ZMP
gpsm2
Ensembl ID:
ZFIN ID:
Description:
G-protein-signaling modulator 2 [Source:RefSeq peptide;Acc:NP_956732]
Human Orthologue:
GPSM2
Human Description:
G-protein signaling modulator 2 [Source:HGNC Symbol;Acc:29501]
Mouse Orthologue:
Gpsm2
Mouse Description:
G-protein signalling modulator 2 (AGS3-like, C. elegans) Gene [Source:MGI Symbol;Acc:MGI:1923373]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25906 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25906
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 > A
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024034 | Missense | 564 | 649 | 14 | 15 |
ENSDART00000056357 | Missense | 563 | 647 | 16 | 19 |
ENSDART00000110108 | Essential Splice Site | 563 | 645 | None | 18 |
ENSDART00000113058 | Missense | 585 | 670 | 13 | 14 |
ENSDART00000131412 | None | None | 83 | None | 3 |
ENSDART00000145634 | None | None | 151 | None | 6 |
The following transcripts of ENSDARG00000017311 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 45547628)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 45639290 |
GRCz11 | 2 | 45492288 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGAGGGCAGGAACGGGGAACAGTTTGCCTGGCCTGCGCACCCTGAA[T/A]GAACACAGCAGCACCAACAACAGACAGATGATCCTCAGCCAGGTCATGGC
Long Flanking Sequence:
AGATTAATTTTGTGTAGCAGTGATATTTTTGTATGAATTATGCACTATAAATGTATTCATTATGTAGCATTTTTCTTAAACCTTTGACTTTGTTTGCCCTCAGCATGGAAGTACAGACATGTTAGGAGACGAGGGCTTCTTTGACTTGCTGAGTCGATTTCAGAGCAACCGGATGGATGACCAGCGCTGTGCCATACAAGATAGCAAGAGCCACCTGTCTGTTAACTCCATCAGCGCTTCTCCACCCACCACACCACCCAGAACCATCAGGAAATGTTAGCTTCTCTTCTTTTACAGTGTTTTCCTTAATTCAACAATCAAGTGGCTTTTTAAATCAACCTACATGCCTGATGTTTTGTTGTCTACCTAGCATTCTCAGAGTCAGCTGCAAGTCCAGGTCAGGAGCCGTTTCTCAGACTGCTGGCGAATGCTCAGGGCAGGAGGCTGGATGAGCAGAGGGCAGGAACGGGGAACAGTTTGCCTGGCCTGCGCACCCTGAA[T/A]GAACACAGCAGCACCAACAACAGACAGATGATCCTCAGCCAGGTCATGGCCAGCACAGACGCCACCGAACCCGACGACCAGTTCTTTGACATGCTCGTCAAGTGTCAGGTATGACGTGAATAAACACGTGGAACCAAACACAAAATGAGAAAAAATAAGTGTAGACAAACAGTCACTGATTAAAGCTTAGTTCACCCGAAACTATAACTTCACACTAGCTAAACGCACCGTACGCTGACATCAAACGAACCTCAGTGCGGACCAAAAGTGCTAGTGTTAAAGCGCTCTTGGTGTTTCAAAGTTCAAAAGGCTCAATTTTTCAGTCACTATCTGTCAGAAGTCATTTTGTTCTGTTACACCATTTATCTCATTATCTATTTTTTTCTGGTCTCTCTCAGGGGTCCCGCCTTGAAGATCAGAGGTGTGCCCCTCCTCCGCCCTCCACTCGTGGCCCCACCGTCCCAGATGAAGACTTCTTCAGCCTCATCATGCGCTCACAG
Associated Phenotype:
Not determined