ZMP

capn8

Ensembl ID:

ENSDARG00000055715

ZFIN ID:

ZDB-GENE-050522-279

Description:

Novel calpain family protein (Zgc:112467) [Source:UniProtKB/TrEMBL;Acc:A5WWC4]

Mouse Orthologue:

Capn8

Mouse Description:

calpain 8 Gene [Source:MGI Symbol;Acc:MGI:2181366]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa5973	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa29806	Missense, Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa5973

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
ENSDART00000078111	Essential Splice Site	544	701	14	21
ENSDART00000144585	Essential Splice Site	544	700	14	21

Genomic Location (Zv9):

Chromosome 22 (position 27216016)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	26609547

KASP Assay ID:

554-3701.1 (used for ordering genotyping assays)

KASP Sequence:

AGATATAGACCCACATTTCAAACGCCTCTTCAGTCARGTTGCTGGAAGCG[T/A]AAGTCACAACTGGTCAATATAAATTTGAATCATTATCATGATTTTTCCCA

Long Flanking Sequence:

ATGTGAAAAAGGTGTGTTTATCTTTGATTTATAGAGTACAAAACACAGACACACTCACACAAATACTTGCAAATATGGTTTATGAAGACTCCAGAGACGCAATGTACTTTAAACTGTAAAAACTGTTTATTAAATGACCGTATCCTACCCCTAAATTTAATCTGGAAACCAAGAAATTGCTAAATTGGTATGCCAAAAGTGTATGCAAGTCCTCATAAACCAGAATAACAGAATACAATTACAGTAGATCATACTCATGTCATTATACAATTTTGAAACATTAATGTATAATTTTACATAACATAATACAAAATAATCCACATAATCAAGTACAGACACATTATATAAATTACATACTGTATATAACACATTTAACCTTGTGTTCCTATTTTCTTTTAAACAAACATTCAAGGTGCATTTTTTTCCTTCCTAGCATTTCATATCTGAGAAAGATATAGACCCACATTTCAAACGCCTCTTCAGTCAGGTTGCTGGAAGCG[T/A]AAGTCACAACTGGTCAATATAAATTTGAATCATTATCATGATTTTTCCCAGTTAGCATGATCTTCTCTTCCCTCTGTAGGACTCTGAGGTCTCTGTATTGGAGCTCCAGCAGATCCTGAACACCGTTGTCTCGAAACGTAAGAAAACACATTAACTTTTTTTTATTGACATATTTTAAATGTCTGAATTTTGCATTGGAAACTGCCTTGAAATAACTTCACCATCCTGCTGATAATTCTCACCTCAGGATCTAATGTGAAGACAGACGGATTCAGTTTGGAAACCTGCCGTCACATTATCAGCCTGCTAGATGTATCCTTACCTCACTGGTTCATTGAATGGAAACTACAGATGTTATTGAAGAAACTAATTTAAAGATATGGCAGCATCTGCCTGTATTCATTTCTCTAGTGTACTTTGCATCATTAGGCATTTTAACCCTTGACCCCAGTGCAGAAAGATGGCAGTGGCAAACTCGGCCTTCTGGAGTTTCACACACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29806

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 > T

Consequence:

Missense, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078111	Missense	564	701	15	21
ENSDART00000144585	Nonsense	564	700	15	21

Genomic Location (Zv9):

Chromosome 22 (position 27215879)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	26609684

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGTCTCTGTATTGGAGCTCCAGCAGATCCTGAACACCGTTGTCTCGAAA[C/T]GTAAGAAAACACATTAACTTTTTTTTATTGACATATTTTAAATGTCTGAA

Long Flanking Sequence:

CCGTATCCTACCCCTAAATTTAATCTGGAAACCAAGAAATTGCTAAATTGGTATGCCAAAAGTGTATGCAAGTCCTCATAAACCAGAATAACAGAATACAATTACAGTAGATCATACTCATGTCATTATACAATTTTGAAACATTAATGTATAATTTTACATAACATAATACAAAATAATCCACATAATCAAGTACAGACACATTATATAAATTACATACTGTATATAACACATTTAACCTTGTGTTCCTATTTTCTTTTAAACAAACATTCAAGGTGCATTTTTTTCCTTCCTAGCATTTCATATCTGAGAAAGATATAGACCCACATTTCAAACGCCTCTTCAGTCAGGTTGCTGGAAGCGTAAGTCACAACTGGTCAATATAAATTTGAATCATTATCATGATTTTTCCCAGTTAGCATGATCTTCTCTTCCCTCTGTAGGACTCTGAGGTCTCTGTATTGGAGCTCCAGCAGATCCTGAACACCGTTGTCTCGAAA[C/T]GTAAGAAAACACATTAACTTTTTTTTATTGACATATTTTAAATGTCTGAATTTTGCATTGGAAACTGCCTTGAAATAACTTCACCATCCTGCTGATAATTCTCACCTCAGGATCTAATGTGAAGACAGACGGATTCAGTTTGGAAACCTGCCGTCACATTATCAGCCTGCTAGATGTATCCTTACCTCACTGGTTCATTGAATGGAAACTACAGATGTTATTGAAGAAACTAATTTAAAGATATGGCAGCATCTGCCTGTATTCATTTCTCTAGTGTACTTTGCATCATTAGGCATTTTAACCCTTGACCCCAGTGCAGAAAGATGGCAGTGGCAAACTCGGCCTTCTGGAGTTTCACACACTGTGGATGAAGATCCAGAAATATTTGGTAAAATTTATATTTCGATCAAATTTTAAATGAATTACTTTCAGCCTTACTTTTTGAATGATGATAATAATAAAATAATAATAATCATCATCATCATCGTTCAGTTTGATGT

Associated Phenotype:

Not determined