ZMP

LOC100332608

Ensembl ID:

Human Orthologues:

C2CD4C, C2CD4D

Human Descriptions:

C2 calcium-dependent domain containing 4C [Source:HGNC Symbol;Acc:29417]
C2 calcium-dependent domain containing 4D [Source:HGNC Symbol;Acc:37210]

Mouse Orthologues:

C2cd4c, C2cd4d

Mouse Descriptions:

C2 calcium-dependent domain containing 4C Gene [Source:MGI Symbol;Acc:MGI:2685084]
C2 calcium-dependent domain containing 4D Gene [Source:MGI Symbol;Acc:MGI:2685505]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43833	Nonsense	Mutation detected in F1 DNA	Not yet available
sa24162	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43833

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
ENSDART00000113168	Nonsense	148	426	1	1

Genomic Location (Zv9):

Chromosome 22 (position 22493581)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	22105217
GRCz11	22	22130195

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCCAATCCGCCATGTCACTTCCTTACATTCCAAAAACTCAGACTTCCTA[C/A]GGCTTTGCTACATTGATGGAGAGTCCCCACACCCGGCGGAAAGAGTCCCT

Long Flanking Sequence:

ACTGTTGAATGTTCTGTTGTGTGTGCTTACAGGCAACCGTGCATCACCCAGTGGGTTAAGCCCAAACGGATCATGTGGGTTCTGGAGAAGATCCGGGACTCAGTTGAAACAAATGTGCTCCGACAAGGAGAGGCGGGTGAAAAAGGAAAGGCTCCTGTTTATAGCAACGTCCTCACACCAGATAAGATCCCAGATTTCTTCATCCCCCCCAAGCTTGTAAGCTGCCCACCAGAGACCGAAGCTTCTGACGTCAAACCCAAAGAGAGTCTGAAACCCTCGACTTCTGAACAGACCATCAGCAACAAAAAGATCAGCAGCCCTCGTAGTCCGCGATTGGTCAGCAAGTTAGCAGGAGACACCAAGAACTTACTGAGGGCGGCGAACCGCCACATCATTCAAATTGAGAGTGCGGATGACGTTGTAGCAGGTGACACCAATGCCGACCCTCAATCCCAATCCGCCATGTCACTTCCTTACATTCCAAAAACTCAGACTTCCTA[C/A]GGCTTTGCTACATTGATGGAGAGTCCCCACACCCGGCGGAAAGAGTCCCTCTTCCACTGTGACCACACAAGCCCAGTAACATCACCCAACACCCAACGCAAGTCCCAAAGCAAGAGTCCTAATGAAGGGAACCACCTCAACCCTCCGGATTTTAACACCTCACATATAAACCCCTACCGATACTTCAGCGGGGGCGAGAGCGACACTTGCTCTTCAGCAGAGTCCTCTCCATTCAGTTCTCCATTGCTCTCCCGATCTGCCTCTCTACTGAAGATCTTTACTCACGAAACTCAAGCCAAGGTCGCAAAAGGAAAGCGGACATTTGCCAGGCATAGTTCCTTGTCTACGGATGAGTGCAGCTCAGCAGAACCAAGCCCTAATGTTCCTAGACGGAGTCACTGTTCGTCCTTGCAAGCCGGCGGAGCTCTGGACCATCTTCATGGCGGGGACCGCCAACACAAAGAGCACACCATCAACATGCATAAAGGAGGCACTGTCCG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa24162

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
ENSDART00000113168	Nonsense	168	426	1	1

Genomic Location (Zv9):

Chromosome 22 (position 22493521)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	22105157
GRCz11	22	22130135

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACATTGATGGAGAGTCCCCACACCCGGCGGAAAGAGTCCCTCTTCCACTG[T/A]GACCACACAAGCCCAGTAACATCACCCAACACCCAACGCAAGTCCCAAAG

Long Flanking Sequence:

CCCAAACGGATCATGTGGGTTCTGGAGAAGATCCGGGACTCAGTTGAAACAAATGTGCTCCGACAAGGAGAGGCGGGTGAAAAAGGAAAGGCTCCTGTTTATAGCAACGTCCTCACACCAGATAAGATCCCAGATTTCTTCATCCCCCCCAAGCTTGTAAGCTGCCCACCAGAGACCGAAGCTTCTGACGTCAAACCCAAAGAGAGTCTGAAACCCTCGACTTCTGAACAGACCATCAGCAACAAAAAGATCAGCAGCCCTCGTAGTCCGCGATTGGTCAGCAAGTTAGCAGGAGACACCAAGAACTTACTGAGGGCGGCGAACCGCCACATCATTCAAATTGAGAGTGCGGATGACGTTGTAGCAGGTGACACCAATGCCGACCCTCAATCCCAATCCGCCATGTCACTTCCTTACATTCCAAAAACTCAGACTTCCTACGGCTTTGCTACATTGATGGAGAGTCCCCACACCCGGCGGAAAGAGTCCCTCTTCCACTG[T/A]GACCACACAAGCCCAGTAACATCACCCAACACCCAACGCAAGTCCCAAAGCAAGAGTCCTAATGAAGGGAACCACCTCAACCCTCCGGATTTTAACACCTCACATATAAACCCCTACCGATACTTCAGCGGGGGCGAGAGCGACACTTGCTCTTCAGCAGAGTCCTCTCCATTCAGTTCTCCATTGCTCTCCCGATCTGCCTCTCTACTGAAGATCTTTACTCACGAAACTCAAGCCAAGGTCGCAAAAGGAAAGCGGACATTTGCCAGGCATAGTTCCTTGTCTACGGATGAGTGCAGCTCAGCAGAACCAAGCCCTAATGTTCCTAGACGGAGTCACTGTTCGTCCTTGCAAGCCGGCGGAGCTCTGGACCATCTTCATGGCGGGGACCGCCAACACAAAGAGCACACCATCAACATGCATAAAGGAGGCACTGTCCGACTTTGTGCAGACTATGATGCTGGAACGGCCCGCTTGCGATTCCGCATTATAGCAGCCGA

Associated Phenotype:

Not determined