ZMP

gfra2

Ensembl ID:

ENSDARG00000042723

ZFIN ID:

ZDB-GENE-040630-1

Description:

Glial cell line derived neurotrophic factor family receptor alpha 2 [Source:UniProtKB/TrEMBL;Acc:B0S

Human Orthologues:

AC144571.1, GFRA2

Human Description:

GDNF family receptor alpha 2 [Source:HGNC Symbol;Acc:4244]

Mouse Orthologue:

Gfra2

Mouse Description:

glial cell line derived neurotrophic factor family receptor alpha 2 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10192	Nonsense	Available for shipment	Available now
sa6102	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10192

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
ENSDART00000062697	Nonsense	158	495	3	9

Genomic Location (Zv9):

Chromosome 8 (position 44223513)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	42176295
GRCz11	8	42183082

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTATGAACCCATGACGCCTCACCGACATTCAGATGCATTTCGCCTGGCGT[C/A]AATCATCTCAGGTAAAGCAGCATTTTCAATACAGTTTATTTGTATTNNGT

Long Flanking Sequence:

AAAGATTGAAGTTGTGCCTACGAGAGTGTAATGTATTGGTTTAGGTGAGGATTGAACCTTCAAAACCTTTTCATTTTTTTATACTGCTAGTCTGACTTAAATAAATTAGTGTTTAGTTGTGAGAATGCAAATGAATTCAAACTGTGAAGTTGATCAACAGTATATTCTCCATGCAGCACATAAGTGCCATTATGAGGGCATTAATGGGCACAAGTAACAAGTAATCGATAAAACAATTGAGTTACTTTTTCATTAAAGTAACTAGTAATTGTAACTACTGTAGTTACTATTTTTCAGTAACTAGCAAAACACTAGCTAGCAAATGAAATGTTTATTGATGCATAGTGCATTTAAAAAAAGAAGAGTTTAGTACAGTTTGTTTGTTCTTAATATGTATCTTAATAGTTTGTATTGTTTCTTTTTAGGTGAAGACTTTTATGAGCCATCTCCTTATGAACCCATGACGCCTCACCGACATTCAGATGCATTTCGCCTGGCGT[C/A]AATCATCTCAGGTAAAGCAGCATTTTCAATACAGTTTATTTGTATTATGTGTTCATTCTGGGAATGTACTGTTAATAATATCTCCTTTTAATTCCACTATTGTATTTGAAACTCAGAAAAGCAAGCACTACATGAATAATTATAATGTTCCAATACACACCACACTAATTAAAGACTAAAGTATTCATCCTAAAGTTTTCTATTTACAAATTACCAGCATTGTAGAAGGAGAAATGAAGATGAATTGCTAACTTTCCTTTCTAGGAAAAAGAGAAGCATGGATAAGTGGTTATTTCACTGGAATAAAAACCATTCTAGACATTTGTCACCTTGGCATGAGTTAAGTCTAATGTTTAATTCACTGACAGCAGTCATTACAGACGGTAGAGGACAGAAACATTGCCTCCAATCCATTATCACAGCCTCGCAGAGCCTGGAACAACTAGAATAACTCATTTTTATTCTGATCCAAAAGAGCGAAATAGCCAGTGAACGACAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa6102

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
ENSDART00000062697	Nonsense	191	495	4	9

Genomic Location (Zv9):

Chromosome 8 (position 44179549)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	42132331
GRCz11	8	42139118

KASP Assay ID:

554-3785.1 (used for ordering genotyping assays)

KASP Sequence:

ACTGACCCGAGCCGCCCTTGCAACCCCTGWCTGGATGCTACCAAAGCCTG[C/A]AACCTGAATGAAAACTGCAAGCGTCAGCGCTCCAACTACATCTCCACCTG

Long Flanking Sequence:

TATGGTAAGCTTTTTTTTGCACTGCAACTGGTGATCAACAGTAAAAAAAATTAAATTGTACCTCTTCTCAACTGGGAAAACCAGTAACATTTAAAAATGCAGAATTATATGGTGTCATTGCTTTCCAATCAAAAATGTCATTATGATGGAAGTCAATGGGCAAACACAGCCACGAACATAATGAAACAGTAAGAAATTTGCCCAAAGTATATTGTTAAATTTTGAAAAAGTTCAAAGCATTTCCTAAAATGTGTCAAAATAAGATTTGCCACCAAAAATCATTCCATTCATCATTCTACAGAGTAACTTGTGGCCAAATCAAGACTTACACTAGAGTGGATGAAAACATCCCTAACAACATTCAAGGGTTAATTTACTCTCATAAACTCATCTGTCCTGTGTCCCCTTGCAGGCATGCATTCAGGCACCAGTAAAGGCCAGCCACACTGCACTGACCCGAGCCGCCCTTGCAACCCCTGTCTGGATGCTACCAAAGCCTG[C/A]AACCTGAATGAAAACTGCAAGCGTCAGCGCTCCAACTACATCTCCACCTGCACACGTGCACAGACACAAGGCCAGCAGCCCTCACAGACGCAGACACAGGAAGGCTGCAACCGAAAGCGCTGCCATAAAGCCCTGCGGCAGTTCTTCGAGCGAGTCGACACGCAGTACAGCTACGGCCTGCTTTTCTGTGCCTGCAAAGATCAGGCCTGTGCTGAGAGGAGGAGGCAGACCATCGTTCCCTCATGCTCCTACCAGGACAAGAACAAGCCAAACTGCCTGCAACTGCGCAACACCTGCCGCCTCGATGTGCACTGCAGGTAAGAGACACAATGTGCTTTATGATGAAAGATGTAAGGTTATTACATCTGACATCACAGTTTATGAGTCCAAATGTTCTATCATAACGAGGAAGTTCTGGGTGATTATTTAAAATGATATTCATGTGCATTTTAGCAGTGAAACTGGCTCTGTAATGAGTTGTAAATCTTCAGGACCTGCTT

Associated Phenotype:

Not determined