ZMP
rbm4.2
Ensembl ID:
ZFIN ID:
Description:
RNA binding motif protein 4 like [Source:RefSeq peptide;Acc:NP_955971]
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 |
|---|---|---|---|
| sa38604 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20916 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38604
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077395 | Nonsense | 260 | 384 | 3 | 5 |
| ENSDART00000112169 | Nonsense | 260 | 384 | 3 | 4 |
| ENSDART00000146368 | Nonsense | 260 | 384 | 2 | 3 |
The following transcripts of ENSDARG00000055080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 23966574)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 22528326 |
| GRCz11 | 7 | 22799483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTAACCAGGGTGCCGACCGGCTATCCTGAGCGGCCTCCTGTGTATGAA[C/T]GAGATCGCTTCGGGAGCATTGACTATTACGAGAAGTTTCGGGCTCATCCA
Long Flanking Sequence:
CGGTGAACTAACCCTTAAAGTGCTGTAAGTACAAAGTAGCTGTCTTGATGCAATAATTCTCTCTTTAAAATGACGGTTTACGTGAGCGGAAGAAAGTTTTACATTGTCTTGCGTGTGTTTTCTTCCTCTCAAAAGGCAAGCTGATCAAAGTACAACTGTCCACGAGTCGTCTTCGTACAGCGCCCGGCATGGGAGACCAAACCGGCTGTTACATCTGCGGAGAACAGGGCCATTGGTCCAAAGATTGCAGGCATAGCCAGAATGGTAGCTATGGCGGAGGCATGGGGGGATACCCCAGTAGAGGCCCTCCAAGAGGCGGCCCGAGTTACGGCATGGGTGGCCCTGGGGGTCATCCTAGTAGAGGTTACCCAGCAGGGCCACTTCCCCCTCCCCCACCCATGAGTCGGCGTCCCAGCTATGGCGAGTATGGAGCAGAGCCTCGAGAACGGTACCTAACCAGGGTGCCGACCGGCTATCCTGAGCGGCCTCCTGTGTATGAA[C/T]GAGATCGCTTCGGGAGCATTGACTATTACGAGAAGTTTCGGGCTCATCCAGCTGCCTCTAGCTACTATGAGGATAGGCCTCACGCCATCCCCCCTCCTCCACCTCCTCCCCCCCTCTCTTCTTCCTCCCTCTCAAGGATGCGATTGGCTCCTCCCAGCCTTGATCCCTATGAGCGACGCTCTCTGGCGCCTCCACCTCCCACAGCAGCAGCAGCGAGCTTCGCGCGGGACCGTAGTCCAATCAGACGTGTGGGCGCCGGTGCGGAAGGCTACTCGTACGAGCGCTCGCGACTTTCCCCGGTCTCAAGGAGCTCATCGGCTTACAGCCTGCCGCGGGCCAGGGAGGGATACACCGAGCGAGTTCGATACGCATACTAAGCCACACACATGCTAAGGTGAGCGAAATGCGGGTCGTTCAATTTGAGATATCAGCGTGATCTGTTCTCTAAGCGTAAACCGTTTCGAGTGCACTAGTAAGCAAAGCCACTTTAATTGGGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20916
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 |
|---|---|---|---|---|---|
| ENSDART00000077395 | Nonsense | 282 | 384 | 3 | 5 |
| ENSDART00000112169 | Nonsense | 282 | 384 | 3 | 4 |
| ENSDART00000146368 | Nonsense | 282 | 384 | 2 | 3 |
The following transcripts of ENSDARG00000055080 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 23966642)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 22528394 |
| GRCz11 | 7 | 22799551 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGACTATTACGAGAAGTTTCGGGCTCATCCAGCTGCCTCTAGCTACTA[T/A]GAGGATAGGCCTCACGCCATCCCCCCTCCTCCACCTCCTCCCCCCCTCTC
Long Flanking Sequence:
AATGACGGTTTACGTGAGCGGAAGAAAGTTTTACATTGTCTTGCGTGTGTTTTCTTCCTCTCAAAAGGCAAGCTGATCAAAGTACAACTGTCCACGAGTCGTCTTCGTACAGCGCCCGGCATGGGAGACCAAACCGGCTGTTACATCTGCGGAGAACAGGGCCATTGGTCCAAAGATTGCAGGCATAGCCAGAATGGTAGCTATGGCGGAGGCATGGGGGGATACCCCAGTAGAGGCCCTCCAAGAGGCGGCCCGAGTTACGGCATGGGTGGCCCTGGGGGTCATCCTAGTAGAGGTTACCCAGCAGGGCCACTTCCCCCTCCCCCACCCATGAGTCGGCGTCCCAGCTATGGCGAGTATGGAGCAGAGCCTCGAGAACGGTACCTAACCAGGGTGCCGACCGGCTATCCTGAGCGGCCTCCTGTGTATGAACGAGATCGCTTCGGGAGCATTGACTATTACGAGAAGTTTCGGGCTCATCCAGCTGCCTCTAGCTACTA[T/A]GAGGATAGGCCTCACGCCATCCCCCCTCCTCCACCTCCTCCCCCCCTCTCTTCTTCCTCCCTCTCAAGGATGCGATTGGCTCCTCCCAGCCTTGATCCCTATGAGCGACGCTCTCTGGCGCCTCCACCTCCCACAGCAGCAGCAGCGAGCTTCGCGCGGGACCGTAGTCCAATCAGACGTGTGGGCGCCGGTGCGGAAGGCTACTCGTACGAGCGCTCGCGACTTTCCCCGGTCTCAAGGAGCTCATCGGCTTACAGCCTGCCGCGGGCCAGGGAGGGATACACCGAGCGAGTTCGATACGCATACTAAGCCACACACATGCTAAGGTGAGCGAAATGCGGGTCGTTCAATTTGAGATATCAGCGTGATCTGTTCTCTAAGCGTAAACCGTTTCGAGTGCACTAGTAAGCAAAGCCACTTTAATTGGGTTCAAATGTATAGCCAAAAATAACCTGTTGAGTGTTTTGTCTCATGAAAATATTTTTTTTCCATTTTTTTTC
Associated Phenotype:
Not determined