ZMP
glis3
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein GLIS3 [Source:RefSeq peptide;Acc:NP_001074076]
Human Orthologue:
GLIS3
Human Description:
GLIS family zinc finger 3 [Source:HGNC Symbol;Acc:28510]
Mouse Orthologue:
Glis3
Mouse Description:
GLIS family zinc finger 3 Gene [Source:MGI Symbol;Acc:MGI:2444289]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17645 | Nonsense | Available for shipment | Available now |
| sa1567 | Nonsense | F2 line generated | Not yet available |
| sa16572 | Nonsense | Available for shipment | Available now |
| sa1286 | Nonsense | F2 line generated | Not yet available |
| sa41564 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17645
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085375 | Nonsense | 47 | 787 | 2 | 12 |
| ENSDART00000142833 | Nonsense | 63 | 803 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 674426)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 671199 |
| GRCz11 | 10 | 687154 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCACCAATGGAAAACWGGGCTTTCCACAGCCATCMCGAGCTCTTCATCAA[C/T]AGGCWCCACAGATTTCACTCCCAGCATCCTCCTCCTCCAAACAGTCTGCT
Long Flanking Sequence:
AAGCCCCACCCCCTACTTAATATTCAGTTTCAGTTGGAAGTACATCAACATACTGTAATAAAGCCCCACCCCCTACTTAATATTCAGTTTCAGTTGAACGTACTTCAGCATACTGTAATAAAGCCCCGCCCCCTACTCAATATTCAGTTTCAGTTAGAAGTACATTAACATACTGAAATAAAAGTCTCAGCAACTTTCAGTTCACCCAGGCTTTAAGACATTGATTCACATGTAACTAGAGAAACATTTAACCGTGTTGTGTCTGCTGTGCTCCTCAGGATCCTGATATATGAATCTGAAGGCCATGTTTTGTGATGGACATGAATGGGAAAGGCTGTAACCTGATGGTTTCTCCGTCCGGCATGGCTCAGATATCTCCGCTGAAGGTCCACACTCCTGCATCTCTCTATCCAGAATCAAACTCAGCTCAGAGTCTCCGCCGGCAGGTGCTCACCAATGGAAAACTGGGCTTTCCACAGCCATCCCGAGCTCTTCATCAA[C/T]AGGCTCCACAGATTTCACTCCCAGCATCCTCCTCCTCCAAACAGTCTGCTCGACAATGCTGTCAGGACAGCGGTATGAAAGGTAAAAACAAGAATTGGCATCCCAGGTCTTGGAGGGCTCCAATTTTGGCCTTTTTAAGATGTAAAATTACTTGTGTCTCCAGAATGTGTCTGACGTTTCAGCTCAAAATACCCTCACTGTTAAGAGCGATTAGTTGACTTTACCTTCAAAATGTGAGTTAACTGGTTGCCTTATAGTTATTAAGTAAACAAATTATGCACATAATTATAAAAGTTAAGTCAATGGCAATTGTCAGAAGGAATTGTAGCTGTTTTGCACCTGTGCCTTTAAATGCAAATGAGCTGTTATCCCCGCCCAATTTCCAAACATTTTGTTTTAGAGAAGTATAGTTAAGGTCAGATATCAGGATAAACCAAGTGGCAACCTCCCGCTCTCCCTTGGGAAGCTAATACGGAAGTAACTGAAACTGCAATTCATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1567
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085375 | Nonsense | 219 | 787 | 4 | 12 |
| ENSDART00000142833 | Nonsense | 235 | 803 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 663606)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 660379 |
| GRCz11 | 10 | 676334 |
KASP Assay ID:
554-1510.1 (used for ordering genotyping assays)
KASP Sequence:
CGGCAGTAGTCCGCGCCTCTCGGCCCGCTCAAAGAAGCGAGCGCTGTCTT[T/A]ATCCCCACTATCGGATGGTTTGGGCCTGGACCTGAACTCCATCATCCGCA
Long Flanking Sequence:
GCTTGCTCCGGCCCTGACGTCACCCATTCTAAGTGAATAGGAAGCGTTGACACTGACGCCCTGTGTGAATAGGGCAATAGGTATCTCAGTATTGGTTGCAAAAATCCCGATCAGAGCACCCCTAATTGTAATTTTAATCCCTGTTTCGGAAACACACAATCAACCAACATGTCTGAAAGCACCCTAAATGAAGGCAGAATGGTGATTTTAACTGATCTCTTGCAGCAGGTGTTTGCTCTCCAGAGAGTCTCTGGCCTCCACCACCCTTAGTCTGGCTGAGACTCAGTCTGTGCGCAGCAGTAAACTGGACTGGCCGTACGGCTACAGGGTCCTTCCTCCACTAGGCCACCAAACAGCCAATCAGTTGTCAGAATCCACTGTCCCTGAATCCTCCCTATCCGAAAGCGTCTCCAACCCTGCATCTCTCCCTCATTACCTCTTCAAGGAAGACGGCAGTAGTCCGCGCCTCTCGGCCCGCTCAAAGAAGCGAGCGCTGTCTT[T/A]ATCCCCACTATCGGATGGTTTGGGCCTGGACCTGAACTCCATCATCCGCACCTCGCCTACATCTCTGGTGGCCTACATCATCGGCTCCAGGATCTCACCAGCGTCCCACAACACCCCGTCCCCACTGCAGGCGGACGTCTGTGGGCATCTGCTGGGCATCAGGGGCAGCGGCATCCCTACATCCAGCAAACATAGCATCTCCGTCAGCGAGAGCCTCCGCATGCAGCCGCTGGAGGACCAGTTCACCAACCTACTAGTGGAGCAGCAGATCCTGCCAGACCCACAAACTGCAAAGGCCAGTCAGACCCATACGGTAATGAAGCATTACCTACGTTACTTGGGGTAAACTTAGAGGGCGCTTTCTACATTTGGTCAATTTAAAAATATGTAACTTAGGCTACACTTTGTTATACATTTCATGTATCCACTAGTGGGCGCTGTCTACACCTGTAGATCGCAAAAAATTAAATATCACTGTCAGATTTTTTCAGTATCGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16572
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085375 | Nonsense | 541 | 787 | 7 | 12 |
| ENSDART00000142833 | Nonsense | 557 | 803 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 648573)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 645346 |
| GRCz11 | 10 | 661301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCCAGCTCACTGCGGAAACACGTCAAATCTCACTCGCTGAAGGAGCAG[C/T]AGGCCCGGAAGAAGGTACKAGAGACAMCAACACACACAAGTCWGTCATCA
Long Flanking Sequence:
GAGACACACATTTCCACACACGTATGTGCACACACACACACTCCAAAAATATTTTTGTTCCTTGTTCAAAGTACTTATTTAAAATAAGCTGAAACAACACAATTCTTGAGATTTTGTCGGGACTGTTTTATGTTCAATTCACTCAAATTAGTAAAAACAACTAAGTTAAATTAATTCCTTCATGTTGTCCCAACACAAATCGATTGTGTGGAACCCAATATTTTTTACAGTGCACACAGAGAGACACACTTTTGGGATTCATTGCCCTACTGGTAAGATCAGGAACAGCAGGGTCCTATAAATGTGTTCCAGCCCCTCCAGGTGTGCAGGAACATGTCATTGCACAGCTCCACACTCACACTCTCTCTAACACACACACACACACACACACTTTGTGTCTGCAGAAACCGTACGCGTGTCAGATCCAGGGCTGTGGAAAGCGCTACACCGACCCCAGCTCACTGCGGAAACACGTCAAATCTCACTCGCTGAAGGAGCAG[C/T]AGGCCCGGAAGAAGGTACGAGAGACACCAACACACACAAGTCAGTCATCATGTACTCGTCACCACAGCCACACACACACAATCGAGAAGCTTTTTGTGTTTTATCCACAGAATTAATCTGCAGATTTATGCGGAGCGATTTTGAGAGCAACTAACAACTTAAAACATGAAATAAATAAACTTTTAACCGTTTGTTTAAGGCAGGGGTCACCATATTTGTTCCTGGAGGGCCGGGGTACCGCAGAACTTAGCACCAACCCTAATCAAACACACCTGAACAGGCTAATCAACAGCTGCGTCCCAAATGGCACACTATGCACTCATGCACTATGCACTTACACACTCAACAGCACAGTATATGTATGTAGTGTCGTCCCAAATGGAGCACTGATGTTTTTTTACTACAAACCGTTTCCCTGATGACGTTTGACGGATGCCAAATCAGTGAAAAAAATGACCGAACTATCAAATAACACCTGCCATGAGTATAATCACATTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1286
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000085375 | Nonsense | 651 | 787 | 9 | 12 |
| ENSDART00000142833 | Nonsense | 667 | 803 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 640714)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 637487 |
| GRCz11 | 10 | 653442 |
KASP Assay ID:
554-1201.1 (used for ordering genotyping assays)
KASP Sequence:
TGACTCACCAGACNNNNNNNNNNNNNNNNNNTCAGACTCATCACATCCAG[C/T]AGATTCATCAGACTCACCTGACTCATCAGATCCAGCAGATTCACCAGACT
Long Flanking Sequence:
ACAGCTTACATGTCTCTCATTTCATTAAAGAAATGCCTTTGCATATTATGAAGGGTAACAGCATAGCATGATACTGAACGCAAAAGACCTGAGCACACGGGTGAAATAAGTCCCTCTATTACATGCCATTCCTCACAGTGAAGGACGGCAGCAGCAGTGCCGTGTAAAGCATGTTCTGTGTAATTGGCTATACAAAGCTTTCAGAATATTTTTGTTGAGTTATTTATACATGAAAGCGTGGGCTAAAGCTAGCTAATCTAACCACTGTTGTGCTTAAGGGTGATGGTTTTCTGTTTTTCTCTTCTGTCGATGGGCAAGTCTTCACCCTGAACCAGCCGAGCCAAACAAACACCCTGAACAGCCCAATGCAGATCGCAGGCGGTCCACAGACTCATCAAAGTCCTCATCAGACTCACCAGGCTCATCAGATCCATCAGACTCAGACTCATCTGACTCACCAGACCCATCAGGCTCACCAGACTCAGACTCATCACATCCAG[C/T]AGATTCATCAGACTCACCTGACTCATCAGATCCAGCAGATTCACCAGACTCATCTCTCTCCACATGGAGCACTGCCACCATTACAGGGAAACAACAGGTGGGATCGCTGTCATCAAATGTGTTGAGCACAAATCAATATTTCACTCAATGATGGAAATGTACTATTAGTTTTTTCCAGACCTGCCCGAGTTTCTTTTTTCTGCTGAACACATGGTTTTATTTTGAATATTGTCAGTAACCGTACAGCTGACCTTATCCATTGACTGCCACAGTATTTTTCCACTTCAGTGGTCTCTTTACCAAATAAACATTGGTTTTAATTCATTCCAGAGGTTTACATCTGACCAGATGGCACTTTTGGATCAATTTCACACCAATTATCAGGAACAATTTATCACTAATTAAGTGTAATTAAGAGAGTCGATTTTCACATCTACATTCATTTAAATGATAAAAGTTCTGATCATGGCAGATTTCGCCAGTACTGCACTACCTGACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41564
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000085375 | Nonsense | 755 | 787 | 12 | 12 |
| ENSDART00000142833 | Nonsense | 771 | 803 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 10 (position 632080)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 628853 |
| GRCz11 | 10 | 644808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATGCTGTGTGTGTTTATGACAGCAGTGCTGGACTGCCAGAGCGGCCCT[C/T]AAGGCTTTATAGGAGAGCAGGAGCCCTCAGTGTCGGAGGACAATTATCTT
Long Flanking Sequence:
ATTTAAAGGCTTCACTAGGGTAATTAGGGTAAAGTTAGGGTAATTAGGCAAGTTATTGTATAATGATGGTTTGATCTGGAGACTATCGAAAAAAGCTTAAGGGGGCTAATAATATTGACCTTAGCATGGCTTTAAAACAATTAAAAACTGCTTTTATTCTAGCCTAAATAAAACAAATCAGACTTTCTCCAGAAGAACAAATATTATCAGACATACTGTGAACATTTCCTTAACCTATTCAACATCATTTGGGAAATATTTAATAAAGAAATAAAATTAAAAGGGGGGCTAAGACTTCAACTGTACATACATAAACATTTATTATTACCAGTTGATGGTTTGATAAGGCGCTTGGACCCGAAAGCCGCTTAGCCTGTCGTCACACTTAACAAGAGAATACTGAATCATACAGGCCTACTGTGAACGCCTGCCATATATTCTCATGCTTGTGGATGCTGTGTGTGTTTATGACAGCAGTGCTGGACTGCCAGAGCGGCCCT[C/T]AAGGCTTTATAGGAGAGCAGGAGCCCTCAGTGTCGGAGGACAATTATCTTCACATCCCGAGATGTCCGAGCCGGATCTCCTGTGTGTTCACTGAAGGCTGAGCGTCTCCGCCACACACTGCAAAATGCCTTTACCTACAGTTTCTGTCTGGATTCCAGTCCAAATACCAGGAAGCGTTTTCTTTCCAGTGCTTCTACAAGAATGTATATTACATTTCATTAAACAGCACTTGGGAGATGTTAGATACTCAGTGTTGGTCTTTAACTGTACACAGCTCACCAACAAACAACAGAAAGCACTTATCACAGGATAAATGTGTATTTTAAACAGACAACCTTTAATAAACCTGTTGATGCATCTCTCTCTCTCTTTATAATAACCGCACAGGCTTTGATATTTGAGTATTTTCCAGCCTCTGTATGTAAACAGATCACAAATAAGCGAAGCTATGAATGAACAGTGACAGCAAAATGCACTTATTAGAGATGAAAGCCATACTG
Associated Phenotype:
Not determined