ZMP

ociad1

Ensembl ID:

ENSDARG00000052334

ZFIN ID:

ZDB-GENE-040426-1100

Description:

OCIA domain-containing protein 1 [Source:UniProtKB/Swiss-Prot;Acc:Q6NYD7]

Human Orthologues:

OCIAD1, OCIAD2

Human Descriptions:

OCIA domain containing 1 [Source:HGNC Symbol;Acc:16074]
OCIA domain containing 2 [Source:HGNC Symbol;Acc:28685]

Mouse Orthologues:

Ociad1, Ociad2

Mouse Descriptions:

OCIA domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1915345]
OCIA domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1916377]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa29350	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa29350

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000103365	Nonsense	117	266	5	8
ENSDART00000128657	Nonsense	117	266	5	9
ENSDART00000141510	Nonsense	117	266	6	9

Genomic Location (Zv9):

Chromosome 20 (position 23237985)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	23351372
GRCz11	20	23250472

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCAAGAAAAGTTTATGAAACTGGAGAACTCTCCACTGGGAGAGGCATTA[C/T]GACAGGGACGTCTGCGTCACGTGTCTTCTGAGTAAGTTTGTGTTTTCGAA

Long Flanking Sequence:

TCTTATTAATTGAGCGATTCAGAAACATGATCCCTGCTTTATTTTATTTATTTAGAATTTATAATTTAGGCTTTTCACATATAAACGTTGATTAAAGCACATACACTGAGTGCATTAAATATGACAAACAGCAGCTCAAATGCTGTTTACTTGTGTTCATCATCTTATCAAAAGTTACATTTTTGGACAAACTAACCCTTTATTTAAAACAAAAGTAAAGAAATTCTCTTATTGTTATTATTTTTCCATAGGAATGCTTTCTCCATCTCCACGATTTGGTGCGCTTCCTAAAATTGCCTGTGAGTATAAAGAACATCAGACAGCACAAAATTATATAGAAAGCAATATAAAAAAAGATTGTACGGAAATTGCCATTTTCAATAAAGGATTGTTGTGCAGTTGCTGGCATATTTGGATACATCGGTGGAAAAATGTCTTACGTGAGGGTCTGTCAAGAAAAGTTTATGAAACTGGAGAACTCTCCACTGGGAGAGGCATTA[C/T]GACAGGGACGTCTGCGTCACGTGTCTTCTGAGTAAGTTTGTGTTTTCGAATACATGCTCGATTCGTTCATTCTAGTCTTTATTTATTTATTTTTTGTTAATTGTTTTGCTTTTTAAAATGTTTTAATGGCTATATTACATTTTCATATTTATTATATAACTTTAAACAATTTATAAAAAGATTCAGCACTTGCTGCAGAAAACGCCACCAAAACATGACACTTCCACATTTCACTGAAGTCTACACACGTTTTCCCTCAAATTAAGATTTGAGGTAAATTAGGGTAATTAATGCCAATGCATTTTATTCAAACTCTTATTGGTACCATTTAACACTGAATAAAGCACATAATCAGCACCTGAGGTGATCATTGCCATTGTAGTGTATGCTGTTATTCCAGCCATGATGTTGCAGAAATATAAACCATTTCTAATGGCCACCATTGGTGGTTGGGGGAGTAACATGGAAAACCTACCTTTAATCGGATGTTGCAGTGCCAC

Associated Phenotype:

Not determined