ZMP
tmem49
Ensembl ID:
ZFIN ID:
Description:
Transmembrane protein 49 [Source:UniProtKB/Swiss-Prot;Acc:Q6NYY9]
Human Orthologue:
TMEM49
Human Description:
transmembrane protein 49 [Source:HGNC Symbol;Acc:29559]
Mouse Orthologue:
Tmem49
Mouse Description:
transmembrane protein 49 Gene [Source:MGI Symbol;Acc:MGI:1923159]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35848 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32025 | Essential Splice Site, Missense | Available for shipment | Available now |
sa10666 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35848
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018461 | Splice Site, Nonsense | 102 | 406 | 5 | 12 |
ENSDART00000111753 | Splice Site, Nonsense | 102 | 149 | 5 | 7 |
The following transcripts of ENSDARG00000012450 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 16369331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17414294 |
GRCz11 | 15 | 17350316 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGCATCTTCTCTTTGTGATCTGGATGTGTTTGCTGTTGTTTGTAGTA[T/A]GTGCAGCACCTGGAGAAGAAGTTCCTGTGGTGTGCCTACTGGGTAGGCCT
Long Flanking Sequence:
CCAATTTTTTTTCCCATATTATCTTAACTGCAGAACTAATATTTTCACTCATTTGACTAATGAGTAGTGCATAGTATTTAGGAGCTTCACGGCCAGTACCTATAATATTGCATAACAATGTCATTAATGATTGCTTACAATATTTAATGATATTAAATTCTGTCTCTTACAGGCTTTGGCAGAGAAGAGGTGTGGTATTTCTGACAGTAGTCCTTTTTTCACTTTTCTCACTGGCTTATTCAATAGAAGGAGCACATCAGGAGGTGAGCTCAACATTGACCTTTTCCCCCGTCACCATTTTGTAATCAGATTCAGGATTGTGTTGTTTAAAAACTCAAGATCAGTCTCTTCTAAACCCCCTGTAAGTTAGTAATTTAATGAAGTAGGTTTATAAGTAAGGTATTAACTTAAAGTGAGTTGAGTTCCCATGCTGTCCTAAAAGAAACACCTTACTGCATCTTCTCTTTGTGATCTGGATGTGTTTGCTGTTGTTTGTAGTA[T/A]GTGCAGCACCTGGAGAAGAAGTTCCTGTGGTGTGCCTACTGGGTAGGCCTGGGTATTTTGTCTTCGGTTGGTCTCGGCACTGGACTACATACGTTTCTCCTGTACCTGGTAAGAGTTCTTGGCTTAAATTTAGACTTTCTCTTGTTCTGCAGAGCATTTTTTAACCCCTAATATAGATATATGACTCTAGATCACATAAACCAAATTGGTGGAACAATTGATGCTTTGCGTGTATGTATTTTTACATGTAGGATTTGTTGGGATAGGACAATATTTGGTTAAGATACAGTGATTTAAAATCTTAAATCTGAGGGTTAAAATAAATTAAATAATGAGAAACTCACCCGTAAAGCTGTCTAAATCAAGTGCTTAGAAATGCAAATTAGTAGTCAAAAATTAAGTAGAAAATGTACTAAATATCTTCATGGAAAATGATCTTATTACTCTAATAATGAATCACTATTATAGTAAAAGGAAAAATGTGTTACTTTTATCCATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32025
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 > A
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018461 | Missense | 134 | 406 | 5 | 12 |
ENSDART00000111753 | Essential Splice Site | 133 | 149 | None | 7 |
The following transcripts of ENSDARG00000012450 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 16369425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17414388 |
GRCz11 | 15 | 17350410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGCCTGGGTATTTTGTCTTCGGTTGGTCTCGGCACTGGACTACATACG[T/A]TTCTCCTGTACCTGGTAAGAGTTCTTGGCTTAAATTTAGACTTTCTCTTG
Long Flanking Sequence:
AGTACCTATAATATTGCATAACAATGTCATTAATGATTGCTTACAATATTTAATGATATTAAATTCTGTCTCTTACAGGCTTTGGCAGAGAAGAGGTGTGGTATTTCTGACAGTAGTCCTTTTTTCACTTTTCTCACTGGCTTATTCAATAGAAGGAGCACATCAGGAGGTGAGCTCAACATTGACCTTTTCCCCCGTCACCATTTTGTAATCAGATTCAGGATTGTGTTGTTTAAAAACTCAAGATCAGTCTCTTCTAAACCCCCTGTAAGTTAGTAATTTAATGAAGTAGGTTTATAAGTAAGGTATTAACTTAAAGTGAGTTGAGTTCCCATGCTGTCCTAAAAGAAACACCTTACTGCATCTTCTCTTTGTGATCTGGATGTGTTTGCTGTTGTTTGTAGTATGTGCAGCACCTGGAGAAGAAGTTCCTGTGGTGTGCCTACTGGGTAGGCCTGGGTATTTTGTCTTCGGTTGGTCTCGGCACTGGACTACATACG[T/A]TTCTCCTGTACCTGGTAAGAGTTCTTGGCTTAAATTTAGACTTTCTCTTGTTCTGCAGAGCATTTTTTAACCCCTAATATAGATATATGACTCTAGATCACATAAACCAAATTGGTGGAACAATTGATGCTTTGCGTGTATGTATTTTTACATGTAGGATTTGTTGGGATAGGACAATATTTGGTTAAGATACAGTGATTTAAAATCTTAAATCTGAGGGTTAAAATAAATTAAATAATGAGAAACTCACCCGTAAAGCTGTCTAAATCAAGTGCTTAGAAATGCAAATTAGTAGTCAAAAATTAAGTAGAAAATGTACTAAATATCTTCATGGAAAATGATCTTATTACTCTAATAATGAATCACTATTATAGTAAAAGGAAAAATGTGTTACTTTTATCCATACAACAAATATTTGGCTAGTTTGTGATCTAAAATATTTTGGAGGATTATTCTGCCCAGCAAGAATTTATTTCTTTGATCAATAGTGCAATAAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10666
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 |
---|---|---|---|---|---|
ENSDART00000018461 | Nonsense | 319 | 406 | 10 | 12 |
ENSDART00000111753 | None | None | 149 | None | 7 |
The following transcripts of ENSDARG00000012450 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 15 (position 16384268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17429231 |
GRCz11 | 15 | 17365253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTGCAGAAACTGTTTGTTATCATTACGTTCAGCAAGCACATAGTGGAG[C/T]AGATGGTGTCTCTGATCGGGTGAGTAACAATGGACAGACAGTGCTAAACA
Long Flanking Sequence:
TCTTGTGTGTTTTGCCACTTCTTGTTGAATTGCTGAATGCCTCCTAAAATGTAAGCCGACTTGGACAAAAGCATCTGCTAAATGACTAAATGAAAACATATTCAGCTATACCTAGGTATATCTAAATTTTATTCTATGGCATCTTTAATCAATGTTTGAGTGAGAGACGATTCCCATAAATCAGAGTGTTTTCGAAGCTGACCATTAGATCATCAGAGACACACCTTCACATGAGTCGGGACTGTTGACTCAGCAGATTATAGACAGATCTCTTTGTTTCATCCAAATGATGGAATCATAAGCCAGTTGCTGATCTCAGCGGGGGTCACATATTTTAATATACACTGAAGACTATCTGCCCTCCACAAAAAACCATCAGACTTTTGCCCCCAGGCCTCGTAAGAGATGCTGTTGATTCATTGTCTGACTATGTTTATCCACTTTTTGTGTCTCTGCAGAAACTGTTTGTTATCATTACGTTCAGCAAGCACATAGTGGAG[C/T]AGATGGTGTCTCTGATCGGGTGAGTAACAATGGACAGACAGTGCTAAACATTATAGCCAGTAAATAAAGACCTACAGCAGTCAAAGAACATCTGAAATTTAGCTTAGTTGTACATGTTTTTAAGATGTAATTAAGATCAAATTATTCATATAAACTAGGGCTGCACTGTATTCTGGAAAAAAAGGGAATTGCGATATTTAAAAAATTTTTAGGTGAATTTTGCCATATGAGTAGTTTTACAAGACAGTTTGAATAGCTCTTTTTGACAGTTTTCTGGGGAGACTAACAGTATTCAGCTACAGATATTAAATAATCACAATGTAAAAAAAAATATTCATACATTGCTTTGTCTTGTTTCTAGTCCAAATATCTAAATAATTCATAGATCAAGTAAAAATATATATTTTTTCAACTTTAGAAAAAATGAAGAGTTTTTCGTTTAAACAAGTAAAATAATCTGACAGTGGGGTAAGTATGTAGTTATTTGGACTAGAAACAGG
Associated Phenotype:
Not determined