ZMP

cep70

Ensembl ID:

ENSDARG00000076965

ZFIN ID:

ZDB-GENE-070705-311

Description:

centrosomal protein of 70 kDa [Source:RefSeq peptide;Acc:NP_001108048]

Human Orthologue:

CEP70

Human Description:

centrosomal protein 70kDa [Source:HGNC Symbol;Acc:29972]

Mouse Orthologue:

Cep70

Mouse Description:

centrosomal protein 70 Gene [Source:MGI Symbol;Acc:MGI:1915371]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa45758	Nonsense	Mutation detected in F1 DNA	Not yet available
sa8774	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa45758

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
ENSDART00000115344	Nonsense	141	609	6	18

The following transcripts of ENSDARG00000076965 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 22 (position 12757291)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	12593221
GRCz11	22	12617998

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCCCTTTATTATAGTGGTTGTTGATGTTTGTGCCCGCACAGAAGTGTTG[T/A]CAGTCTGTGGAGCAGAAGCTGATTCAGGAGCAGCAGCAGGCCTCTCGGCT

Long Flanking Sequence:

CTATAGGTGAATTGAATAAACAAAATGGTCTGTATTGTGTGTGCGCGAATGAGAGTGAATGGGTGTTTCCCAATCCTGGGTTGCGGCTGGAAAGGCATCCGCTGCGTAAAACTTATGCTTTCACTGTATCAACCACTAAAATAGAGACTAAGTCGAAGGAGAATGAATGAATGAATGAGAGTGCGTCACCTACAGGTGGTTTGTAAGGCTCACTCACCTGTGTGAAGCCCACTCAGAATTGCCAGTTGTTTTCCAGAAACATGAAGAGTTGATAAGAAAGCTGATCATTTTCAGCAGCTGATTATAGTAATTGTGTACGTAGTGCTAGCTGTTTTGCCACTGAACGTCAGTAGGCAGGGCTTATAGTGGGATGATTAATCTCTTGTCTGTTCTGAAGTTGGTTGTAGAGTATGTACATATGAACAGTTTTTGGAGCTTTAATTGAATGCTTGCCCTTTATTATAGTGGTTGTTGATGTTTGTGCCCGCACAGAAGTGTTG[T/A]CAGTCTGTGGAGCAGAAGCTGATTCAGGAGCAGCAGCAGGCCTCTCGGCTGCAGAAGAAGCTCCAGTATGCAGTGCGGGAGGAGGAGAGACGGGCGACCCGACAGAAGCAGACCTTCCAGCAGATCCTCCACAGATCAGCGCGACCCAACTCCACCAATGACCAGCAGTGAGTCTCACACTTATTACAAATATTTGTGAATTGGGGTGGAAAAAAAGCGGTCATTTCAGAAAATTATGGGGAACTATTTTAACTTTCAATAAACTGTTTAAACTCTGTAAATTTATTCATTTTCCTTAAGCCTTGTCCCTTATTTATCAGGGGTCACTACAGAGGAATGAACCTCCTACTATTCTGGCATATGTTTTACACAGCAGATGCCCTTCCAGTCTTAATAATAATAAACACACTAATATAGCAATACATTTTTATATTTATGTTTATTATTAAAATTGTCATTTTCAGCAACAGAACATTGGATAAAAGTATTGAAATAATTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8774

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115344	Essential Splice Site	566	609	16	18

The following transcripts of ENSDARG00000076965 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 22 (position 12746625)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	12582555
GRCz11	22	12607332

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGTCTGGACAGGAGATCTGCAGCCTTCTGGAAAGCMGCGACATTGACAG[G/A]TATGTGCGTCTSTTCATTTGAAYATCTKTWAACCTTTTCCGTTWTGACTC

Long Flanking Sequence:

ATCTTCAGTTATACGTCATATAAAAGTTACTGTTGTTATAAGAAATATTTAAATATTTGTTTATAGTATATACAAAATAAACCATTAAAAAAATGTCTGCATGGCTAATTTCTGAATTACAGAGCGCAATAAGATTTCCATATTCCTCCTTTATAAAAACCTTTGGCTCAACAAAAAAAAAATTACTCAACTTGCTGAATAGTCAGATTTGTGCACTAAAAATGTATGCAAATTAGCACATGTTGAAATAATGTATTATTTGCATATGTAAACATCACACTTTAAAAAAACTTAAATGCCTTTTATGTTGTTGTTTGAATTATTGATGTAATTAATCAGCTGGGAAAATGTGGAGATCACGATGAGCTGATGCTTTGCTCCTCTTCTGCTGTTGTAGATGATAAAGCTCCTGCTAGTGAGGTGGTCAGCAGCGTCTCCAGTGTCCTGTCTCAGTCTGGACAGGAGATCTGCAGCCTTCTGGAAAGCAGCGACATTGACAG[G/A]TATGTGCGTCTGTTCATTTGAATATCTGTAAACCTTTTCCGTTATGACTCAGTTCAGGGACGTCGGCTGATGGCGGTCCACATCTACCTGATGCTTTAAGTTCATATTTGAATCATCCGAACACATCCACACAGTTAATGACGGCATTTAATGGTCAAATGAAATAGGAGTAAAACACAAATTATTTCTTTTATTTTAATCATATTATTTTCAGCAGGTCTAAGACTAGAATAGCTATAGGAAATGTACTTTTTATTCTGTAAACTACTGTGCTGATACTGCTGGTAAAAAAAAAAGTTTAATAGAGAACATAGAAACATGTTTAGTAGAGACTTTTTGGTGAAAATATATTTGTTTTTGCAAAAGATAACAAGGAGCCATGTTTTCATACATTAAATACATTTTTTAGACAACAAAATGCCTTTTTCAACTAAAGAAGATACTCTCCACATTTTCATGCAACATTTTGCCGTTACAGAATTTACTAATGTCCATTTTAG

Associated Phenotype:

Not determined