ZMP

TMEM128

Ensembl ID:

ENSDARG00000059150

Description:

transmembrane protein 128 [Source:HGNC Symbol;Acc:28201]

Human Orthologue:

TMEM128

Human Description:

transmembrane protein 128 [Source:HGNC Symbol;Acc:28201]

Mouse Orthologue:

Tmem128

Mouse Description:

transmembrane protein 128 Gene [Source:MGI Symbol;Acc:MGI:1913559]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22395	Nonsense	Available for shipment	Available now
sa28220	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22395

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

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082184	Nonsense	6	152	1	8

Genomic Location (Zv9):

Chromosome 14 (position 146849)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	215195
GRCz11	14	39171

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCAGCCGAGCGCCATGGCGGACTTCAGTGAGGTGATGAACCTGCGGCGG[C/T]GATTCAAAACAAACGAACAAGAAGAGGAGAGAGAGCAGAGTGAGACACAC

Long Flanking Sequence:

CTAGAGCTGCAGAAAACTACAGGGCTGCCTCATTTGTTTATGCGACAACAGTTATTGTGTTACCATAGCAACTGTAGAATCACCACAGCATGAATCAGCGGTGTTTTATTACAGTATGGGTTAGGGTTAGTGTTTATGAGTTGGTTTGTGTCATCATAAACAGCACACACACACACACACACACATATGATAACTATAAGCAGAGATTATGAACTGAATGTGCGCCCAGTCAGACTGCAGCCTCTCTCTATAACGCCAGAGCAGATCAGGTGTCAGCTTTAACAGCTCTACTCTACTGGCACGACGAGCTCTTAATGTGACATTAAACCGCCGTGCTCCCTGACGCAAGTTCGCAGATTCGGGTCGGTAATCGGTGAAACGAATCCGACTCGGTTCGGACCCGGCGACTCACTTGAATCTCCCGAGCCTCCGTCGCTGGAGAGTGACGTCATCAGCCGAGCGCCATGGCGGACTTCAGTGAGGTGATGAACCTGCGGCGG[C/T]GATTCAAAACAAACGAACAAGAAGAGGAGAGAGAGCAGAGTGAGACACACACACACACACACACACACACACACACACACACACACAGCAGCGCTGTTCTTTAACTAATGTCGTGATGTGTTATGTGGACGTTTGTCGTTAAAGTATTGTGTTATTCTGTGTTGTGCCTAAGTTGTTGTCAGGTTGTGTTAGTGTTGTAATGCTGAGCTGGAGCTGTGTTTGTGCTGATGTGCTGTTGTCTGTGTTCTCATGTTGATGTGTTGATGTCGAGATGTGTCAGTGACGTCATGTGTTATGTTGTTGTTGTTTTCATGTTGTGTTAGTATTGTTGTGATGATGTTGTTGTGTTGTCATGCTTGTGTTACGAGTTGTTGTTGTTGTTGTTGTTGTTGTTGTGCAGGCTCTGGTGCTGATGCGGCTGAGGAAGTGAAGACGTCGGCTCGGATCAACCGTCACTCAGTGTTCTGGATCGTGTCCGCCGCCGCCGTCACCTACTATGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28220

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
ENSDART00000082184	Nonsense	12	152	1	8

Genomic Location (Zv9):

Chromosome 14 (position 146831)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	215177
GRCz11	14	39189

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGGACTTCAGTGAGGTGATGAACCTGCGGCGGCGATTCAAAACAAACGAA[C/T]AAGAAGAGGAGAGAGAGCAGAGTGAGACACACACACACACACACACACAC

Long Flanking Sequence:

ACAGGGCTGCCTCATTTGTTTATGCGACAACAGTTATTGTGTTACCATAGCAACTGTAGAATCACCACAGCATGAATCAGCGGTGTTTTATTACAGTATGGGTTAGGGTTAGTGTTTATGAGTTGGTTTGTGTCATCATAAACAGCACACACACACACACACACACATATGATAACTATAAGCAGAGATTATGAACTGAATGTGCGCCCAGTCAGACTGCAGCCTCTCTCTATAACGCCAGAGCAGATCAGGTGTCAGCTTTAACAGCTCTACTCTACTGGCACGACGAGCTCTTAATGTGACATTAAACCGCCGTGCTCCCTGACGCAAGTTCGCAGATTCGGGTCGGTAATCGGTGAAACGAATCCGACTCGGTTCGGACCCGGCGACTCACTTGAATCTCCCGAGCCTCCGTCGCTGGAGAGTGACGTCATCAGCCGAGCGCCATGGCGGACTTCAGTGAGGTGATGAACCTGCGGCGGCGATTCAAAACAAACGAA[C/T]AAGAAGAGGAGAGAGAGCAGAGTGAGACACACACACACACACACACACACACACACACACACACACACAGCAGCGCTGTTCTTTAACTAATGTCGTGATGTGTTATGTGGACGTTTGTCGTTAAAGTATTGTGTTATTCTGTGTTGTGCCTAAGTTGTTGTCAGGTTGTGTTAGTGTTGTAATGCTGAGCTGGAGCTGTGTTTGTGCTGATGTGCTGTTGTCTGTGTTCTCATGTTGATGTGTTGATGTCGAGATGTGTCAGTGACGTCATGTGTTATGTTGTTGTTGTTTTCATGTTGTGTTAGTATTGTTGTGATGATGTTGTTGTGTTGTCATGCTTGTGTTACGAGTTGTTGTTGTTGTTGTTGTTGTTGTTGTGCAGGCTCTGGTGCTGATGCGGCTGAGGAAGTGAAGACGTCGGCTCGGATCAACCGTCACTCAGTGTTCTGGATCGTGTCCGCCGCCGCCGTCACCTACTATGTGGACTTCATCTCTGTGCT

Associated Phenotype:

Not determined