ZMP
si:ch211-172j10.2
Ensembl ID:
ZFIN ID:
Description:
transmembrane protein 184C [Source:RefSeq peptide;Acc:NP_001139068]
Human Orthologue:
TMEM184C
Human Description:
transmembrane protein 184C [Source:HGNC Symbol;Acc:25587]
Mouse Orthologue:
Tmem184c
Mouse Description:
transmembrane protein 184C Gene [Source:MGI Symbol;Acc:MGI:2384562]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39644 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38277 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39644
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111566 | Nonsense | 115 | 447 | 4 | 10 |
The following transcripts of ENSDARG00000078789 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 36433520)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 35993378 |
| GRCz11 | 1 | 36725405 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAGTATCCCAACATTGCCATCTATGTAGACACATGTAGAGAGTGCTA[C/A]GAGGCCTATGTCATTTACAACTTTATGATCTTCCTTCTCAACTACCTGGG
Long Flanking Sequence:
AACCAAAATAAATGCAAAGTAGGTGCAGTATTGTACTGACATTATTATCTGTCCTACATTTTTTTCTGGTTCTCACTTGCTCCCTCTGATTTTTTTATTGTTTTACACCCTCAGAATATTATGGATGGTTCCTATTTACAGCCTGGACAGTGTGAGTATCCAAATGTTGGTATTTGAATCACAAATGGCAACTCTGATGTTTGTTATCCAATATAAAGTCTCTTGACTTTAGCACTGACCTTTTTCTGTTTGACAATCAGTTAATATGAGGCCTGATGTTGCAGATGCTCATGACTTGATTACTTTAAGAGTTCAACCAGAAAAAGTGACTCGTTTGAGCAATCTCATGTGCCTCCAATCTTTTTTTATTTTATTTTTTTGAGGAGCATGATGCAATTTGTCATGTCTATTTTTTTCTAACATCTATTATTATTTTCACAGTGGATCGCTTTGAAGTATCCCAACATTGCCATCTATGTAGACACATGTAGAGAGTGCTA[C/A]GAGGCCTATGTCATTTACAACTTTATGATCTTCCTTCTCAACTACCTGGGGAACCAGTATCCTAGTCTGGTGCTCATGCTGGAGGTCCAGGAGCAACAAAAGCATCTGCCCCCACTTTGCTGTTGCCCACCGTGGCCCATGGGAGAGTGAGTTTTTGCCGAAATGCATTAAAATATGTAAATATATTGATTCTGATTTGTTTATCTTTTAATTAGTTTTTGATTTGATTGTAGATTTAATACTATTTATATTTTTAAAAAAAATCAGTCAACGCTGCAGTACACATGTAGCAATTGTTCTCACTTTAGTCATGGCTGACTGTTTACATATGCATTTCAAGATTTAAGTGTGCATTTGACTGTTCAATTTACAATAAGCAGCAAAAGTGAGGAGAATTCAGCTCTCGCACACTTATGTCTCTTTCTTTGTGGCGCTTCATGTTCGTGCCACAGAAAAGTGCCTGTTAAACATTTTTAAATGACTCATCACTCACATATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38277
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111566 | Nonsense | 312 | 447 | 9 | 10 |
The following transcripts of ENSDARG00000078789 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 36443244)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 36003102 |
| GRCz11 | 1 | 36735129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGGAAATGTTTTTGGCAGCCATTGCCCATCACTTCAGCTTCACTTA[C/A]AAGCCCTACATACAGGAAGCAGAGGAAGGTTCCTGCTTTGATTCCTTCCT
Long Flanking Sequence:
ATATTTTCCCTATTTTTTTCTTTTATTATCTTTTGTAGGCAAGCTGTGTTCATTGCACTTTTAGTGAAGGTTGGTGTAATCTCAGACTCTCACACCTGGGACTGGGACAGTGTGGAGGCTGTAGCTACAGGTTTACAGGTATGTACAATCTATAGATGAGATTCAGAAGTCTAAACTGTATTCCACTAGAATCAAATACATTAACATCCCAGTCTCTTTGAGAGTTGTCTTAACAAAACCCACATTTGTAAATGTGGTCAATGGCTGGATAGCAGCTAGTAAAGCACCAGTCTAGGTATTTTAGAAAATAATCATTCATTGTCTGGCCTATCATGCATTCCACGTTCGACTGATGCTGCACAGCCGTTAATAGACTAATGGTTGCACAGATGGAAGTAACCTTCAAGATTAAGACTCTGTGATTCTCTTTTCTAACAGGACTTCATCATCTGTGTGGAAATGTTTTTGGCAGCCATTGCCCATCACTTCAGCTTCACTTA[C/A]AAGCCCTACATACAGGAAGCAGAGGAAGGTTCCTGCTTTGATTCCTTCCTGGCCATGTGGGATATTTCAGACATACGGGCTGACATCTCAGAACAAGTGCGCAATGTTGGTGAGTCAACAAAGTCTTTTCAACAAAAGTGTTTGCCCTAAACCTAATAACTGGTGGGGCGATTTTTAGCAGTAACAACAGCAATCAAGCATTTTCAAGGACTTCAAAGTGTCCACGGGATCTTAAAAAGTATTGAAAGTTGATAAATCAATGTAGAGAAATTCTTGTATGCTATTTTGCAAGTATTACATTTTATATCATTTAATTTTTATTTTTGATTATGCAATGTATGGTTGTATGCTAAAGTTTGCCTGAATTAAATCTGCAAATATCAGGATGCTGTTGAGTTTATGAAAGCACTTAAATCCTACTAGATTTGACATCATGTTGCTTTGTTTACTGCAGTAACCAAGGCAACATCATTATTTCTGCAGTTCTAAACATTCAGGAT
Associated Phenotype:
Not determined