ZMP
gps1
Ensembl ID:
ZFIN ID:
Description:
COP9 signalosome complex subunit 1 [Source:RefSeq peptide;Acc:NP_001071227]
Human Orthologue:
GPS1
Human Description:
G protein pathway suppressor 1 [Source:HGNC Symbol;Acc:4549]
Mouse Orthologue:
Gps1
Mouse Description:
G protein pathway suppressor 1 Gene [Source:MGI Symbol;Acc:MGI:2384801]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45144 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33237 | Essential Splice Site | Available for shipment | Available now |
sa11784 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45144
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059506 | Nonsense | 168 | 487 | 5 | 14 |
ENSDART00000141106 | Nonsense | 171 | 490 | 5 | 14 |
The following transcripts of ENSDARG00000040650 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 36240795)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36112079 |
GRCz11 | 3 | 36241677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTCCTGCGTGTGTTCAGGAGGGGTCACGATGACCTTGGAGATCACTA[T/A]CTTGACTGCGGTGACCTCAGCAATGCCCTGAAATGCTACTCCCGAGCCAG
Long Flanking Sequence:
AGCTACGAGTGGAAGCACTGAAGATGGCCCTGTCCTTTGTCCAAAGAACCTTTAATGTTGATGTCTATGAAGAAATCCATCGCAAACTCACTGAAGCCACAAGGCAATTCCTGTTTTATTTTCCCCTCCATGCTTAACATTGAATCCTAATATGGAAAAACAAGCATGATTTTTACTAAGTCTGAATTTTAAACTCTGTTTCACCACAGGGAAGTGCAAGGAGTCCCAGATGCGGTACCAGAGGGGGCAGTTGAACCCCCTCCTCTCGACACAGCCTGGGCAGAATCTACCAGGAAAAAAGCCCTGCTCAAACTGGAGAAGCTGGATACTGACCTTAAAAACTATAAGGGAAACTCCATCAAAGAAAGCATAAGGTATGCCATACTAGTTGTCTCTTTCTCATTAGTATTATTTCCAATTATTGTTTAGCTGTTGTATTGAATATCTGAACATGTCCTGCGTGTGTTCAGGAGGGGTCACGATGACCTTGGAGATCACTA[T/A]CTTGACTGCGGTGACCTCAGCAATGCCCTGAAATGCTACTCCCGAGCCAGAGACTACTGCACTAGCGCCAAGCATGTCATCAACATGTGTCTTAATGTAATCAAGGTGCGGACTCATCTTCCTACGTGGTCATTATCTGGTTTATTGGTTCATTTTATTCAATATTACTCTTCAGTAGTTATAAATTTACCCACATCAAAAATAAATAAGTATTTTTTCATGTGGGTATCTTGAAAGGTACATTTACTACCTTTTTGATCCAATTGCAATGTTATAACATTTTACATCAAAAACATTATAATTTGAGATTAAAGGCTGTTTTCTGTCCTTTTCTAAATGCCATCATCAGAACACACTCTTTAAATAGGAGGGATTGATGGTAGACTCAATGGTAAACGTCCATTGATGTAAATGTCTAATAGTTTGCATGTTGGAAAGGACCACTGAGGTAAACCTATGCATGTATATATGACAGCATACAACTGCTGTGATTTTTAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33237
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 |
---|---|---|---|---|---|
ENSDART00000059506 | Essential Splice Site | 310 | 487 | 9 | 14 |
ENSDART00000141106 | Essential Splice Site | 313 | 490 | 9 | 14 |
The following transcripts of ENSDARG00000040650 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 36238482)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36109766 |
GRCz11 | 3 | 36239364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTACGTTTGACAGACAGGAATTGCAGCGAAATGTCATCTCAAGCAGG[T/C]GAATTTAAATGTTTAGCATTTGCAGTCTCTTTATATATGAGGTATATTTT
Long Flanking Sequence:
CAAGCCAATTGATTTGAAGAATTGATACAAATTATAAAGATTAAAAATGATGATGATTTAGTATTTTGGGGGCTGTGATGTGATCGTAAAATAGCCTTTTAATATGGCATTGAATACATTTACTGGTGTTTACATTGCATTGACTCTTGTGGAAGTATGAATTGATGTCAACATCTTTCTCTGGTCACTGTAGGATTGGCAGAACTTGCATCAAGAAAGTATAAACCGGCTGCCAAGTGCTTCCTGCAAGCCTCCTTTGACCACTGCGACTTTCCTGAGGTTGGTGCCATTTCTGACCCTGCTCTAATGCTGTGTCATATTGAATTGCATTATAAGTTGAAATGAAGATGAGTAGATGCAGTGCTTTCCTACAGTTTGTAATGATATTTTTTTTCTCTCTTTAGTTACTTTCTCCCAGTAATGTAGCTGTGTATGGGGGGCTCTGTGCCCTGGCTACGTTTGACAGACAGGAATTGCAGCGAAATGTCATCTCAAGCAGG[T/C]GAATTTAAATGTTTAGCATTTGCAGTCTCTTTATATATGAGGTATATTTTTGGTTGTGGATCAAACCTCACTGATTTGTAATTTACTCTTATTTTTGTTTCAGCTCCTTTAAATTATTTTTAGAGTTGGAACCTCAAGTCCGTGATATTATCTTCAAGTTTTACGAGTCAAAGTATGCATCTTGTCTGAAAATGCTGGATGAAATGAAGGTAAGATTGACTAAGCAGAGTTTCAGATAGTGATTTCTGTCTCTTGTGGTTGGAATATTGTGATTCTTGAGTGTTTACTCTCTGTATTTCAGGATAATCTCCTCCTAGACATGTATCTGGCCCCTCATGTAAGAACACTGTACACACAAATCAGGAACAGAGCCCTCATACAGGTACGTAAAAGGATAATTTGTGTTGATTTGTGATCTTGATTTACATGTTAACCTTGACTTATGGTTAATAGGATTTAGATTTTTGTTGAATTGAGAGTAAGAGGTTGTTTTTATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11784
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059506 | Essential Splice Site | 345 | 487 | 10 | 14 |
ENSDART00000141106 | Essential Splice Site | 348 | 490 | 10 | 14 |
The following transcripts of ENSDARG00000040650 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 36238272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 36109556 |
GRCz11 | 3 | 36239154 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTAYGAGTCAAAGTATGCATCTTGTCTGAAAATGCTGGATGAAATGAAG[G/A]TAAGATTGACTAAGCAGAGTTTCAGATAGTRATTTCTGTCTCTTGTRGTT
Long Flanking Sequence:
TCAAGAAAGTATAAACCGGCTGCCAAGTGCTTCCTGCAAGCCTCCTTTGACCACTGCGACTTTCCTGAGGTTGGTGCCATTTCTGACCCTGCTCTAATGCTGTGTCATATTGAATTGCATTATAAGTTGAAATGAAGATGAGTAGATGCAGTGCTTTCCTACAGTTTGTAATGATATTTTTTTTCTCTCTTTAGTTACTTTCTCCCAGTAATGTAGCTGTGTATGGGGGGCTCTGTGCCCTGGCTACGTTTGACAGACAGGAATTGCAGCGAAATGTCATCTCAAGCAGGTGAATTTAAATGTTTAGCATTTGCAGTCTCTTTATATATGAGGTATATTTTTGGTTGTGGATCAAACCTCACTGATTTGTAATTTACTCTTATTTTTGTTTCAGCTCCTTTAAATTATTTTTAGAGTTGGAACCTCAAGTCCGTGATATTATCTTCAAGTTTTACGAGTCAAAGTATGCATCTTGTCTGAAAATGCTGGATGAAATGAAG[G/A]TAAGATTGACTAAGCAGAGTTTCAGATAGTGATTTCTGTCTCTTGTGGTTGGAATATTGTGATTCTTGAGTGTTTACTCTCTGTATTTCAGGATAATCTCCTCCTAGACATGTATCTGGCCCCTCATGTAAGAACACTGTACACACAAATCAGGAACAGAGCCCTCATACAGGTACGTAAAAGGATAATTTGTGTTGATTTGTGATCTTGATTTACATGTTAACCTTGACTTATGGTTAATAGGATTTAGATTTTTGTTGAATTGAGAGTAAGAGGTTGTTTTTATTATTGTTATTATTATTAACAATTACTGTATTTATAAAATTATTCAAACACAAAAAAGTAATGATATACAATGCAGTTTTATTTTTTATTTCTTTAGTGTTGTTCTAACTGTTGGTTATTAATTGTAAGATGATTTTGGTTAGTTTTAGTCTTTATGGTTGTTGTTTTGTGTCTTAATTTATTATATATCTATGGTTGTCTTTTTTTATTGGTCA
Associated Phenotype:
Not determined