Busch Lab

ZMP

LOC100002045

Ensembl ID:
ENSDARG00000089439
Human Orthologues:
TMEM132A, TMEM132B, TMEM132C, TMEM132D, TMEM132E
Human Descriptions:
transmembrane protein 132A [Source:HGNC Symbol;Acc:31092]
transmembrane protein 132B [Source:HGNC Symbol;Acc:29397]
transmembrane protein 132C [Source:HGNC Symbol;Acc:25436]
transmembrane protein 132D [Source:HGNC Symbol;Acc:29411]
transmembrane protein 132E [Source:HGNC Symbol;Acc:26991]
Mouse Orthologues:
Tmem132a, Tmem132b, Tmem132b, Tmem132c, Tmem132d, Tmem132e
Mouse Descriptions:
transmembrane protein 132A Gene [Source:MGI Symbol;Acc:MGI:2147810]
transmembrane protein 132B Gene [Source:MGI Symbol;Acc:MGI:3609245]
transmembrane protein 132B Gene [Source:MGI Symbol;Acc:MGI:3609245]
transmembrane protein 132C Gene [Source:MGI Symbol;Acc:MGI:2443061]
transmembrane protein 132D Gene [Source:MGI Symbol;Acc:MGI:3044963]
transmembrane protein 132E Gene [Source:MGI Symbol;Acc:MGI:2685490]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa39669 Nonsense Mutation detected in F1 DNA Not yet available
sa19551 Nonsense Available for shipment Available now
sa32736 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39669
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
ENSDART00000126296 Nonsense 229 971 4 11
Genomic Location (Zv9):
Chromosome 1 (position 45445176)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 44288395
GRCz11 1 44989698
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGAGAAGGCATCCGCATATGCCAGCAGGACACAGGGCCCGGCCTGAT[C/T]AAATTCAGCTTTACTACTCATCCTTTGGCATCCTGTCCATTAAAACCGGA
Long Flanking Sequence:
CCAGTAGAGATCGCTCATTTTTAAAGAAAACAGACCTTAAACGCGCCGATTTTGCGTTGGCACACAATTCACAGGAAACTATTAACCCAGGTTACTGGCAAATTAAAAGTCCTATTAGCATGCTTCAGCATATTCCCTATAGATGGGTCAGGACTGCAATATACTAGAATTCAAAGTTATAAACAAAGCTCTTATCTAACTCTTTAATTAAACAACACATACAAAATATTAATTGTGGTTAATCGTATTTAAAATATATATATTTGAATAATAATTATTTATTTGTTTGTGTGCTGTTTTCAATATCTTCTCAGCCACCGTTTGGGTTGTGTGTGGTTACTCTAACATTTCCAAACGACTGGTTTGAGCCCGCTCAGAACACAGAGGCGAACCTGGACCAGACTTTCAAGCAGCGTTACATAAGCAGAAACCGCTCTCGCTCCCGCAGCCGAAAGAGAAGGCATCCGCATATGCCAGCAGGACACAGGGCCCGGCCTGAT[C/T]AAATTCAGCTTTACTACTCATCCTTTGGCATCCTGTCCATTAAAACCGGACCCCCGCGGTGCGTGGAGGACACAGTAGAGCAGTCAGAGAGAAAGCTTCTCTACATTGGTCCTGTGGGACTTGAGGATCAAGAGATCAACAAAACCAAACAAAGCCCTGCATGTTTAGACACAAAGGCAGAAGAGAAGTTCTGGTTGGATTCCAATGTGTTAATCGTCTACAGCAAAGGGCCTGTGCCTGCCGGACAGCCAATCAGAGTGTCTGTAAACCTAAGGGGAAATTATAGTGAGGAGTCTCTGACCATTAGGTAACATTGTTGCTTGACATAAATTTGCTTATTTATTTTAATGTATCTTTAATATTATCATTATTTTACCTTCAGGCTGAAAGTGAAAAAAGGATTGCTATCTCTGGAGGTCCATCCCGTCACACATTCTGACCTGTGGATGGTTAATGTAGAACAGACGACAGGTTCAAAACACGATGTTGTTTCCATCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19551
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
ENSDART00000126296 Nonsense 748 971 11 11
Genomic Location (Zv9):
Chromosome 1 (position 45452132)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 44295351
GRCz11 1 44996654
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGTCCTCTTTGGCAGAATCTGTGGTTGCAGTAACGCCTGCTCCATCC[C/T]AACGCATTTTGGCACAAGGTGATGGCGGAGGACCTCTTGTTAAAGCCGAG
Long Flanking Sequence:
AACTAGTCTTCTGTTTGTTTGTGTATTGATGAGCTTGCTCTTTAAGTACTGGCCTGTCAGATTTCCTGATTTCCTCCCTAATCCTTTTCCTGCTTTTCAAGGTGGTTTCCAGTCAGTGGGATGGAGTGCTTGGAAGGGCTAACGTGATTGTAACCTCTGAACCTGTGACTCCCGCTGACCTCTCTGTTCAGCTGGTGGGAGGGCTTGGCCTGTCTGTTAATCCCAGCCCATCTCACCCTTCTGTTGTCACAGCAACAGTGAATGCTCACAATACACTCTACAACCACGGACAAGTAAGTTTCTGGTATTCAAGCTCCTAAAAATTCGTCCAGATTTGTAACTTATGATGTCCACCCTTTCATTAGGAGGCGTCTATCAGTGTCTGGATCCAGTTCAATGATGACTCTGCCATATTGATGTCTGCATTTAATGAGGTCCCCTATACTCTACGGCTGTCCTCTTTGGCAGAATCTGTGGTTGCAGTAACGCCTGCTCCATCC[C/T]AACGCATTTTGGCACAAGGTGATGGCGGAGGACCTCTTGTTAAAGCCGAGCTTCTGGTTTCCAGCTGTGACCCAGCATCTAACCATGTTGAACTGGAGGCAATTCATAAAGCAAGCGAAGCCAAAAGACTGGCTAAGGGGTCTGGCTGGATAAGGGTGAACCTAAACATGGACTTTTGGCCAATAGGGAGTGAGGAAACCAACTTTGAGATGCACGATGTGACTGATATGCTCGTCGATTCCAACAGTGATCTGTATGATGACTTTGAAGATCATGACAGTACAGTAAATGCCACAAGTGATTATGATAGTGGCAATGACATATTTAAACGAAAAAACGTGGAGCAGGCGGTGTTGATCCCCAACCATGAAGAGAACGCTGTCTATTTGTCTCCTGGTGTGGAAAAGGAGAGGAAAGAGGTTAAAACAGCTGATAGACAGGTAGAGATTGGCATTGGAGCTGTCCTGTCTCTGCTTTGTCTCTCATCCCTACTTTTCCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32736
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126296 Nonsense 946 971 11 11
Genomic Location (Zv9):
Chromosome 1 (position 45452726)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 44295945
GRCz11 1 44997248
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGACGAGAGGGAAATGTGAAAGACACTGTGGAGGAGGAACCTGGAGAA[G/T]AGCAAGAGGAGAATAGACAAGAGGAAAAACAGTGCAGAGCAGTGATAACA
Long Flanking Sequence:
TGGAGGCAATTCATAAAGCAAGCGAAGCCAAAAGACTGGCTAAGGGGTCTGGCTGGATAAGGGTGAACCTAAACATGGACTTTTGGCCAATAGGGAGTGAGGAAACCAACTTTGAGATGCACGATGTGACTGATATGCTCGTCGATTCCAACAGTGATCTGTATGATGACTTTGAAGATCATGACAGTACAGTAAATGCCACAAGTGATTATGATAGTGGCAATGACATATTTAAACGAAAAAACGTGGAGCAGGCGGTGTTGATCCCCAACCATGAAGAGAACGCTGTCTATTTGTCTCCTGGTGTGGAAAAGGAGAGGAAAGAGGTTAAAACAGCTGATAGACAGGTAGAGATTGGCATTGGAGCTGTCCTGTCTCTGCTTTGTCTCTCATCCCTACTTTTCCTGGTCAACTGCCTACCATGTGCACTAAGAGAACAAAGATATAGAGAAAGACGAGAGGGAAATGTGAAAGACACTGTGGAGGAGGAACCTGGAGAA[G/T]AGCAAGAGGAGAATAGACAAGAGGAAAAACAGTGCAGAGCAGTGATAACAGGGAATAATGACAAAATGGAAATTCAATGACCCTTTGACTTTACAAATATCTCATGTTGCACATTATCTTGTGCATATTCTGGAGAATGTTGCTACATCTTTATATGTCCATTGCAGTCACATAGGTGATTTTGTAATTGTGGGTACATTCGGCATTTCAAAACCCAATTTTTTATAGAGCAAATAAAACTCTTTATAAACAGCAATTCCTTACAGTATCTTATTGAAAGAAAATTACATTTTAATCATTTAGTGCTTACCAAACACAAATAATATATATACATATATATAATTATTAAGTATTTATTTTGGGAATAATATTGACATAAAATTGAACCAGATTTTGGTAAAAACCCAAACAATACAAAAATAAAACTATAAAAAAAAAAAAAAATAATAATAATAATAATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined