ZMP

cx28.1

Ensembl ID:

ENSDARG00000041792

ZFIN ID:

ZDB-GENE-070320-1

Description:

Gap junction protein [Source:UniProtKB/TrEMBL;Acc:Q5TYN8]

Human Orthologues:

GJA1, GJA3, GJA4, GJA5, GJA8

Human Descriptions:

gap junction protein, alpha 1, 43kDa [Source:HGNC Symbol;Acc:4274]
gap junction protein, alpha 3, 46kDa [Source:HGNC Symbol;Acc:4277]
gap junction protein, alpha 4, 37kDa [Source:HGNC Symbol;Acc:4278]
gap junction protein, alpha 5, 40kDa [Source:HGNC Symbol;Acc:4279]
gap junction protein, alpha 8, 50kDa [Source:HGNC Symbol;Acc:4281]

Mouse Orthologues:

Gja1, Gja3, Gja4, Gja5, Gja6, Gja8

Mouse Descriptions:

gap junction protein, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:95713]
gap junction protein, alpha 3 Gene [Source:MGI Symbol;Acc:MGI:95714]
gap junction protein, alpha 4 Gene [Source:MGI Symbol;Acc:MGI:95715]
gap junction protein, alpha 5 Gene [Source:MGI Symbol;Acc:MGI:95716]
gap junction protein, alpha 6 Gene [Source:MGI Symbol;Acc:MGI:95717]
gap junction protein, alpha 8 Gene [Source:MGI Symbol;Acc:MGI:99953]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa37127	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37127

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000061251	Nonsense	66	247	1	1

Genomic Location (Zv9):

Chromosome 20 (position 40771892)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	40843051
GRCz11	20	40740161

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCAGAATGGTCTGCAACATCAACACTCCTGGTTGCCTGAACGCCTGTTA[C/A]GACCACATCTTCCCCATATCTCACATGCGATTCTGGGTGCTCCAAATCAT

Long Flanking Sequence:

GATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGAATAGATAGATAGACAGACAGCTATTATTAGCCCTCCTCTGAAATTTTAATTCCTCAAAATATTTCTCATCAGCCGTTTAACAGAGCGAGAACATTTCAAATGTATTTTGTTATTTATTTTTAAAAAGATTATGATGTTATTATGTTGGATTTTTATTGTTAAAGTAAGTGGTAATTCCTAATAATTATGTAAGTCTTCCACATCACATAGTTACCCTCTGATGTCTTCTAATTTTCAGACACTGTAAATCATGGGCGACTGGGGATTCCTCTCCAAACTTTTGGACAAAGTGCAGTCTCACTCGACCAGCATTGGAAAGGTTTGGCTGACAGTTCTGCTGATCTTCAGAATAATGGTTCTAGGTGCCGGACTGGATAAAGTCTGGGGAGACGAACAGTCCAGAATGGTCTGCAACATCAACACTCCTGGTTGCCTGAACGCCTGTTA[C/A]GACCACATCTTCCCCATATCTCACATGCGATTCTGGGTGCTCCAAATCATCTTCGTGGCCACTCCGAATCTGGTCTACCTCTTTTATGTTCTGCATGTCATCCATAGAGAAAACAAACTGAGGCAGCGTTTAGAAAATCAGGCAGAGAAGCACGGTGTCAAGCTACCGAAATACACAGACGGCAATGGGAAGGTTTATTATAAAGGGAACCTTCTCGGTTGTTATATGTTTAGCCTCATTGTGACTATTTTGTTGGAGGCTGGCTTTCTTGTAGGCCAGTATTTTTTAATTGGCCTTTTGATGCCCATGCAGCTTGACTGTAATGTAGAGCCATGTCCTAGTGTTGGTCTGCATTGTTTTACGTCCCGTCCAACTGAAAAGAGCATCTTCATTGTGTTCATGCTCATTGTGGCTTGCGTGTCTTTAGCTCTGAATATTGGAGAGATTTTTTATCTGATTGGTCGCAGGAATGTGTATAAAGCAAGGACTCGTTCGAATGC

Associated Phenotype:

Not determined