ZMP
pob
Ensembl ID:
ZFIN ID:
Description:
Transmembrane protein 111 [Source:UniProtKB/Swiss-Prot;Acc:Q7SXW4]
Human Orthologue:
TMEM111
Human Description:
transmembrane protein 111 [Source:HGNC Symbol;Acc:23999]
Mouse Orthologue:
Tmem111
Mouse Description:
transmembrane protein 111 Gene [Source:MGI Symbol;Acc:MGI:1913337]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12923 | Nonsense | Available for shipment | Available now |
sa33938 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12923
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025441 | Nonsense | 71 | 261 | 2 | 8 |
ENSDART00000129302 | Nonsense | 71 | 261 | 3 | 9 |
The following transcripts of ENSDARG00000020607 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 42306549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42377603 |
GRCz11 | 6 | 42375139 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTTATCAGGAGCAGAGTTTTACGAGAAAATGGCAAATACATCCCTAAA[C/T]AAGTGAGCCTTCTTMAANCTTTTTTGCATTTTKCTTGCGAWGTGATCRAA
Long Flanking Sequence:
TTGGAGATAGTTGTCCTTTACTCAAACACAAAACTATGAATGATAAATTCAATTGATTGTTCCTTCATTTTGTCCACAGCTCACAATGAATGATCTTGTTGTTAATTTAAGGATTCAGTTGAACATAAAATCCAGGAGATTATTACATTAAAATGTGTTGTTTCCATGTTCCAGGGTGGTGAAATTCCATCAGCATCTCTTCCTAAAAAGCATGGCTGAGCCCGAGCTCCTCCTGGACTCCAACATCCGTCTTTGGGTTGTGCTGCCAATTGTATTTATTACTTTTCTCGTTGGTGTGATCCGCCATTATGTCTCAATTCTGTTACAAAGTGATAAGAAGCTTACATTAGAGCAGGTTTCAGACAGGTAACATTTATCGTCCGTCTACTTTTATTTCTAAAACACACAAAATATTTCAAACTATTTTTGAATGTCCTCCACACAGCCAGGTTCTTATCAGGAGCAGAGTTTTACGAGAAAATGGCAAATACATCCCTAAA[C/T]AAGTGAGCCTTCTTCAATCTTTTTTGCATTTTGCTTGCGATGTGATCAAAGTAGAACGTCTGATTTGTTGTATTGTGCTAAAACAGTCTTTCTTGATGAGAAAATTCTACTTCAATAACCAAGAAGATGGGTTTTTTAAGAAGACTAAGAGAAAGGTGGTCCCACCGTCTCCGATGACTGGTGAGTTTTTCTTGAAACAGACACAAGAGGTCAAAGATTTGCCTTTTATGAAGAGAAACTGAGCAAGAAAGGAGTGACGAGATTAATTGAATGTTTTTCACTCTTTTAGATCCGAGCATGTTGACCGATATGATGAAAGGCAACGTGACAAATGTCCTGCCTATGATTCTTATTGGTGGTTGGATCAACTGGACCTTCTCTGGGTTTGTTACAAGTAAGACATACAATATTCAGAATAAAATATGGCTTGTTGAGGTGTATTCTTACAAGACGTGTCTTAACGCATTTGTAATTCTTGCTTTCTCCTCCAAGCAAAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33938
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 |
---|---|---|---|---|---|
ENSDART00000025441 | Nonsense | 168 | 261 | 6 | 8 |
ENSDART00000129302 | Nonsense | 168 | 261 | 7 | 9 |
The following transcripts of ENSDARG00000020607 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 42305882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42376936 |
GRCz11 | 6 | 42374472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGCTGTCTTTAAATAATCTCCTGGTGTATTAATCTGCAGGGTGAGCT[C/A]AGCATCTTGGTATTTCCTGAATGTCTTTGGTCTCAGGAGTATGTATTCCC
Long Flanking Sequence:
GTCTCCGATGACTGGTGAGTTTTTCTTGAAACAGACACAAGAGGTCAAAGATTTGCCTTTTATGAAGAGAAACTGAGCAAGAAAGGAGTGACGAGATTAATTGAATGTTTTTCACTCTTTTAGATCCGAGCATGTTGACCGATATGATGAAAGGCAACGTGACAAATGTCCTGCCTATGATTCTTATTGGTGGTTGGATCAACTGGACCTTCTCTGGGTTTGTTACAAGTAAGACATACAATATTCAGAATAAAATATGGCTTGTTGAGGTGTATTCTTACAAGACGTGTCTTAACGCATTTGTAATTCTTGCTTTCTCCTCCAAGCAAAAGTACCGTTCCCTCTCACACTCCGCTTCAAGCCAATGCTGCAGCAGGGAATTGAGTTGCTCTCTCTAGATGCCTCCTGGTTAGTGCTCTTTCACCCTTGAGTGTCACTTTCCTTTTTACCTAAAGCTGTCTTTAAATAATCTCCTGGTGTATTAATCTGCAGGGTGAGCT[C/A]AGCATCTTGGTATTTCCTGAATGTCTTTGGTCTCAGGAGTATGTATTCCCTGATTCTTGGACAGGATAATGGTAATTATATGCAATAGAACAACATATTTGACAGACTTAACCCCAGCAGTGATGGCTTGTTGTAGTATTATATAAAGATTTGCTGATTTATTTAGAATCTTAAACAAATATGACTTTGTTTATTATTTGAAAACTTTAAACATATGCTTGTTTATTTATTTAAAATTGGACTGTTGCCATAGCTATTGCCTTTAAATTTTGTCTTAAAGTGAGAGTTGCACTTCCCTTTACACTATCAGGTTTGATTAAAAAATATCTCTATCTGCTCTCTATTTGGCTTTTTCAGACCTTATCTTAGATGTAGTGTGTAATATACTTGTTTGTGAATGTAAAAGTCTGCAAAAAAGAACCAGTTTAGCCTGCCTGAAATGAGTCTACATTCATTTCATTCTAACTTTTTGCACAAACATAGGTTTGCACCATATTTGC
Associated Phenotype:
Not determined