Busch Lab

ZMP

GIGYF1 (1 of 3)

Ensembl ID:
ENSDARG00000075647
Description:
GRB10 interacting GYF protein 1 [Source:HGNC Symbol;Acc:9126]
Human Orthologue:
GIGYF1
Human Description:
GRB10 interacting GYF protein 1 [Source:HGNC Symbol;Acc:9126]
Mouse Orthologue:
Gigyf1
Mouse Description:
GRB10 interacting GYF protein 1 Gene [Source:MGI Symbol;Acc:MGI:1888677]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa34046 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa31566 Nonsense Mutation detected in F1 DNA Not yet available
sa20912 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa34046
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
ENSDART00000109594 Essential Splice Site 55 1017 2 25
Genomic Location (Zv9):
Chromosome 7 (position 22018665)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 20609101
GRCz11 7 20882402
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGATACGGCCGAGAGGAGATGCTAGCACTTTATGTCAAAGACAACAAG[G/A]TAAGAAAAAGATTTAAACAAATCGGCCTAATTTTTAAGCTTAGGTTATTT
Long Flanking Sequence:
TATTTTAGATAAACCTAAGAGCCTAAATATCTATATAAATATTATTGGCCAATTGCAGTATTTTTACTGCAGCAAAAAGAACTCATGATGGCAGAAGGATTCTAAATTATTTGTTTTACATATCTTAAAACGGTCTGGTTCTTAGTATTTTCACTGACCAGACATTAACACAAGCTTCAGTATCATTTTGATGGGAAAAAAAAAACGGTTGCGATGCATCCTAAATGAAGCAGGATGAAGAGTCAGCACTGACAGGGCCATCTCTGGGCAAGAGCCAGGACTAGAGCACTTCTCAATGGAAGCTTCCAGATTGTTGCTGCTGAACATCTTTTGATCGGATTTTTCTTTCTCTCTCTTCTCTTTCTCTCAGGCTTCGTGCACTTTCCAGTGGAAGCAGCTTGTCTTCCCCTCCTGCCTCTCCTGCTATGCCAAAGTACAAGCTGGCCGAGTACCGATACGGCCGAGAGGAGATGCTAGCACTTTATGTCAAAGACAACAAG[G/A]TAAGAAAAAGATTTAAACAAATCGGCCTAATTTTTAAGCTTAGGTTATTTCCCGGCATTCAGCGTGCCATGATTAGGCCTGCTTGTATACCTCATAACAAGTCTAAATATCATAAGGGCTTGCTTATAGTTAGATTAGTTACCATCTTTTGATAAATGGGTGTTTTTCATTTCTCATTGCTGATTTGCCGTTGTGTTCACATGCTCAATAGAAATGACTGTGATTGGTCACCAGTTCACCAAATTCTCTGCTGTTTACTAGGGTTGGGTGATGTCGACCAATTTGGCATCGTATAATGTCTAATGTGAAACATCGCGATGGACAATGGCATCATCGTTGTAGGTGGTGGTGAATCTATTGTTTATGAATGATTAATTCATTCATAACGTATTAGTTATTTGTAGCCTACTGTTTCAACTACCTGACCCTCATAGTCTTTGTTTTACCCATAACCAAATCATAAATAGATAAAGATAAGTTACACACAAATTTCCACCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31566
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109594 Nonsense 427 1017 10 25
Genomic Location (Zv9):
Chromosome 7 (position 22028951)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 20619387
GRCz11 7 20892677
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCCGCCACCGGGGGGTGATATTGAGGACGACGAGGGCATGAAGCACCTG[C/T]AACAGGTACTAGAAAACAGATGGGATAATATCTGACTAAAATTCATAAAG
Long Flanking Sequence:
TAAAGTAGCATTTGTTGCTGATCATCGTTATCATCATCATTTTTTGCATTGGTTTTATGGCTGTCTCTCACGCTCTCTTTCTCTCGATAGATGTCATCGACTCTGCTGCTGTCTCTGAAACTGAAGTGAAACTGGTTTCTCCTTCAACTCCTCCTCCTCCTTCTCTTCCTCCCTCTCTTCCTGCTCCCATCTCCGAGGCTGTGCCCTCTGCAGCCCCCTCTGGCCTGGAGGAGTCTCCACCTGCCCCCTCCATTCCCCACAAACTACCAAGTGAAGGTAAAAAGGATTTTTTTTTTTATCATCTCCTACAATTGAATAGATGATTTGTGCTTTAATTATGCATGTTTTGTGTGTGTGTAGTGTTATCAGAGGCCATGTTAGATTTGAGCCCCAGTGCCTCCTCCAGTCTGCCTTCATCGCCTCCCTCTTTGTCCTCTGCTGCTACTGACCTCCCGCCACCGGGGGGTGATATTGAGGACGACGAGGGCATGAAGCACCTG[C/T]AACAGGTACTAGAAAACAGATGGGATAATATCTGACTAAAATTCATAAAGGGTCTAAAAAGTTAAGGTTATTGATGTAATATCAATTGAATGTTAAAGATGATGTATGTAAGATTGACACCCAGTGGTTGAACTCGGTATTGCACTCCAAATTCAAAACACTTCTTCACATGGTCGCTCCTCAGACAACTCCATACAGTTGCCAGATTTATGACACCAACAGGAATGAGCGTGCCTGACTATTAAGCCCACACTGTGACTACTAGCAACGACACGCAATAGTAGTATTTTGTATGTTAAAAGGTCAAAACCATCGCCTGAAAATTCCATTTTAGAAATGGTTTTTATTTCTCGTAGCTGAAAACATCATTTGACAATGATCACCTCAGGTTCATGTGCTTCATTCAGTTTTAAATGCCAGAAATGCTAGTTTGAATACAGTTTTACATGACAGTTATAGCCATACTGAAAGCAGCAGCAGATAGATTATCTCAGATCTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20912
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109594 Nonsense 761 1017 19 25
Genomic Location (Zv9):
Chromosome 7 (position 22047587)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 20637963
GRCz11 7 20904301
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCCCTCAACCTCCTGGATGTCCAGCAGGAGGCTGACAGAATGCACAAA[C/T]AACAGCACAGAGTCCAGCAGCAGAGGGTAAGACACACATACATACACACA
Long Flanking Sequence:
GATTTGATGCGAAACTGACTAAAGAAGTGGCGTGAATAAAACCGTTGATCCATTAAGGCGAAAAACTGCAAGCTTTACAAGTTTTTTTTTCAGTCTTTTTGAGCACACTGGCTTATAGATATCCTAAAAACTAAAACTACCGATTCTAACGTCTAAAAAAACAACAATATTTTAATTGCATTAAAATCGTGTGAAAATCCTGTCAGTGGTTGTTATATTTTTTATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTATTTATTTTTTTTTTGTAATTGTTTTCTTCACATCTTTTCCCAAGCAACAGGATTTGCTGATGAAGTTGCTCCAGCAGGCTCCCCGTCAGGGCTCCTCTGGCTCCGGGTCGAGCTGGAGTTCAGGACCCATCTCTGGACTGGGAAAGCAGTCCAAGCCCCTCAACCTCCTGGATGTCCAGCAGGAGGCTGACAGAATGCACAAA[C/T]AACAGCACAGAGTCCAGCAGCAGAGGGTAAGACACACATACATACACACATGCACTGATGTTCAGTCCTGCAAAAAGGAAAAAAACATTTATTATGAATGTCCCGCTCTGCAGTGGAGCGATGCCTCTTCACTGTGGGGCGCAGCTGGATCTTTGGATGGAAAGGTGGGAAGCAGTGGCAGCTCCTCTGGAGGAGGAATGGGCGTCTGGGATGAGGCCCTCAAGAACCAGAGTGCTCTTCGTAACAACATGGGCCTGAAGAACAGCCGCAGCAGCCCTTCGCTCAGGTAAACCCAAAACCACATGCCAAGAGATGACTAGAATAGGGTTTTCAGTGGCTCATGCCAGAGCTGAACGGCTTATGTGTGTGTTTCTTCAGCGAACAGTACATGATGAGGGGCCGTAAACGCACTGAGGAGGAGGATCGGCTGCTGAAGCTCCTGCAGGGGATGAAGTCTCAGGACGGCTTCACCACCTGGTGTGAACAGATGCTGCATGCGC
Associated Phenotype:
Not determined