ZMP

kcnc4

Ensembl ID:

ENSDARG00000061288

ZFIN ID:

ZDB-GENE-060503-773

Description:

potassium voltage-gated channel subfamily C member 4 [Source:RefSeq peptide;Acc:NP_001182125]

Human Orthologues:

KCNC1, KCNC2, KCNC3, KCNC4

Human Descriptions:

potassium voltage-gated channel, Shaw-related subfamily, member 1 [Source:HGNC Symbol;Acc:6233]
potassium voltage-gated channel, Shaw-related subfamily, member 2 [Source:HGNC Symbol;Acc:6234]
potassium voltage-gated channel, Shaw-related subfamily, member 3 [Source:HGNC Symbol;Acc:6235]
potassium voltage-gated channel, Shaw-related subfamily, member 4 [Source:HGNC Symbol;Acc:6236]

Mouse Orthologues:

Kcnc1, Kcnc2, Kcnc3, Kcnc4

Mouse Descriptions:

potassium voltage gated channel, Shaw-related subfamily, member 1 Gene [Source:MGI Symbol;Acc:MGI:96
potassium voltage gated channel, Shaw-related subfamily, member 2 Gene [Source:MGI Symbol;Acc:MGI:96
potassium voltage gated channel, Shaw-related subfamily, member 3 Gene [Source:MGI Symbol;Acc:MGI:96
potassium voltage gated channel, Shaw-related subfamily, member 4 Gene [Source:MGI Symbol;Acc:MGI:96

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa7136	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa7136

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087293	Nonsense	481	603	2	4
ENSDART00000146805	Nonsense	481	581	2	3

Genomic Location (Zv9):

Chromosome 8 (position 25792581)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	24920499
GRCz11	8	24939638

KASP Assay ID:

554-5181.1 (used for ordering genotyping assays)

KASP Sequence:

AAAGCTGCCCAAGAAGAAGAAGAAGCACAACCCAAACCCAGGTATGGTGT[T/A]GGACTCTGGCTCATTTGGGAAGTCTGAAAGCAACTCGCCACGGAACAGCA

Long Flanking Sequence:

CAAAGCTGCCAAGGATGTCCTGGGGTTTCTGCGCGTGGTCCGTTTTGTCCGAATCTTACGGATCTTTAAGCTCACGCGACACTTTGTGGGTCTCAGGGTTCTCGGGCACACCTTGAGAGCGAGCGTCAATGAGTTTTGCTTGCTCATCATCTTTCTTGCTCTCGGGGTGCTCATCTTCGCCACCATGATCTACTACGCCGAGCGTATCAGCGCAGATCCGGACGATCCTAGTGGCTGCAACCACACGCATTTCAAGAACATTCCCATCGGCTTCTGGTGGGCAGTGGTCACCATGACGACACTTGGTTATGGGGACATGGTTCCTAAGACGTGGCTCGGCATGATAGTGGGTGCGTTATGTGCTATAGCGGGCGTGCTTACTATCGCCATGCCGGTGCCTGTTATCGTTAACAATTTTGGTATGTACTACTCGCTGGCTATGGCCAAGCAAAAGCTGCCCAAGAAGAAGAAGAAGCACAACCCAAACCCAGGTATGGTGT[T/A]GGACTCTGGCTCATTTGGGAAGTCTGAAAGCAACTCGCCACGGAACAGCACACAGAGCGACACATGCCCACTCGCTGCGGAGGAAAACATCACAAGAAACCGCTCAGGTAAAACATGACGATTACAAGACAAGGGGGTTTCTCAGAGGCAAAAATCTATGAAATGATACTGTATAGTTGCCAGGATTATGAGGCCTGTTTTTCTCCTCTGAAAAACTACATACCATGTTAAATTGATGTGCAAAGTTCAACTGAGTCCTGTCTACAAAGTTTAAAGTAACTCTAAACTAGTGTTGAAATGAATGGAACATCTTCAGAAGGCCTAAGAGATCATTAACATAGAATCAGATTTAGTTTTATTGGAAGTGCTTCATTTGAAGTCACCATTAAGATCGGTTTGTCACGATAAGAAAACCCTGGAGGAAATATGAGAGTGGTACTGGCTAATTGTAACAACAACAACAACTAAATCATCCTACAGTGTAGTAGCCACTGACTGGG

Associated Phenotype:

Not determined