ZMP
tmem205
Ensembl ID:
ZFIN ID:
Description:
Transmembrane protein 205 [Source:UniProtKB/Swiss-Prot;Acc:A1L2F6]
Human Orthologue:
TMEM205
Human Description:
transmembrane protein 205 [Source:HGNC Symbol;Acc:29631]
Mouse Orthologue:
Tmem205
Mouse Description:
transmembrane protein 205 Gene [Source:MGI Symbol;Acc:MGI:3045495]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40012 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa7317 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6148 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40011 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40012
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064028 | Essential Splice Site | None | 188 | None | 4 |
| ENSDART00000137099 | Essential Splice Site | None | 188 | None | 4 |
| ENSDART00000139990 | Essential Splice Site | None | 188 | None | 5 |
The following transcripts of ENSDARG00000043604 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 13605234)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 14349390 |
| GRCz11 | 3 | 14499190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGGATTAACCCAAACTGATCACACAGAACCAGGCGTAGAGCGACCGGG[T/A]ATGTATTTTCTATAAACCGACAGAGTTTACAGTTGGAGGGAAATTGCTTA
Long Flanking Sequence:
CAGCACTACCTACTGCATCACCGCGTCGGCCCGATTTATATACTCACTCCTTTATATATTTGCGTATTTATTTATATAATGTTTTGCAGGTTTCATCCTCCCTTAGAAATGGCAAAAAAATGAAGTAAATTGTTAGAAATATAAAATTGCTTAAATTAAGAATTAATTATAAAATCTTAATTTTAAAATATTAAATTAAATATTTTATCAGTATATACCTAACACTAACCACTCCGTGTCATAATGTTATTTTTTAATGTTATATTGTAAAACGGTGTGAGACTGGACTTCAGAACGACAAACAGCTCGTGATTGGTTCGTTTTCGTTCATGTGTTTGGATAGTAGAAAGTGATTGGATGTCGAGGTCACGAGGGCGGGACTAACACGGTAGGTGTGATATCAGGCGAAAAGAGCAACCAACAGAACATTTGTGCACGACAAGACAAGTTGCAGGATTAACCCAAACTGATCACACAGAACCAGGCGTAGAGCGACCGGG[T/A]ATGTATTTTCTATAAACCGACAGAGTTTACAGTTGGAGGGAAATTGCTTAAGCGTGTCATGCTTGCCCAAGTAACAGAAATTTTGTGAACGACCATTACGGAAGTCTTGAAACGCTGTGCTTATTAACGTCTTATTAACGGAGTATTAAAAATAAACTGATGCAAACATAAATAAATGGATCAAAAACATACGCTGTCAGGATCTCAGGTGAGGTTTATGAACGCACAAACACAGGCTCTGTGTTGAATTAGTATGTTGCTGTCATGTTATCAACATCAGCCCATGCTTAAAACTCCTCTTATCTACACTAACACACTTGATATGCATGTGCGTTCATAATACATGTTAGGCCTATATAGCCTACTAACTGTGAGCTGTTATGCACTATGCAGATAGGAAAATATTCATCCATTTATCTCTATTAATCAAGTTCAAAAGAGCTGTTTTGGCATGACTTGTCAAGTATCGGCAAAACATTGCAGGTTACATAATCGATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7317
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 |
|---|---|---|---|---|---|
| ENSDART00000064028 | None | None | 188 | None | 4 |
| ENSDART00000137099 | None | None | 188 | None | 4 |
| ENSDART00000139990 | Essential Splice Site | None | 188 | 2 | 5 |
The following transcripts of ENSDARG00000043604 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 13604440)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 14350184 |
| GRCz11 | 3 | 14499984 |
KASP Assay ID:
554-4390.1 (used for ordering genotyping assays)
KASP Sequence:
CCGCCAACTWTTCCAGCATTTGTTTTACGCAGTGGATGGCCTTCCAGCCG[T/C]AAGKCAGTACTGGAAAACACCTATAAACACTCATTCTCNNNNACACACACACAC
Long Flanking Sequence:
CTCCTCTTATCTACACTAACACACTTGATATGCATGTGCGTTCATAATACATGTTAGGCCTATATAGCCTACTAACTGTGAGCTGTTATGCACTATGCAGATAGGAAAATATTCATCCATTTATCTCTATTAATCAAGTTCAAAAGAGCTGTTTTGGCATGACTTGTCAAGTATCGGCAAAACATTGCAGGTTACATAATCGATAAATAAAATCGAATAACGATTATTATAAAAATCGAGTGATTATAAAATACATTGATTTATAAATACATGTATACATACAGAAAAGGGAAAACACAATTAATATTTTGATAAATGCATGCATAAATAAGAAAGATAAAAGCATTAATATGAGGATTTAAAGGACAATGAAGGAGAAAAATTCATTCGTTTATTAATTTTCCTTCAGTTTAATCCCTTATTTATCGGGGGTCCCCACAGTGGAATGAACCGCCAACTATTCCAGCATTTGTTTTACGCAGTGGATGGCCTTCCAGCCG[T/C]AAGTCAGTACTGGAAAACACCTATAAACACTCATTCTCACACACACACACACACACATCCTATGGCCAGGGGGAAACCGGAGCAGGGAGCACTCAGAGTAAACCCGGGCCAACACTGGGAGAACATGCAAACTCGAAATAGAAATGCCAACTGACCCAGCCAGGACTCCAACCAGTGAACTTCTTGCTGTGAGGTGACAGTGCTTACCACTGAATTGGCTCAGTCCCTTTATTGATCTGGGGTCGCCACAGCGGAATGAACCGGCAACTTATCCAGCACATGTTTTACGCAGCGGAGGCCCTTCCAGCAGTTACCCATCACTGGGAAACATCCATACACACTCATTCACACTCATACACTACAGAAAATTTTAGCTTACCCAATTCACCTATAGTGCATGTCTTTGGACTGTGGGGTAAACCGGACCACCCGGAGGAAACCCACTCCAACATGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6148
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000064028 | None | None | 188 | None | 4 |
| ENSDART00000137099 | Essential Splice Site | None | 188 | 2 | 4 |
| ENSDART00000139990 | None | None | 188 | None | 5 |
The following transcripts of ENSDARG00000043604 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 13601667)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 14352957 |
| GRCz11 | 3 | 14502757 |
KASP Assay ID:
554-3769.1 (used for ordering genotyping assays)
KASP Sequence:
TGCTCTTTGAGGTTTTAATCTTAATTAAATTGCTTCTTTTTCTATTTATA[G/T]AACATTTTTTCTTTACAGAAAGATAATTATGGCTACTGAGGGAGATCCGA
Long Flanking Sequence:
TTTATTCTTAAGAATAATTCATGTAATTGCAGTCATTTTAACTATTTAATAATGATGCATTGGAATCAGAATGTGAAAACGCAAATCCTAAATAAATAATAATAAATGTTAACAAAAAAACTTCAATGTAAAAAGTAACAGAGGCTGCGATATCTGCTACCAGATCTATATTCAGTTGTCACACACTTGTATAAAAATATACTATAGTAATTTATAGTAAATACTGCAGTGTTTTTTTAACCGTACTGACACTGACAGCTCCAATACAGATAGAGATGTTGCACAATCAGCTAAAGTGTTGCTAGAATTGTTTTTTAACGTCTGGGCGATATATATTGCATCAGCAAAAATGATTGAGCTCATGTCCATGTGTTAATTATATGGTGACAGGCCTTTTATTTAATTAGTAATGTTTGGTGATTGGATAGTGTCCTGCCATATTTTGTAATTTGCTCTTTGAGGTTTTAATCTTAATTAAATTGCTTCTTTTTCTATTTATA[G/T]AACATTTTTTCTTTACAGAAAGATAATTATGGCTACTGAGGGAGATCCGACTGACTTTGTGAAAGTTCTTCATCTGCTGGTGATTTCCTTCACTTGGGGAATGCAGGTGTGGGTGTCTTTCATAGCAGGTAAGCAAACTTGTATGAAAACTAAACAGAAATACAGTCGATGCATGCCATGTACCCGTAATTCTGCTTTTGTCTTTCTTAGGTTTTGTGCTGATTTCTCAGGTGTCCATGCACACATTCGGTCTTGTGCAAAGCAAGCTGTTCCCAGTTTATTTCTACTGTCTGCTGGGTGGCAATGCAGTCAGCCTCGCCGTATATGCTGTGTATCACCCTAGAGAACTGCTCGATTGGCATGAAGGCATACAGGTGACAGATTGAGTCATTGTTTTTGGGCTTGTTACGCGTTGAAGTTTTTAAGTTATTAAATGGATAAAACAAAGCAATCAGTAAGTCTGTAATGATGCTAGATGAAAAATTAAAAGACAAAGCGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40011
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 |
|---|---|---|---|---|---|
| ENSDART00000064028 | Nonsense | 127 | 188 | 4 | 4 |
| ENSDART00000137099 | Nonsense | 127 | 188 | 4 | 4 |
| ENSDART00000139990 | Nonsense | 127 | 188 | 5 | 5 |
The following transcripts of ENSDARG00000043604 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 13597299)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 14357325 |
| GRCz11 | 3 | 14507125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACAGAGAATATGCTGGTCATGCAGGAGATCGAGAAGGAGCACGGTCTG[G/T]GAAATCAAGTGGGCATGAGCTCCAACAGGGAAGGATACACCAAACTGCGT
Long Flanking Sequence:
AATAAAAACTGAATATACAGCCGAAGTGGTTGGGTGCGGAATAAAAGTTAACAGGAGCGGGACTAAAAAATCTGTCCAGCGCAGACCTCTAGATTACACTACGCTGTTAAAAAAAAAAGCTTAATTCCACACAAATGCTTTATGTTGTTCCAATGCAAATCGATTAAGTTAGCTTAATCATTTTTACATATTTAAGTGAACTGAACTTAAAACAATTAAGTTGTCCCCTCAAAAAATTAAGAATTGTGTTGTTTCAACTCATTTCAAATAAGTAGTTTGAACTCAATCTCACTTGTGCTTTCATTTCATCACCCAGTCTTAACTCTGTGTGTACTCCAATGTTTGGATACCCTCTATTATCATTCAGTTTGTATTGTCCTCGACAGATGAGCCTGTTCTTTGTGGCTGTGATTATGGCTGGTCTGAATGCGCAGTGGTTTGGTCCGTCTGCCACAGAGAATATGCTGGTCATGCAGGAGATCGAGAAGGAGCACGGTCTG[G/T]GAAATCAAGTGGGCATGAGCTCCAACAGGGAAGGATACACCAAACTGCGTGAACAGGACCCCAAATACAAGGAGCACAGAAGCACCTTCTACCGCTACCATGGTCTGTCCAACCTCTGCAACCTCATTGGCTTTTTCTGCATTACCGTCAATCTCATCTACCTGGCCCTCAATTTGGGAACTATATGAGTACAGACAGACAGATATTTTTCAAGATGATACGTTGTCTGTTTTCTACTGTCGAGTTTTTTTAAGTATAACAATAAGGCTTCTAGTTTTTATATCGAAACACCAAGGATGATGAATATTACAAGAATGATTGCTAAGGGACAGTTCATCCACAAATGAAAATTCTGTCATAAAATAATCACACTGTACTTAAGACCTGTTTGAGTTTCTTCTGTTGAACACAAAGGAGATATTTTGAAGAAAACTGGAAACTGGTAACCATTGACTTCCATAGTATTTGCAACCATGGAAGTTAATGATTACAGGTTTTTT
Associated Phenotype:
Not determined