ZMP
wrb
Ensembl ID:
ZFIN ID:
Description:
Tryptophan-rich protein [Source:UniProtKB/Swiss-Prot;Acc:Q6DRM0]
Human Orthologue:
WRB
Human Description:
tryptophan rich basic protein [Source:HGNC Symbol;Acc:12790]
Mouse Orthologue:
Wrb
Mouse Description:
tryptophan rich basic protein Gene [Source:MGI Symbol;Acc:MGI:2136882]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35806 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa30987 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35806
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114134 | Essential Splice Site | 30 | 170 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 5795885)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 5914222 |
| GRCz11 | 15 | 5902073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCTGTGCAACCTCGTCAAAACATTCCTGCCATCCATTTCTTCATTT[G/T]TAAGTACTCAATTAAAACGAGTTTTAGGGACGCTTAAGCACATATATATT
Long Flanking Sequence:
TGAGCGGCGATTGGCTGAAACGTCCTGGCAACCACATTTCAAACCAAAGCAAAGTACCTGTTTGGATAGGTTGAGGTGCCAATCACAGATTTACTTGTATATTCTTTAGGCGCCACTCTTAATAATTTTTGTGTAGGTACGCTTACAAATGTAACATTTAACAGCGGAAGTGTTGAGTACATATTCAAGCATTGCAAACGATTTAAATGCATTTAAAGATATTGTAAACAATAAACGCGAAAACAATACTTTTTATCTTACAAACATGGGGGTTTAAAACACATTTGTATGCAATTGCATGTTTTTAAACAACACAAGTGAACAATAACCGTCTAATCCAAGGGACCACTTTAAAACAGGGCTATAGTCCGTTTGAATAATTGGGGGAGGATCAGGCTGATGAAAAGAAAATGGCTGCCGGGTTTAACTGGTTTCTTGTACTGAGCTCTGTGTTTCTGTGCAACCTCGTCAAAACATTCCTGCCATCCATTTCTTCATTT[G/T]TAAGTACTCAATTAAAACGAGTTTTAGGGACGCTTAAGCACATATATATTTTATTTAAAACGTGTTTTCGTTGTAACATAACGTGACGCCACAATGCACAGTGATACAGCATGTCTGCTACCCCTACCGGAGCTTCTTGTAGGCACAGCGAACAAAAGCTTCCCTGTTAAACAAGCACAGTATCTTCATTTTGCTTTGTTCTAATTCACTCATGAATTACATTAAGATGTTCTACCGAACAAACATTTTATATGAGGTGTTGTTGCTTTGACAAATCAATTAAAACAGGTCAATTCGTTCATAACAGTACATACTTGTATAATGTTTCTAAACTACTGCTAATTCATATTACATTCTATTTCGTGTACGTGGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCCACCGTGTGTGTCTTAAATATACATCACACAGTTTTTAGCACAGCCATATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30987
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000114134 | Essential Splice Site | 86 | 170 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 5798607)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 15 | 5916944 |
| GRCz11 | 15 | 5904795 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTGGAACGCAAGATCAACAAGATGACTGATCAACTCAAAACTCTTGG[T/G]AAATAAAACTCGTTCTTATTTTGCACATTACATGCATACGCAGCAAGGTG
Long Flanking Sequence:
ATTCATTTTTAGATGTTAAAATGGCTTGTTTTGTTGCTTGATGTTGCAAACTGATATTTTCTTATTATATTATTCTACTTTTATGTATAATTATGCAAACACTTGTTTGTAGAGCAAGTAGTTTTACAGTTTAGGCAACTGAATCGGAAGTTCTAAAATGATCGCACTTCCGCATTAAAGAATAAGGTCAATGGCAGAAAATTTTGGCGGTTTTAAAACCTTGACTTTTACAAACCGCTGTATATTGAAAACGGTTATCGTCCCATGCCTAATATATAATAAACACACGTGCATGTATATTAAAACTTTTTATTTGTGTGTTTGTTCTCATAGTTGTCAAAGATCTTCCATAAAGATGCAGATCAGGAGATGGAGATGAGGACTGAGATCCAGAACATGAAGATGGAACTGTCAACCATCAGCATGATGGACGAGTTTGCCAGATATGCTAGACTGGAACGCAAGATCAACAAGATGACTGATCAACTCAAAACTCTTGG[T/G]AAATAAAACTCGTTCTTATTTTGCACATTACATGCATACGCAGCAAGGTGGTGGACCAAGCTTTCTTACCAGCACACATGTGGTAAGAAAGAAGCCCACTAACTAAAGCAGACAAAATGTGTAGCAACATGTATAATATTGATTCCAGAAAAAAACAAGGAGCAAAGGGTACGTGTTAAGATGTTTACAGCCAACAGAACACTTCACTGGAAGCAGATGAAAGTCAAAATAGCATCAAAGCTTTGAAAATGTACCTTTGTCCACTTTAAAGTGGGGTGGGAACAACTAAGAAACCAAAAGTTTTTCACTTTACCCTAGAGGACTCAGCCCAAGTGTGGAAAATGGCAGGTGGGTTTCAGATAACGGCTTCAGTGTTCATGAAGGGAGACAAATGGCTCAGCTGCTGCCTGTTGCTGTCCTTCATGTCCAGCATAGTAAGTTTATTGTGGGTAAAATGGATGAAACTTAGTTTACCCATAATTTAAAACGGTCATGACTCT
Associated Phenotype:
Not determined