ZMP
lrwd1
Ensembl ID:
ZFIN ID:
Description:
Novel protein (Wu:ft31b04) [Source:UniProtKB/TrEMBL;Acc:B0R160]
Human Orthologue:
LRWD1
Human Description:
leucine-rich repeats and WD repeat domain containing 1 [Source:HGNC Symbol;Acc:21769]
Mouse Orthologue:
Lrwd1
Mouse Description:
leucine-rich repeats and WD repeat domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1918985]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14204 | Nonsense | Available for shipment | Available now |
| sa16789 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14204
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000050906 | Nonsense | 152 | 763 | 4 | 15 |
The following transcripts of ENSDARG00000035147 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 64550123)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 60802783 |
| GRCz11 | 5 | 61487504 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTSTAAANNGTGTTTTCTTGACYGCCTTTAGGTGATTGGTGTGTGGGAA[C/T]GAGACTTTAGTCTTCCTGATCCCATTTCAGCAWAAAGCCTTGCTGCTGTT
Long Flanking Sequence:
TGCTTACACACAACACATTAAATAAAATACACATATACTCACAATTGAGCGATAACTTTAAATGTTCTCAACTATTGAACTAAATGTGAAGGCCGGTAGCGAAAGTGATCCATGTGGTGGTCACTCTACCAAACACTCCTTCTTACTCTATGGTAAGTGACTTTTTATACAGATGCGAATCAACCTAGTGCCCCTGGAGGTCGGAAGCAGTATTACATGTCCACATACCAAACAAAACACAATGCAAGAAAATAAATAAATCAGAAAATAATACTAGTAACATTTAACATGTTACATAGTTTTAGCACTGAAGTCAATACTTTTGACAACTCTACTGTCTACTAACTGTACTACTACTACTGTAACTTTACTATGTAATAATCCTGCCGGAAATTTTGTTACATTTCTTATTACTTGCATATTTTTTAAAACCCTTTAAAAGTGATCCTATTTGTAAAGTGTGTTTTCTTGACTGCCTTTAGGTGATTGGTGTGTGGGAA[C/T]GAGACTTTAGTCTTCCTGATCCCATTTCAGCAAAAAGCCTTGCTGCTGTTGAGAAGAGCTTTGTTAACGCTGCCTGCACACAAGTCAAGTATGGCCCCAATTCCTTGAGTGATTACACAAAGTGGAGGGTCAGTATTATGTGAATGTTGTGTTCCTGAGACAGATTTTAAGTTTATAGGTCAGTGTTTCTCAACCACGTTCCTGGAGTACCTCCAACACTGCATGTTTTGGATGTCTCTTTTGTCACACCCATTACAGGTCTTTCAGTCTCTGCTTATGAGCTGATGATCTGATTCAGGTGTGTTTAATTAAGGAGGCAAGAAGAATGTGCAGAGCTGGTGGTCCTCCAGGAAAGTGGTTGAGATATATTGTTTTAGAGCATCTAAACTGTTGTGGTTTCAGCAGATTTTAACTTTTCAACTCATCCTGTTTCTGCTTATTCAGGTTGAAAAGATTGCAAAGGAGTATTTGAAGTCACTGACCAGTAGTGAGGAGGAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16789
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000050906 | Nonsense | 163 | 763 | 4 | 15 |
The following transcripts of ENSDARG00000035147 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 64550156)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 60802816 |
| GRCz11 | 5 | 61487537 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATTGGTGTGTGGGAAYGAGACTTTAGTCTTCCTGATCCCWTTTCAGCA[A/T]AAAGCCTTGCTGCTGTTGAGAAGAGCTTTGTTAACGCTGCCTGCACACAA
Long Flanking Sequence:
TATACTCACAATTGAGCGATAACTTTAAATGTTCTCAACTATTGAACTAAATGTGAAGGCCGGTAGCGAAAGTGATCCATGTGGTGGTCACTCTACCAAACACTCCTTCTTACTCTATGGTAAGTGACTTTTTATACAGATGCGAATCAACCTAGTGCCCCTGGAGGTCGGAAGCAGTATTACATGTCCACATACCAAACAAAACACAATGCAAGAAAATAAATAAATCAGAAAATAATACTAGTAACATTTAACATGTTACATAGTTTTAGCACTGAAGTCAATACTTTTGACAACTCTACTGTCTACTAACTGTACTACTACTACTGTAACTTTACTATGTAATAATCCTGCCGGAAATTTTGTTACATTTCTTATTACTTGCATATTTTTTAAAACCCTTTAAAAGTGATCCTATTTGTAAAGTGTGTTTTCTTGACTGCCTTTAGGTGATTGGTGTGTGGGAACGAGACTTTAGTCTTCCTGATCCCATTTCAGCA[A/T]AAAGCCTTGCTGCTGTTGAGAAGAGCTTTGTTAACGCTGCCTGCACACAAGTCAAGTATGGCCCCAATTCCTTGAGTGATTACACAAAGTGGAGGGTCAGTATTATGTGAATGTTGTGTTCCTGAGACAGATTTTAAGTTTATAGGTCAGTGTTTCTCAACCACGTTCCTGGAGTACCTCCAACACTGCATGTTTTGGATGTCTCTTTTGTCACACCCATTACAGGTCTTTCAGTCTCTGCTTATGAGCTGATGATCTGATTCAGGTGTGTTTAATTAAGGAGGCAAGAAGAATGTGCAGAGCTGGTGGTCCTCCAGGAAAGTGGTTGAGATATATTGTTTTAGAGCATCTAAACTGTTGTGGTTTCAGCAGATTTTAACTTTTCAACTCATCCTGTTTCTGCTTATTCAGGTTGAAAAGATTGCAAAGGAGTATTTGAAGTCACTGACCAGTAGTGAGGAGGAAGAACGGGTTGCAGACACAACTCCAACAAAGGAGAA
Associated Phenotype:
Not determined