ZMP

si:dkey-190l1.2

Ensembl ID:

ENSDARG00000061042

ZFIN ID:

ZDB-GENE-060503-620

Description:

gamma-aminobutyric acid type B receptor subunit 2 [Source:RefSeq peptide;Acc:NP_001137515]

Human Orthologue:

GABBR2

Human Description:

gamma-aminobutyric acid (GABA) B receptor, 2 [Source:HGNC Symbol;Acc:4507]

Mouse Orthologue:

Gabbr2

Mouse Description:

gamma-aminobutyric acid (GABA) B receptor, 2 Gene [Source:MGI Symbol;Acc:MGI:2386030]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39253	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43313	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39253

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086617	Nonsense	666	935	15	19

Genomic Location (Zv9):

Chromosome 19 (position 36223228)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	35087748
GRCz11	19	34674868

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGCCTGTGATGATAAATATTCTTGCCCTTTTCTCTTTGTCTAGTTGTTC[G/T]GATGTTTCTTGGCCTGGGAGACGAGAAACGTGAGCATCCCAGCACTGAAC

Long Flanking Sequence:

ACATCAGAGCACCTTAGAAACCACTTAGAAACATGATTTCAAAACACTCAGAACAACTTAGCAAACGTTATAAGAGAGGATAAAACCCACAGAACACCATAACAACTACTTTGAATCATAGTAAAAAAGATCAGAGCACCTCAGAAACCCCTTTAGAAACATGATTAATATAAACTCTTAACACCTTAGCAACCAATTAAAATTGTGATAAAACCCTCAGAACACCATGGCAACCACTTAGAAACAACGTAAAACATCAGAACTCCTAAAAAAACACTTAGAAACATATTAAAAACCCTCAGAAAACCTTAGTAACCACACATAATAAAAAATAAGATAGAAACTACCTAAAATACCTTAGCAACAATGTGGCAACATCTATTCCTGGGTTGTGTCACCAACTTCCTTCAGATAAGGTAAACATCTGCTTGCAAATCTGCCCCTGCCTCTATGCCTGTGATGATAAATATTCTTGCCCTTTTCTCTTTGTCTAGTTGTTC[G/T]GATGTTTCTTGGCCTGGGAGACGAGAAACGTGAGCATCCCAGCACTGAACGACAGCAAGTACATCGGTATGAGTGTGTACAATGTGGGCATCATGTGCATCATCGGGGCAGCGGTGTCCTTCCTGACTCGGGATCAGCCTAATGTTCAGTTCTGCATTGTGGCCCTGGTCATCATTTTCTGCAGCACCATCACGCTGTGTCTGGTATTTGTGCCAAAAGTAAGTACTGCAATGCTCCGCCTGATCCGGCCCAATGGGAAAAGAATTGTAGAGGTCAGCGAAAGGCCCTTTCTGGCATTTGATTTGTGCAAATCCCTAGCAAGTTCACCTGAATATAATTGAGAACCGTGCTTACTTTGCATCCCCTGGAGCTCTCTGGAAATAAACACAACGGAATTTGAAAGAGTAGAAAGATTAGACTCTCTCTCACTCTAAACAAATACATCTTACATCGAGTTAGCCTCACCATCTCAACTGTCTGCCTTTGTCTTCTCTCTCTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43313

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086617	Nonsense	922	935	19	19

Genomic Location (Zv9):

Chromosome 19 (position 36228054)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	35092574
GRCz11	19	34679694

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACGCAAGTTGCAGCAGTCCCACAAGCAGCCCATCCTCCAGTCCCCGCCAC[A/T]GACACATGCCTCCCTCCTACAGGGTCATGGTGTCCGGCCTGTGAGCCCTT

Long Flanking Sequence:

ACACCTTACTCCTTTGCCATGCAACCAGAAACCGCCAAACTAGATACATATTGAATTTTAGTTTAGTCCTGGCTGATGGCACAAGAAGAACAAGATCAGGACCAAATCCTTTACAAGCAACTATTGTAAAACGACCTCAAACTTTTAAATAATAGTGAAGGTCTAGATGGTGTAGTTAGGGCAACTACCAGCAGGATCTAATGGTGTCATAGTAACCCTAAACCCTATATTAAGACGAGAATGCAACGTGCAAGGCAAAATCACTGTTGCTTTAAATGTACTCTGTAAACTTCTGTTCTAAAAATCATCACAGGAAATGGAGAATTTTCTGCATTTTATGCAAATAAATCATTTTCTTCCCTGTCATTTGTGTTCGCAGCATACAGCGCCGGCTATCCTTGCAGCTGCCAATCCTGCATCATGCCTATCTACCCTCCATAGGAGGTGTGGACGCAAGTTGCAGCAGTCCCACAAGCAGCCCATCCTCCAGTCCCCGCCAC[A/T]GACACATGCCTCCCTCCTACAGGGTCATGGTGTCCGGCCTGTGAGCCCTTGCCCTGACCTGCACTACACTCCGAGGAAGCGATCAGCTTTTTTATTTTAAGACAGACTGAGCAATATCAGCGGTTAACAGAAGCGTGTGAGCAACCCGGGGGGGTCCAAGTCCTCATGCATCCATGACCCCCTTCCACCATCCATGGCCACATCAGAGCAGAACTGATCTTTCAGGCTAGGAGGGAGGTGACTGGAGGTCCTCACACAGCAACTCAACCCAGACTCCAATCCTCTCGTTCCTGTCACCTCCCAATCCTATCTCAATTAACTCAACACTCCCCCAAAACAGCAACACGGACCAATGGAGGACAGGAGCTGTAGCCTTACCAGCTAATAAAAAGACACTTCTGTTGTTAGCCTTTCTGTGCACATCAGTTCTGCTGGAACTTGTGGGAAAGGGGCAACGGATGTGACCGAGAACTCCTCCTCATTACTCACCACTTCAACAG

Associated Phenotype:

Not determined