ZMP
golim4a
Ensembl ID:
ZFIN ID:
Description:
Golgi integral membrane protein 4 [Source:RefSeq peptide;Acc:NP_001091662]
Human Orthologue:
GOLIM4
Human Description:
golgi integral membrane protein 4 [Source:HGNC Symbol;Acc:15448]
Mouse Orthologue:
Golim4
Mouse Description:
golgi integral membrane protein 4 Gene [Source:MGI Symbol;Acc:MGI:1920374]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39514 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30471 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39513 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39514
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 |
|---|---|---|---|---|---|
| ENSDART00000109191 | Nonsense | 43 | 645 | 1 | 15 |
| ENSDART00000127546 | Nonsense | 10 | 520 | 1 | 14 |
Genomic Location (Zv9):
Chromosome Zv9_NA331 (position 76185)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150030.1 | 22314 |
| GRCz11 | KN150030.1 | 22314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGAGCAGGAGACCAGGGATCATGGGCAACGGCGCGTGCTCCAGGAAG[C/T]AGAAGAAGATTTTCCAGTCTCTTTTTCTGGTCACGGTGGTTTTTGGCATG
Long Flanking Sequence:
CAATTACAAAAGATTTCCATCTCAGACACACGGCCCTCCCATCAGAACCAACATCTTTTGACTGACATGACCTTTGACCAATCACAGCAATGGAATGTTGCCGAGGGGCGGGATTTCCTTCTGTTTCAGGCAGCGCTGGATGATCTTCTGCAGCGCTAGGTGACACGTAATGAAAGGTGCGATCAGGCCTCTCTAAAACTAAGGTAATTAGTTAAAAAAGACTGCTTTTCATTATGTAGACAACTTCAGAGAGCGCTGACTAAACACGAGAACCGAATTCAGCCGGATACGTTACTTTTCTAACTACTGAGCGTCTTTGGAAAACTTGAGGGAACGTTCGTTTACTTAGCTGCTGTCTGGGAATATAATGTTTCATGAGGAATTTCGGAGGGGAAAGCGTTGTTTCTTTGCTGAAGAGTGAAGATAAATTCATTCCCGGGAAAGTTTGTGTGGAGAGCAGGAGACCAGGGATCATGGGCAACGGCGCGTGCTCCAGGAAG[C/T]AGAAGAAGATTTTCCAGTCTCTTTTTCTGGTCACGGTGGTTTTTGGCATGATCTATGGAGGGATGATGTCTTATGAGATGCACAAACAGCTGAAGAGGACAGAAGAGCTGGCCGTCAAATATCAGCAGCACCAGGAGTCACTTTCGGCTCAGCTTCAAGGTACGGTAAAAACACACTTCGTCGTGATGACGTCACATTGTAAAAAAACTGCCTTGCTTTCTTACCTCGGTGTTGCCTTCTTGATGTTTTTCCCATTTATTATGATGCTCACGGATGTATTTTGTGCTTGAACGTATATTCATGTTTATTGTAATGCTCAAATACTTATAAAAAATTCGATCACACTTTACAATAAGGTTGTATTATTTGTTAATGTATTTACTAACATGAACTAAGTGTAAACATTTACATTTAGCAGACATTTAGCCAAAGCGACTTACAAATGAGGTCAAGAAAGCAATTTACACAACTATAAGAGCAACAATGAATAAGTGCTGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30471
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109191 | Essential Splice Site | 96 | 645 | None | 15 |
| ENSDART00000127546 | Essential Splice Site | 63 | 520 | None | 14 |
Genomic Location (Zv9):
Chromosome Zv9_NA331 (position 76024)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150030.1 | 22153 |
| GRCz11 | KN150030.1 | 22153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGTCAAATATCAGCAGCACCAGGAGTCACTTTCGGCTCAGCTTCAAGG[T/C]ACGGTAAAAACACACTTCGTCGTGATGACGTCACATTGTAAAAAAACTGC
Long Flanking Sequence:
GACACGTAATGAAAGGTGCGATCAGGCCTCTCTAAAACTAAGGTAATTAGTTAAAAAAGACTGCTTTTCATTATGTAGACAACTTCAGAGAGCGCTGACTAAACACGAGAACCGAATTCAGCCGGATACGTTACTTTTCTAACTACTGAGCGTCTTTGGAAAACTTGAGGGAACGTTCGTTTACTTAGCTGCTGTCTGGGAATATAATGTTTCATGAGGAATTTCGGAGGGGAAAGCGTTGTTTCTTTGCTGAAGAGTGAAGATAAATTCATTCCCGGGAAAGTTTGTGTGGAGAGCAGGAGACCAGGGATCATGGGCAACGGCGCGTGCTCCAGGAAGCAGAAGAAGATTTTCCAGTCTCTTTTTCTGGTCACGGTGGTTTTTGGCATGATCTATGGAGGGATGATGTCTTATGAGATGCACAAACAGCTGAAGAGGACAGAAGAGCTGGCCGTCAAATATCAGCAGCACCAGGAGTCACTTTCGGCTCAGCTTCAAGG[T/C]ACGGTAAAAACACACTTCGTCGTGATGACGTCACATTGTAAAAAAACTGCCTTGCTTTCTTACCTCGGTGTTGCCTTCTTGATGTTTTTCCCATTTATTATGATGCTCACGGATGTATTTTGTGCTTGAACGTATATTCATGTTTATTGTAATGCTCAAATACTTATAAAAAATTCGATCACACTTTACAATAAGGTTGTATTATTTGTTAATGTATTTACTAACATGAACTAAGTGTAAACATTTACATTTAGCAGACATTTAGCCAAAGCGACTTACAAATGAGGTCAAGAAAGCAATTTACACAACTATAAGAGCAACAATGAATAAGTGCTGCAGGCAAGTTTCGGGTATGTAAAGTGTAAGACGCAAAACATTAGTAATTATTATTATTATTGTTTTTTTTTTGTAGTACAGTTAGTGGTAGAACCAGAGAGGGAATTGCAGATTAGGAAGGGAAGTGGAGACTAAATAGTTGAGTTTTTAGTAATTTCTTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39513
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109191 | Essential Splice Site | 120 | 645 | 2 | 15 |
| ENSDART00000127546 | Essential Splice Site | 87 | 520 | 2 | 14 |
Genomic Location (Zv9):
Chromosome Zv9_NA331 (position 60474)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150030.1 | 6603 |
| GRCz11 | KN150030.1 | 6603 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAAGTCTCTTCAGAAGGAGCGAATTGACCATAAAAAAGCCAAAGAAG[G/A]CAAGTGCATTTTTAACAAATGACAACATCACTGACTTGATAATAATGGCA
Long Flanking Sequence:
GATAGGGATAGGGAAATTTATTTATTTAAATAGATTTATTTTAAAGCATGACTGTAACACACATACACCATAATGAACATGTTAAAACATATGCTAAAATTTCTGAATAATGGCAAAAAATACTTGTGCAACTCCTTTTTTGTGTGTACAGCCATGCTTTTCATACCTATTGGTTTCTAGTGTGGTCCTGTAAAATCTCAGTTTCAGGGGCTATCTAACCTTTTCCTTTAGCCCTACACTTTTAAGCTAAAGAGAACTGAGGATCCTCTACCCCTTCACATGAATGCACAAAGCAATGGGTAAGGGGAAGGGCTAAGAGGTAGAATTGGGATTGGGCCTTACTGACCCTTATAGCAACTGCAGCTTTTCTAAATATTCATTTAATATACATAATCCCAAATCTCTCTTTCTCTCTTGTCTCTCAGTTGTGTACGAACATCGCTCAAGGTTGGAGAAGTCTCTTCAGAAGGAGCGAATTGACCATAAAAAAGCCAAAGAAG[G/A]CAAGTGCATTTTTAACAAATGACAACATCACTGACTTGATAATAATGGCATCCCTGATGGATAAACCGGTACAACCCAATAGAGCTGGATTATACTAAGCTAACAGTATACGAAGATCAGTGTTGGGTAAAGTTACTTTTAAAAGTAGCATATTAAAATCTTTGGTCCCACTTTATATTAAGTGGCCTTAACTAATATGTACTTACACAGGAACTAATAGTTTGTTACAATGTACTTATTGTGTAAATACATGCATTTACTTTGAACTTTTGCTTGATTAAATACATGTATGTATTTACATCTGTAATTAACTTTTGTAGTTACATTTGTAAATACACTGTTGACCATCCCTTACACCTTAACCCACCCTTAAACCCACCCATGCCACCAAACCTGTCCATAACCCAACCTCTATCCCAACTCAAGAGCACCACAAGTGTTCTCAAATACTTCATGAACACAGTAAGTACATTGTATTTATTTTTTTTGATGTAAGTACA
Associated Phenotype:
Not determined