ZMP

ENSDARG00000060688

Ensembl ID:

Human Orthologues:

TRIM50, TRIM62, TRIM72, TRIM73, TRIM74

Human Descriptions:

tripartite motif-containing 50 [Source:HGNC Symbol;Acc:19017]
tripartite motif-containing 62 [Source:HGNC Symbol;Acc:25574]
tripartite motif-containing 72 [Source:HGNC Symbol;Acc:32671]
tripartite motif-containing 73 [Source:HGNC Symbol;Acc:18162]
tripartite motif-containing 74 [Source:HGNC Symbol;Acc:17453]

Mouse Orthologues:

Trim50, Trim62, Trim72

Mouse Descriptions:

tripartite motif-containing 50 Gene [Source:MGI Symbol;Acc:MGI:2664992]
tripartite motif-containing 62 Gene [Source:MGI Symbol;Acc:MGI:1914775]
tripartite motif-containing 72 Gene [Source:MGI Symbol;Acc:MGI:3612190]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41728	Nonsense	Mutation detected in F1 DNA	Not yet available
sa44730	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa41728

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
ENSDART00000085792	Nonsense	366	548	5	6

Genomic Location (Zv9):

Chromosome 10 (position 42214479)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	40927188
GRCz11	10	40848374

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCGGGCCCCTGCAGTACAGAGTCTGGAAGTCACTCAAGGGCAGCATCTA[T/A]CCAGGTCAGAGAAAAGAAAAAGATAAATAACTTTAAGGGAAGAAAAACAT

Long Flanking Sequence:

CATTTTTGAGTGAACTGTCCCTTTAAATCATCACTGCAACAGTTAACCGGACAGTGAGATTTCATCACTCAGATCAGCACAGGACTCAATCTAATGACCTCACCCTCGCAATAGGAAGATAATGCCATTAGTTCAGCGCAGGGGGATTTTCCAGATCGGCGGATAAAGAAAGGAGAGCAGTTCACTTACAAAACACTGATCTCATGTGGAAAACTTGTGGCCCTCGAGCCTCCGCCGCTTTCACCAATCTGCTCTTTCCTGTCTTTCTGCAGAGCATTAAGGGTCTGCTTCAGAGGTGAGTGGCTCTTTTCCATTGATACGCTCTCTAATGTTTTGATGAGGATCTGCGTGAATTGTTTTGGTGTCTGGGCTTCTGTTGTTTTAAGCAGGCAGCCACCCAAGTTCGAGAGGCCGACGCTGACGCCGCCCAGCCTGTGCGAGGGCCGATTCGCCGGGCCCCTGCAGTACAGAGTCTGGAAGTCACTCAAGGGCAGCATCTA[T/A]CCAGGTCAGAGAAAAGAAAAAGATAAATAACTTTAAGGGAAGAAAAACATACAGTTGATATGCAATTATTCAGGCGAGGCAGTGGCGCAGTAGGTAGTGCTGTTGCCTCACAGCAAGAAGATTGCTGGGTCGCTGGTTCGAACATCGGCTCAGTTGACATTTCTGTGTGGAGTTTGCATGTTCTCCCTGCCTTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTTCAGGTGAATTGGGTTGGCTAAATTGTCCGTTGTGTATGAGTGTGTGTGAATGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGAATGAATGAATGCAAATATTCACCCTCCTGTGAATATTTTTCTTTAATATTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa44730

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
ENSDART00000085792	Essential Splice Site	367	548	5	6

Genomic Location (Zv9):

Chromosome 10 (position 42214484)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	40927193
GRCz11	10	40848379

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCCCTGCAGTACAGAGTCTGGAAGTCACTCAAGGGCAGCATCTATCCAG[G/A]TCAGAGAAAAGAAAAAGATAAATAACTTTAAGGGAAGAAAAACATACAGT

Long Flanking Sequence:

TTGAGTGAACTGTCCCTTTAAATCATCACTGCAACAGTTAACCGGACAGTGAGATTTCATCACTCAGATCAGCACAGGACTCAATCTAATGACCTCACCCTCGCAATAGGAAGATAATGCCATTAGTTCAGCGCAGGGGGATTTTCCAGATCGGCGGATAAAGAAAGGAGAGCAGTTCACTTACAAAACACTGATCTCATGTGGAAAACTTGTGGCCCTCGAGCCTCCGCCGCTTTCACCAATCTGCTCTTTCCTGTCTTTCTGCAGAGCATTAAGGGTCTGCTTCAGAGGTGAGTGGCTCTTTTCCATTGATACGCTCTCTAATGTTTTGATGAGGATCTGCGTGAATTGTTTTGGTGTCTGGGCTTCTGTTGTTTTAAGCAGGCAGCCACCCAAGTTCGAGAGGCCGACGCTGACGCCGCCCAGCCTGTGCGAGGGCCGATTCGCCGGGCCCCTGCAGTACAGAGTCTGGAAGTCACTCAAGGGCAGCATCTATCCAG[G/A]TCAGAGAAAAGAAAAAGATAAATAACTTTAAGGGAAGAAAAACATACAGTTGATATGCAATTATTCAGGCGAGGCAGTGGCGCAGTAGGTAGTGCTGTTGCCTCACAGCAAGAAGATTGCTGGGTCGCTGGTTCGAACATCGGCTCAGTTGACATTTCTGTGTGGAGTTTGCATGTTCTCCCTGCCTTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTTCAGGTGAATTGGGTTGGCTAAATTGTCCGTTGTGTATGAGTGTGTGTGAATGTGTGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGAATGAATGAATGCAAATATTCACCCTCCTGTGAATATTTTTCTTTAATATTTCCTAA

Associated Phenotype:

Not determined