Busch Lab

ZMP

gata4

Ensembl ID:
ENSDARG00000035759
ZFIN ID:
ZDB-GENE-980526-476
Description:
transcription factor GATA-4 [Source:RefSeq peptide;Acc:NP_571311]
Human Orthologue:
GATA4
Human Description:
GATA binding protein 4 [Source:HGNC Symbol;Acc:4173]
Mouse Orthologue:
Gata4
Mouse Description:
GATA binding protein 4 Gene [Source:MGI Symbol;Acc:MGI:95664]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa45720 Nonsense Mutation detected in F1 DNA Not yet available
sa44950 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa45720
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
ENSDART00000049129 Nonsense 210 338 7 12
ENSDART00000099559 Nonsense 213 352 2 6
Genomic Location (Zv9):
Chromosome 20 (position 53591186)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 53151578
GRCz11 20 52956995
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTACCATAAGATGAACGGCATCAACCGGCCGCTGGTCAAACCACAGAGA[C/T]GACTGGTGAGAAAATTGCAATACTTTTTATTCTTAGTTGTTTTTATTTCT
Long Flanking Sequence:
ATTCAGTTATTAGAGATGAGATGGAGAGATGGGCACTAGTGGGCGGGGCTTTCCCCCACTAATGACATCATACAAAGGGAGAATGTCCATCACAGTGTTTCTGCAGACTGTTTTCATCAAGTCTGATTATGAACAATAGAATTAATTCATGATTACCATTAGAGGCTGGATATATTCACACACTGCTGACAAACAACTGTGTTTAAACCCCTTATGAAATAGATTTTTACATAATAGATGTCCTTTAAATGTTCTTCCGATGATCCTGTGTCTGATATGGTTGTTCATTTACAGTATTTTTGTTTATTTATTTGCATGTGTGTGTGTTTGTTTTATCAGAGTTTTTTGATGATCTGGGCGAGGGCCGGGAGTGTGTGAACTGCGGGGCGATGTCGACTCCTCTGTGGCGGCGGGACGGCACCGGTCATTACCTGTGCAATGCCTGTGGACTCTACCATAAGATGAACGGCATCAACCGGCCGCTGGTCAAACCACAGAGA[C/T]GACTGGTGAGAAAATTGCAATACTTTTTATTCTTAGTTGTTTTTATTTCTCATACTTGTTTCTTTTATCATATATATCTAAATAATAATTTATTCCTAAACTGTACACCTATAGGATTGTGCTTTAGACGCCATCTTGTGGTCAAATGCAGAAATTCATTCAGCACTATAGCTTTATTGGTATTAGCTGTTAAGTGTGCATGGGTTGGAGAGTGCATTGAGGGATTGATTGAGTGCACTTGAGAATGTCCACTATGGTTTCGGACACGAGAAATGGCTGCTCCCTCAAATAGTGCACTATTAAGGGCATAGGGGGCAATTTCGGATGTGGCCCCAGTTCACTCTACACAAGATCACCACTTTACAATTAACAAACAGCATTGGCATTCCATCATTGTGCTTTTGCACACTTATTAGTGTTATTTTGCACACTTTTGCTGTGAATTGTTATTTTGCATGCTAACGGTCATGTTTAATGTTGTTTTGCACACTTATTACATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44950
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049129 Essential Splice Site 281 338 9 12
ENSDART00000099559 Essential Splice Site 284 352 4 6
Genomic Location (Zv9):
Chromosome 20 (position 53587386)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 53147778
GRCz11 20 52953195
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAGACACGAAAGCGCAAACCCAAAAACATCAGCAAAACCAAACCCGG[T/G]GAGTGTCCTGTCTGCTGTCAGATATCCCCAACTGTTTATTGTAAACTGAA
Long Flanking Sequence:
TATTATTTTTGCATATTTTGTATTGTTATTTTGCACACTTACTGTAATGTTTATTGTTATTTTGCATGCGTATTGTAGTGCTTTCTGTTATTTGCCATGCTTTATGTTATTTTGCATGCTTATTTGCACTGTTTACACTCTATATTCCATCTCTTCCTCACTGCTCTCTCCCCCTTTTTCTCTCAGTCTGCGTCCAGGCGGGTGGGTTTATCCTGCACAAACTGTCAGACTACCACAACAACTCTTTGGAGACGCAATGCAGAAGGAGAGCCAGTCTGCAACGCCTGTGGACTCTACATGAAGCTCCACGGGGTCAGAAATCTCTTTATCTGCAGTACTACATGTGTCCAGCAGATGGAGATAGAGAACCAGTAAAACCACAGCTCTGAGTGTTTGTTCTGCTGTTCTTCTGCTCAGGTTCCTCGTCCTCTCGCCATGAAGAAAGAGGGCATTCAGACACGAAAGCGCAAACCCAAAAACATCAGCAAAACCAAACCCGG[T/G]GAGTGTCCTGTCTGCTGTCAGATATCCCCAACTGTTTATTGTAAACTGAACGTCAAAACCTTTTCAATTGATTTTGAATTAGCTTTTTATATCTGTTGAGAATTTGTCCAAAGCTTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTGGTGTGGGTTTCCTCCGTGTGCTCCGGCTTCCCCCACAGTCCAAACACATGTGCTATAGGGGATTTGATTAACTAAGTTGGACGTAGTAGTGTGTGTGTTTGTGTGTGTGTGAATGGGTGTTTCCCAGTACTGGGTTGCAGCTGGAAGGGCATCTGCTGCTTAATACAAATGCTAGAATAGTTGGCGGTTCATTCCGCTGATGCGATGCGACCCCTGATAAATCAGACTCTAAGCTGAAGGAAATTGAATGAATGAATGGCTAAAAGTGATGGTGACCTCTGACCTTTCACCTGTGTGTGTTTTGAAGGCTCCTCTGAAGGTCAGTCGGCGATCAGCGCTGTGAACTCCAGT
Associated Phenotype:
Not determined