ZMP

LOC796278

Ensembl ID:

ENSDARG00000078627

Human Orthologue:

TMEM151B

Human Description:

transmembrane protein 151B [Source:HGNC Symbol;Acc:21315]

Mouse Orthologue:

Tmem151b

Mouse Description:

transmembrane protein 151B Gene [Source:MGI Symbol;Acc:MGI:2685169]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa2891	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa2891

Status:

F2 line generated
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Availability:

Not yet available

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110361	Nonsense	332	505	2	2

Genomic Location (Zv9):

Chromosome 17 (position 31645724)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	31569651
GRCz11	17	31586614

KASP Assay ID:

554-2447.1 (used for ordering genotyping assays)

KASP Sequence:

CAGAAACGGTGGACAGTACAGAGCTGGAATGGCACATCCGCTCAAACCGC[C/T]AGCTTATTCCAAGCTACTCAGAGGCCATGCTGATGAACCTGGGGGCTTCW

Long Flanking Sequence:

GCCGGTGTGGAATGAAAGATGTTTCACGCAACTTACGTGGACTGGAAGGTCACGCGGCGACGCGGTTGCATTTCTCCAAATGCTTCAGCTTCGCGGGAGCAGGACCTGAAAATGCATACCTCAATCAGCGTGCCAGGTTCTTCTCAGAAATTGAGGGCCTTGATGACTACATGGAAGCCCGTGAAGGGATGCTTTTAAAGAACGTCGACTTTAAAGAGCACCTCATAGCTTATGTGGATCCTGACCAGCTGCCGTGGTACACATCACGGGTCACCTTCTGGATGGCAGCTCTCCTCATGCTCTCCTGGCCACTGCGAGTGCTGATTGAGTACCGGACAGCATTTGTGCACTACCAAGTTGAGAAACTATTCGGATTGGAGTATACAAACAACAGCCCATCTCCAGAGGGCGATGACACCACGAGGAACAATCGCTATGGCCTTCCAAGAGCAGAAACGGTGGACAGTACAGAGCTGGAATGGCACATCCGCTCAAACCGC[C/T]AGCTTATTCCAAGCTACTCAGAGGCCATGCTGATGAACCTGGGGGCTTCAGGGTCAAACCACAGAGACAGTATCTCCTCCAACCGTTTACTGTTGGACAGTTGCTCAACACAGAGCTACGGGACGCTGGTGCAGAACTGTGAGCACTGTTGCCAACAAGAAGGAGGGGAAAGGCGGCCAACCATCAGCTCCAGCTGTTCCTCCATCTTCTCTCGGCACACCTTCCACTCGCGTTTGTCCCTGGACACCTCACACTTCTCGCTCTGCCGCATGTATGGCTCCAGACGCACCGTAGGACTGTGGAGAAGCCGCAGTAGCACCCTAACAGAGCGATGCTGCCCTGACGAGCAGTGCTGTAGGTCTTACACCAGTCAGCTGGCTCTCAATGACAGCCCACCAAACTATCAAGACGCTCGATTCTTTCCAGTCCTCATAGTACACCGGTCTGAGGGCTGCGGAGAGTCCTCTGAGGTCAGGAGGTATTATGTCCGCAGAGGCTCC

Associated Phenotype:

Not determined