ZMP

si:dkey-202b22.5

Ensembl ID:

ENSDARG00000073965

ZFIN ID:

ZDB-GENE-041210-175

Description:

Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RH03]

Human Orthologue:

C12orf63

Human Description:

chromosome 12 open reading frame 63 [Source:HGNC Symbol;Acc:24777]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20256	Nonsense	Available for shipment	Available now
sa2158	Essential Splice Site	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa20256

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From EZRC

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000036401	Nonsense	391	1085	9	28
ENSDART00000110028	Nonsense	99	279	3	7
ENSDART00000135276	None	None	188	None	4

Genomic Location (Zv9):

Chromosome 4 (position 17548590)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	18491430
GRCz11	4	18480406

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTGCACACTCCTGCTGGACTAAAGCTCTAGACTGTGCTCTTCAAAGCTA[T/A]GGAGTTCTGGAGTCTTGGGATGGAGACACCTGGGGCAGCAGTTCGTCTCA

Long Flanking Sequence:

TAGGTTGCCAGTTCAATAGGATTTGTAAGATAATTAAGGAAATTACAACAGTTGCAAGATTAACACTAATAACTGTGATGATTTGAAAGTGTTCGCTAATTTTGATCAGTAATGTTTTACAGATATCTCATTTAAGCTTTTATACTGTGCTTCAAAATATACGTAACTGCTTTTTTTACTCTGGTGAGCATAATATTCTCCTTTTTTTATCTCCGCCATTTTGTCATGTCATGAAGAATATCTCAAAGCAAATAAGTGCAACTCCTTCCTGGTGCAAGCTCACCATGACCTTGGAAACCTGCATTTCTACAATGGAAATCTAAAGTAAGATGTGTGCATTTAAATACTGACCCCAAACATTTGAACCTTAGTCTAATTCAGTGATTGCACAGTAAAAAAAAAAGGGAAAAAAGGCTTGTATTAGTGTCTTTATTTTTGTTTATGTATAGGTCTGCACACTCCTGCTGGACTAAAGCTCTAGACTGTGCTCTTCAAAGCTA[T/A]GGAGTTCTGGAGTCTTGGGATGGAGACACCTGGGGCAGCAGTTCGTCTCAGGAAACACTGAGGCATGCTGGGATATGGGGCTGTCTCCAGGGAGCTGTGCTTTCAGCCAAGATCGCACAGTGAGTGAAAACCCAAAAGGTGTTTTTGAGACAGCTTTCCATTACAGCTGTATAATTTCTGTTTTTTCTCCTGACAGGCATATCCTTACCTTAAACATCCACCAGCGCACAAAGTGCTGCCTTCTCTCTGCCAAACTCTTCAAGGTAAGAATTGAGTCACTTTTTTATTCTTAACCCGATTATACTTCATGAGTTGGCAGCGCACGAGGTCATGTAAATGTATTAACTTGTTTTCCTTTATTGAAATAAGATCATAAATTGTTTAAGGATAAACAGATTGCCACAGATTGATTTTTCGCCAATAATTTCACGCATGTAAATGGATCAACTGTTTTGAGTCAGTTTATTGAAGTGTGCATGTGTGATATCTGACAGAAACAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa2158

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000036401	Essential Splice Site	431	1085	9	28
ENSDART00000110028	Essential Splice Site	139	279	3	7
ENSDART00000135276	None	None	188	None	4

Genomic Location (Zv9):

Chromosome 4 (position 17548711)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	18491551
GRCz11	4	18480527

KASP Assay ID:

554-2836.1 (used for ordering genotyping assays)

KASP Sequence:

GGATATGGGGCTGTCTCCAGGGAGCTGTGCTTTCAGCCAAGATCGCACAG[T/C]GAGTGAAAACCCAAAAGGTGTTTTTGAGACAGCTTTCCATTACAGCTGTA

Long Flanking Sequence:

GATATCTCATTTAAGCTTTTATACTGTGCTTCAAAATATACGTAACTGCTTTTTTTACTCTGGTGAGCATAATATTCTCCTTTTTTTATCTCCGCCATTTTGTCATGTCATGAAGAATATCTCAAAGCAAATAAGTGCAACTCCTTCCTGGTGCAAGCTCACCATGACCTTGGAAACCTGCATTTCTACAATGGAAATCTAAAGTAAGATGTGTGCATTTAAATACTGACCCCAAACATTTGAACCTTAGTCTAATTCAGTGATTGCACAGTAAAAAAAAAAGGGAAAAAAGGCTTGTATTAGTGTCTTTATTTTTGTTTATGTATAGGTCTGCACACTCCTGCTGGACTAAAGCTCTAGACTGTGCTCTTCAAAGCTATGGAGTTCTGGAGTCTTGGGATGGAGACACCTGGGGCAGCAGTTCGTCTCAGGAAACACTGAGGCATGCTGGGATATGGGGCTGTCTCCAGGGAGCTGTGCTTTCAGCCAAGATCGCACAG[T/C]GAGTGAAAACCCAAAAGGTGTTTTTGAGACAGCTTTCCATTACAGCTGTATAATTTCTGTTTTTTCTCCTGACAGGCATATCCTTACCTTAAACATCCACCAGCGCACAAAGTGCTGCCTTCTCTCTGCCAAACTCTTCAAGGTAAGAATTGAGTCACTTTTTTATTCTTAACCCGATTATACTTCATGAGTTGGCAGCGCACGAGGTCATGTAAATGTATTAACTTGTTTTCCTTTATTGAAATAAGATCATAAATTGTTTAAGGATAAACAGATTGCCACAGATTGATTTTTCGCCAATAATTTCACGCATGTAAATGGATCAACTGTTTTGAGTCAGTTTATTGAAGTGTGCATGTGTGATATCTGACAGAAACACATCGCAGGAACAAATGTAAGCTCATTCAGAACAAACCAAAAGTTTAGCATTAAGGGAGGTGGAAACTCAGAAAGTTTATACTACCTAAATATTTATAAAACTCTATTCTCATCTTGTACAG

Associated Phenotype:

Not determined