ZMP
tmem9
Ensembl ID:
ZFIN ID:
Description:
transmembrane protein 9 [Source:RefSeq peptide;Acc:NP_956160]
Human Orthologue:
TMEM9
Human Description:
transmembrane protein 9 [Source:HGNC Symbol;Acc:18823]
Mouse Orthologue:
Tmem9
Mouse Description:
transmembrane protein 9 Gene [Source:MGI Symbol;Acc:MGI:1913491]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34410 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34411 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34410
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062403 | Splice Site, Nonsense | 38 | 193 | 1 | 5 |
ENSDART00000137899 | Splice Site, Nonsense | 31 | 186 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 26614992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25742910 |
GRCz11 | 8 | 25762049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGGCGTTTCTTGTTCTCATAGAAGTGGTGTCGTTTGCTTCTGCAGAT[A/T]AGGTACAGTTTTACTGGCTTATTTTCACCTGTATTCTTATGTTTTAAAAC
Long Flanking Sequence:
AGTCTTTTATTTTGCTTTTCGCCGGTTATGAAGGCGGCATAGATCTATCTATGCGAAGGCGGGACATGTAGAGTGTCATCGTCACGTGACAGTGTGACGTAAACATTCATGAACTTCCGGGAAAAGTCAACAAATGCGTTGATGTAAATACTGTCTGTATGTTTGTGCGTTTAGTTTTGCATTTCTGCGTGTAACATTTTATGTATTTGTACCTCCTTATGTAATTTTATTTCCTCTAAAATACGCAATATAGACAGGAGAAGGCCTAAACGGCGAAACCGGTTGTCTGCCAGCCTCTTATTAATGCGGCATAGACCATTTACTAACTGATTATAAGTACATTGTTTACAGTACAACCATCACCTTTAGCTAAACGACAAATAATTTAAATGTATTATTTTACAGGCGTCATGTCCTTCATTGCACAAAGTCTCCGGACACCAGTAATTTTCCTGGCGTTTCTTGTTCTCATAGAAGTGGTGTCGTTTGCTTCTGCAGAT[A/T]AGGTACAGTTTTACTGGCTTATTTTCACCTGTATTCTTATGTTTTAAAACCTCTATATGTAAATAAACGTGAAAAAAGGCAACATTTCGAATGTTACCAGGTTTTGACATGTTATTAATGCAATTAGCATTTTTCATTCATTTTCCTTCGGCTTAAGTCCCTTATTTATCAGGGGTCCCCACAGCGGAATGAACCGCCAACTTATCCAGTAGATGTTTTACACAGCAGAAGCCCTTCCAGCTGCAACCCAGTACTGGATTAGCACTTAGCATTTTTTTATAACAAAAAAAAACTAAAACTAAATCTTTGGAGTATTAACCTATACAAACTACTCCAGAAAAGAAACCTTAATAGTTTGTCAATAGGTTTACATTTGCACGTTAATCAGCAAAATTGTGTAAAAGATGTCTGAGATATGGAGGAAGGACTTACTGAGGTTGATGATATGATTTAACAAAAGTTTTTTTGACCCCCTATATTTATACTAATGTGCTTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34411
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062403 | Essential Splice Site | 105 | 193 | 3 | 5 |
ENSDART00000137899 | Essential Splice Site | 98 | 186 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 26617019)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25744937 |
GRCz11 | 8 | 25764076 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGCTGTGTGAGTGCAAGTATGAAGAACGAAGCAGCAACACCATCAAG[G/A]TGAGAAGAGACTTTTATTATCTAATCATGCATTTAAAGGAAATTGAGGAG
Long Flanking Sequence:
AAATCTTAAAAAACTGTTTTAGATTTTTATCTTGTATATTATCATTATTATTATTATTATATATGTATTTTACCTTGTACATTATTTATTGCTGTTGAATACTTTTATTTATTCGAATATTTTTATAATTATAGAAAATTGGTGTTTATAAAACGTGATAAACTTGATCTATTTTCTTTTTGCCATGACATAGCCATAGAGGCTGAAATGGCAATAAAATTAAAACTCTCTCTCTCTCTCTCTGGGCCAACTTTGGCCTGCGGGTCCTAGTTTTGGCCATCTCTGCTCTAGACAGACTGGTACTGTCTGTAAAAGATATATTTTATAGATTATGTACATTATATCTTGATAGTTTTTTTCCATTTATATTTATGAATGTATTGTCTTATAGTAACTGTCTGCATGTGGTGGAGCCCATGCCAGTGCCTGGTCATGATGTGGAGGCCTACTGTCTGCTGTGTGAGTGCAAGTATGAAGAACGAAGCAGCAACACCATCAAG[G/A]TGAGAAGAGACTTTTATTATCTAATCATGCATTTAAAGGAAATTGAGGAGTATTAATATTCTGATAAATTTCCCAGGTGACCATTATCATCTACTTGTCAGTGGTCGGAGCTCTTTTACTGTACATGCTATTCCTGCTTCTGATTGATCCTCTGATTCGCAAACATGATCCGTACACCATGCCACTGCAGAATGAGGAGGATTCAGAGGTATGTGGAAATTGTTTGAGAAAAGTTACACAAACGCAGAAATTACATTTTTATGTGGCCTCAAAATACAGTTTTTAGCAAAACATTTTTGTCCAAAATCAAAATATTATATAAATAATAAAAGTTCTCCACAAATCCTCTGCAAAAAAAATCAATTTCTTTTTTTCAAGATTGACCATTTCTATATTAGTCAATCACAAAATATCTAATCAGCCAGTTACATGACTGCACCTCATGCATTTATGCATGTAGATGTGGTCAGTATAATCTGCTGAAGTTCAATGTGAGTATC
Associated Phenotype:
Not determined