ZMP

LOC564883

Ensembl ID:

ENSDARG00000076401

Human Orthologue:

CACNG3

Human Description:

calcium channel, voltage-dependent, gamma subunit 3 [Source:HGNC Symbol;Acc:1407]

Mouse Orthologue:

Cacng3

Mouse Description:

calcium channel, voltage-dependent, gamma subunit 3 Gene [Source:MGI Symbol;Acc:MGI:1859165]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa25255	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa33230	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa25255

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
ENSDART00000110126	Essential Splice Site	70	309	1	4

Genomic Location (Zv9):

Chromosome 3 (position 35384719)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	35169915
GRCz11	3	35299423

KASP Assay ID:

554-7828.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGAGGAAGTCATGACCCATTCAGGGCTTTGGAGAACCTGCTGTCTAGAAG[G/A]TAAGGCGTCTCATGTGCTTCTGAAAGTGAAAGTACTCCTATCTATCTATC

Long Flanking Sequence:

GATGAGAGACTGCTCGTCTGTGACAGTTTTTCCACAGCCCACAATGAGAAACAAACAGCTCTCCGCGTAAGCGATGGAAACACTGTGAGGCTTCTTGCTGAACTTGAGAAGCAGCAACAGCGACTGCAACAGTCTCGACACCCCAGAAATCAACACATGATAATGGTATGGGCTTCTGAAGTCGATTGGAGCATGGAGTCCGCGCACCAGGCAGGCTAGGAGGTTTTTCAATTTTTTGCGAGACGCGCTAAGAACCCTGTTTTAACCCCCCATCCTGAAATGAGGCAAAATGTTGATGTGTGACAGAGGAGTCCAAATGCTCATCACCACAGTGGGCGCTTTCGCCGCGTTCAGCCTGATGACTATCGCTGTGGGAACGGACTACTGGCTGTACTCTCGAGGAGTGTGCCGGGTCAAAAGTAATAACGAGAACGAGACGAGCAGGAAGAACGAGGAAGTCATGACCCATTCAGGGCTTTGGAGAACCTGCTGTCTAGAAG[G/A]TAAGGCGTCTCATGTGCTTCTGAAAGTGAAAGTACTCCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTCTTTTCTAGGATACACTAGCGTTCATTCTAATTGAGGATTATTTAATGTGACACATTGGAAGCACTACTAACCTCAATCTATCACCAGAATTTATTTGAATGCTCCGATATTTAGATCATTCTGAAGGGTTTAAGATAATTGAAGCTTTGTTGAAGTCACAAATCAAGTCATTTTAATAAGCAGTATGATGATTGCAGTCATCTTATAACTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33230

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110126	Essential Splice Site	146	309	3	4

Genomic Location (Zv9):

Chromosome 3 (position 35456123)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	35241319
GRCz11	3	35370827

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGCAGACACAATGTCATCCTCAGTGCCGGAATCTTCTTTGTCTCTGCTGG[T/A]AAGAGATTAAAACCACTGCATCACTGCTAGCAAGCTCCGTTTGTTTATGT

Long Flanking Sequence:

ATGGTAAAGGAACAAATGTTAATTTAATTTCAAGCCAATTCTTTGAGTGGCACCATTCTGCTAGACATGAAATATTTATTGTTTTATCCTAAGTGACTTACAAAAGAAAATTTGATTCTGGCCAGAACAGTGAGTGAGTGGAGAGAGTTCAGGAAGAGTATGACGTGGGTAAAATATAGTTCCTGACACACCATTGCACAGGGTTTTTTTTATTTATTTTTATCTATTTAAACATAAATGAACCCTTATGTAAGATGTAATTCACATAAAACTGTTTTCTGACCCCGTGTACAGCTAGTTTTCTCAGTGCTGTTTGCAGTGTTACTAATGTGTTTGGGTTTGCTTGTATGTCCCTCAGGAGCAGTGAGAGCGTCCAGCATCTTCCCCATCATGAGCGTCGGGCTCCTGTTCATGGGAGGTTTGTGTGTGGCTGCTAGCGAATTTTACAGGAGCAGACACAATGTCATCCTCAGTGCCGGAATCTTCTTTGTCTCTGCTGG[T/A]AAGAGATTAAAACCACTGCATCACTGCTAGCAAGCTCCGTTTGTTTATGTTTGTGGCTGTTTCTGAACCACAGTCAATTGTTCAGTTGTAGGAAAGAGTAGGGCTGGATGATTCATCGGAAAGAAACAGAAATTCATCACCTTTAACTGATTAATTCCCCCTTTTTTAAGGTGCAGTATATAAGTTTGACACCCAGGTTGCCAGATTGAGGGCAGGAGCGAGTGATTTAAGTCATCTTGCACCTGATAGAAGGACAATTTTCCACATATAAAAGTTTTTGTGCCAACCAACACCTCAAATTGATATATTAGAAACGGCTTCTATTTCTCAGGTGAACAACAGAACTATGCCAATGATCACCTCAGGTGCGAGAAGGGGAAATGCCGATTTTGGAGGGACTATTTTGGCTAATAAGTGCAAAAAGCGCACTTCGTTGGAATAAGCTATTTGAGCAATTTCAGTCTATCACGTTTGATCAACGGAGACAACATAACTGTAGA

Associated Phenotype:

Not determined