Busch Lab

ZMP

eif2ak4

Ensembl ID:
ENSDARG00000077010
ZFIN ID:
ZDB-GENE-090302-1
Description:
GCN2 protein [Source:UniProtKB/TrEMBL;Acc:B5U809]
Human Orthologue:
EIF2AK4
Human Description:
eukaryotic translation initiation factor 2 alpha kinase 4 [Source:HGNC Symbol;Acc:19687]
Mouse Orthologue:
Eif2ak4
Mouse Description:
eukaryotic translation initiation factor 2 alpha kinase 4 Gene [Source:MGI Symbol;Acc:MGI:1353427]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa24807 Nonsense Available for shipment Available now
sa38198 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24807
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
ENSDART00000112556 Nonsense 196 553 4 13
Genomic Location (Zv9):
Chromosome Zv9_NA561 (position 71287)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150326.1 71287
GRCz11 KN150326.1 71287
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGTGACTCTGCTGTCGCGGCTCAACCATGAGAACATCGTGCGCTATTA[T/A]AACGCCTGGATCGAGCGGCAGGAGATGTCTTCTGGAGCAGAGCTGACCAG
Long Flanking Sequence:
TTCTGTGTGTTTGTAAATGCGTGTTTTGATAATACCTGCGATCCAGTGCGTCTCTTTATCGAGAGTAAACGTGGCACAGACCATGTAACAGTAGCTACAAATTAAAATTAAAGCTGCAGTAGGTGATCGTCTTTAAAAACGTGTGCTGTTGTGCTGGTTGAAAGTCTCTTCACATTCCAATAGTACTGATTAAAGTAAATGATCTAAATGTGTTTATGTGTGTTTTTATATCCTGGATCAGGCATAAGACTAAAAAATGTTCGTCCAATTAAATATTGTTGGACCGACAAACATTTCCATTACGACAGTCATCTCAAATTAAAAATTGAGTTTCTGCGGATGCTCACTTTTGTCTCCTTACAGGTGCAGAATAAACTAGACGGCTGTTATTACGCGGTGAAGCGGATCCAGGTGAACCCGGCCAGCAAACAGTTTCGCAGAATTAAAGGTGAAGTGACTCTGCTGTCGCGGCTCAACCATGAGAACATCGTGCGCTATTA[T/A]AACGCCTGGATCGAGCGGCAGGAGATGTCTTCTGGAGCAGAGCTGACCAGCGACAGTTCTGAGGCCCTGAGCACACCTGAGCGTCCTTCCCGACCTGCCGCTCCCTCCCGCAGAAATGAAGATCTGAGTCTGCTGGGACGCCTAGAGGAGGAGGCTCCGCCGCCGGCTCTGGCCAGCTCTGTGGAGTGGAGCACGTCTCTGGAGAGATCCAGCAGTGCTAAATGCAGCACCGCAGACTCTGAAGATGAAGAGGAGGAGGAGGAGGAGGATGTCTTCTGTCCATCATTCCTGTGAGATTTGGACAACACTTACACTTAATACACAAATACACTTTATTAAACATGTATACAGATACAATGACATCACATACAGTTGAAGTCATAATTATTCGGCCTCCTGTGAATATATATATACATAGCACTGTCAAAATTAACGCGTTAACGCATGCGATGAATTTTAAATAATTAATGCGTTAAAACAAATTAACGCAGTTCAGGTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38198
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
ENSDART00000112556 Essential Splice Site 498 553 11 13
Genomic Location (Zv9):
Chromosome Zv9_NA561 (position 51807)
Other Location(s):
Assembly Chromosome Position
GRCz10 KN150326.1 51807
GRCz11 KN150326.1 51807
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGAGCACCGCATCAGAGCGCATATTTGTGCTTAGTCAACTCAGGAAA[G/A]TGAGTTTCATCAAACACATCCCACTGTCATCAGTTTATTCTTCATCATCT
Long Flanking Sequence:
GTGAATTAGATTTATGCACAAATCTGTAATATGGCATTAATCATTAGTCAATAATCAGCGTGTCCAGTCAGTGAGAAACACAAGAGCATTACCTCCCCAGCTCCTGCTGCTCCTGCACAGATATCACTGAGAGGAGTGTAGTTTGCTGCACTGTTGGGATTCTCCACTGTAGTGTTTGTTCTCCTCTAATAAATGAGCCTCAGAAAACCAAGACCAAACGCAATGAATGCAGTGAATGCGGTGGCTTCTGGAGGCTTGAAACGGGAGCGAAGACAGATGCTCAGGACCGTTCTGGAGGGAATAATAATAGAAGAAGAAGAATACTGACGCACCGTGATGACGGACTGACATAGCTACTGTCTGGCTCTCTCTCTCTCTTTCTCTCTGTGTGTGTGCAGAAAGTGGATCTGTTCAGTCTGGGCATCATCTTGTTCGAGATGTCCTACAGGCCCATGAGCACCGCATCAGAGCGCATATTTGTGCTTAGTCAACTCAGGAAA[G/A]TGAGTTTCATCAAACACATCCCACTGTCATCAGTTTATTCTTCATCATCTGTCGCTCAGAACAAACACACACATGATGAACATTAGGGATGTATTGAAAGTAAAATCCTCGTTCTGTTTGTCCTGCAGGAGTCCATTACTTTCCCTGAAGATTTCTGCAAGTATGAGAGTGGAACGCAGGTGACACACGTTTTTTTTTTAATGTTTTTCTTTTTGTTAGTTTATCTACAATAACTTTTCAGCCTTATAGTAGTGTATTTATTTGGCACATTATGTGTATAACCACAGTTTTAGTGGTTATTTGAGGAGCAAACAGGGCAAACAGAGCCCAACAGAAACAGAAACGTACACTGTGCCAGAATTACACTGCAAAAAAATGTTTTTTTTGTTTTGTATCTTGTCCGAATATCTAAAGATTCTTAAATCAAGAAGCATTTTCCAGACAAGCAAAGCTAATGTGCTTGTATTCAGAAATAATTTGCCAAAATTAAGCGAGTTTTT
Associated Phenotype:
Not determined