ZMP
tmem176l.1
Ensembl ID:
ZFIN ID:
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7299 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18185 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7299
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 |
---|---|---|---|---|---|
ENSDART00000121522 | Essential Splice Site | 96 | 235 | None | 6 |
ENSDART00000132112 | Essential Splice Site | 96 | 236 | None | 7 |
ENSDART00000136568 | Essential Splice Site | 96 | 236 | None | 7 |
ENSDART00000145814 | Essential Splice Site | 96 | 236 | None | 7 |
The following transcripts of ENSDARG00000086230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 49585462)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 46554491 |
GRCz11 | 16 | 46521207 |
KASP Assay ID:
554-5371.1 (used for ordering genotyping assays)
KASP Sequence:
KTGGAACAACCTTACTGGTTGTGATGCTGTTTTTTGGTTCGGTGGTACGG[T/C]AAGAATTAATGTCTTWTTCTTCTCCTTTTAAATATTTGATGTAGAGGTGT
Long Flanking Sequence:
ATTATGTACTATAATACTCATTTCTTTGTGTTTTATACAGCAGGTTTGGACTTCATCAGTTGTGTGAAGATTGAAGTGCATCGTTTCCACCCGCAGCATGTCTCTGACACTGGCTCAGGGTGAAGGCATTACTGTCATCACCGTCACCTCAAACCCGAAGAGCAAATGGCCCATTCTGTGTCAGATCCTGGGCACTTTATGCTACACTCCAGTATATTCTGTGTCTCAGGCTGTGAAGGAGAAGCTGAAGAGCGTTTACACTGCTCTTGGGGTGAATTAAACCACTGTCTTTTCATTGCGTTTCCATTACAATTATTTTACATTTTAAGATGCATTATCGGTTTTGAGGCATTCAAGCAAAAATCTGTTTATTTTTATTCCATAGACTATGCAGATAATATATGGAGTCCTCTGCATTGTGTTGGGGGTTCTGATTGACAGACTTTGGTATTGGAACAACCTTACTGGTTGTGATGCTGTTTTTTGGTTCGGTGGTACGG[T/C]AAGAATTAATGTCTTATTCTTCTCCTTTTAAATATTTGATGTAGAGGTGTAAACCTACACTTAGGGTTGTGCCTATCAACGATAGTATCGTGTATCGACGATAGGCAAAGATATCGCCAAGAGCTGAAACCTATGACGATTTTAAAGACGATGCTTGCACACAGTTATTTTTTGTTCACCATTTTTTCTTTCATTGGCATTCTACTTACCAGCAAAACCGAAATGTGCTCACACTGCAGATTTGAAAGACGATGGCGCTTCCTCATACTGTTACCTCAGCCTCACTTCATCGCCGCTCGCCATGTTAAAGTGTGGAATAATGGTCAAGCGCCATATTTACTCGCGGGGAGGAGTTTCCTTATCTGAGCTCATGGATTTAGAGGCACACAAAGTCAATTCGGGGAGATATAAAACACACATAAATTATTTAAATGCAAAACTGAGAAACCGCAATTCACAAGCGCGTATTGAACCGTGAAAGTCATACCGAATGGTTCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18185
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 |
---|---|---|---|---|---|
ENSDART00000121522 | Nonsense | 153 | 235 | 4 | 6 |
ENSDART00000132112 | Nonsense | 153 | 236 | 5 | 7 |
ENSDART00000136568 | Nonsense | 153 | 236 | 5 | 7 |
ENSDART00000145814 | Nonsense | 153 | 236 | 5 | 7 |
The following transcripts of ENSDARG00000086230 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 49584178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 46553207 |
GRCz11 | 16 | 46519923 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTCAATAGACCTGGYCAGKGGAAATTATCTATACWGCRATGATTATTA[T/G]GATTMTTCAACACCTTCCCCTGAACAGAGGAGTGATAGAGAGACCTGCAT
Long Flanking Sequence:
AAACAATATAGGTTAAAGGGGCTAATAATTTTGACCTTAATGTTTTTAAAAAAATTAAACGCTTTTATTCTAACTGAGATTAAAAAGAAACTGAAATTCTCCAAAAGAAAAAATATTATTAGACAATGTGAAAATTTTCTTGCTCTGTTAAACATCATTTGGGAAATATTTAAAAAAAGAAAAAAAAATCTAAAGGGGGGCTAATAATTCTGACTTTTTTAAAATTTGGTTGCTTTTCAGGCCATTGTATTTGGAATCGTGACTATTCTTACAGCTTGGTTTCCCAGTTCTTGTCTGGTAAGTTTCTGTCAAAACCATAAAGTATCAAAAAAATCTGTTCTGGAATTATTTGAAGCATCACCAATTTATGTTGCTTGTGTTTTACAGCTGGCCTTCACACTGCTTCTGAATGTAGTCAGTGGTGCGCTGGCCATCACAACTGTAGTCATGTGTTCAATAGACCTGGTCAGTGGAAATTATCTATACTGCAATGATTATTA[T/G]GATTCTTCAACACCTTCCCCTGAACAGAGGAGTGATAGAGAGACCTGCATGAAATACATGGAGACCAATCAGGTTCTGATTAAATTTGTTTTATTTATAATAAAAGGTTCAATTAAAGCCTTTGGGATTCTACTTTATAATTCATACTGCTAATTTAAAATAGTTATTTAATGTAATGTTTATAATGATTTTTTAATAATATATTTTTATTATGGATTTTTAAAATGCAGTAAAATAATAACAGTTATGAAACTTAAGATATTTATGGAAACATTTTATATGCAATTATTAAATAGAAAAGTTCTACTTTTTGTTCATTAAAGAATCTTGGGGGATAAAGTATAAAATAATGCAGAAAAAAAATGACACAAAAATGACATTTTTTGACAACTATTATGATTAATTAACTACTTGATCTTAGTAGCCTAAGTGTCTATGTGGCATATTAAAATTCTAAAAAATTATGTTACACTGAAAACTGAAGTAATAATGCTACCACA
Associated Phenotype:
Not determined