ZMP
tmem178
Ensembl ID:
ZFIN ID:
Description:
Transmembrane protein 178 [Source:UniProtKB/Swiss-Prot;Acc:Q08CE6]
Human Orthologue:
TMEM178
Human Description:
transmembrane protein 178 [Source:HGNC Symbol;Acc:28517]
Mouse Orthologue:
Tmem178
Mouse Description:
transmembrane protein 178 Gene [Source:MGI Symbol;Acc:MGI:1915277]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41870 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9980 | Nonsense | Available for shipment | Available now |
sa1210 | Nonsense | F2 line generated | Not yet available |
sa27806 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41870
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 |
---|---|---|---|---|---|
ENSDART00000008594 | Nonsense | 91 | 301 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 31389823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 30267185 |
GRCz11 | 11 | 30514369 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGGCGCTCATGAAGCCCATTCACGTTGGGAGTCGAGAGGAGGAACTGT[T/A]GGAGAACTGGAGGGCGATTTTGGGCATGGGCATTTTGGAGACGGAGTGCG
Long Flanking Sequence:
GCGGCTAAAAGAAGATGCACAGACGCCGAAGGCAGTGCAGGTAAACACGCACGCACGGCCATCGCGCATCCCCATATAGATGCCCACGGCACCGCACGCGCAGACACACTCCGCTCATCCACCTGTAATGACAGATCGCTGCCCAAAGCGGTGCATTGTCCCAGGAAACGGCGAGGAAAGTCCGCTTCGCGTGAGAGATGACTGAGTGAGTTGCGCGGATGTTGGAGACATGGAGAAACGGGCTCTTGTAACGGCGATCAGCTTGTCCATGAGCCTGCTCGCGCTCATGCTGCTGGTCACTGCGATCTTCACCGATCACTGGTACGAGACCGACACCAGGAGACACAAGGAGAACTGCGACCAGTACGGGTCCGAGTCCAACGACCAGAAGAACAGGGAGATGCCCATCTATCACCTGCCTCTGGTGGACAGCGGGAACGCGAAGCGCAACCTGGCGCTCATGAAGCCCATTCACGTTGGGAGTCGAGAGGAGGAACTGT[T/A]GGAGAACTGGAGGGCGATTTTGGGCATGGGCATTTTGGAGACGGAGTGCGGGCGCCCGCTTTTCTCCACCTATTCGGGACTATGGAGGAAATGCTACTTCCAGGGAATGGACAGGGATATTGACAAACTCATTTTGAAGGGTAAGGCTTAGGTGGAAAGTTCATTTCGATGCAAAATATACAGAGGAAAAAATGTGTGCTTAGTTGGGTGTGAAGCGGTTTAGTGCCAGCCAACAGAACTAAACGAAGTTCGAGACTTTTCTTTTTTCTACTACCCTAACACAAAAGAGTTCCCTGCGCTAAATCTAACGCACGTCCGAATGTCAAACAAATAATTCTCATGAGTCGACTCTAACAGCATTCAGCGCAACCAGAGTAGTTCCATTAGTTCCAAACGAATGATTGTAATGAGCTGGCTATGTAATAGTTGTTTTTGATGAATCAACACACCTACAGTAGCTATTAACCAATCAATAAATAAGACAGACAGGTTTTAACCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9980
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008594 | Nonsense | 116 | 301 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 31389898)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 30267260 |
GRCz11 | 11 | 30514444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGGGYATTTTGGAGACGGAGTGCGGGCGCCCGCTTTTCTCCACCTAYT[C/A]GGGACTATGGAGGAAATGCTACTTCCAGGGAATGGACAGGGATATTGACA
Long Flanking Sequence:
ATAGATGCCCACGGCACCGCACGCGCAGACACACTCCGCTCATCCACCTGTAATGACAGATCGCTGCCCAAAGCGGTGCATTGTCCCAGGAAACGGCGAGGAAAGTCCGCTTCGCGTGAGAGATGACTGAGTGAGTTGCGCGGATGTTGGAGACATGGAGAAACGGGCTCTTGTAACGGCGATCAGCTTGTCCATGAGCCTGCTCGCGCTCATGCTGCTGGTCACTGCGATCTTCACCGATCACTGGTACGAGACCGACACCAGGAGACACAAGGAGAACTGCGACCAGTACGGGTCCGAGTCCAACGACCAGAAGAACAGGGAGATGCCCATCTATCACCTGCCTCTGGTGGACAGCGGGAACGCGAAGCGCAACCTGGCGCTCATGAAGCCCATTCACGTTGGGAGTCGAGAGGAGGAACTGTTGGAGAACTGGAGGGCGATTTTGGGCATGGGCATTTTGGAGACGGAGTGCGGGCGCCCGCTTTTCTCCACCTATT[C/A]GGGACTATGGAGGAAATGCTACTTCCAGGGAATGGACAGGGATATTGACAAACTCATTTTGAAGGGTAAGGCTTAGGTGGAAAGTTCATTTCGATGCAAAATATACAGAGGAAAAAATGTGTGCTTAGTTGGGTGTGAAGCGGTTTAGTGCCAGCCAACAGAACTAAACGAAGTTCGAGACTTTTCTTTTTTCTACTACCCTAACACAAAAGAGTTCCCTGCGCTAAATCTAACGCACGTCCGAATGTCAAACAAATAATTCTCATGAGTCGACTCTAACAGCATTCAGCGCAACCAGAGTAGTTCCATTAGTTCCAAACGAATGATTGTAATGAGCTGGCTATGTAATAGTTGTTTTTGATGAATCAACACACCTACAGTAGCTATTAACCAATCAATAAATAAGACAGACAGGTTTTAACCTAAGGGTGTTGGGCAGGGGGTGGATCTGAGTAACAGGGGCCTTGGAGAGAGAGAGTGGGGGTCAGCATAATGATACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1210
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008594 | Nonsense | 155 | 301 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 31395491)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 30272853 |
GRCz11 | 11 | 30520037 |
KASP Assay ID:
554-1119.1 (used for ordering genotyping assays)
KASP Sequence:
GTATTGCAGAGCGATGCACATCTGTCAAGTACCATTTCTCCCAACCCATC[A/T]GACTCAGGAACATCCCTCTCAACCTGACGAGGACCATACAGCAGGACGAG
Long Flanking Sequence:
GTTCAGAAAGGGTACATTTTAATTTCACCCACACATTTCGGATCCAGCCAGCTTGAATTCATGTCTCTGACTGAATGAATTGACCGTATCCCCCCACACTATGAGTCCAGAACGTGTTTTAAAATATTATTAATTACCTAATGCTTGCTGCATGATCACTGCAGTCTCATTCCAGCTCGCAGAATTAGCTCCCAACGCCGGCCAAATCTGTGTGGTGTTGGTGTGAACTCAGGCGGAAATAATGACAGAAGGTCACTCTGTCGGGGAGGCTGGAGTTTCAGCAAAGCTTGAAACGTCTAGGGAAAAGACAAACAATAAAACAAAGAGTCGAGAAGATTAGTGCAAACAGAAAATGCAATATACCAGCAGCGTGTCGTTTTATTTGTGTGGGATTTCAGCTTGGTTTGAAGGTGGGAGTTTGTCCTAAATGAGTGTGCGATCTGTGCGCAGGTATTGCAGAGCGATGCACATCTGTCAAGTACCATTTCTCCCAACCCATC[A/T]GACTCAGGAACATCCCTCTCAACCTGACGAGGACCATACAGCAGGACGAGTGGCACCTCTTACGTAAGTTGCCCAAAGCTTCCTCACCACCGCCTTGTGCAGCTCTTGATATGCCATGAATATTAAGCAGAGCTCGCAAGCTGGAGTTAAGTGTGCTTTGCATGGAGAAAACTGCAGAGAAAATCCTTGTAAAATAAAACCTAAAGGCTGATGCTTTTCTGCTTAGTTTGATTTTGATCAATGCTGTTCAGTTTCTTAAAAGGATAGTTCACCCCAAAATTTAAATTCTGCCATTGTATATTAAATGTATGATAATTTACTCACTATTTGCTCTCCCTCAAGCGGTTCCCAACCTTTATGATTTTTCTTTCTTCTGTTGAACACAAAAGAAAATATTTCAAAGAAAGTTGGAAACCTGTAACCATTGACTTCCATAGTATCTGTTTTTTTTCTACTATGGATGTCAATGGTTACAGGTTTTCAGCTTTCTTCAAAATATC
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:
sa27806
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008594 | Essential Splice Site | 176 | 301 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 31401635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 30278997 |
GRCz11 | 11 | 30526181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGATAAGGTGTGAGTTGGCTAAGTGGGCGATATGTGTGTGTGTGTTTC[A/T]GATCTGCGGCGCATCACGGCAGGGTTTTTGGGCATGGCAGCAGCCGTAAT
Long Flanking Sequence:
AATGGATTTGCTCTTCAATGTTTAGACTTTCAGCAGTGAAATTAAACCACACTGAACTGAACTAAACTGAACGTCAACTCTGAAAACTGGACTGACACAGTTTCAATTTACTAGAACTTCTATGCTAAGCTGCTTTGACACCATTTACATTGTAAAAGTGCTATAGAAATAAAGATGAATTGAATTATTATTATGTTTGCACAAGATTTTATTAAGTGAATGAAATATATAACCACTAAATAGAAATGTTCACAAAATCTAAACAATAAAAGAAATTTGAATAAAAATGATATTAAAAATACACCTTTGCATCAAAATGTTTCATTTGGAGTTCATGGCAAAATATGGAGAATAGAGCCTCATAAAGCTTTGGAATCACCAGATGATAACGAAATGTTCATTTTTGGGTGAACTATCCCTTGAAATCCTCACATTTCAGTGAAAGTTCCTAAAGATAAGGTGTGAGTTGGCTAAGTGGGCGATATGTGTGTGTGTGTTTC[A/T]GATCTGCGGCGCATCACGGCAGGGTTTTTGGGCATGGCAGCAGCCGTAATGCTGTGTGGAAGCATCGTGGCCGCGGTTGGATTTTTCTGGGAGGAGAGCCTCACTCAGCATGTGTCTGGACTCCTGTTCCTTATGGCAGGTACATCATTCTGTTCATTCGCTCTTCCTTGGATCTTCTTTTTTCATACTCAGCTACTTGTTACTCGTTTCTCCCAGTCGCAGTGTTTCTTGTAGGTGGTTCTTTTTCCTTTCCAAGTTGTTGTCTACCTTGTTCATTCTCCCACGTCTTGTATATTCATCTGTTTTTCTCCTTCTGTCTCATTTGTCTTGGACTTATACAGTACTGTACATATGTACACACATTACACACACACACACGTCCCCACCGGGAAATAAAAACAAGTACACATACACACACATATACTTCTGGTTTATGAGGACTATCCATAAATATATTATGTTTTATACAGTAGAAAACAAGTACACATTCACACACACAC
Associated Phenotype:
Not determined