCTCCTTTGTTATTCTTTTCAACATTTTCATATTCAATGGAATTTACATTTACTGTGTGTGTATTGTGCCTTTCACTGTACATATACTTTAAGTATACATTTATATTAAATGCATGTTTCTGCGTTGCATTTAAAATGCTCCTGACACAAAATGTAAAGTTTTTTTAATGTTACTCACTGACAGTACTCTAGCAGAATTCATATTACAGAAATTACTTGGGATTATGTTATATTTAGGGTAAGTTAGCTCGAATAAACTAGTGAATAGTTACGTTTATCATAAGACTCAATTTATTAAAACTGGCTAACTGCATAATTTATTATGAACTACAAGTGGGAAATATTGTATCAACTGTAATGTAATGGGACGCTGACAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8781

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000058415	Nonsense	85	158	1	2

Genomic Location (Zv9):

Chromosome 13 (position 20624807)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	20326546
GRCz11	13	20425258

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGCTATGGCATGCTGTACTGCTCCTGTCCTCTAGGGGACCARTCAGCCTG[T/A]TCTGAGCGCAGGCGCCAAACCATCGTGCCAGCTTGTTCATATGAGGACAA

Long Flanking Sequence:

GCATGTCACTTTCACTATCCACTTTCACAGTTGGAATTTTATATATAGCTGTGTAATGGATAACAAATGGTTTGTGCAAAGCATGCATACAGAGATCAATGTATTTTATTTCCACTGTAAAATATATACTAATATATATTTGTAAATTTGTAAAAATGTAAATGCTGAGCAACTATTAAATTTGAAAACAGACGCAGTGCCTGGTGATTAAAAAAACTCATATTGTTTCTTACACTATGTATCTTTATCTTTGCAGGTGAGCCAGCGCTTGCAAAGGAGAACAACTGTCTGAATGCAGCAAAGGCCTGCAACCTGAATGACACCTGTAAGAAATACCGCTCTGCGTACATCAGCCCATGCACGAGCAGAGTCTCAACAGCTGAAGTCTGCAACAAGCGGAAGTGCCACAAAGCCCTGCGGCAGTTCTTTGACAAGGTGCCACCCAAACACAGCTATGGCATGCTGTACTGCTCCTGTCCTCTAGGGGACCAGTCAGCCTG[T/A]TCTGAGCGCAGGCGCCAAACCATCGTGCCAGCTTGTTCATATGAGGACAAGGAGAGACCCAACTGCTTGACACTGCAAGCTTCATGCAAGACCAACTACATCTGCAGGTTTGAATGCCTCCTTTGTTATTCTTTTCAACATTTTCATATTCAATGGAATTTACATTTACTGTGTGTGTATTGTGCCTTTCACTGTACATATACTTTAAGTATACATTTATATTAAATGCATGTTTCTGCGTTGCATTTAAAATGCTCCTGACACAAAATGTAAAGTTTTTTTAATGTTACTCACTGACAGTACTCTAGCAGAATTCATATTACAGAAATTACTTGGGATTATGTTATATTTAGGGTAAGTTAGCTCGAATAAACTAGTGAATAGTTACGTTTATCATAAGACTCAATTTATTAAAACTGGCTAACTGCATAATTTATTATGAACTACAAGTGGGAAATATTGTATCAACTGTAATGTAATGGGACGCTGACAACTGAGGT

Associated Phenotype:

Not determined