ZMP
si:dkey-19f23.3
Ensembl ID:
ZFIN ID:
Description:
transmembrane 6 superfamily member 1-like [Source:RefSeq peptide;Acc:NP_001074130]
Human Orthologues:
TM6SF1, TM6SF2
Human Descriptions:
transmembrane 6 superfamily member 1 [Source:HGNC Symbol;Acc:11860]
transmembrane 6 superfamily member 2 [Source:HGNC Symbol;Acc:11861]
transmembrane 6 superfamily member 2 [Source:HGNC Symbol;Acc:11861]
Mouse Orthologues:
Tm6sf1, Tm6sf2
Mouse Descriptions:
transmembrane 6 superfamily member 1 Gene [Source:MGI Symbol;Acc:MGI:1933209]
transmembrane 6 superfamily member 2 Gene [Source:MGI Symbol;Acc:MGI:1933210]
transmembrane 6 superfamily member 2 Gene [Source:MGI Symbol;Acc:MGI:1933210]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11951 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11951
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 |
---|---|---|---|---|---|
ENSDART00000040601 | Nonsense | 251 | 374 | 9 | 11 |
ENSDART00000145260 | Nonsense | 251 | 321 | 9 | 11 |
ENSDART00000040601 | Nonsense | 251 | 374 | 9 | 11 |
ENSDART00000145260 | Nonsense | 251 | 321 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 22 (position 18031801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 17782736 |
GRCz11 | 22 | 17807714 |
KASP Assay ID:
2261-6710.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGTCCTGGATTGCCCGCTGGAAATCCTCAACAAATATGTGACYGAGTA[T/A]GAACCGTATCTAAAGGATCCCGTGGGCTTCCCCAAAGTTATGGTGAGATA
Long Flanking Sequence:
ATATAGAAATAACAAACTTTAATCCTTTATTAGTGAAAATACTAGCGGTCTAAAACTTTTAGGCTGTATAGTACTGTATATCCCAGACATCTGCACAAACTTCCTCTGTAACAAAGCACAGACACATTCGAGGATATATGTCAACACTTGAATGTGCGCAATATACTGACACTGAAAGGAAGTAATGTTTGAATAAAGCCTTTATTTTTTTTAGTGTGCACTCTTGTAGCTTCATAATATTCAGATTAAACCACTGAAGGTCTGTTATGAGGATGTTTTTTGGTATCAGGTCTCAGGTGTTAGAATGACATAAGGGTGAGTAACATAATTTTCATTTTTGAGTGAACTAACCCTTTAAACATGGTGCCTGTATTATGTTTTGTGAAAATAATGCCTACAGTTCAACAAAAAATAATTGCCACAACAAATTTCCCATCTCTATCCACACAGGCAGTCCTGGATTGCCCGCTGGAAATCCTCAACAAATATGTGACCGAGTA[T/A]GAACCGTATCTAAAGGATCCCGTGGGCTTCCCCAAAGTTATGGTGAGATACTCTGACATTCAGCTTATGGCGGCCCTCGAGCACACTTTGCTTCTTAACAGCCTTGGCTTTATAACATTAAGCTCCTCTAAATGACTGGTTTTTCTCATCATTAGCACTCAATAAGGTTGTCACCTTGAGTAGTCCAAGAATATCTCTACTGTCTCGACCGACCGCGCGGGTTTGGAAGGTGATGTTTTCGGTTTAGATTGGGGTTTCACTTCGGTCAATAGGTTATCAAAAGTCCTTGTTCTAGCTAGAGCCCAGGCACAATGGAGGCCCATCGATTAGCTAGGAGATGTGCTGCGAGTACTTGATAAGCTAATCCTACCCATGAGTCCTGGCTGAAAACCTCCCGTCAGCTCAAACAAGGGGACGTGACGGAGAGATTGTGACATGGGTGGTAATGTGTTTGATAAGGAATGAGGGAGCAGAAACACGTATGTTTGTACTGAAGACCG
Associated Phenotype:
Not determined