ZMP
SGSM1 (2 of 2)
Ensembl ID:
Description:
small G protein signaling modulator 1 [Source:HGNC Symbol;Acc:29410]
Human Orthologue:
SGSM1
Human Description:
small G protein signaling modulator 1 [Source:HGNC Symbol;Acc:29410]
Mouse Orthologue:
Sgsm1
Mouse Description:
small G protein signaling modulator 1 Gene [Source:MGI Symbol;Acc:MGI:107320]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18376 | Essential Splice Site | Available for shipment | Available now |
sa45194 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40390 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17936 | Nonsense | Available for shipment | Available now |
sa26440 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18376
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 |
---|---|---|---|---|---|
ENSDART00000047841 | Essential Splice Site | 27 | 1069 | 2 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21831209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19544081 |
GRCz11 | 5 | 20047881 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCATTAATGCAATATTGTCCATTTTCTCTGTYCATAAATGTGTRTGTA[G/A]CTGCCGTCGAAGCCTGTGTGCTTCATGGRKTGAAGAGGAGAGCTGCTGGT
Long Flanking Sequence:
TTCATCGCTTACATCTCTAAAACAATCATTTTAATCGCAATACCTGCTCATTGGAACTTTCACTTATTTAACTTTTCACTTAAGCCGTTACATTGTTATCCTGTAAATAAATGGTGATGCATTTTTCCCTCAGTCCTTTGAATAGAAATTTCAAAAAACACTTATTTGAACCAGAATCATAAACAAAAGATGAAAAAAAGAACAGCTTTACAAAACAATATACATGTTATTACTGTCACTTCGATTACTTTAGTGCACCCTTGCAGAATAAAATGTAAAAAAGACATATTGCAAATGTCTGAACAGTAGTCTACTTTCTGGAAGAGTAGTTGAAAGTATGATTCTTGAAAGCGTGGTCACTTTTTGCAATCATCCCTGTTTTTCTGTTCCTCAGATACACAAAAAGCCTTTGATGGACTGGTGTAATGTGTTCGGTCTTGTTGGAAAATGATCCATTAATGCAATATTGTCCATTTTCTCTGTCCATAAATGTGTATGTA[G/A]CTGCCGTCGAAGCCTGTGTGCTTCATGGATTGAAGAGGAGAGCTGCTGGTTTCTTAAGAAGCAACAAAATAGCGGCGCTGTTCACCAAAGTGGCCAAAAACTTCCCTCCGGCTGAAGAGCTGTGCAGAAAAGCCCAGGAACTGGAGCTGGTCTTTGAGAACAGGTCAGACCATACTTTACAACACACAGCTAAGACTCATTCAGATATAGAGAAAATAAATTAACACAACAGGTGTATATGTAATGGGTATAGGGTTTTGGTGAACACACTGAGGAAGGTATTGTGTGTTTTCCATCCTTTGGTGCTAGATGCACATCTAACTTCAAAGGGAAAACTGATTCTGTGAGTTTAGATTTAATTCAATTCAGTTAATCTTTATTTGTATAGCGCTTTTACAATGTAGATTGTGTCAAAGTAGATTCACATAGAAGATAATAGTGAATTGAAACAGTGTCAGTTCAGTTCAGTAGATCATACTTTCATATGCAGATTTCCTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45194
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047841 | Essential Splice Site | 81 | 1069 | 2 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21831374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19544246 |
GRCz11 | 5 | 20048046 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAGCTGTGCAGAAAAGCCCAGGAACTGGAGCTGGTCTTTGAGAACAGG[T/C]CAGACCATACTTTACAACACACAGCTAAGACTCATTCAGATATAGAGAAA
Long Flanking Sequence:
TTGAACCAGAATCATAAACAAAAGATGAAAAAAAGAACAGCTTTACAAAACAATATACATGTTATTACTGTCACTTCGATTACTTTAGTGCACCCTTGCAGAATAAAATGTAAAAAAGACATATTGCAAATGTCTGAACAGTAGTCTACTTTCTGGAAGAGTAGTTGAAAGTATGATTCTTGAAAGCGTGGTCACTTTTTGCAATCATCCCTGTTTTTCTGTTCCTCAGATACACAAAAAGCCTTTGATGGACTGGTGTAATGTGTTCGGTCTTGTTGGAAAATGATCCATTAATGCAATATTGTCCATTTTCTCTGTCCATAAATGTGTATGTAGCTGCCGTCGAAGCCTGTGTGCTTCATGGATTGAAGAGGAGAGCTGCTGGTTTCTTAAGAAGCAACAAAATAGCGGCGCTGTTCACCAAAGTGGCCAAAAACTTCCCTCCGGCTGAAGAGCTGTGCAGAAAAGCCCAGGAACTGGAGCTGGTCTTTGAGAACAGG[T/C]CAGACCATACTTTACAACACACAGCTAAGACTCATTCAGATATAGAGAAAATAAATTAACACAACAGGTGTATATGTAATGGGTATAGGGTTTTGGTGAACACACTGAGGAAGGTATTGTGTGTTTTCCATCCTTTGGTGCTAGATGCACATCTAACTTCAAAGGGAAAACTGATTCTGTGAGTTTAGATTTAATTCAATTCAGTTAATCTTTATTTGTATAGCGCTTTTACAATGTAGATTGTGTCAAAGTAGATTCACATAGAAGATAATAGTGAATTGAAACAGTGTCAGTTCAGTTCAGTAGATCATACTTTCATATGCAGATTTCCTATACCCAATTCATATAGTCATTTTATTTTAAATTTATTTTGTGCACACAACCTAGAAACCTGCAATGCATTTGCATTTGGCAACAAATTTTTTGAATGTTTGCATCTCATCTCGTTTTTATTATTAATCCTTTGTTTAGCCAGGAAGTCACATCTCTTTGATCCACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40390
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 |
---|---|---|---|---|---|
ENSDART00000047841 | Nonsense | 679 | 1069 | 17 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21868972)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19581844 |
GRCz11 | 5 | 20085644 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGAGCAAATCGAGTCTGAGCCCAAGAACGATGTTGGCAAACAGGTTTGC[A/T]AAATCTCAAACGGAACCCCTCAAAATGGCACCAGCTCTCCAGACTCCGGC
Long Flanking Sequence:
TTATTACTTATGTCCCATTTGACCAGTAAATTGGAATAGTCAGATTGACTAGTCATCGCTTAATTTTTAGAGCTGCTGTCTTCCAGTCAAAATCGAGTCACATAAAGAAACAAAGCATTCAGTGGTGCAAAGTCCGACGAAATATCTGAACATCTACATTTTGGGGCTTGGACCTGGAAACAGTATTCCATACGTCACAACTTTATAAGAAGATAGTAATAAACCTTTAAAGTGAAAATGGCAACCTAATAGCATAATAGGGGCACTGAACATTTTGATTTTTTTTTTTTGCTTCAAATTGCATGTGATAACAAAGGAGCTCCTCTTTGACTGATGTTCCTCACCCTCACACTCTTTCCTGATAGTTCATCACTTCCCAAAAGCCCTTTCCCTGGAGTAGCTTGCTTCCCTTTGGTTTGTTTCTCCAGGTGTTTGAGTCTGTTGAAGAGGTCGAGCAAATCGAGTCTGAGCCCAAGAACGATGTTGGCAAACAGGTTTGC[A/T]AAATCTCAAACGGAACCCCTCAAAATGGCACCAGCTCTCCAGACTCCGGCCACCCCTCTTCCAGAAACTTCTCCGTCACCTCTGGTCAGTCGGACTCCTTGAGTACAGAGGACAGCGGAATACATGAGCCAAACCTTAAAAGTCAACCGCAACTAACAGCATCAAAGGAAAAGGCTGCATGCTGCGGAGAGGAAGGTAAGGAGACTGAGGAACGTGAGACCAAAATGGTGATGAAACAGGGGGTAAGAGAAGATAATAAAACTGAGGTTAACAAAGTGTTATTAGATGAAGTGGTTACACAGGAAAGCAAAAAGGCCACTGAGGACTCTGAAGTCAAGATGGATATTTCAAAAACAGCCCGAGATGCCTTTGTGGCTTCTACAGCAGATCACAGCCAGGTGACCAAAATGGAAGTGGGCGAATCTCTGGAGAGGAGTTTGACATCGGAAAATGATGCACTGACACGGCATACTGAGCCAGATATTCCCAAAGCAACAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17936
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047841 | Nonsense | 792 | 1069 | 18 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21869483)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19582355 |
GRCz11 | 5 | 20086155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACACGGCATACTGAGCCAGATATTCCCAAAGCAAYAGAGGTCATGGAAW[C/A]KACTCCTCYAGAGCGGAAGATGAATGAGACTCRAGTAAGAGCGGACATCG
Long Flanking Sequence:
CGGAACCCCTCAAAATGGCACCAGCTCTCCAGACTCCGGCCACCCCTCTTCCAGAAACTTCTCCGTCACCTCTGGTCAGTCGGACTCCTTGAGTACAGAGGACAGCGGAATACATGAGCCAAACCTTAAAAGTCAACCGCAACTAACAGCATCAAAGGAAAAGGCTGCATGCTGCGGAGAGGAAGGTAAGGAGACTGAGGAACGTGAGACCAAAATGGTGATGAAACAGGGGGTAAGAGAAGATAATAAAACTGAGGTTAACAAAGTGTTATTAGATGAAGTGGTTACACAGGAAAGCAAAAAGGCCACTGAGGACTCTGAAGTCAAGATGGATATTTCAAAAACAGCCCGAGATGCCTTTGTGGCTTCTACAGCAGATCACAGCCAGGTGACCAAAATGGAAGTGGGCGAATCTCTGGAGAGGAGTTTGACATCGGAAAATGATGCACTGACACGGCATACTGAGCCAGATATTCCCAAAGCAACAGAGGTCATGGAAT[C/A]GACTCCTCCAGAGCGGAAGATGAATGAGACTCGAGTAAGAGCGGACATCGAAAGGCCCCACAAGGGAATTAAAGATATTACAGCAATCCGAGAGCAACCTTTGATAGCAAAAGATCTTAAGGTATCAGATGCACTCGAGCAGAAGGTTGTAGCTGACATTCAAGTGTCTGTTTCAGAGGATACAGAGAAAGAAGCAACAAAAACCAATGAAACAAGCAAAGATAATGACTCTAAGACATGGATGGATGAGGAGAACAATGTTAGAGTGTTGAAACCAATTGATGAGAAGACCAGTGATTTAGCCGATGAAGCTGGTCCGACAGGAAAAAGAAAAGCAGATATGCAAAGGAAAGCTCCTGTGGTTGAGGAGACAGTCCCATTGGTGCATGAAGCTTTTAGCAATAGAAAGATGAGTGAAGCCCAAGATGAAACCGAATCAGACGAGTCTCCCTCTGCCATCGAGATGGAAGAGATTCCTACGGCTAAAGTGTGGGAAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26440
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 |
---|---|---|---|---|---|
ENSDART00000047841 | Essential Splice Site | 1041 | 1069 | 25 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 21876434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 19589306 |
GRCz11 | 5 | 20093106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTCACTGGGCGGTTGATTTGAATAATTATGTCCTGTTTTTTTATTCC[A/T]GAAATGGCTGAGCATCACAATATCAAGCAGATCCTGACTCTGTCTCGAGA
Long Flanking Sequence:
ACCTGATATTTTATTGCATATAGGTGATGTCTATGTGCACATGTTTAATGAAGTGTATTTGTGTGTTAAGTGCCTGTGTTGTACTCAAAGTCTTCGATGCAAATGACTTTTTAAAATATTAAAATTAATCATTTTATATATATATATATATACATTTGATGAAGATTGTAGTGATGTAATATTATTTTTATTATGAGTGGGGTTTAATTACAGTTTAAATATGGAAAATCCTTATATACTCTGAAAATCTATACCTTTATTCACATTACACCCTGCTGTTAGATAAAGATTTAGATTAAGGTTAGGAGAAGGCTACAAAAACACTTCAAATGCTGGAAAAGTTATTTGAAGTTTGTGATTTGATCTTAGGCTATATGTGTATGACAAGTAAAGTAATTATTTTAAAGGGATATGATTATTTTTCTATACATACTGTATTTCTGGTTTATTCAGTTCACTGGGCGGTTGATTTGAATAATTATGTCCTGTTTTTTTATTCC[A/T]GAAATGGCTGAGCATCACAATATCAAGCAGATCCTGACTCTGTCTCGAGACCTGGTGTGCAAAGTGCAGACACTTATAGAGAACAAGTAGCTCTGAAACCTCTCGTGTTCACAGATGTATCCCATCAGCCCTTACTGCAAAACAGGGAACATTTGACCAAATCAGTTTCAAGTAGGTATAGTGAAACATTTCCAATGCCAACCATCTCGATCTACCTGCAGTCAGTCAGTGTGCAATTATTAAGAGTCGTTTGGCTCTTTGATCAGGTTTTACAGTACATTACATTTTATAAGTAGGTGCTGCTAATGAGTGCTCATCCACTGCATGACACCGAGTTTGATCTTGTTGTAAATGCAGTCAGGATTACTGGGGATTTTGTAGGCTCCGTTTCAAAACCTAGTGAACTGCCTTGCTATTTACTGCCTACATTAACTGAAACAAAACCTCATAAAAGACTAAGATAATGCGATACTGATACGTAGCTCACACAAAAAGTGGGT
Associated Phenotype:
Not determined