ZMP

LOC100148094

Ensembl ID:

ENSDARG00000020039

Human Orthologue:

MAD2L1BP

Human Description:

MAD2L1 binding protein [Source:HGNC Symbol;Acc:21059]

Mouse Orthologue:

Mad2l1bp

Mouse Description:

MAD2L1 binding protein Gene [Source:MGI Symbol;Acc:MGI:1913841]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42246	Nonsense	Mutation detected in F1 DNA	Not yet available
sa2699	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa42246

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
ENSDART00000004779	Nonsense	123	385	2	3

Genomic Location (Zv9):

Chromosome 13 (position 33923251)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	33346522
GRCz11	13	33698676

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAATATACTTACTAAATAATGGCACCGAAATGTTTTATTTCAAGGTTGT[C/T]AGGAGACTGATTCTTTGGCCAGTGCTTCTGGCAGTCATAAGGATTGTGAA

Long Flanking Sequence:

AGAGGAAAAATCAAGAGAAGCAAATAAAAAGGAAAAATTTGGTTAATTTTGTAGGTTGCAATTTTTTTCAGTATTTTTCTTGAATTTAAGTTAATTAACCTTAAATCTCTCAATGTTTGGACACTAAAATATTATTTAAATATAAATCTGTTTTGTTTAAATGTACCAGAACACATTGCCTATATTCACTGAGAAATGGATACAAATATACATTTTTAAAACGGGGTGTACTCAAATATGCTGAGCTGAGAGAGAGAGAGAGGGGGGGGGGGGGGTCCATTTGAACTGACTAAATGCGTATAAATGTGATAATCGAAAAATGTTCATAAAAAGTAAATGACACAAATTTTCCTTAAACCTTATATGCTTTGAAAATCTCAATATTATTTTTTATCTCAATAATAATTTATTTTCACATATTTATTATACAGAAAGTTACTAAAAATATTACCAATATACTTACTAAATAATGGCACCGAAATGTTTTATTTCAAGGTTGT[C/T]AGGAGACTGATTCTTTGGCCAGTGCTTCTGGCAGTCATAAGGATTGTGAATCAAATGGAGTGCCTCCACACTCTGTAGATGATGAAGAAATATTCAGAAGAGCGAGAGAGGAAGGACGAGTGAATGTCATCTTCCCTGGATGCATCACTCAGGATGGTTGCTGTCGATTTGTTGGCGAGCTTCTGAAATGTGTCCTTTATCAGCGCCAACAGATGCCCATGACATACGACCAAATGGTGTTCCTTCAGAAACAGCAGCATAATGCCTCTCAGGTATTGCAGAAGGGTTGATCTATGTTTCATGTTGTTCAATCCTAATTTTAAAAAACAAAAGTTTTATAAAAGTATTTAAAGAAATAACAGTAATGTATTGTTAAAGGCGTAGTTCACACAAAAATGTTAATTGTCATCATGTGCTTTAATTTTAATCACTTACCCTTTACTTGTTCCAAACCTGTTTGAAATTATTTTTCTGTTGAACACAAAATAAGATATTTAGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa2699

Status:

F2 line generated
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
ENSDART00000004779	Nonsense	162	385	2	3

Genomic Location (Zv9):

Chromosome 13 (position 33923134)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	33346405
GRCz11	13	33698559

KASP Assay ID:

554-3018.1 (used for ordering genotyping assays)

KASP Sequence:

CACACTCTGTAGATGATGAAGAAATATTCAGAAGAGCGAGAGAGGAAGGA[C/T]GAGTGAATGTCATCTTCCCTGGATGCATCACTCAGGATGGTTGCTGTCGA

Long Flanking Sequence:

TGGACACTAAAATATTATTTAAATATAAATCTGTTTTGTTTAAATGTACCAGAACACATTGCCTATATTCACTGAGAAATGGATACAAATATACATTTTTAAAACGGGGTGTACTCAAATATGCTGAGCTGAGAGAGAGAGAGAGGGGGGGGGGGGGGTCCATTTGAACTGACTAAATGCGTATAAATGTGATAATCGAAAAATGTTCATAAAAAGTAAATGACACAAATTTTCCTTAAACCTTATATGCTTTGAAAATCTCAATATTATTTTTTATCTCAATAATAATTTATTTTCACATATTTATTATACAGAAAGTTACTAAAAATATTACCAATATACTTACTAAATAATGGCACCGAAATGTTTTATTTCAAGGTTGTCAGGAGACTGATTCTTTGGCCAGTGCTTCTGGCAGTCATAAGGATTGTGAATCAAATGGAGTGCCTCCACACTCTGTAGATGATGAAGAAATATTCAGAAGAGCGAGAGAGGAAGGA[C/T]GAGTGAATGTCATCTTCCCTGGATGCATCACTCAGGATGGTTGCTGTCGATTTGTTGGCGAGCTTCTGAAATGTGTCCTTTATCAGCGCCAACAGATGCCCATGACATACGACCAAATGGTGTTCCTTCAGAAACAGCAGCATAATGCCTCTCAGGTATTGCAGAAGGGTTGATCTATGTTTCATGTTGTTCAATCCTAATTTTAAAAAACAAAAGTTTTATAAAAGTATTTAAAGAAATAACAGTAATGTATTGTTAAAGGCGTAGTTCACACAAAAATGTTAATTGTCATCATGTGCTTTAATTTTAATCACTTACCCTTTACTTGTTCCAAACCTGTTTGAAATTATTTTTCTGTTGAACACAAAATAAGATATTTAGAAAAAAGGCTGGAAACCATTGTCTTCTATAGTATTTGTTTTTCATACTATGGAAGTCAATAGTTACTGCTTTCAGCTTTTTTTATATTTCCTTTTAGACAAAAGGTTTTTTAAAAGGCT

Associated Phenotype:

Not determined