Busch Lab

ZMP

LOC565651

Ensembl ID:
ENSDARG00000074582
Human Orthologues:
AC144571.1, GFRA1, GFRA2, GFRA3
Human Descriptions:
GDNF family receptor alpha 1 [Source:HGNC Symbol;Acc:4243]
GDNF family receptor alpha 2 [Source:HGNC Symbol;Acc:4244]
GDNF family receptor alpha 3 [Source:HGNC Symbol;Acc:4245]
Mouse Orthologues:
Gfra1, Gfra2, Gfra3
Mouse Descriptions:
glial cell line derived neurotrophic factor family receptor alpha 1 Gene [Source:MGI Symbol;Acc:MGI:
glial cell line derived neurotrophic factor family receptor alpha 2 Gene [Source:MGI Symbol;Acc:MGI:
glial cell line derived neurotrophic factor family receptor alpha 3 Gene [Source:MGI Symbol;Acc:MGI:

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa12119 Nonsense Available for shipment Available now
sa22469 Nonsense Available for shipment Available now
sa38993 Nonsense Mutation detected in F1 DNA Not yet available
sa38994 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12119
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000108987 Nonsense 123 431 3 8
Genomic Location (Zv9):
Chromosome 14 (position 23685937)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 22385727
GRCz11 14 22682972
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGCTTAACCTGGTAGAGAACTATCCGTATGAAACAGTGGAGAAAGGCTA[T/A]GAGTTTGTCCGTCTGGCTTCCATCACTGCAGGTAAGGTAATAGCTTGATT
Long Flanking Sequence:
AATGACTGTGTAAAGTCTGTCAATTGGATGACTAGTCTATTTTTAGACGACTGTTAGATGTCACTGACAGTGCAGATTTAGCTTTGTTTCTGCCCAAACATCTATATTTAGATGTCTATTAGGCAAGAGTGGCTAAGAATGTCAGATGTAAAGGGAATCACATTTAAAGTCAAGCCCAAAATTATTTATACCCCAGGGATATGAATAATTATGGACTTGACTGTATTTACATCCAATCAACCAAAGTTCATATTAATAATATCGTTTATATGAATACCAGGTGTAAACAGTGCCTGATAATCACGTCACAGTAGGAGCATTGTAAAAAAAAAAAACTAATTATGCACATTTCTTTTTAAAAACCCTAATTATATATTGTTGGAATGTATTGTTCTTTATGAATTATTAAATGTACACTTTCATTGCTGAAATTAGCTCTTTGTAATTGCAGGGCTTAACCTGGTAGAGAACTATCCGTATGAAACAGTGGAGAAAGGCTA[T/A]GAGTTTGTCCGTCTGGCTTCCATCACTGCAGGTAAGGTAATAGCTTGATTCTGGCACTGAATGTTTTCTTTGTATTCTGTAATTCAAGAAAAACAAAGTTTAAATTACTGGCTGTTATAAAGCATAGCAGCTTAACACTAGCTACATGAAATTCTATTGTTATTAATAGGAATATGCACTATTTGTTTTATAAGTGACAATGATTGATAGTGGAAAAGATGATCAGCTAGGATTTTGTGTGACAATGCTTTGCTGAATTTCTGAAGTTGAACATTTAGCATTAGCTCTACAGAAATAATTCAGATAATATTACAGTATAAATAATTTTTCAGAAAGTGCAGTTTAGAAAATCTAGAAACTCTAAAATGCTAAATGGATGTAACAAAAAATACAAATAAAAGAAAATGCACTTTAAAAAAGCATTATTGTAAAAAGAAACAGCATTTGTAATAGCTTGACATACATGTGACATAACACAGATAGTGTTCCTGCAGTTTCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22469
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
ENSDART00000108987 Nonsense 165 431 4 8
Genomic Location (Zv9):
Chromosome 14 (position 23692651)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 22392441
GRCz11 14 22689686
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAAAGCTTGCAACATTGATGACGTTTGCCAGAGACTGCGCACCGAGTA[T/A]GTGTCAACATGCATCAAGCCCTCCACCAAATCGGGTTTGTGTAACCGATC
Long Flanking Sequence:
CAAAACAATTCTCTTTAGGTGATTTAATTTCTTCCCCCTCCTTTTGCTCTTTCAATTGCGTAATATATACATCTCCAGTAAAATCTATGATGCAAAATGAAATCACGTCTTTTTAATGTCTTCTCTCCTCCAGCTATCTATTTTATAAAATGTCTTAATCGAATTTGTCGTCACTTCACTTCTCATGTAACTTCAGAGATCCTAGTGATGGAGTGAATGCAACACCGAAAATAGGCTGAGGGGGAAATTAAGTTCTGTGGAGAATGCCCTGGTTGCTACAGTAGTTCCTATAACTATCTGGTGCAAAAACTCATAATATAGCCCGTTCTGGCCATGAGCTGCCAGTATATATACTTTTAATCACTTCAGTCAGTCCTAACGACTGCAACGTTTGAATTCTCCACAGATTCTGAAATCGGGATGAGCACAGTGAACCGTTGCCTGGATGCGGCCAAAGCTTGCAACATTGATGACGTTTGCCAGAGACTGCGCACCGAGTA[T/A]GTGTCAACATGCATCAAGCCCTCCACCAAATCGGGTTTGTGTAACCGATCAAGGTGCAACAAGGCCTTGCGGCGATTCTTTGACAGAGTCCCTGCAGAGTACACCCACGAGCTGCTTTTCTGCCCTTGCAGCGACATGGCCTGTTCGGAGAGACGACGACAGACCATCGTGCCCAGCTGCTCCTATGAGGGAGAAGATAAACCCAGCTGCCTCTCGCAGATGAGGATCTGTAAGGCCGACTATGTTTGCAGGTCAGTTTCAGAGGCTTTGACAGCCACATACCATGTGGGCGGCAGGATTAAACAACTCACCTTGCATGCACTTCTTTTTTCAGAGTAAATAAAGCCTCAGCTTTTCTATAGCTGTCTAGAGAAAGAAACACTCGCATATTACTGGTGATAAGAAAAAAAGCTGTTCTTCGCCATCCTTGTAATCCATGTTTGAATAAATGGTCATTGGACAGAGTTATGAGACCCTGAAATGTTTTAGAAGTCAGATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38993
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
ENSDART00000108987 Nonsense 176 431 4 8
Genomic Location (Zv9):
Chromosome 14 (position 23692683)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 22392473
GRCz11 14 22689718
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACTGCGCACCGAGTATGTGTCAACATGCATCAAGCCCTCCACCAAAT[C/A]GGGTTTGTGTAACCGATCAAGGTGCAACAAGGCCTTGCGGCGATTCTTTG
Long Flanking Sequence:
TCCCCCTCCTTTTGCTCTTTCAATTGCGTAATATATACATCTCCAGTAAAATCTATGATGCAAAATGAAATCACGTCTTTTTAATGTCTTCTCTCCTCCAGCTATCTATTTTATAAAATGTCTTAATCGAATTTGTCGTCACTTCACTTCTCATGTAACTTCAGAGATCCTAGTGATGGAGTGAATGCAACACCGAAAATAGGCTGAGGGGGAAATTAAGTTCTGTGGAGAATGCCCTGGTTGCTACAGTAGTTCCTATAACTATCTGGTGCAAAAACTCATAATATAGCCCGTTCTGGCCATGAGCTGCCAGTATATATACTTTTAATCACTTCAGTCAGTCCTAACGACTGCAACGTTTGAATTCTCCACAGATTCTGAAATCGGGATGAGCACAGTGAACCGTTGCCTGGATGCGGCCAAAGCTTGCAACATTGATGACGTTTGCCAGAGACTGCGCACCGAGTATGTGTCAACATGCATCAAGCCCTCCACCAAAT[C/A]GGGTTTGTGTAACCGATCAAGGTGCAACAAGGCCTTGCGGCGATTCTTTGACAGAGTCCCTGCAGAGTACACCCACGAGCTGCTTTTCTGCCCTTGCAGCGACATGGCCTGTTCGGAGAGACGACGACAGACCATCGTGCCCAGCTGCTCCTATGAGGGAGAAGATAAACCCAGCTGCCTCTCGCAGATGAGGATCTGTAAGGCCGACTATGTTTGCAGGTCAGTTTCAGAGGCTTTGACAGCCACATACCATGTGGGCGGCAGGATTAAACAACTCACCTTGCATGCACTTCTTTTTTCAGAGTAAATAAAGCCTCAGCTTTTCTATAGCTGTCTAGAGAAAGAAACACTCGCATATTACTGGTGATAAGAAAAAAAGCTGTTCTTCGCCATCCTTGTAATCCATGTTTGAATAAATGGTCATTGGACAGAGTTATGAGACCCTGAAATGTTTTAGAAGTCAGATGTTTTCAGATAAATCACATGATTGTGAATTCAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38994
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
ENSDART00000108987 Nonsense 188 431 4 8
Genomic Location (Zv9):
Chromosome 14 (position 23692719)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 22392509
GRCz11 14 22689754
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCTCCACCAAATCGGGTTTGTGTAACCGATCAAGGTGCAACAAGGCCT[T/A]GCGGCGATTCTTTGACAGAGTCCCTGCAGAGTACACCCACGAGCTGCTTT
Long Flanking Sequence:
ACATCTCCAGTAAAATCTATGATGCAAAATGAAATCACGTCTTTTTAATGTCTTCTCTCCTCCAGCTATCTATTTTATAAAATGTCTTAATCGAATTTGTCGTCACTTCACTTCTCATGTAACTTCAGAGATCCTAGTGATGGAGTGAATGCAACACCGAAAATAGGCTGAGGGGGAAATTAAGTTCTGTGGAGAATGCCCTGGTTGCTACAGTAGTTCCTATAACTATCTGGTGCAAAAACTCATAATATAGCCCGTTCTGGCCATGAGCTGCCAGTATATATACTTTTAATCACTTCAGTCAGTCCTAACGACTGCAACGTTTGAATTCTCCACAGATTCTGAAATCGGGATGAGCACAGTGAACCGTTGCCTGGATGCGGCCAAAGCTTGCAACATTGATGACGTTTGCCAGAGACTGCGCACCGAGTATGTGTCAACATGCATCAAGCCCTCCACCAAATCGGGTTTGTGTAACCGATCAAGGTGCAACAAGGCCT[T/A]GCGGCGATTCTTTGACAGAGTCCCTGCAGAGTACACCCACGAGCTGCTTTTCTGCCCTTGCAGCGACATGGCCTGTTCGGAGAGACGACGACAGACCATCGTGCCCAGCTGCTCCTATGAGGGAGAAGATAAACCCAGCTGCCTCTCGCAGATGAGGATCTGTAAGGCCGACTATGTTTGCAGGTCAGTTTCAGAGGCTTTGACAGCCACATACCATGTGGGCGGCAGGATTAAACAACTCACCTTGCATGCACTTCTTTTTTCAGAGTAAATAAAGCCTCAGCTTTTCTATAGCTGTCTAGAGAAAGAAACACTCGCATATTACTGGTGATAAGAAAAAAAGCTGTTCTTCGCCATCCTTGTAATCCATGTTTGAATAAATGGTCATTGGACAGAGTTATGAGACCCTGAAATGTTTTAGAAGTCAGATGTTTTCAGATAAATCACATGATTGTGAATTCAGTATTGAGCAGTGCAGGTTAGATGGTCCTTCATCAAGA
Associated Phenotype:
Not determined