ZMP
zgc:113334
Ensembl ID:
ZFIN ID:
Description:
Transmembrane protein 182 [Source:UniProtKB/Swiss-Prot;Acc:Q5CZV0]
Human Orthologue:
TMEM182
Human Description:
transmembrane protein 182 [Source:HGNC Symbol;Acc:26391]
Mouse Orthologue:
Tmem182
Mouse Description:
transmembrane protein 182 Gene [Source:MGI Symbol;Acc:MGI:1923725]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34551 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41351 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34551
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 |
---|---|---|---|---|---|
ENSDART00000059092 | Essential Splice Site | 48 | 248 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 6968701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 6948794 |
GRCz11 | 9 | 6927185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCATCTGAGACCTGCAATTCATATTCAAATAGTCCAGTTACTTCTGAG[G/A]TGGGTGTGTTGCTTCAAGTGTTTTAATATGGGGGGTAATATGAAAATATG
Long Flanking Sequence:
CTCCTCTCTCTCCTGCAATCTCATTCTTAAACCACTCCTCTGAGAGCGACAGCAGGCACCTTCACTCAACTGACCAAAATAGCCCAATGGGCAGCCTTACACTGGTGTGCTATCATAAAGCCCACTCCAAACCCAGTGTCAGGTCTTGAATCACACATATAGACACACACCGGAGCGAAGAAGAGTCCTAGAAAAGCCACTTGTGTCCACATGCCATAAACCTTGCTGAGTAAAACCAGACTATTTTTTCTGACAAATTGTGAGGAGTTACATAATTTCAGTGCCTACTTCATGTGGGAAGGAGGAGAGACTGTTTAACAAGCAGTGAACGGGTGGAAAGGTTGCACTCTGAGATCATGAAGATACATGTGGCTGGATTTTTCGCTGGGCTCTTCGGTGCCTTGGCAACTCTGTTCATCCTCCTGTCTTTTGGCACGGACTATTGGCTCCTGGCATCTGAGACCTGCAATTCATATTCAAATAGTCCAGTTACTTCTGAG[G/A]TGGGTGTGTTGCTTCAAGTGTTTTAATATGGGGGGTAATATGAAAATATGGGCATTTTTGAGTATTTAATTGACATCATGAATGATGTCGTTTCCAAAATGCGAAAGATCTGAACTGTCTGATTAACTGTATCTTTTAGATTTCTGTGTACTTAACTTGAGCTCTTTGATCCTCCCTGATCCTCTCGCAGTAATGGGCATATTTGGTTTCCAAGCTGTGGCAGTCATATGACATCCACGTACGTCATTATTTACAGTCTCAGAGATTCAAGACTGTAGACTATCACATGCTGCAGTGTGATACTACACTTAATACTGAACAGCCAAACTGGAATCTCAGCGCAGTGGCTATTCATAGCGGTCACACAAGTCTGGTTTCCCCCATAAAGATTTGGGAGAGAAAATGAGATCCAAGTTAAAGGGATAGTTATTACTATATTTACTCACCCTTCACTTGTTGCAAACCAGTTGAACACAAACGAAGATATTTTGAAGAAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41351
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 |
---|---|---|---|---|---|
ENSDART00000059092 | Essential Splice Site | 95 | 248 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 9 (position 6963343)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 6943436 |
GRCz11 | 9 | 6921827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTCGATGACGTCATGAACGATGGCAATCTGTGGAAGTTCTGGTTTGG[T/C]AAGAGATTGTGTTTTAGCTTTTGAGCAATATACATTCGGAGATGTCTTTA
Long Flanking Sequence:
TCTTCAATAGATTTTTTAAAATGGTGGGGTCATTTTAAAGAAAAAGTCAACCAAACTTCATGATACAAACTGAAAAAAGTTATTTATGAAATTTTTCTGCTGTTAAAATGGTGTTTCAGCTTTGACCCCTAAGTCAACATGGTTTCTAGTCAACAAGCTAGTTTACATTGGGTTTCTCATCAATGTTGGAAATAATGTCTTTGGCATCTACTCGAAACTTGCATGCAAATGCATAAATAACATTACCCATCCACAGTCCGCCAGTGTCTGTCCTCCAGCAGTTTGGGATTTTTGTCATTTTCTCTGGCTCCACAACAGGTGTGGATTACTCTCTGACCTCTGCTCTCTGCTCCTTCACAGCGAGGTGATATTCTTGTCAACCAGGTTCCCGACCCCAATAGTGAAGCCCCGAACTTCACCTTTCATCATGAGGGCTTCTTCTGGCGCTGTACCTTCGATGACGTCATGAACGATGGCAATCTGTGGAAGTTCTGGTTTGG[T/C]AAGAGATTGTGTTTTAGCTTTTGAGCAATATACATTCGGAGATGTCTTTAGTTTTTCAGCTTTTTTAGCTGATGTATGCCAATGTTTATTTCTACACAATGTTGGGTAGGTTACTTTAAAAAGTATTTAATTACATTATTAAATTTTTTAATTACATTTTAATTACATTATTTAATTACATTATTAAATTTGTATTTCTGAAAAAGTAACTAAATTACTTAAGAAGTAACCAGTTAAACTCTGCGGACCCGGTACCATGATGTCATCGACTTTCGCTTAAGGATTTAAAGGGCTAGCATTGCACCAGACCCCTTTAAGTGGTTTCGTTTGAATGTGTAAAATCTATATTTTATGCACATATGCAACACTTTTTTTTTTGTTTTTGTTTTTTTGGTATATTATTTACATTTAAATACACAGTATTTTGGATACCCCAGCTGGATATTGAACATTGGTTAATTTTCATATATTTCATATGGTTCATATATATGACACAAGTA
Associated Phenotype:
Not determined