ZMP
tmem206
Ensembl ID:
ZFIN ID:
Description:
Transmembrane protein 206 [Source:UniProtKB/Swiss-Prot;Acc:Q7SY31]
Human Orthologue:
TMEM206
Human Description:
transmembrane protein 206 [Source:HGNC Symbol;Acc:25593]
Mouse Orthologue:
Tmem206
Mouse Description:
transmembrane protein 206 Gene [Source:MGI Symbol;Acc:MGI:1914200]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1880 | Nonsense | Available for shipment | Available now |
sa42999 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42998 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1880
Status:
Available for shipment
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:
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010975 | Nonsense | 74 | 298 | 4 | 8 |
ENSDART00000141182 | Nonsense | 74 | 181 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 45550359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 45399591 |
GRCz11 | 17 | 45382843 |
KASP Assay ID:
554-1870.1 (used for ordering genotyping assays)
KASP Sequence:
CATTCTTTTGTTTGCAGGAATTGTTTTATTTCCTGGAAAGGCACATTTAT[T/G]AAGCTGCATGCATCACTATCACGACAACATTCCACCTCTTGTTGCATTGG
Long Flanking Sequence:
ATTTCAGACTTCATGGACAAACTCAACCACCCAGTGATGTCCGTTTCATACAAAGAGGTTGAAGAGTTTGCTGCACCAGGTGAGTGTTTCTATTTATATGTTTAGTTCACCTCAAAAAATAACCTTTGTTCATCTTCAGAACACAGATTAAGCTATTTTAGATGAAGCGTCCTCATCCTCTATAGGCAGCAAGTGTCTTGAGGTGTTCAATAGAGCACCTTTGGGATGTGGTGGAACAGGAGATTCGCATCATGGACAAATCTGCCGCAACTTCGTGATGCTATCATGTCAATATGGACCGAAATCTCTAAGGAATATTTCCAGTACCTTGTTGAATCTATGCCACGAAGGATTAAGGCAGTTGTGGGGGCAAAAGGGTTCCAAGCTGGTACTAGTAAGGTGTACCTAATAAAGTGGCCAGTGAGTGCAATCTTTTAAAGTATGTTTGATCATTCTTTTGTTTGCAGGAATTGTTTTATTTCCTGGAAAGGCACATTTAT[T/G]AAGCTGCATGCATCACTATCACGACAACATTCCACCTCTTGTTGCATTGGAAAATCTTGCGAAAAGAGAGTGTATGAAAGAGGAAGTCATCTACCATGGGCCGTATTCAAACCAGACAGAAGTATGTTTTTTAGATCGGAAGTTTTTCTAAAGAAATGGTACTATTATTAATCTTTTTTATGTAACATTTCTCTTTTTTTGGCAACAGAAGCGAGCTTTGGTGTTCAGAGGGCCGACTGACGTGAGGAACCGAGAGCTTATATTCCTTCAGCTTAGCCGAAACGAAACAGAAGAGGATTTCAGCGCAATCAGCTATATGATTTTTGCTAAATTCAGTGACATGCTTGAAAGGTAGATCCTAGATAGGAATGTTTACCATGAATTGGGTTTGTTTTACTGTTTGAATAAATTGTACTTTTTATTTCTAACCAGCTCAGATAAAGCTGCATTTATGATGGACTGTGAAAGGAACTACTCGATGTGGACCTTCTCTGGAGGCT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa42999
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 |
---|---|---|---|---|---|
ENSDART00000010975 | Nonsense | 80 | 298 | 4 | 8 |
ENSDART00000141182 | Nonsense | 80 | 181 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 45550340)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 45399572 |
GRCz11 | 17 | 45382824 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTTTTATTTCCTGGAAAGGCACATTTATTAAGCTGCATGCATCACTA[T/A]CACGACAACATTCCACCTCTTGTTGCATTGGAAAATCTTGCGAAAAGAGA
Long Flanking Sequence:
AACTCAACCACCCAGTGATGTCCGTTTCATACAAAGAGGTTGAAGAGTTTGCTGCACCAGGTGAGTGTTTCTATTTATATGTTTAGTTCACCTCAAAAAATAACCTTTGTTCATCTTCAGAACACAGATTAAGCTATTTTAGATGAAGCGTCCTCATCCTCTATAGGCAGCAAGTGTCTTGAGGTGTTCAATAGAGCACCTTTGGGATGTGGTGGAACAGGAGATTCGCATCATGGACAAATCTGCCGCAACTTCGTGATGCTATCATGTCAATATGGACCGAAATCTCTAAGGAATATTTCCAGTACCTTGTTGAATCTATGCCACGAAGGATTAAGGCAGTTGTGGGGGCAAAAGGGTTCCAAGCTGGTACTAGTAAGGTGTACCTAATAAAGTGGCCAGTGAGTGCAATCTTTTAAAGTATGTTTGATCATTCTTTTGTTTGCAGGAATTGTTTTATTTCCTGGAAAGGCACATTTATTAAGCTGCATGCATCACTA[T/A]CACGACAACATTCCACCTCTTGTTGCATTGGAAAATCTTGCGAAAAGAGAGTGTATGAAAGAGGAAGTCATCTACCATGGGCCGTATTCAAACCAGACAGAAGTATGTTTTTTAGATCGGAAGTTTTTCTAAAGAAATGGTACTATTATTAATCTTTTTTATGTAACATTTCTCTTTTTTTGGCAACAGAAGCGAGCTTTGGTGTTCAGAGGGCCGACTGACGTGAGGAACCGAGAGCTTATATTCCTTCAGCTTAGCCGAAACGAAACAGAAGAGGATTTCAGCGCAATCAGCTATATGATTTTTGCTAAATTCAGTGACATGCTTGAAAGGTAGATCCTAGATAGGAATGTTTACCATGAATTGGGTTTGTTTTACTGTTTGAATAAATTGTACTTTTTATTTCTAACCAGCTCAGATAAAGCTGCATTTATGATGGACTGTGAAAGGAACTACTCGATGTGGACCTTCTCTGGAGGCTTTAGGACGTGGGTCAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42998
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 |
---|---|---|---|---|---|
ENSDART00000010975 | Nonsense | 224 | 298 | 7 | 8 |
ENSDART00000141182 | None | None | 181 | None | 4 |
Genomic Location (Zv9):
Chromosome 17 (position 45547322)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 45396554 |
GRCz11 | 17 | 45379806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTCTAGTCTAGTGTGGTGAAGTACATTGACAAAAGGCCTCCACTGGAG[C/T]AAACCAACGAGCTTTTCTTCATCGTGTTCCAATGGCGGGATCCATTTATA
Long Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTATATATATATATATATATATATATATACTTTTTTATTAATAGAATCAATAAAAAAGTGTGTGTGTATATATGTATATATATACATATATATATATACACTAGAAGTTACAAATGCATAACTTTTTAACATCCCAAAATGAAAAGACTGAATTTTGAGGTATAAACTCTGTTGTAATTTTGTAAACTCAGAATTTGTAGAGTAAAGAAGTTCAGAACTGTGTGATATAAACAGACAATTCTGACAGTTAAAAAAGCCAGTGTTGTGAGATGTAAACATAGCCTAATTAGATAAAAGGCAACATTTTGAGAGGGAAAAAAATGTCAATCACAACCCCGCAATTGTGTGAGGGAAAAAAAAACTGTGAGATAAAAATAAGCACTATATTTTTTAAATCCATATTCTGTTTTATTTTTACCCGACATGTTAATTCTAGTCTAGTGTGGTGAAGTACATTGACAAAAGGCCTCCACTGGAG[C/T]AAACCAACGAGCTTTTCTTCATCGTGTTCCAATGGCGGGATCCATTTATACAGCAAGTTAAAGACGTAAGTGAACACGCCTTCAAATATTCAATTAATACTTCAGATGCTTTGTAGACTGTCTAATTAAGTATACTTATATCTTCTTTTTAACAGATAGTGACAGCAAACCCGTGGAACACCATTGCCATTTTGTGTGGCGTCTTCATGGCCCTGTTTAAAGCAGCAGACTTTGCCAAACTCAGCATTAAGTGGATGATCCGAATCCGCAAAAGACACAAAAGGGCAAAAATGAGAGAAATGAACCAAATCAGCTAAAACCGGACAACATTACACATCTGGAGATTTTAATTAGGACCATTGGGACTCCTGAACTGCTGAACCATTTCAGATATACATTTTCTTAATGAATGTATTGCGTTTTAACTGGAGTGATTTTAATATTGTACAGTATTGTACAAACTCTGAGGCACATGATCAACAGTACAAGAGCAAAGTTTA
Associated Phenotype:
Not determined