Busch Lab

ZMP

gnav1

Ensembl ID:
ENSDARG00000043006
ZFIN ID:
ZDB-GENE-081031-92
Description:
Guanine nucleotide binding protein alpha subunit v1 subtypeNovel protein similar to vertebrate guani
Human Orthologues:
GNA11, GNA14, GNA15, GNAQ
Human Descriptions:
guanine nucleotide binding protein (G protein), alpha 11 (Gq class) [Source:HGNC Symbol;Acc:4379]
guanine nucleotide binding protein (G protein), alpha 14 [Source:HGNC Symbol;Acc:4382]
guanine nucleotide binding protein (G protein), alpha 15 (Gq class) [Source:HGNC Symbol;Acc:4383]
guanine nucleotide binding protein (G protein), q polypeptide [Source:HGNC Symbol;Acc:4390]
Mouse Orthologues:
Gna11, Gna14, Gna15, Gnaq
Mouse Descriptions:
guanine nucleotide binding protein, alpha 11 Gene [Source:MGI Symbol;Acc:MGI:95766]
guanine nucleotide binding protein, alpha 14 Gene [Source:MGI Symbol;Acc:MGI:95769]
guanine nucleotide binding protein, alpha 15 Gene [Source:MGI Symbol;Acc:MGI:95770]
guanine nucleotide binding protein, alpha q polypeptide Gene [Source:MGI Symbol;Acc:MGI:95776]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa14474 Essential Splice Site Available for shipment Available now
sa24095 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa14474
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063143 Essential Splice Site 106 362 3 9
ENSDART00000137537 Essential Splice Site 107 363 3 9
Genomic Location (Zv9):
Chromosome 22 (position 11690148)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 11550316
GRCz11 22 11579998
KASP Assay ID:
2261-6500.1 (used for ordering genotyping assays)
KASP Sequence:
GCATGGGATGGGTGTCCTTCGCATCAACCTCGCCAACCCAAAAAACAAGG[T/A]CTGTTGCTKTCTTCACTACACTTTACAGACACAATATGTRCTTNTTTTTCA
Long Flanking Sequence:
ATCTGATTTAATCACGATTAGTTATTGCCCAGCATTCATTTGAATATATGTAAATGAACAGAAAAAAAAAACAGTAAATCATTATGCATAATACATAAGTGCATTGAGCTGCAGTAGAGCGTTTGATGGCTGCACAACGATGAGGTCACTTCCTGTCACTCAGGTGGATGAGAGACAATCAGGATCACTTGAGCAGAAGTGAATTCAGGAAGTGGATGCACATGTTTGCTTCAGTGGTTTCTGCGTAATGCTTTTACTTTAGGACGTCATTGTAGCGTTTGAAAAGACAAACACAACCTGCCAGTCATGTTTTTATTCAGCAGATGCATTCAGAATATAAATATGCTTTGTTTAGTTTTTTTTAGCTAGATACTCAGAAGGATCTTGTGTGTTTTTATATTTTCAGCCGGCGGTGCTTGATAATCTGCTGACCTCCATGAAGTTTGTCCTGCATGGGATGGGTGTCCTTCGCATCAACCTCGCCAACCCAAAAAACAAGG[T/A]CTGTTGCTTTCTTCACTACACTTTACAGACACAATATGTACTTTTTTTCATTAAAATGTCTAATAACCACTAGAACTGTGTTATATAAAGTATAAATATGCCGTTGAAGTTTCTTTTTACTTTTTCAAATATTTTCCAAATGATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTCCCATAATATTTTTTCTTCTGGAGAAAATCTTATTATATTTATTTAGGCTAGATTAAAAGCAGTTTTTTATTTTTTAAAACTATTTTAAGGTCAATATTATTAGCACCCTTAAACAATATTTGTTTTCGAGAACCATCATTATACAATGATTTGTATGATTACTCTAACTAGCCAAGTAAACCTAATTATAGTAAAGCCTTTAAATTGCATTTTAAGCTGAATACTAGTATGTTTGTTGTGAATACGAGCAAGCTGTTGCAGGATAACTGGGAAACAGCAAGCTGTTGCAGAATAACTGGCACTGGTGAAAATCAACTGTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa24095
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063143 Nonsense 260 362 7 9
ENSDART00000137537 Nonsense 261 363 7 9
Genomic Location (Zv9):
Chromosome 22 (position 11657609)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 11517777
GRCz11 22 11547459
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGTTCAGAATCGCCTGCAGGAGAGTCTCAAGCTCTTCTCTTCAATCTG[C/A]AACAACATCTTCTTCAGGGGCACCTCCATGGTAAGAGACGAGTCTATTAG
Long Flanking Sequence:
AAGCTAATGGAAGTCAAAAACTATATTAATTCTTTTTCCACTGCATTATGACTTTGTATTCAATACGGAACATTAAATCTGTTAAGTGACAAGACTTTTGTCTAAGCAAAGTCCTAATTAAATAATTTAAAAATCAAGGCATGATCATGTTTTATTGTGGTAAAATAAGCGTAATCTAGAAGTCTTTGCCTTTCATGTAAACCACTTCTGATACCAATTGATCAACTAGAAGTCAAGTTATTATTTGTTGTTCCTAAAACTTGGATAGGCGACAAGACTGTTGTCAGGTGGTGTAGTGCAATCTTTACAATTCAAAATCAATATAAACAATAAAAAAAAATGTTAACCAAATTTATTCGACTTGCTATGAGCACACAACTGTACCCGGCCTTATCTTTTTAAACACAGGAGAGAGCATGATGGGAAGTCTGACGGCTTGTGTGTTTTTGCCTTGTTCAGAATCGCCTGCAGGAGAGTCTCAAGCTCTTCTCTTCAATCTG[C/A]AACAACATCTTCTTCAGGGGCACCTCCATGGTAAGAGACGAGTCTATTAGCAGTGAGAGCTCCTCCAATCTCCTCCATTTAACTCAAGAGGCCACGCTAAACATATGAGGCCAAAACAATTCAAAAACTCTTCATTTGATGCAGACAAGCACACCGACATGAGCTATAATGCCAAAGTTATTTTCCAGATTAAAATGAAGTGGCCTTTTTGGTTTTTGCAGAAGACTGGATGTACGTCTAATGTACATTTGTATGAAAGCAGAATTTATTTCATAACAATAAAGTGTTTAAACTTTTTTTTTTCTTCTTCCTACCGCCTGTTAATAAATTATTATTACTTTTGATTAATATTTTTCTGTATTTTTTTTTCTTAGCGATTTGTTCAAGGAATATTTATTTTTTAATTTAACACAAATGTTATATGTTGAAAACTTTCTCTGTTTTTGGCATTGAAACAGTGGCATATATTTTGCTTTAGCAGGGTTTCCGCTGGGTCTTAA
Associated Phenotype:
Not determined