Busch Lab

ZMP

grhl1

Ensembl ID:
ENSDARG00000061391
ZFIN ID:
ZDB-GENE-030131-3665
Human Orthologue:
GRHL1
Human Description:
grainyhead-like 1 (Drosophila) [Source:HGNC Symbol;Acc:17923]
Mouse Orthologue:
Grhl1
Mouse Description:
grainyhead-like 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2182540]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa14528 Essential Splice Site Available for shipment Available now
sa6488 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14528
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087454 Essential Splice Site 70 613 3 16
Genomic Location (Zv9):
Chromosome 17 (position 32628358)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 32470089
GRCz11 17 32422600
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATRCTATTGGATGTGGTCAGACTTACACAGAGTTTGTTTGCTTTCCCC[A/T]GGTGCCACGGGACAAGAGAACAATATCCCAGCAAAAGACTGACGTCCTGG
Long Flanking Sequence:
TCATGTTTGTTAGTCCAGTAAACAGAACTTCTTTGAGGGATGTAAATTTATAGTAGCAAAAAACTTTTTTTTTCATGCTGTTTAAAGGCTAAAAATATGATTATTTCTAAACATAAAACTAAAAAATAAATGTATATTTAGCATTAAATATTAACAAAAAAGTATTTATTAATACTGTAATCACTGCTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACTATAACTAAAATAGTTTTTTATTAACATGTCTAAGACCAGAATATGGTTATTATTTGAGAACCACATTGAGTTTAATGATGTCTGATGATGTCCTATTTTTGCACCAAATGCTGATTGTATGTTAAATATGTTGGCTGGCAGATATAATAGGTAAAGCTGATGCTATTGGATGTGGTCAGACTTACACAGAGTTTGTTTGCTTTCCCC[A/T]GGTGCCACGGGACAAGAGAACAATATCCCAGCAAAAGACTGACGTCCTGGGCTCTGATGTGGATCCCAACAAAAGGTGAAGCTCTCATCAAAGATGCCTTAGTCAATGCCATTTTTTTCTCTCATACTGGGAAGATGAGACCCTACATTTTCATTATTCTGTACTATGGTTGCAGTAACTAATAGATTAGAAAATAGTCATCAGTCATTTAAGAATGCAAGAGTGAATTCCATTTCTTCCTCATATTTGGAAGTTGAGGTCTTACTTTTATTTTTAATATTGGTGCTGGAGGTTTGAATTAGTAATAATAGTAAAGAAGATAGTTGTCAAATATTTATACGGTTGATCTGTCATGTCTGTTTGTCCAGCATGCAGAAGCTCAATATACAGTAAGTGACCTCAATTTGAAGTGCTTTTTTCAAAGAATATGAAGTGCTTAAAATATGTTTATGTACATGTTTAATGGTGCTGCACTGTTTAAAAGTATGTATTATACAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6488
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087454 Essential Splice Site 361 613 9 16
Genomic Location (Zv9):
Chromosome 17 (position 32614447)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 32456178
GRCz11 17 32408689
KASP Assay ID:
554-5306.1 (used for ordering genotyping assays)
KASP Sequence:
TGCATTAAATAACTTGAACACTTCTTTCTCTCTCTCCCTCTTTCCTCCTC[A/T]GATCTTCATCTCRGTGAACTGCCTGAGCACAGACTTCTCGTCTCAGAAAG
Long Flanking Sequence:
AACAAGTTGAGGATGAGTAAATGATGACACGGGGCAAACTATTCTTATAATGCAGGTGTACAGTAAACAAGCCCTGGAAGCAACAACCACTGAATTGACATGAGCCAATAATGATTTCTTTACATGATACTTCATCCAAAAATTCCATTTACTCACTATTATTTACTCACCCTTATGTGTTCAATCTTTCTTCTGTTGAACACAAAATAATATATTAGAATATATGTATTTTTATTAGCCTGAAAACCATTGACTTCTGAAGATTTCCACCTTTCTTCAAAGTATCTTCTTTTGTGTTTAACAGAAGAAATATTTTCAGTCTTGAATGAACTGCCCCTCAAATTATATTTTTCTCCTTTTTGAGGTTTCCCCACTGCTTATTGTGCATTTATTACTGTAAAGCTATATACAGTCATTTTAAAGGCTCCAGTACTCTCTAAGAAATCGATTTGCATTAAATAACTTGAACACTTCTTTCTCTCTCTCCCTCTTTCCTCCTC[A/T]GATCTTCATCTCGGTGAACTGCCTGAGCACAGACTTCTCGTCTCAGAAAGGAGTGAAAGGCCTGCCGCTGAACATACAGATCGACACCTACAGCTACAACAACCGCAGTAACAAGCCCATCCACCGCGCTTACTGCCAGATTAAAGTCTTCTGCGACAAGGGTGCCGAGCGCAAGATTCGTGACGAGGAGAGGAAACAGTCCCGGAGGAAGGGCAAGTGTCCTGACGTCAACCCTCCTTTGGGAAACTGTAAGCACAAGCTTTAGGCTTTTGCTTTTAACTGATGCAATGGTGGTTTGTAGTAGAAATAGAAGCCTAGAGCCCCGGAGAGTCTTGTTTTTCACTTTGTCCTTGTTCGTTTTGTGCAGTCGGGGCAGATGTCAAGGTGCCGCTCCTGCACAAGCGCACAGACATGACAGTGTTCAGGACACTGACGGATTTCGAGACGCAGCCTGTCCTTTTCATCCCAGACATCCACTTCTCTACCTTCCAGCGACATGT
Associated Phenotype:
Not determined