Busch Lab

ZMP

si:ch211-152p11.4

Ensembl ID:
ENSDARG00000079705
ZFIN ID:
ZDB-GENE-060503-764
Description:
Novel protein similar to vertebrate regulator of G-protein signalling family [Source:UniProtKB/TrEMB
Human Orthologue:
RGS1
Human Description:
regulator of G-protein signaling 1 [Source:HGNC Symbol;Acc:9991]
Mouse Orthologue:
Rgs1
Mouse Description:
regulator of G-protein signaling 1 Gene [Source:MGI Symbol;Acc:MGI:1354694]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa45674 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa25092 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa36856 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa45674
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114301 Essential Splice Site 148 322 2 6
ENSDART00000136414 Essential Splice Site 148 322 3 7
Genomic Location (Zv9):
Chromosome 19 (position 28026094)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 27956206
GRCz11 19 27540429
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCAAGCTGGCAGCTGCTAAATTACACATTAAAAGTTTGTTTGGACAG[G/A]TGAGTTCTAATGCTTTTAGTTAATGAAGTTCATTGAATTGTAATAATCAT
Long Flanking Sequence:
CTTTCTGCAGGCCTCTGTCATTTTCCTTATCAATCTGTGTTTTGGAACCCATCAAAATGCTTCGTAAGTCCAGTTCAGTGGGTACATTAGTAGAGCTGGATGGATGGGAGCAGGTGGATAGAGATGATCGCCCAGGCAGCTCAGAGGATGAGATGGACGGGGCTTCAGCATCCTACCCTTGCACCCCAGATGCAAAGTCAAAGAGTGCAGGAAAGGGTGGGCTGATCCGAGAACACAGTTTTAGTGTGGAAAATCTGGTTGGCTTGGATAAGGACTCTGATCTACTGAGAGTTACGAATCTTAATGAGAGTTTTAAAGCCTACAGTGACAGCCAGCTCACTTCCAATGCCAAAGGCAGCAGTGAGAGTGTGGAGAAGTGTTGCACTCTTCCTGGCTCTTTCCCATCCAAAGAGAAATCCGAAGAAACTCCTCATCACCGGCTGCAAGCTCACTCCAAGCTGGCAGCTGCTAAATTACACATTAAAAGTTTGTTTGGACAG[G/A]TGAGTTCTAATGCTTTTAGTTAATGAAGTTCATTGAATTGTAATAATCATTCAATCTTTGATATGACCATTTAAATAGTTCAGTTCACATGATGATAAGGTGACTATAAAATGTTTTCTTCTACTGCAGTTTGATGTTTTAATACTGACAAAGGCTACGTTTGTTTGGTCAGAAATGCAGTAAAACACCAATATTGTGCAATTTTATTGCTACTAAAGTAACTTTTAAATTTAAGTATTTAAAAAAAAAGTAAGTTATTAGTATGATCAATTTTAGCATCGTCTCTTGAATCTTTAGTGCCATACACACTTTCAGAAATCATACTAACATGCTGATTTGGTTCTCAAGAAACATTTTTTTCACTAAGTCCATTTTGAAACTTCTAATTTCAAAACTTCCCTTTATAACACAATGGTTGGGTTTGTCCATATTTAAGTGTTTGACAAATAGAAGTTGAAAATAACAATTTCTCTGGAAATTAACAGCATACAGTTGAAATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25092
Status:
Mutation detected in F1 DNA
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
ENSDART00000114301 Essential Splice Site 167 322 3 6
ENSDART00000136414 Essential Splice Site 167 322 4 7
Genomic Location (Zv9):
Chromosome 19 (position 28023960)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 27954072
GRCz11 19 27538295
KASP Assay ID:
554-7667.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATTCCTCGCATACGAATTTGAAAGAGCACCGAGAGAATGTAACCAGG[T/C]AAAAGACATCACCTCCGCAAATAATCAAATCACATTTTTGCACTCTTTTG
Long Flanking Sequence:
GTCTTGCTTTTTTCAAATCTGCAAGCCAAGTGTGATGATGTGAAAAGCCACGAATGCTTTTGTATTACACAATTAGTAAAGCTTGCTTTTACTCAGTTCTACCCCTTGAGATATAATGTTGCTTTGTCCAAACAGTAAAAGGAGAACCAAGCAGTGAAAGAGGAACTGGATGTTCTGGTTTTATATAAAGGGAATCACACTAATGATGTAAAATGTGTGTGGTTTTTTATCTATTGTGACAGTGCAAGTGATACAATTAAAACTTTCACTTTCTGGAATATTTTGGCATTTGATATAGTATCTGGCTTTGTCAGAAAGATTTCCATGACGTAACACTGATATGACATTTGTTTAAGTCATGGAACATTTTCAATCAAGCCGGTTATCATCATGATGATGTTGTGCGTATCATTGACCTTTAATTGTTTTTTTTTCCACACAAGAATTCACCACATTCCTCGCATACGAATTTGAAAGAGCACCGAGAGAATGTAACCAGG[T/C]AAAAGACATCACCTCCGCAAATAATCAAATCACATTTTTGCACTCTTTTGCTTTGGGCCTATCTTTTGTCCCCCTCTTGCAAAACTCCTCCTAGTCCCCTGTTTTGGCCCAGTGTTATTAATTCCACAATTTTTCAATGTGCTTTTTTGTCACGTATCCTCTCACACTCTTGTTTCTCTCAGCACGAAAGAGAAGCGTTCTCGAAAGCCTTTCCTCCGGCAGTGGAGTCAGGTTGGCCATGGCAGAGGTCGACTCAGCAGGAAAGAAGTGGAGAGCTGGGCCAAGTGCCTTGAAACTTTGCTGGCCAGCAGAGGTGAGCACTCCTTTATAAACTGCTTGAGTCGCCAGGCAGCTGGTCAAAGGACGCTTGCGAGACACCATAGCGTCACATGCTAATGAACCGCTGTTGCGCTACCAACTTTGACCTGGAACGCTGTTCTTGGAAATCAAGATATTTGTGGCCGACTGGCCGTTCATGCTTGAAATGTTGTCCTAATGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36856
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000114301 Essential Splice Site 210 322 4 6
ENSDART00000136414 Essential Splice Site 210 322 5 7
Genomic Location (Zv9):
Chromosome 19 (position 28023646)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 27953758
GRCz11 19 27537981
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAGTGGAGAGCTGGGCCAAGTGCCTTGAAACTTTGCTGGCCAGCAGAG[G/A]TGAGCACTCCTTTATAAACTGCTTGAGTCGCCAGGCAGCTGGTCAAAGGA
Long Flanking Sequence:
AAAGATTTCCATGACGTAACACTGATATGACATTTGTTTAAGTCATGGAACATTTTCAATCAAGCCGGTTATCATCATGATGATGTTGTGCGTATCATTGACCTTTAATTGTTTTTTTTTCCACACAAGAATTCACCACATTCCTCGCATACGAATTTGAAAGAGCACCGAGAGAATGTAACCAGGTAAAAGACATCACCTCCGCAAATAATCAAATCACATTTTTGCACTCTTTTGCTTTGGGCCTATCTTTTGTCCCCCTCTTGCAAAACTCCTCCTAGTCCCCTGTTTTGGCCCAGTGTTATTAATTCCACAATTTTTCAATGTGCTTTTTTGTCACGTATCCTCTCACACTCTTGTTTCTCTCAGCACGAAAGAGAAGCGTTCTCGAAAGCCTTTCCTCCGGCAGTGGAGTCAGGTTGGCCATGGCAGAGGTCGACTCAGCAGGAAAGAAGTGGAGAGCTGGGCCAAGTGCCTTGAAACTTTGCTGGCCAGCAGAG[G/A]TGAGCACTCCTTTATAAACTGCTTGAGTCGCCAGGCAGCTGGTCAAAGGACGCTTGCGAGACACCATAGCGTCACATGCTAATGAACCGCTGTTGCGCTACCAACTTTGACCTGGAACGCTGTTCTTGGAAATCAAGATATTTGTGGCCGACTGGCCGTTCATGCTTGAAATGTTGTCCTAATGAAAATGTTACATGCAGAGAGGACTAATACATCATGTGGTTAATGAGAGATACACCACTGTTCAGATTAGGGTAAAATAACTTTGTACGTTTAGGGTCAAACAAAAGTGTGATTCGTTTGACAGTGTTGCATTACCCTCTTGTTTTGGTTCAGGTTAAAATGGCAAAATTCCAGAATGTGATTATGCAAATCATATGTGGGTACAACTGTACTCTCATTGGTCCGAGAGCATCTTGATATGCTGCACAATATATTGTTTCAGTGTCAATATCACAATGTCACATTCAGGATCTTTATAGTCATGTTGGGATTAGAAT
Associated Phenotype:
Not determined