ZMP
rgs7bpa
Ensembl ID:
ZFIN ID:
Description:
Regulator of G-protein signaling 7-binding protein A [Source:UniProtKB/Swiss-Prot;Acc:Q08BU8]
Human Orthologue:
RGS7BP
Human Description:
regulator of G-protein signaling 7 binding protein [Source:HGNC Symbol;Acc:23271]
Mouse Orthologue:
Rgs7bp
Mouse Description:
regulator of G-protein signalling 7 binding protein Gene [Source:MGI Symbol;Acc:MGI:106334]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21336 | Essential Splice Site | Available for shipment | Available now |
| sa31663 | Nonsense | Available for shipment | Available now |
| sa1911 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21336
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085573 | Essential Splice Site | 48 | 248 | None | 6 |
The following transcripts of ENSDARG00000060601 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 32762614)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31905340 |
| GRCz11 | 8 | 31914572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGCCTGTACTTTCTTAGCTTGTTTGCCTTTGTTTTCCTCTCTTCCAAA[A/G]GGTTGTCCAGGAGTTCAATACACTTGTGGCCCTCTATAGGGAGTTGGTTA
Long Flanking Sequence:
TTTTTTTAAATAAAGAAAAAAAAATGACAGATTTATTATAGCATTTATAAACTGCACCTCTCTGATGATTTGAAGTGCTTACTGTATTCTTACCTGCAATATAAGCCACTTTGAATAAATGAGTTAATTGAATAAATGTAAATTTGCTATAAGTTATGTCCTAATAGCATAAAAATGGATACTACTTGTAAAGTAAGGCATAAATGTTAAAACTGCTTGCCATTGAACGCTAATCCTTTATACCAAATATTGATAAAATGGCATGAGCATCTGTCGCCTGAGGCTCTGCTCCCCAGCAAATAGCCTGTTTTACCTTTGTGAAACTGTCTGGATGTTTCAATGTTAAGAATGAAAAATGTCTAGGCAACTTGGATGCATGTCATCTCCTCAAAGTTAAAAACCTCTTTAATTTATCGGCTTGATACATTTTCAAGGTTAAAATAGATTTGTTCAGCCTGTACTTTCTTAGCTTGTTTGCCTTTGTTTTCCTCTCTTCCAAA[A/G]GGTTGTCCAGGAGTTCAATACACTTGTGGCCCTCTATAGGGAGTTGGTTATCTCTATTGGAGAGATTTCCGCTGATTGTCCTTCTCTTCGGGCGGAAATGCACAAGACACGCACAAAAGGCTGTGAGATGGCACGAACAGCACATCAGAACCTTTCTGCAATATCAGGGTAGGATGTGCAATTTCACAATTTTGATGTATTTGTTTATTGCATGTTAATGTGTGGGACTAAGAATTAGAATTTTTTTTCCTTTTCGGCTTAGACCCTTTATTAAGGGTCTCCACAGCAGAATGAATCGCCAACTTATCCAGCATATGTTTTACGCAGCGGATGCCCTTCCAGCTGCAACCCTTCTCTGGGAAACATCCATACACACTACTTTGTCATACACACTAATTCATACACTATAGACAATTTAGCCTACCAAATTCACCTGTACAGCATGTCTTTGGACTTTGGGGGAAACTGGAGCACACGGAGGAAACCCACACGAACACAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31663
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 |
|---|---|---|---|---|---|
| ENSDART00000085573 | Nonsense | 213 | 248 | 5 | 6 |
The following transcripts of ENSDARG00000060601 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 32754796)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31897522 |
| GRCz11 | 8 | 31906754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGACAGAAATGAAAAATCTGCTAAGCAAACTCAGGGAGACAATGCCTT[T/A]ACCGCTGAAGAACCAAGGTAATGTTCACTTACACAAGTTCCCTCGCTGAT
Long Flanking Sequence:
ATTTTCTACACAATCTGTTTTTGTTGAGACAACATGAAGAAATTAAGTTAACTTATTAGTTTTTGCAAATTTTTGTGGATTGAACATAAAACAATTAAGTTGTCCCCCCAAAAATAAAAACAATTGTGTTGTTTCAGATCAATTTAAATACAAAGTTTAAACAAACAACAAGTGTTACTTTTTAGAGTGTACGTACTATGAAAGTAATGTCTCACTGTATGTGTTCCAGGAAAACATTACTTAGGAGCTACAAAGTTGGACAGTAGGAAGGAGGACAGTTCTGACATTCCGATCCTGGAAGACACGTCCTCCACTCCACCGGACTGTCCGCACACGTACTTCCTGGTGGCCACAGACATTGAGAACATCGAGAGGTAAATAGTCTGAGCAGAATCGCTCAGTGTTAAACTGATAGTTTGAATCTCAAACACATTCTTGATGTTCTAGGGACATGACAGAAATGAAAAATCTGCTAAGCAAACTCAGGGAGACAATGCCTT[T/A]ACCGCTGAAGAACCAAGGTAATGTTCACTTACACAAGTTCCCTCGCTGATATTACAGACTAATTCACTGAAAGCTTGAAAAAATTGGGTTTTCAAAACTTTCAATAACAGCAAGGTCTCAGTTGTACCCAAGCGTTCAAAAGTTTGGGATTCTCCTTTTAATTTTAGTTGTAGGTCTTTTAAATGCTAGCAATTCGTTAAAAAGAAGATTTAAGACCTCTACCTGTTTTGTAATGTCTCAGAAGCTCAGCTATGTACTGTATGTACCCAGAATGTTTAAGGCTGTTGAAGTCAGTAAGAATATATTTAAATCACTCATTCAATGAGCAGACATTGTGTACTGATTGAAAATGCAATACATTACAATGATTCAAAATATTAAACAACGAAATACAATTAAACAAAAAATGACAGGAAGAAATTTCATTTACAGAAGTGTTCAAAAGTTTGGGTTTCTTCTTTTAGTTTTAGTTGTAGGTCTTGTAAATGTGATTAGTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1911
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085573 | Essential Splice Site | 219 | 248 | 5 | 6 |
The following transcripts of ENSDARG00000060601 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 32754777)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31897503 |
| GRCz11 | 8 | 31906735 |
KASP Assay ID:
554-1901.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCTAAGCAAACTCAGGGAGACAATGCCTTTACCGCTGAAGAACCAAGG[T/C]AATGTTCACTTACACAAGTTCSCTCGCTGATATTACAGACTAATTCACTG
Long Flanking Sequence:
TTTGTTGAGACAACATGAAGAAATTAAGTTAACTTATTAGTTTTTGCAAATTTTTGTGGATTGAACATAAAACAATTAAGTTGTCCCCCCAAAAATAAAAACAATTGTGTTGTTTCAGATCAATTTAAATACAAAGTTTAAACAAACAACAAGTGTTACTTTTTAGAGTGTACGTACTATGAAAGTAATGTCTCACTGTATGTGTTCCAGGAAAACATTACTTAGGAGCTACAAAGTTGGACAGTAGGAAGGAGGACAGTTCTGACATTCCGATCCTGGAAGACACGTCCTCCACTCCACCGGACTGTCCGCACACGTACTTCCTGGTGGCCACAGACATTGAGAACATCGAGAGGTAAATAGTCTGAGCAGAATCGCTCAGTGTTAAACTGATAGTTTGAATCTCAAACACATTCTTGATGTTCTAGGGACATGACAGAAATGAAAAATCTGCTAAGCAAACTCAGGGAGACAATGCCTTTACCGCTGAAGAACCAAGG[T/C]AATGTTCACTTACACAAGTTCCCTCGCTGATATTACAGACTAATTCACTGAAAGCTTGAAAAAATTGGGTTTTCAAAACTTTCAATAACAGCAAGGTCTCAGTTGTACCCAAGCGTTCAAAAGTTTGGGATTCTCCTTTTAATTTTAGTTGTAGGTCTTTTAAATGCTAGCAATTCGTTAAAAAGAAGATTTAAGACCTCTACCTGTTTTGTAATGTCTCAGAAGCTCAGCTATGTACTGTATGTACCCAGAATGTTTAAGGCTGTTGAAGTCAGTAAGAATATATTTAAATCACTCATTCAATGAGCAGACATTGTGTACTGATTGAAAATGCAATACATTACAATGATTCAAAATATTAAACAACGAAATACAATTAAACAAAAAATGACAGGAAGAAATTTCATTTACAGAAGTGTTCAAAAGTTTGGGTTTCTTCTTTTAGTTTTAGTTGTAGGTCTTGTAAATGTGATTAGTTAAAAAGAAGATCTAAGATATCT
Associated Phenotype:
Not determined