ZMP
si:ch211-241d21.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens GLIS family zinc finger [Source:UniProtKB/TrEMBL;Acc:B8JJK6]
Human Orthologue:
GLIS1
Human Description:
GLIS family zinc finger 1 [Source:HGNC Symbol;Acc:29525]
Mouse Orthologue:
Glis1
Mouse Description:
GLIS family zinc finger 1 Gene [Source:MGI Symbol;Acc:MGI:2386723]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31640 | Nonsense | Available for shipment | Available now |
| sa10106 | Nonsense | Available for shipment | Available now |
| sa38681 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31640
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000029255 | Nonsense | 376 | 902 | 3 | 10 |
| ENSDART00000140941 | None | None | 226 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 18620877)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 18065765 |
| GRCz11 | 8 | 18101477 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTCTCATACAGCCCGCTGCATTATTGGATGGCTGCACCCCAACGCTG[A/T]AACAAGAACCGGCGGATGAGTTCTCTCCAAGTGAGGAGGAGCTCTTTCAG
Long Flanking Sequence:
ATGATGGTAACTTAGCAACTGTTCTGTCGTTGTCGGCGATGGCGGTGACTGTGTATCCATTTAATAATGAAGATGGCTCCACCCCGCTGGCTTTGTCCCCGAGCTCACGTCACTCAGCAAGGCCAAACGCGAGCGGACTGAAGAGACGGTGCCTCTCGGTGGCCTCCCAGTCCGCCTCAGAGGGAATCGATACCGTCGCCAACATCTGCTCCTCCCAGATGTCCTGCGTTAACGGCCTGCGCACCAATTCGTCATCGCCCTCCGCCGGCACGTTCTCCCACAGGTCTCTCTCCGCACCCAGCCCTCAGTTGCCGTCACCCTCCACCTCGTCCTGTCTCCTGCCCCTCTCCTCTTCGTCATCGTCCTCCTCGGTGTCCTCAGTTGAGCATTGTGAGGACGTGGGCTCCATGCAGCCTGGACCCACTGGTGTGGGGAGCAGCGACGGGCTCGGACTTCTCATACAGCCCGCTGCATTATTGGATGGCTGCACCCCAACGCTG[A/T]AACAAGAACCGGCGGATGAGTTCTCTCCAAGTGAGGAGGAGCTCTTTCAGCATCACTATCAGCATCTGACGAGCCGCGCAAGCCACTGCGGTGGGCATTCCCAACATCACCACCATCACCACCACCATCAGACAGGCCCCCCACGGCCGCCCATGCCCCCTCCCTACCACCTGCACCAGTACATGGGCTCCGGCCCAGGAGCCCTACTGCATCTTCAGAGCCAACAGCAGTCTCCACCCTCAGGCCTGCTGGCACAGCCCAAACAAACAGGCCTGGTAGAGCAGCAGGTGGGCGACAGGGAGGACGTGTTTAGCGATAAACAGGTTTGTCGTTGGATCGACTGCAGCGCAGCATATGAGCAGCAGGAGGAGCTGGTTAGGCACATCGAGAAGGTCCACATCGATCAACGCAAGGGCGAGGACTTCACCTGCTTTTGGGCCGGATGCGTCCGACGCTACAAACCATTCAACGCCCGATACAAGCTGCTCATCCACATGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10106
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 |
|---|---|---|---|---|---|
| ENSDART00000029255 | Nonsense | 450 | 902 | 3 | 10 |
| ENSDART00000140941 | Nonsense | 32 | 226 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 18621099)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 18065987 |
| GRCz11 | 8 | 18101699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCACCAGTACATGGGCTCCGGCCCAGGAGCCCTACTGCATCTTCAGAGC[C/T]AACAGCAGTCTCCACCCTCAGGCCTGCTGGCACAGCCCAAACAAACAGGC
Long Flanking Sequence:
CCTGCGTTAACGGCCTGCGCACCAATTCGTCATCGCCCTCCGCCGGCACGTTCTCCCACAGGTCTCTCTCCGCACCCAGCCCTCAGTTGCCGTCACCCTCCACCTCGTCCTGTCTCCTGCCCCTCTCCTCTTCGTCATCGTCCTCCTCGGTGTCCTCAGTTGAGCATTGTGAGGACGTGGGCTCCATGCAGCCTGGACCCACTGGTGTGGGGAGCAGCGACGGGCTCGGACTTCTCATACAGCCCGCTGCATTATTGGATGGCTGCACCCCAACGCTGAAACAAGAACCGGCGGATGAGTTCTCTCCAAGTGAGGAGGAGCTCTTTCAGCATCACTATCAGCATCTGACGAGCCGCGCAAGCCACTGCGGTGGGCATTCCCAACATCACCACCATCACCACCACCATCAGACAGGCCCCCCACGGCCGCCCATGCCCCCTCCCTACCACCTGCACCAGTACATGGGCTCCGGCCCAGGAGCCCTACTGCATCTTCAGAGC[C/T]AACAGCAGTCTCCACCCTCAGGCCTGCTGGCACAGCCCAAACAAACAGGCCTGGTAGAGCAGCAGGTGGGCGACAGGGAGGACGTGTTTAGCGATAAACAGGTTTGTCGTTGGATCGACTGCAGCGCAGCATATGAGCAGCAGGAGGAGCTGGTTAGGCACATCGAGAAGGTCCACATCGATCAACGCAAGGGCGAGGACTTCACCTGCTTTTGGGCCGGATGCGTCCGACGCTACAAACCATTCAACGCCCGATACAAGCTGCTCATCCACATGAGGGTTCACTCGGGAGAGAAACCCAACAAATGCATGGTGAGTCTCCACAGTTTTTTAATGGCTGTCAAAAGTGCAGCATTTTCAACAGTTTCCTATGATGAAGTTCATTATAAGTGGCAGCTAAAATGGCCTTGAAAAGGCATAAGCAGCTTTTCGGAGTGAAATGTTTTCGTTGGAATTCACAGTGAGTTTAATTTAAGTGGAAAGCTGGTGAAAGCTAATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38681
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000029255 | Nonsense | 716 | 902 | 7 | 10 |
| ENSDART00000140941 | None | None | 226 | None | 3 |
Genomic Location (Zv9):
Chromosome 8 (position 18684500)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 18129388 |
| GRCz11 | 8 | 18165100 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCAGGCCTGTACGCTGGCTCCAGCACGACACACAATGGAGCCCCACTT[G/T]AGTTGCTCTCTTCTGGACCTGACCTGCCACCCAGGCAGCCCCGCATGGAC
Long Flanking Sequence:
CATTTCAACAATCACTTGCTGTGTGTACAGGGTATTATTCAGATGAATCAATGATTGATTGACTTCCTCATTGTCCATCATTTTTTTCAGCTTTTTTTTTTTTTGGCTGAAGATACAGCCTACCTGTTATATTCATTTTTGTAGCAATTCAAAGCAGATCTGCCTTTGCTTATTATTTCTGCCGCTCCATTCAGATATAGTCAATCTATTAAGGATGTTCTGTTAAAATCACTCAGTCAAATCCATTCTGCACGGCAACATTTATCATTGACAGTAAATAGCGAACAGCAAGAAACAGGAACAGTTAATTTAATCCAAAGGGCCTTGGTGTGTTTGTGTTGTCATAACAAGTGCCTGTTGCCATTAAGAGTTGTTTGTGGAGATTTAATTTGGTCAATGTGCCGCTCTTGAGGTTTATCAGGCATGTTTTGCACATTAGTATTGTTTGTCTTCCAGGCCTGTACGCTGGCTCCAGCACGACACACAATGGAGCCCCACTT[G/T]AGTTGCTCTCTTCTGGACCTGACCTGCCACCCAGGCAGCCCCGCATGGACCGTGACATTGGCAGCCCCCATCATCTCTCCCCGCTGTCCGGCCTCGAGAACACCCGAGAAGGGTAAGTATTGAACCCGCCGAGCTTCATTTTTACTCCCAGTTGCTCTGACATACATGCAGGGCGGATGAGCTCAATGAAAATGATGTCAGGGGGTTGTCATCAGTTATGGATATCACTGTAGTAATAGTTACACATGCTGGGACTGTTCCAATTAGTGAGCTGTCGCAAAAAGGCTGTTCCAAGAGATATCTCCTTTTGACCCGATTCCACAAACGCAATTCCACAATTCACTATGATGTTCTTTGAGTGATTCATCCAGGATGTCTGAGTGAGAAAACATTGACTTTTCAATAAATGACAAAAATTAAACACTCACTTAGTAATCTCTACTGAATGAATCATGAATCAGTTCAGTGAATGATTCATTAGTATACTCATAGCCTGTTGT
Associated Phenotype:
Not determined