Busch Lab

ZMP

gnat2

Ensembl ID:
ENSDARG00000094180
ZFIN ID:
ZDB-GENE-011128-10
Description:
Guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2 [Source:Uni
Human Orthologues:
GNAT2, GNAT3
Human Descriptions:
guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2 [Source:HGN
guanine nucleotide binding protein, alpha transducing 3 [Source:HGNC Symbol;Acc:22800]
Mouse Orthologues:
Gnat2, Gnat3
Mouse Descriptions:
guanine nucleotide binding protein, alpha transducing 2 Gene [Source:MGI Symbol;Acc:MGI:95779]
guanine nucleotide binding protein, alpha transducing 3 Gene [Source:MGI Symbol;Acc:MGI:3588268]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa41206 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa25395 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41206
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
ENSDART00000132697 Essential Splice Site 2 179 2 6

The following transcripts of ENSDARG00000094180 do not overlap with this mutation:

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 26085943)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25213861
GRCz11 8 25233000
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATAGGTGCTGGTGAATCAGGGAAGAGCACCATTGTAAAACAGATGAA[G/A]TGAGTTGAAACACATGCGATATACAAAACACATGCTCAGATATGACAATT
Long Flanking Sequence:
AGCTCAAAGGCGAATCAAAGTGTCAGTGATCTTCTGAGAAGCTTTCCCTAACACAAATCCAATTGGGTCACTTTATAAGCAGGCTCATAAGCCTTCCTCTGACCTGCCCATCAATGGCAATCTATGAGTTTTTCTTGACAGGTTATCTACAGCTTAACATTGACCTTGTTATTAAAATCAATATCCATAGAGAGGAAAACAAATGGTTTAAATTCAGGAAAAATTCAGGCATTATGTTATCTGTATGAAGTGATACATCAATGTCACAATGGAATATGTAACCAAGGGACTAAGATTCAGCTCAATGTGGTTTGTTCAAAGACCTTCGAATGAAGTTAAAAGTTACAGATGGAGTTCATCGTGCCAAAACTTTGTGTGATGTTTGGTTTAAAAGCGTTTGAGGACTCGTTTGTCCTTTATTTGCTCTACATCATGTTTTTTCCCCTTTGTTTTATAGGTGCTGGTGAATCAGGGAAGAGCACCATTGTAAAACAGATGAA[G/A]TGAGTTGAAACACATGCGATATACAAAACACATGCTCAGATATGACAATTTGTATCTTTGTAGACAAGCTGTGTAAGCTCTTGAATTGAGATTTAGGTTTCTTGCATTCTAACTGAATTAATCCTTAACATTTAGTGTGCATTTGGGGAATACCAGCGCTTACCTACAGTAGAGTTGAGACCCTAAACTGTTATCACTAGGTGGTAGTGAATGAGGAGCCTGTCCTTTATCTTCAAATCATTAATAAAAACCCCTCTTGTTCCTGTCCAAGGATTCTCCATCAAGGTGGTTATACAAAAGAAGAACAAATGGAGTTTCGATCTATTATTTTTGGCAACATCCTGCAGTCTGCTCTGGCCATCATCAGGGGCATGGAGATGCTGTCAATCAACTTTGGATCGCCATCTGCACAGGTCTGCAGGACTGCTCTAAAACAAACAGAACAATTATTAGTGTGAAAATGATTCTCTAAAAAGCATGTTATGATGTTCAGTACAAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25395
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
ENSDART00000132697 Nonsense 56 179 4 6

The following transcripts of ENSDARG00000094180 do not overlap with this mutation:

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 26082296)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 25210214
GRCz11 8 25229353
KASP Assay ID:
554-7833.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAACAGTGCCCCCTTTTTCTGTCTCTTGTAGGAGGATAGTCAAAAGCTC[C/T]AGAACCTGTCTGACTCCATTGAGGAGGGCACCATGCCTCCAGAGCTGGCA
Long Flanking Sequence:
ATTCATTGTTGCTCTTGGTTGTGTAAATTGCTTCCTTGTCCTCATTTGTAAGTCGCTTTGGATAAAAGCGTCTGCTAAATGACTAAATGTAAATGTAAATGTAAGTGTAGTTACCACATAAAGGCTGCCAAGTGCTAATTCCCTGCAGATTTTCCCATGATCGCAGACCGATATGTTTGCAAACTTGTTAACTTGCAGCATACTAAAATCAGGCTCAAAATCCTGTAGTGTGAACAGGCAATAGTACAAATAACTGATGTAAAAATGCACTCCACTTGTGAGTACTACTGAAAATCCAATCAAGAACAGTTTCATAAAAGTCAACCATTTTCTCAATTTGGATGATCCATTCCACCTGGATCATGTACATCATAATAACGAAATCTAAATCTGAAGCTATGTCTATGCAACTTAATGAGTAATAGAATCAGCTGACTTACCACATGGTGCCTAACAGTGCCCCCTTTTTCTGTCTCTTGTAGGAGGATAGTCAAAAGCTC[C/T]AGAACCTGTCTGACTCCATTGAGGAGGGCACCATGCCTCCAGAGCTGGCAGACGTCATCAAAAGGCTATGGAAGGATGCAGGCGTGCAGGCCTCTTTTGATAGAGCTGCCGAGTACCAGCTGAACGACTCTGCTGGATAGTGAGTAAAACACTCAAAAGGCCCAGCAACACACATAAAGTTGAATTGTGCCTGAGGAAGCGATTAGACCATGCTTATTTGATGTTGAATGCCGTTTTCATGCTTTGGTGACTTTCAGTACTTTAGCAGATGAATAATTCAGGTGTGTCTGTACATGAATTGCTGACTCATCTCCCACAGCTACTTGAACGAAATGGACAGAATCTGCAAACCTGACTACCTTCCCACCGAGCAGGATGTGCTGAGATCTCGAGTCAAGACCACTGGTATCATTGAGGAACAGTTCGGTTGCAAAGAGCTCCACTTTAGGTGTGTCTTACCAGACTGAGAGGATGGAAGCAATAGTTGGTTCAAACTTAGA
Associated Phenotype:
Not determined