ZMP
tm9sf2
Ensembl ID:
ZFIN ID:
Description:
transmembrane 9 superfamily member 2 [Source:RefSeq peptide;Acc:NP_997893]
Human Orthologue:
TM9SF2
Human Description:
transmembrane 9 superfamily member 2 [Source:HGNC Symbol;Acc:11865]
Mouse Orthologue:
Tm9sf2
Mouse Description:
transmembrane 9 superfamily member 2 Gene [Source:MGI Symbol;Acc:MGI:1915309]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19513 | Essential Splice Site | Available for shipment | Available now |
| sa18297 | Nonsense | Available for shipment | Available now |
| sa32695 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19513
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
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019743 | Essential Splice Site | 52 | 658 | 1 | 17 |
The following transcripts of ENSDARG00000003866 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 28743676)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 28994505 |
| GRCz11 | 1 | 29798436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTAAGAAAGAAGCGGGCGACAAAAACAGCGAAGTCCCAGACTGCAAGG[T/A]AAATATTCACATTTAGAAGTGTACTAAATTAGTTTGCTTAAACGTATGAG
Long Flanking Sequence:
AAATGAGTACTTCACTATTTGCTTATATTGCATGGCAATAATAAAACAGTAGTGCAAAGATCTGTAATTTAGAGATCCTGTCATTTTATAAGAAATACGAGGCAGTCTGCATAAAACAAACGAGTTCTGTCATTTCTATCGCTTCCGCGTTGAAGTCCTCCTCTATCCCATCATGCACTTCGTGACGGATGACGTGTCTAAGGAGTCAGATGCTGCTACGCAGGCAGCGGTTACGCTAACGCTTGTGCTTAGACATCACCAATGTCTAAATTTTGACACCCATATCTACATTTCACGCATGTAAATACATCTACAGATTACTTAATTAGTCGGTCGTGGCAAAATGGTCGAGTTCCACCGTGTCCGTGTTGTATTTGTGTCGCTTTTCGTGTGCGGGTTGTTGCGGGACGCGTTGAGTTTCTATCTTCCTGGTTTGGCCCCGGTCAGCTTCTGTAAGAAAGAAGCGGGCGACAAAAACAGCGAAGTCCCAGACTGCAAGG[T/A]AAATATTCACATTTAGAAGTGTACTAAATTAGTTTGCTTAAACGTATGAGATGTCTCTTGGTTTTTGTTTAGTTTTTTCTTTATTGCCGTCCGTATGTTGCGTGATGCTAGCTCGAAATGCTATTCCGGGGTCAGTTGTGAAAAACCTATGATCTTAACTCACTTAAAGAATAGCCGTTTTATCTCTTTTATTCATTTTAGCGTCGTAAAGGGTAAGTTTAACGTTAGTCAAATGGTTTGTGTGGCCTAACGTTAACGTTACATGATAGAGGCGCGGTTCTTACTCAACTGTCACTCTCGAACTAAGCTTAGACTTTCAATTTGTTCGTTAACGTTACTTTTTTATTGTAAAATTCGGGTTTTATTTACCGTTTTTCTGTGAAAGCCTTGGCTTTTGTTTTGAGATTAATTAGCAATTGGGTACGTTGACAAAAAGATCAATAACTTACCTGACAGGATCAGTAACCGTGACGTTAACTTGCTTGCATTGAATGGAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18297
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019743 | Nonsense | 73 | 658 | 2 | 17 |
The following transcripts of ENSDARG00000003866 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 28746406)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 28997235 |
| GRCz11 | 1 | 29801166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTTTGTGAACAGGCTGGATTCTGTGGAGTCAGTTTTACCCTATGAATA[T/A]ACTGCGTGAGTTTAACATGTTTGTCATTTTTTTGTTCATKCAACATTTTT
Long Flanking Sequence:
ACAAATGAAATCGTATGAATTTGTACAAATTAAAATACCACTTTACCACTTTAAAATAATTTTAATTACTAAATAATTAAATAATTTTAGTTTTGTAGTTTCCACCCACCAAACTGTACAATAAAACTGCAGTAAATCACCATAGAGGCAGTAAAACCTTCTCAACCCTGTTTGTGCAGTTTTAAATTTGGGATTTTTACAGTAGTAACATTAACTAAAGTGTCTGGTAATTTGTTGGAGAATTTAGTGTCTAGTGTCTTTATTTTAATCCTTTATAAGGGCATTGAATAGTAAATCATATATCATACGAATACTTGTATGTTAACAGGAAATGTCAATGAAAGTAAACAGTCATCATTAAACAGTGATGCTTTTATTACAAAAAGACGGATATGCTGTGGACATTGCTCTTACATTTGCTGCTTCTCTTTTCAACAGTCAACCATTGAGCTCTTTGTGAACAGGCTGGATTCTGTGGAGTCAGTTTTACCCTATGAATA[T/A]ACTGCGTGAGTTTAACATGTTTGTCATTTTTTTGTTCATGCAACATTTTTATTTCAGTAGCATTTATATGCTGATACATTGGTTATACATATATAACTTATCAAGGTTCGAAATTAACTTTTTTACTTGGCAGCACCAGTGCTCCTAACTTAAAAAGTTTAGGAGCACCAGAAAATAATTCGGAGCACCCACCAAAAATGAATGAGCAGTACCACTGCAAATTGTACATTAACAGATTTATTGTATTTGAAAACAACATCAATTAGGAGTAACAAAAAAGTGAAACAATTGTCTAACTAACGCTGAGATGACATTGATATTTGTGCAATAATTCCAAAATAAATGTCTAATAATTATAAAACATTAATGATGACGATGATGACAATAATACTGATAATGAATTACATTTCTCATTATCATGCATCTGTGAATGTGCTTGAATGTGAGTTGTGTGCTATGTAAAGACCTACTGTTACTTTATAAAAAATAAATTCATGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32695
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019743 | Nonsense | 327 | 658 | 9 | 17 |
The following transcripts of ENSDARG00000003866 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 28754532)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 29005361 |
| GRCz11 | 1 | 29809292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAATGGTCGCTATGATCATGCTTCGAACACTTCATAAAGATATCGCT[C/T]GATACAACCAGATGGACTCTGTGGTGAGTTCCACTCTACAAGATTACATC
Long Flanking Sequence:
TACAAGTTTATAGCAAATAGCGTTTAATTTATTTTCAGCAAAAGAAAAGCTTTAAGGCCTTCCAAAGTTTTTTGCCTAAATAAAAGCTTAGTTTTAACTTTGGAAAGCAATTATATTATGTCATACATATTAGTATTCTAGTTTTACTGTTGTTCTTTAAAATGTTTTTTATTAAACACAGATAATACATGCTTAATATAGTAATATACTTCTTTAGTGATTACCAATAAACAGAAAAATCTGTTTAATAATAACTGTTCTAATTAAAACCTTCTTTTCCGTTTAACAGCACAATAGTGTTATTGAAATATATTGTGACAATTTCAGTAACCAGTATTTATTTATTAAATTAAATGGTAATAATAGTTGAAGTCACAAAACATGAATGCTCAGCTGTTTTGTTCTCTTCCACCAGTATCATGAACTCTCTGGTCATCGTACTCTTCCTCTCTGGAATGGTCGCTATGATCATGCTTCGAACACTTCATAAAGATATCGCT[C/T]GATACAACCAGATGGACTCTGTGGTGAGTTCCACTCTACAAGATTACATCATAATCTTATATGATCTGTATATATGTTTGTGTGACTGTTGTAGTTTATGCATTTTAGTACAGCCAACATTTTGTCTTTCAGGTGATTGATCATATTTATGTATACATGTGTTTGAGTCTGTCTGTGGTTAATCAGCATAATGGCAAAAGAATACTGTATTTCACTGTGTTACAGTGGCAGTGGCTTAGTGCTGGTGTTAATGAAGAATCTGCCATGCGTTTTGCTCATAATGTGAAATAAATCCACACTTTGTTGATCAACAGTTGAACACTTGAGGCAACAACAGTATTTACTTTGCCATTTTGTGTGTTTGTTTATGCTTTCCTTTAATCTGCACCTCCGTAAACATGTGCCTCGCACGTGCATGATGTCATCGTTTTCGAAGACTCGTTTTCAGAAATGACAACAACAGACAATTTTCAAAAACTTGTAGACCAGGATTGCCCAAA
Associated Phenotype:
Not determined