ZMP

si:dkey-210e6.1

Ensembl ID:

ENSDARG00000078817

ZFIN ID:

ZDB-GENE-081104-369

Description:

Novel protein similar to human and mouse ring finger protein 165 (RNF165) [Source:UniProtKB/TrEMBL;A

Human Orthologue:

RNF165

Human Description:

ring finger protein 165 [Source:HGNC Symbol;Acc:31696]

Mouse Orthologue:

Rnf165

Mouse Description:

ring finger protein 165 Gene [Source:MGI Symbol;Acc:MGI:2444521]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa34268	Nonsense	Mutation detected in F1 DNA	Not yet available
sa27119	Nonsense	Mutation detected in F1 DNA	Not yet available
sa21168	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa34268

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
ENSDART00000109989	Nonsense	141	347	3	8
ENSDART00000147753	Nonsense	121	327	2	7

Genomic Location (Zv9):

Chromosome 8 (position 763023)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	629533
GRCz11	8	695276

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATGCTCCAGACAGAACCCTTCCCCATCCACAGACGCTGCGGCCGCCGTA[T/A]GAATATCCTCCATCCATTCACATTCCCCCACCGGTACCACAGCAGCCACG

Long Flanking Sequence:

AGCTTAAAGTGACATTTAAAGGCTTCACTAGGGTAATTAGGGTAACTAGGTAGGTTATGGTAATTAGGCAAGTTACTGTATAATGATGGTTTGTTCTGTAGACTATCCAAAAAAATTAGCTTAAAGGGACTAATAATATTGACCTTAAAATGGTGTTTAAAAAATTAAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATAAGACTTTCTCCAGAAGAACAAATATTATCAGACATACTGTGAAAATGTCCTTGCTCTGTCAAACATCATTTGGGAAATATTCAAAAAAGAAAAAAAATTGAAAGGCAGGCTAATAATTCTGACTTGAAATGTACATACTTTATTTTTAAAAACTTGGTTTCATTTTAGGCTTTAAGATGGGGAAGAGAATCCCACTGAGTGTTTTTGAGCAACGGTAAAGTATTTGATTGTGATTCTCCCCAGCAGACATGCTCCAGACAGAACCCTTCCCCATCCACAGACGCTGCGGCCGCCGTA[T/A]GAATATCCTCCATCCATTCACATTCCCCCACCGGTACCACAGCAGCCACGCTACCTTGCAGAAGGAACAGACTGGTACGTGTGTATTCAACTGTGGCTAACACTGTGTCCTGAATACACACGACACGACACTGTGATGCAATAAAAGCTCAATATTTCATATTGAAAGGAGTATTGTCCTAACCCACACGCAAAATTTCAATAGACTTTCTATTCCTGCAAAGTCACAGCAGAACTACAGCATAAACTTCACTTAATCACCTCGGTACTGATTATGTGCTTTATTCAGTGTCAAATGCTTCTAATGTGAGATTAGGGGATTAAATTTCGAGAGAAGCATGTGATATGATATGAGCACGACTGGCTTCTCATCTGTATTCAGTAATAATCCAATCAGAGTGATCCAAACTTACAATAAATGTACTGTTTTTCCCTACTGCTCTATCTTTGCTGGAAGAATCCCCCCTTCCACCCTATCTCCTCCTGTTCCTCCCTTTTCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa27119

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
ENSDART00000109989	Nonsense	217	347	5	8
ENSDART00000147753	Nonsense	197	327	4	7

Genomic Location (Zv9):

Chromosome 8 (position 769051)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	635561
GRCz11	8	701304

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTGTTGTTGTTGTGCACAGGTGGTCCATGAGATCAGAAATTATCCATA[T/A]CCTCAGTTACACCTGCTGGCTCTTCAAAGCCTCAGTCCATCTCGGCACGC

Long Flanking Sequence:

ATTTTTGTAAACCAACAATGCTGTCCATTATTTAAAACAGTCATACTTTAAATGACTTTAACTGTCCTTATTTAAAACAGTAAAAACATGGTCAGCCGTTTGGTTGAGGAGCAGTCAAAGGGTTAGAATATTATCTCCAAATAGAGCAATTCAATTAATTTGGTGAAATCATTTTCATATGGCAATATGTGTTGCCTTTCCCAGACATGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATATGATGGATAAATTGGCGACCCCTGATTAATAAAGGGACTAAGCCTAAAAGAAAATGAGTGAATGAATATGTGTAAATTTTGCAATGTCAGATCTCTCCACTATCGCCGAGCTCTAGTTCTAAGTATCATTAAATTTGAAGGATTTGTTGTATTTTACATAGTTAAGCAACTCCAACTGGAAAACAGAGAATTTCCCACTCACACTGCTGTTGTTGTTGTGCACAGGTGGTCCATGAGATCAGAAATTATCCATA[T/A]CCTCAGTTACACCTGCTGGCTCTTCAAAGCCTCAGTCCATCTCGGCACGCGACGGCAGTGCGGGAGAGTTACGAGGTGCGGATCATCATCATCATCATCGCTTCAGTTAAAGTACAGCTAATTCTGCAGCATCTCTCACACGTGTTTCTGTCTGCTTCTGAATCCAGGAGCTCCTGCAGTTGGAGGACAGACTGGGAAATGTGAACAGAGGCGCCGTGCAGGCCACCATCGAGAGGTTTACCTTTCCTCACAAGTATAAAAAGGTAAAAACTGTGTAAAGGAGACCTAATATGCAAATATCACATTCATTAGGGGTTTAAACACAGCGGCAGCATTGAGTGAATATCTCCAGCAGCCTCTAATGGTCAACATGAATTAACTGTGTTTGTTCTAATCAGACTTGATGAATGAAACACTTTGATTGACATTCTCCCTTTGTACGTGTCATCAGAGAGGTAAAGCCCCGCCCACTACTCTCTCTGCATAAACAGCAGCCCTGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa21168

Status:

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

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109989	Essential Splice Site	242	347	5	8
ENSDART00000147753	Essential Splice Site	222	327	4	7

Genomic Location (Zv9):

Chromosome 8 (position 769127)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	635637
GRCz11	8	701380

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAGCCTCAGTCCATCTCGGCACGCGACGGCAGTGCGGGAGAGTTACGAG[G/A]TGCGGATCATCATCATCATCATCGCTTCAGTTAAAGTACAGCTAATTCTG

Long Flanking Sequence:

ACAGTAAAAACATGGTCAGCCGTTTGGTTGAGGAGCAGTCAAAGGGTTAGAATATTATCTCCAAATAGAGCAATTCAATTAATTTGGTGAAATCATTTTCATATGGCAATATGTGTTGCCTTTCCCAGACATGGGTTGCAGCTGGAAGGGCATCCGCTGCGTAAAACATATGATGGATAAATTGGCGACCCCTGATTAATAAAGGGACTAAGCCTAAAAGAAAATGAGTGAATGAATATGTGTAAATTTTGCAATGTCAGATCTCTCCACTATCGCCGAGCTCTAGTTCTAAGTATCATTAAATTTGAAGGATTTGTTGTATTTTACATAGTTAAGCAACTCCAACTGGAAAACAGAGAATTTCCCACTCACACTGCTGTTGTTGTTGTGCACAGGTGGTCCATGAGATCAGAAATTATCCATATCCTCAGTTACACCTGCTGGCTCTTCAAAGCCTCAGTCCATCTCGGCACGCGACGGCAGTGCGGGAGAGTTACGAG[G/A]TGCGGATCATCATCATCATCATCGCTTCAGTTAAAGTACAGCTAATTCTGCAGCATCTCTCACACGTGTTTCTGTCTGCTTCTGAATCCAGGAGCTCCTGCAGTTGGAGGACAGACTGGGAAATGTGAACAGAGGCGCCGTGCAGGCCACCATCGAGAGGTTTACCTTTCCTCACAAGTATAAAAAGGTAAAAACTGTGTAAAGGAGACCTAATATGCAAATATCACATTCATTAGGGGTTTAAACACAGCGGCAGCATTGAGTGAATATCTCCAGCAGCCTCTAATGGTCAACATGAATTAACTGTGTTTGTTCTAATCAGACTTGATGAATGAAACACTTTGATTGACATTCTCCCTTTGTACGTGTCATCAGAGAGGTAAAGCCCCGCCCACTACTCTCTCTGCATAAACAGCAGCCCTGAGTGAGAAGCAGCCGTCTGTCCATTAGCCATTAGAGTGTTTGAGCTGCTGAAGATGATGTCAGCATAGACTAAGAGG

Associated Phenotype:

Not determined