ZMP
zgc:85682
Ensembl ID:
ZFIN ID:
Description:
somatostatin receptor type 5 [Source:RefSeq peptide;Acc:NP_998462]
Human Orthologue:
SSTR5
Human Description:
somatostatin receptor 5 [Source:HGNC Symbol;Acc:11334]
Mouse Orthologue:
Sstr5
Mouse Description:
somatostatin receptor 5 Gene [Source:MGI Symbol;Acc:MGI:894282]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa5992 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa37851 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5992
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061674 | Essential Splice Site | None | 383 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 24 (position 16787705)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 11146433 |
| GRCz11 | 3 | 11112976 |
KASP Assay ID:
554-3810.1 (used for ordering genotyping assays)
KASP Sequence:
ACCTTTTTACACTTGAGATGATAACACCATTGYGTTCTCATTTTGCTTTC[A/T]RCCCCCCYGGTGACCAMATTTGCRCCTKTATCCAAACATGGCAACCCAAG
Long Flanking Sequence:
TGGGTTTATGGAAGGAGGAATTTGGGTCAGTCGATCGGTAAGTCAGTCAGTCAACAGCAGCCTTTGGTGGATTTATGCAAAAAGAGCAGGCGCGAATGGCAATCACGAGACAAATCTGAGATCTGATCAAGCATATACAACAGCCTCTGGTGGATTCGTGAAAACAAGAACTGCAAAAAAAAAAAAAAAAAAAAACATACCTCCTGGGATGTATTTGGTGCTCTCCAAAAATGTATATAGGGGTGCATTTTCAAAATGAAAATAGGTTGGTAAAACACAATAAGAAAAATCAGTAAAACAGAGCAATGCATTGTGTTGTAAAGATTGCCAGTGTTGATGTGTATGCTGAATGAATTACGTCTCAAAGGAATGTCAACAAAACAGATAAAGCCATTCTCCAAAGGATTTTTCAATCACACAGTGTGCGCACAAGCATGCAATTCCAATTGAACCTTTTTACACTTGAGATGATAACACCATTGCGTTCTCATTTTGCTTTC[A/T]GCCCCCCTGGTGACCACATTTGCGCCTTTATCCAAACATGGCAACCCAAGAGCCGATATACAACACATCCCTCTCAAACCAAACCACCAATTCCTCCAGTGACCCTAATGAAAATCTGCTGGCTGAAGAAGAAAGCACTAAAGCCCTGGCTGTGATCTACCTCGTGGTGTTCATCGTGGGTCTGACAGGAAACTCTCTGGCCATTTTTGTAGTTCTCCGCTACACCAAAATGAAGACGGTCACCAACATGTACATCTTAAATCTAGCCGTGGCTGATGAGCTGTACATTCTGGGACTCCCGTTTCTCACCACCCACAATGTGCTCTCTTACTGGCCCTTCGGAAACTTCCTCTGCCGTATCCTGATGTGGGCCGACTCCATCAGTCAGTTCACCAGCACATTCTGCCTGACAGTAATGAGCATTGATCGCTACATGGCTGTGGTGCATCCTATCCGTAGTGCCAGGTGGCGGAGACCCAGCGTTGCCAAGGTTATAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37851
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061674 | Nonsense | 35 | 383 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 24 (position 16787845)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 11146573 |
| GRCz11 | 3 | 11113116 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCCTCCAGTGACCCTAATGAAAATCTGCTGGCTGAAGAAGAAAGCACT[A/T]AAGCCCTGGCTGTGATCTACCTCGTGGTGTTCATCGTGGGTCTGACAGGA
Long Flanking Sequence:
CAGCCTCTGGTGGATTCGTGAAAACAAGAACTGCAAAAAAAAAAAAAAAAAAAAACATACCTCCTGGGATGTATTTGGTGCTCTCCAAAAATGTATATAGGGGTGCATTTTCAAAATGAAAATAGGTTGGTAAAACACAATAAGAAAAATCAGTAAAACAGAGCAATGCATTGTGTTGTAAAGATTGCCAGTGTTGATGTGTATGCTGAATGAATTACGTCTCAAAGGAATGTCAACAAAACAGATAAAGCCATTCTCCAAAGGATTTTTCAATCACACAGTGTGCGCACAAGCATGCAATTCCAATTGAACCTTTTTACACTTGAGATGATAACACCATTGCGTTCTCATTTTGCTTTCAGCCCCCCTGGTGACCACATTTGCGCCTTTATCCAAACATGGCAACCCAAGAGCCGATATACAACACATCCCTCTCAAACCAAACCACCAATTCCTCCAGTGACCCTAATGAAAATCTGCTGGCTGAAGAAGAAAGCACT[A/T]AAGCCCTGGCTGTGATCTACCTCGTGGTGTTCATCGTGGGTCTGACAGGAAACTCTCTGGCCATTTTTGTAGTTCTCCGCTACACCAAAATGAAGACGGTCACCAACATGTACATCTTAAATCTAGCCGTGGCTGATGAGCTGTACATTCTGGGACTCCCGTTTCTCACCACCCACAATGTGCTCTCTTACTGGCCCTTCGGAAACTTCCTCTGCCGTATCCTGATGTGGGCCGACTCCATCAGTCAGTTCACCAGCACATTCTGCCTGACAGTAATGAGCATTGATCGCTACATGGCTGTGGTGCATCCTATCCGTAGTGCCAGGTGGCGGAGACCCAGCGTTGCCAAGGTTATAAATAGCATGGTATGGGCCCTTTCGTGTCTGCTAACGCTGCCAGTCATTATTTATTGTGACGTCCAGCCGGGACTCAACACCTGCAACCTGAGCTGGCCTGAGCCTCGTGACGTTTGGTCCACAGCTTTCATCCTCTACACCGCC
Associated Phenotype:
Not determined