ZMP
tmem41b
Ensembl ID:
ZFIN ID:
Description:
Transmembrane protein 41B [Source:UniProtKB/Swiss-Prot;Acc:A1A5V7]
Human Orthologue:
TMEM41B
Human Description:
transmembrane protein 41B [Source:HGNC Symbol;Acc:28948]
Mouse Orthologue:
Tmem41b
Mouse Description:
transmembrane protein 41B Gene [Source:MGI Symbol;Acc:MGI:1289225]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25375 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25375
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098277 | Nonsense | 280 | 282 | 7 | 8 |
| ENSDART00000110614 | Nonsense | 280 | 282 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 66966165)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 64881149 |
| GRCz11 | 7 | 65105177 |
KASP Assay ID:
554-7566.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCCGTCGTCTCCATCCTGCCGGTTTGCTTTCAGAAGAAACTCCAGCAA[A/T]AGCTCGAGTAGAGAGAGGTCTCCCACCCCTGCTTGATTCAACTCAGGAAT
Long Flanking Sequence:
TTGTTTTATTTCGGCAAGAATAAAAGCAGTTTTTAATTTTTTAAAGACCATTTTAAGGTCAAAATTATTAGCCCCTTTAAGCTATATATTTTTTTTCTGATAGTCTACAGAACAAACCACTGTTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAATCTAATTAACCTGGTTAAGCCTTTAAATGTCACTTTAATCTGTATAGAAGTGTCTTGAAAAATATCTAGTCAAATATTATTTACTGTCATCATTTATCCATTATGTATCTTCAATATATAAGATCAACTGATGAGTGAATCATCTAATAGTTTTTGGATGTGTTTAATATATTCACAGGAGTGGCTCCTCCGTCCTTTGTGGCGATAAACGCAGGGACGACGCTCTACAAACTGACCACCGCTGGCGAGGCCGTGTCCTGGAACTCTCTTCTGGTGCTGGGGGTTTTGGCCGTCGTCTCCATCCTGCCGGTTTGCTTTCAGAAGAAACTCCAGCAA[A/T]AGCTCGAGTAGAGAGAGGTCTCCCACCCCTGCTTGATTCAACTCAGGAATGATACTGATCCTCTAAACTTCTCCTCATTTTCGACTTCTTCTTTTATGCATGTATGACCGACCCCTCATACAAAGGGCAGGACCGGCCTTCCATAGTTTCAACAGCACTGTCACGCAACGAAGATTCAATCGTCACTGATTTTCTCTAGCAATATATTCCACGTCGACGTCTTCAGTGGATTTTAAAGTTCATATAAAACAGCAGTGATTCATGTGCGATACACTGGAGAAAGAGCCGTTCACTCCCTCTCAAGTCGCTGAGCTGAAATGGAAAGTGCCAACTTTTGTGCTCTACTTTGACGATGAAGTATTACATGCTTCAGAAACCTTTTGAGGGGGAGCTTTGTGAGTTTAACCGAGTTCGATGTTATTTCGTAAGCCAGCTGAGACTGTGAATGGATTATGCAACAGTGCCCTGTGTAGTGTGTGCTGATGCTAACTATAGACCAC
Associated Phenotype:
Not determined