ZMP

ENSDARG00000091482

Ensembl ID:

Human Orthologues:

C20orf118, NCOA7, OXR1

Human Descriptions:

chromosome 20 open reading frame 118 [Source:HGNC Symbol;Acc:16112]
nuclear receptor coactivator 7 [Source:HGNC Symbol;Acc:21081]
oxidation resistance 1 [Source:HGNC Symbol;Acc:15822]

Mouse Orthologues:

Gm1332, Ncoa7, Oxr1

Mouse Descriptions:

nuclear receptor coactivator 7 Gene [Source:MGI Symbol;Acc:MGI:2444847]
oxidation resistance 1 Gene [Source:MGI Symbol;Acc:MGI:2179326]
predicted gene 1332 Gene [Source:MGI Symbol;Acc:MGI:2686178]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38216	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa32565	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38216

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
ENSDART00000128563	Essential Splice Site	37	160	2	4

Genomic Location (Zv9):

Chromosome Zv9_NA816 (position 10082)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	KN150645.1	10082
GRCz11	KN150645.1	10082

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTGGTGCATCTGAACCGCCTTTACTCTCACAGCGTCGTACCTGGACAG[G/A]TGAGATTACCAGAGCTACACTTAAGATCTAATCAAGAGTCAAAATAACAT

Long Flanking Sequence:

TTATTAATTAATTAAATTTGTGTAGCTTCTTTTTAAATTAAATAAATTTAATAAAAAAATAGATTAATCAATTGAAATAAATAATAATAATTTTTGGAGGGGTTTTAAACTGAAGTGAATCCAGCAGGACTGAATCTATAATATATGAACTTAATCTGAAAGTGTTTATTTTTCTTAAAAGTGTGTGTGTGTGCGCGTTCGTTCGTTCGTTCAGTAAGTGCTTTGAACCTTTTTCTTTCAGACAACAGCAGTAAATCTGGCACGCAGACCAAGAAGGAGAAAACCCGGCCTCCAGGAACAGTTGAATACATGGTGAGTTTCCTTTAAATGTGTGTCTGAACTCTTTTTAGTGTGTTTCTGTGTGTTTACCGAGTGTGTGTGTGTGTGTTCAGGTTGAACCGAAAGACACACTGAACAGCATTGCCCTGCATTTCAACATCACCCCAAATAAACTGGTGCATCTGAACCGCCTTTACTCTCACAGCGTCGTACCTGGACAG[G/A]TGAGATTACCAGAGCTACACTTAAGATCTAATCAAGAGTCAAAATAACATCATAATTTGGAAGTAATCAACTGTTTTCTGTGCTGCTTTTGAGCCTCATCTGAATGCTGTTTGAGTGGGCGTGGCCAACTGTAGACTAAGAAGTAAACGCCCACTTTGATTGGCTGGCAGTTTTGCATATTAAAATGCTTAACAGGCACTGAGGTAAATGTGGCTGTCAGTTTTCTGTGGAGGCGGAGCTTATCAACTGTTACATTCAGTGTTGGGAGAAATTAATTTCAGATTAACTCATTACTGTAATTAAATTACATTTCTGCAGAAATAAAGTCAACAAATGGATTACTTTTTATTTAATTTACTTAGGTACTCTTAAATACTGTACAAAAGCACGCACATCTCTATTAATTGGGTGCTCAGCCAAAACCGCAAAAAGTGCAAATTAAATGTAAATCAAAGGCGGCAACACCAAGGCTCCAAAAATACAAATTTATTAAATTAATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa32565

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000128563	Nonsense	131	160	4	4

Genomic Location (Zv9):

Chromosome Zv9_NA816 (position 16830)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	KN150645.1	16830
GRCz11	KN150645.1	16830

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTAGACGCCATCACAGGTCCTCATGGATCCCAAAACCCATGGGCCGACCC[A/T]AGATCCGAGCCGGTTCAAGGCCAAAGCTTCGAATTGTGCCTCGGATACGG

Long Flanking Sequence:

GGGTAAAGTTAGGGTAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGGAGACAATCCAAAACTAATATTGCTGAAGGGGGCTAATAATATTGACCTTAAAATGGGTTTAAAACTATTAAAAACTGCTTTAATTCTAGCCGAAATAAAACAAACAAGACGTTCTCCAGAAGAAAAAATATTATAGGAAATACTGTGAAAAACTCCTGAATCTGTTCGACATCATTTGGGAAATATTGAAAAAGAAAATAAACAGGAGAGTGAATAATTTTGCCATTCATATCTATTGTGGTCACACGTTTACTCTTCTGTCAGGATGGTGAGTACAGCAGCCGGCCGGGACGTCCTGTGTGCAGAGAGACGTCACCGCTGTCTGAAGACGAGAGTCCGGCCACCGTCAAATTCATCAAGATGAGCTGCAAATACTTCACTGACGGCATGGTGAGAACTAGACGCCATCACAGGTCCTCATGGATCCCAAAACCCATGGGCCGACCC[A/T]AGATCCGAGCCGGTTCAAGGCCAAAGCTTCGAATTGTGCCTCGGATACGGGTCGGCTTTGGTATGAATTGCCTCAGGTCTCAGGTAATCTAAAATAAATGTGCGTTTATAATGGGGCCAATCAGACTTGATGTTATTACTAAAGGAACAGTAGGGCAGAGCGATATGATAAATATCTCAATATATGTCATCTCATATCCTGTTAACGATATACAGACTTATGCAAAAGTTTGGGCACCGCTGTGGCTGCATAATTATGCAACCTTTCTTTATAAGAGAAAATCACAGTGAAATGCCATCCAGTTTCTAGAGAAAGCTAGATAATGTCATGTTTTTCAGACAGAAATTCGTAGTGCAGCAGTACTGAGATGTGTGAAATTTAAGTAAAATTGGAAAATAGGCTGTGCAAAAATGCAAAAATTTGGGCACCCAATGCAAAAATTTGTGCAAAAATATGTAGTCACTTAATGCTGATTGGTTACAACAGTGGTCCCCAACCTT

Associated Phenotype:

Not determined