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