ZMP
rbm4.1
Ensembl ID:
ZFIN ID:
Description:
RNA-binding protein 4.1 [Source:UniProtKB/Swiss-Prot;Acc:Q6IQ97]
Human Orthologues:
RBM4, RBM4B, RP11-658F2.1
Human Descriptions:
RNA binding motif protein 4 [Source:HGNC Symbol;Acc:9901]
RNA binding motif protein 4B [Source:HGNC Symbol;Acc:28842]
RNA-binding protein 4 isoform 1 [Source:RefSeq peptide;Acc:NP_002887]
RNA binding motif protein 4B [Source:HGNC Symbol;Acc:28842]
RNA-binding protein 4 isoform 1 [Source:RefSeq peptide;Acc:NP_002887]
Mouse Orthologue:
Rbm4b
Mouse Description:
RNA binding motif protein 4B Gene [Source:MGI Symbol;Acc:MGI:1913954]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa2347 | Nonsense | Available for shipment | Available now |
| sa9445 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2347
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 |
|---|---|---|---|---|---|
| ENSDART00000052862 | Nonsense | 120 | 419 | 2 | 4 |
The following transcripts of ENSDARG00000036386 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 23970612)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 22532364 |
| GRCz11 | 7 | 22803521 |
KASP Assay ID:
554-2517.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTGGTTGAGTGCGATATTGTGAAGGACTATGCTTTTGTTCACATGGAG[C/T]GAGTGGAAGATGCTATGGAAGCCATCAGTGGCTTGGACAACACAGCCTTT
Long Flanking Sequence:
TCTATCCCTTTAAATGTGCCTTTTATGGAATTATAAACTTGTATGAAGCTTACCATTCTTTTTAAATGTGCACTACATGTTCTTGATTTTTCTGTTTTCTTTTTCTCTCAACAGATCCTGAAATTTGAATTTACATTATTAAAATGGTGAAAATCTTTGTTGGGAACCTCTCGCCGAACACTACGGCTGAGGAGATCCGTTCCCTCTTCTCTCAGTATGGCAAGATCTCAGAGTGTGACATTGTGAAGAACTTTGGCTTTGTGCACATGGATAGCAAATCGGAGGCAGATGAAGCCATTCAAAATCTTCATCATTACATGCTGAATGGTATGGCCATGAATGTGGAGATGAGCAAAGGGAAACCCAAGACCTCTACAAAACTCCATGTGGGAAACATCAGCAGTAGCTGCACCAACCAAGAACTCAGGGCCAAGTTTGAGGAGTACGGACCTGTGGTTGAGTGCGATATTGTGAAGGACTATGCTTTTGTTCACATGGAG[C/T]GAGTGGAAGATGCTATGGAAGCCATCAGTGGCTTGGACAACACAGCCTTTCAAGGTGAACCAGTATGGTCCTTTGACCTGTTTAAATAAAGAAAAATAATATTATCTTGTTACATTACCAAAAGTGAGCATTTCAGGTTGGTAAGTAGAAAAATTGGTAAGTGATAAGTGAGTATAATTTGGTTTATTTACTGCTAGCTTACTATACAGAGATCTATGGAGGATGTGAATGTAGTTCTAAAATGGCATTTTTTATATCAGCCAAAAACACAGGACAAAATGGACAATGGGATGACCTTAGTGTAAATTATTTGAAGTAAGAGTAAATGTGTCTTTTTTTTCCCACACAGACAGTTCATTGTTCAATGTTAATGTTAACATGAAATTGACTGTTTTAAAGTCCATAGGTTTCTTTACTAGTAATTTCTTAATTTAGTCATTATGAGGGCCTCATATTTAAATTACCCAGTACACTTCTATTATTATTATTCTTTTCAAATT
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa9445
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 |
|---|---|---|---|---|---|
| ENSDART00000052862 | Nonsense | 417 | 419 | 3 | 4 |
The following transcripts of ENSDARG00000036386 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 23973139)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 22534891 |
| GRCz11 | 7 | 22806048 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTGCTGCGTATGACGTGCCGCGGGAYCCATACGCTGAAYGGGCGCGCTA[T/A]GCTTACTAGCCTAATTCCTGTGCGCACTCAGGTGAGATCTTTTTAGGATC
Long Flanking Sequence:
GGTATGCCAGCGGGCTACGGTGTTGGCGCGGATAATAGCATGGCTCCAGTGTACGGAAGCGAGGCTGCGTATGGGACTAGTGGCATGGCCTACCCCGGTGCGTTGCCTGCGTACCCGATACGACGACCACCTTATGAGGAAAGAGATCCGTATGGTGTAGTGGACTTCTACGAGAAATATCGGGCACGTCCGTACGGAGGCAGTTATTTCGAAGATAGACGCGCGGTTCAACCTCCTGTCCCTCCTCCCCCCACTTCTACGCCAGTTGTGAGAGAGCGCCTGCCCTCTAACCTTGTCGACCCATATGAGCGCCATCCCCTTCCCCCTCCTCCGGCTCCCACCTCTTCATACTATGTCCGTGAACGGAGCCCGGTCCGACGAGCTCCACACGAGGCGGAGGGATACGCGTATGAGCGGTCGCGCCTCTCTCCCATCTCTGTGCTTCCCAGGACTGCTGCGTATGACGTGCCGCGGGATCCATACGCTGAACGGGCGCGCTA[T/A]GCTTACTAGCCTAATTCCTGTGCGCACTCAGGTGAGATCTTTTTAGGATCATAAAAGGTTAGGGCACAAACTAAAAGCTGTTTTCAGGGGAATTACTATCATCATTTATTCACCCTCAGATACTATATAAAAAATATATATATATACATATACATACATAATGTCAAGACATACTGATTTGAAATGGCATGAGGGTTAATAAATGATGATGGAATTTTTTTTTTGGATGAAGTAGGTTTTTTTAAATGCTGTCTATCATTGGGAAGCAATTTTTATTCATGTCAAATTACCTGAATCTCACATTTTGCAATGTCCATATTACAATTATTTATAACCTCATGTATTTAAACTAGAGGCCAAATATGGTCATAAATATTTGACACATTATTATTTTTAGATGTAATGAATGTATTACTTTACCTATCAAGTGTCTTATTTACATTTCAGGTATGACAGTATTGGCACGTGGAAGTCCACTAAACTAAAGCCGGAATGATTGA
Associated Phenotype:
Not determined