ZMP

LOC794222

Ensembl ID:

ENSDARG00000074669

Human Orthologue:

CACNG4

Human Description:

calcium channel, voltage-dependent, gamma subunit 4 [Source:HGNC Symbol;Acc:1408]

Mouse Orthologue:

Cacng4

Mouse Description:

calcium channel, voltage-dependent, gamma subunit 4 Gene [Source:MGI Symbol;Acc:MGI:1859167]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa40189	Nonsense	Mutation detected in F1 DNA	Not yet available
sa18642	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa40189

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
ENSDART00000112043	Nonsense	171	322	4	4

Genomic Location (Zv9):

Chromosome 3 (position 61573274)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	60846966
GRCz11	3	61079554

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCATCGGTATAATTGTCTACATCTCCAGCAATGCCGGCGACCCCAGCGAC[A/T]AAAGAGACGAGGACAAGAAGAATCAGTATAACTATGGTTGGTCGTTCTAC

Long Flanking Sequence:

TGGATGGTGGGAGGAAACTGGGGAACCCGTGGGAAACCCACGTGAGCATTGGAAGAACGAATAAACTCTGCACAGAATCGTTGACTGGATTGGTAACGACTAGAACCAGTGACGTTCTTGCTGTGAGGCAACAGTGCTAACTACTGGGCCACTGTGCCACCCATCTAGGGAAGGAGGAGGAGTGAGGTGGAAGTGGGGATTCTTCAAAATGAAGATGGCTGTTATATGGAACTTATGGTAATTATAGTGGTTTTAGAATCGTCTGATTGGTGAATCATAAATTGAATAATGCGGAGCCGGCTGCAAGCAATCATAAGCACGTGATCTACGATGAAACTTCACTTAATCCACATTTATATGTACCTTGTTATATCAAATGACAAATTAAATAAAACTTATGTTACTTATCAAGACATTTGCTTGTTTTGTGTCTGGCAGGTTTGAGCAACATCATCGGTATAATTGTCTACATCTCCAGCAATGCCGGCGACCCCAGCGAC[A/T]AAAGAGACGAGGACAAGAAGAATCAGTATAACTATGGTTGGTCGTTCTACTTTGGAGCGCTCTCTTTCATTGTGGCCGAGGCGGTGGCCGTTCTGGCAGTCAACATCTACATCGAGAAGAATAAAGAAGTGAGGTTTAAAGCACGACGTGAGTTCATCAAGTCTACCTCCTCCTCTTCGCCATACTCCCGCATGCCCAGCTTTCGCTATCGTCGACGGCACTCGCGGTCCAGTTCGCGCTCCACAGAAGCATCCCGCGAGGCGTCGCCTGTGGGCATGAAAATGATTAGCTCGGTGCCTGTAGGAGAGATCAACATGTACACACTGACGAGAGACCCTCTCAAATCAGGCACGGATAGTTCTTACAGTCCAGATCATGATTCTGGATTCCTCCAAGTGCACAACTGCTTTCCTAAAGACCTTAATGATGGTGCCAACAGGAGGACAACACCTGTATGAGGGTACTCAATGGAACGGAAGAGATAAAGGCCATATTAATTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa18642

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000112043	Nonsense	184	322	4	4

Genomic Location (Zv9):

Chromosome 3 (position 61573315)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	60846925
GRCz11	3	61079513

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CCCAGCGACAAAAGAGAYGAGGACAAGAAGAATCAGTATAACTATGGTTG[G/A]TCGTTCTACTTTGGAGCGCTCTCYTTCATTGTGGCYGAGGCRGTGGCYGT

Long Flanking Sequence:

GTGAGCATTGGAAGAACGAATAAACTCTGCACAGAATCGTTGACTGGATTGGTAACGACTAGAACCAGTGACGTTCTTGCTGTGAGGCAACAGTGCTAACTACTGGGCCACTGTGCCACCCATCTAGGGAAGGAGGAGGAGTGAGGTGGAAGTGGGGATTCTTCAAAATGAAGATGGCTGTTATATGGAACTTATGGTAATTATAGTGGTTTTAGAATCGTCTGATTGGTGAATCATAAATTGAATAATGCGGAGCCGGCTGCAAGCAATCATAAGCACGTGATCTACGATGAAACTTCACTTAATCCACATTTATATGTACCTTGTTATATCAAATGACAAATTAAATAAAACTTATGTTACTTATCAAGACATTTGCTTGTTTTGTGTCTGGCAGGTTTGAGCAACATCATCGGTATAATTGTCTACATCTCCAGCAATGCCGGCGACCCCAGCGACAAAAGAGACGAGGACAAGAAGAATCAGTATAACTATGGTTG[G/A]TCGTTCTACTTTGGAGCGCTCTCTTTCATTGTGGCCGAGGCGGTGGCCGTTCTGGCAGTCAACATCTACATCGAGAAGAATAAAGAAGTGAGGTTTAAAGCACGACGTGAGTTCATCAAGTCTACCTCCTCCTCTTCGCCATACTCCCGCATGCCCAGCTTTCGCTATCGTCGACGGCACTCGCGGTCCAGTTCGCGCTCCACAGAAGCATCCCGCGAGGCGTCGCCTGTGGGCATGAAAATGATTAGCTCGGTGCCTGTAGGAGAGATCAACATGTACACACTGACGAGAGACCCTCTCAAATCAGGCACGGATAGTTCTTACAGTCCAGATCATGATTCTGGATTCCTCCAAGTGCACAACTGCTTTCCTAAAGACCTTAATGATGGTGCCAACAGGAGGACAACACCTGTATGAGGGTACTCAATGGAACGGAAGAGATAAAGGCCATATTAATTGGATAGCCATTGGGGATAAGTGGCAGACGCCAACGAAGGGGA

Associated Phenotype:

Not determined