ZMP
tmem33
Ensembl ID:
ZFIN ID:
Description:
transmembrane protein 33 [Source:RefSeq peptide;Acc:NP_998828]
Human Orthologue:
TMEM33
Human Description:
transmembrane protein 33 [Source:HGNC Symbol;Acc:25541]
Mouse Orthologue:
Tmem33
Mouse Description:
transmembrane protein 33 Gene [Source:MGI Symbol;Acc:MGI:1915128]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa9069 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa19098 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9069
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060577 | Nonsense | 229 | 252 | 8 | 8 |
| ENSDART00000060577 | Nonsense | 229 | 252 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 14 (position 49300474)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 47378033 |
| GRCz11 | 14 | 46351973 |
KASP Assay ID:
2260-7917.1 (used for ordering genotyping assays)
KASP Sequence:
TTCACAGAGCTGCGCATCTTACTGGAGCATTTTGTGATGAAGCCCAGCTG[T/A]CCCGTCTTCTTCAGGAGGATGTGCCTCAACAGCATTGCCTTCGTTAGCCG
Long Flanking Sequence:
GGATTCTGATTAGTCAGTGTAATAATTCAGAATAACATATCCTGGAATATTGCAACTGACCAATCAGAATCCAGTATTTCAGATAGCTGTGTAGTAATTCAGAATAACATACCTTGGAATGTTGCGCTGTTATCTGATATACTGGATTCTGATTGGTCAGTCTAATAATTTAGAATAACATGCTTTGGAATCTTGCAACTGACCAATCAGAATCGAGTATTCCAGACAGCTGTGTAATAATTCAGAATAACATGCTTTGGAATGTCACGACTGACCAATCAGAATCCAGTATTCCAGCTGTGTAATAAATCTTCATAATGCACACTTTTATATCAAAACATCATGCTTTTTGCTTCCACCCTAAAAAAAATTTGCATTTACCACATGCTGTAATAAACAATGGCCAGAGTACCATCATCTGATGAGTGTTTTTCTTCCGTCAGGACGCTGTTCACAGAGCTGCGCATCTTACTGGAGCATTTTGTGATGAAGCCCAGCTG[T/A]CCCGTCTTCTTCAGGAGGATGTGCCTCAACAGCATTGCCTTCGTTAGCCGCCTCGCTCCAACCGGCGTCTAAATACTCTCTCTGAACACACATACACACACTACCACACACTCTTCACTGATCTGGACTAGTAAAACAAGCTGGCGGTTCAGATGTTGATGATTTTCTCCTCTGCACTGAAGCTTGGCTATGTTTGGAGAGACTCTATCCATCTGACAGACTGACTGCATCCCAAAAAAACAGAAGGAAACCGCCAGATGATGTGTATCTGTGCTCGGTTAAAGGGCACAACTGTTCATTACTGCTTTTATATCTTGACTCATGGTTTTTTTGGGGGGGTAGAGAGGAATTCTTAAGATATTTAATGTAACTGCTAGGCTAAATAGACATAGCTTGTATTTCTAATGAGATCAAATTAGCATCGGCAAATCAAATTTGAGCTGCTGTTGTACTTCTGTTTGATTCCATTTGATTTTCTTTGTTTTTTTTTTAAGTTGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19098
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000060577 | Nonsense | 229 | 252 | 8 | 8 |
| ENSDART00000060577 | Nonsense | 229 | 252 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 14 (position 49300474)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 47378033 |
| GRCz11 | 14 | 46351973 |
KASP Assay ID:
2260-7917.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACAGAGCTGCGCATCTTACTGGAGCATTTTGTGATGAAGCCCAGCTG[T/A]CCCGTCTTCTTCAGGAGGATGTGCCTCAACAGCATTGCCTTCGTTAGCCG
Long Flanking Sequence:
GGATTCTGATTAGTCAGTGTAATAATTCAGAATAACATATCCTGGAATATTGCAACTGACCAATCAGAATCCAGTATTTCAGATAGCTGTGTAGTAATTCAGAATAACATACCTTGGAATGTTGCGCTGTTATCTGATATACTGGATTCTGATTGGTCAGTCTAATAATTTAGAATAACATGCTTTGGAATCTTGCAACTGACCAATCAGAATCGAGTATTCCAGACAGCTGTGTAATAATTCAGAATAACATGCTTTGGAATGTCACGACTGACCAATCAGAATCCAGTATTCCAGCTGTGTAATAAATCTTCATAATGCACACTTTTATATCAAAACATCATGCTTTTTGCTTCCACCCTAAAAAAAATTTGCATTTACCACATGCTGTAATAAACAATGGCCAGAGTACCATCATCTGATGAGTGTTTTTCTTCCGTCAGGACGCTGTTCACAGAGCTGCGCATCTTACTGGAGCATTTTGTGATGAAGCCCAGCTG[T/A]CCCGTCTTCTTCAGGAGGATGTGCCTCAACAGCATTGCCTTCGTTAGCCGCCTCGCTCCAACCGGCGTCTAAATACTCTCTCTGAACACACATACACACACTACCACACACTCTTCACTGATCTGGACTAGTAAAACAAGCTGGCGGTTCAGATGTTGATGATTTTCTCCTCTGCACTGAAGCTTGGCTATGTTTGGAGAGACTCTATCCATCTGACAGACTGACTGCATCCCAAAAAAACAGAAGGAAACCGCCAGATGATGTGTATCTGTGCTCGGTTAAAGGGCACAACTGTTCATTACTGCTTTTATATCTTGACTCATGGTTTTTTTGGGGGGGTAGAGAGGAATTCTTAAGATATTTAATGTAACTGCTAGGCTAAATAGACATAGCTTGTATTTCTAATGAGATCAAATTAGCATCGGCAAATCAAATTTGAGCTGCTGTTGTACTTCTGTTTGATTCCATTTGATTTTCTTTGTTTTTTTTTTAAGTTGTTG
Associated Phenotype:
Not determined