Busch Lab

ZMP

tmem195

Ensembl ID:
ENSDARG00000025595
ZFIN ID:
ZDB-GENE-040426-2207
Description:
Alkylglycerol monooxygenase [Source:UniProtKB/Swiss-Prot;Acc:Q6NYE4]
Human Orthologue:
TMEM195
Human Description:
transmembrane protein 195 [Source:HGNC Symbol;Acc:33784]
Mouse Orthologue:
Tmem195
Mouse Description:
transmembrane protein 195 Gene [Source:MGI Symbol;Acc:MGI:2442495]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa22691 Nonsense Available for shipment Available now
sa35954 Nonsense Mutation detected in F1 DNA Not yet available
sa44828 Nonsense Mutation detected in F1 DNA Not yet available
sa35953 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa22691
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000034746 Nonsense 58 446 2 13
ENSDART00000139934 Nonsense 42 330 2 10
ENSDART00000147582 Nonsense 70 458 2 13
Genomic Location (Zv9):
Chromosome 15 (position 33700782)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 34546558
GRCz11 15 34404527
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCACGCCATATTTCATTGGCTTGATATTATTGGAGATTGTGTTGGGCTG[G/A]TTAAAGACAGATGGCCCTCACATTAAGATCAACGACTTCATTACGTCTTT
Long Flanking Sequence:
TATGCATATGTCAGTGTACTTCTCAGTCCTACAATATTACCGGGACATTCATTCATTTTCTTCCATTACATAAATAAAAGATCAGCTGATCGCTATTAAAATTCTGGTAAACATCTACAGTATGCGTGCTTGTATACCTTGCATTGCTAGGAATTTATCCCATGACTTTGCTACAGAACCAATGCATATCCTTATGCAAACAAAGAATCACTTCATTTGCTGACAGACGCTTAGTATATTAGATTTTTATGCTTAGTTTGACATGCATTGTAGGGCTCTTACAGAAGGTCATGTGTAAAACTTATAAAGCTTAATGTTTTATAATGTAATGCTTCACTTTCTGTCTGATATACTAAAGTGTACAGTTTTACCATAATGTTTATTTAAATTACTGTAATTGTGTTATGTTGGTGTTTACTCACTGCTGAATTCATGTTTTTTGTGCTGTAGGCCACGCCATATTTCATTGGCTTGATATTATTGGAGATTGTGTTGGGCTG[G/A]TTAAAGACAGATGGCCCTCACATTAAGATCAACGACTTCATTACGTCTTTGTCCGCAGGGATGATGTCCCGTCTGCCTCAGTGAGTTCACAACAACTTCCCAATCTCATACAAAATCGAATTATTAAAATTGTTGGAAAATCCCGGAGTAGTATTTTTTTTAATAATATGTTAATAGTAATTTATAATTTGAAAGTTGTTAATATTATCAAAATTGTATTTTGTTATTTATTTATTTTTATGTGTCTGTGTGTATTTTATGTTGACTATTTTCAGGACAAAAAGGTTTATATAATTTTAATATAGCCAGTGTTGCTAAGTAAAGTTAAATAAAAATGTAATTCAATTATAAAATAAAATTGAAATAGTTAAATAAAAGTAAAGTTGAATAAAAAATAAGTAAAAAAAAGTACAATTAAATCAAATTAAACATATTTAAATAAAATAAAGGTAACTAAAATAAAGTTAAATACAAATAGTTAAATAAACATAGTTAAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35954
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
ENSDART00000034746 Nonsense 165 446 4 13
ENSDART00000139934 Nonsense 149 330 4 10
ENSDART00000147582 Nonsense 177 458 4 13
Genomic Location (Zv9):
Chromosome 15 (position 33671663)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 34517439
GRCz11 15 34375408
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTTCTGAATACTACAATCTGTCGACAGCTCTGCGCCAGTCTGTCACA[C/T]AGCAGTTTTCCTCATGGGTATGAAGCACCTGCGTCTGTCTCATTCATTTA
Long Flanking Sequence:
TCTCTCCATCTAAATCTGAGGTGCAGTAAATGTTTTATGAACTTAAGGAAATGTTTTGAAGAACATGTAATATCCAAAGAAAAGTACCTCAGCCATTTAGACACTGATGAGTGCTATTAGACTGACTGAGGCACACCGGCCTAAACATTTAACCTTTTAATGTCCATTTCAATTAGTTTCATAGTTAAGTGCATAATTAATTAATGCACTAATCCAACTCATTGCAATCTTGTCTCTTATTCAGTCAGTATAGGGGTTACAAACGTGAAATAAAGTAAGTAAAATAGTAAATAAAATAGATTAATATGTCCAGAAAGAGCAATAGATGAAACCAGGTCCAGCACAGGTCAAATGGTAGAGCATTTGTAAATGTCAAAAACGGAATAAAATCTCACATTCATCTTGTGGTTTCAGAGTTAAACATCCTCTGGGCGGGCCATCAGGTTCATCACAGTTCTGAATACTACAATCTGTCGACAGCTCTGCGCCAGTCTGTCACA[C/T]AGCAGTTTTCCTCATGGGTATGAAGCACCTGCGTCTGTCTCATTCATTTATGATCATTTTTGCCATGAAACATGGTTGATCAAATAACAGTTGTTAGTTAATGAGCTCAAGCTGGTAGCTAATGATGTGTTATGACGTGATAATATTCGATGTGTTTTATCAGATATTTTACTCTCCGTTGGCGCTGCTGATTCCTCCTTCAGTGTTTGCGGTACATATACAGTTCAACCTGCTGTACCAGTTCTGGATTCATACTGAGGTATTGTGGGATTTGTTATTATTAATGGTTATAAAATTTTTGGGGTAAAAAAATACTGTCAAGGCTTACAGGATTAATGAAATGATCTTTAAAGGGGTCTTAATGTAAAATGTTTATTCTTCAATAACAGATTTACTGCTCATATTTGAACAGCTTGTTATGAATTTTACAAAAAGATGACATATAGGACTTTATAGGTTTTCTATAAATTTATATAAACTTTTTTTATGTGAAGGACTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44828
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
ENSDART00000034746 Nonsense 190 446 5 13
ENSDART00000139934 Nonsense 174 330 5 10
ENSDART00000147582 Nonsense 202 458 5 13
Genomic Location (Zv9):
Chromosome 15 (position 33671442)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 34517218
GRCz11 15 34375187
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCTCCGTTGGCGCTGCTGATTCCTCCTTCAGTGTTTGCGGTACATATA[C/T]AGTTCAACCTGCTGTACCAGTTCTGGATTCATACTGAGGTATTGTGGGAT
Long Flanking Sequence:
TTGCAATCTTGTCTCTTATTCAGTCAGTATAGGGGTTACAAACGTGAAATAAAGTAAGTAAAATAGTAAATAAAATAGATTAATATGTCCAGAAAGAGCAATAGATGAAACCAGGTCCAGCACAGGTCAAATGGTAGAGCATTTGTAAATGTCAAAAACGGAATAAAATCTCACATTCATCTTGTGGTTTCAGAGTTAAACATCCTCTGGGCGGGCCATCAGGTTCATCACAGTTCTGAATACTACAATCTGTCGACAGCTCTGCGCCAGTCTGTCACACAGCAGTTTTCCTCATGGGTATGAAGCACCTGCGTCTGTCTCATTCATTTATGATCATTTTTGCCATGAAACATGGTTGATCAAATAACAGTTGTTAGTTAATGAGCTCAAGCTGGTAGCTAATGATGTGTTATGACGTGATAATATTCGATGTGTTTTATCAGATATTTTACTCTCCGTTGGCGCTGCTGATTCCTCCTTCAGTGTTTGCGGTACATATA[C/T]AGTTCAACCTGCTGTACCAGTTCTGGATTCATACTGAGGTATTGTGGGATTTGTTATTATTAATGGTTATAAAATTTTTGGGGTAAAAAAATACTGTCAAGGCTTACAGGATTAATGAAATGATCTTTAAAGGGGTCTTAATGTAAAATGTTTATTCTTCAATAACAGATTTACTGCTCATATTTGAACAGCTTGTTATGAATTTTACAAAAAGATGACATATAGGACTTTATAGGTTTTCTATAAATTTATATAAACTTTTTTTATGTGAAGGACTCTTAAGGGAAAAGAATTGGGATGTTTATACTTCCAAGAGCCACTTCAAGCTGCACTCTGAAAAGCAATAAGTTGACTTTGCTTGAGTGGGTAAACTGATGTCTTACATTTCTTTTACAAAGTATACTCTAACTTAGCCAGATGTATGTTCACTACCTGACAAAGTCTTGTTGTCAATCTCCGTTGTAAGAGCAGCAAATAATAACTTGTCTTGACTTCTAGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35953
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000034746 Essential Splice Site 225 446 6 13
ENSDART00000139934 Essential Splice Site 209 330 6 10
ENSDART00000147582 Essential Splice Site 237 458 6 13
Genomic Location (Zv9):
Chromosome 15 (position 33664410)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 34510186
GRCz11 15 34368155
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTGGAGTTGATCCTAAATACTCCAAGCCACCACAGAGTTCACCACGG[T/C]AAGCATCATTACCCTTTGAAAGTAGATTTGCATTGGTGTGTGTTATCTTT
Long Flanking Sequence:
CAGCAGTGTTTAGGAGCGTGCTCAACAGTGCTCAAATGTTAATGGGAAATGGATGTTTTTAAAATGTCAGCACCAATTGTCAATTTTAATACTTGCATTTATTTAAAGACAGTCACAATTTGTTCAGAAGCCATTGTTTAAAAAAAAAGCTACAGCTCTAGTAAAAGCTATTAGTAAAAGTTCATTGCTTAAAAATGTTTACTTTTAATAAACTGGAGCAACTGATTCAGTGTAAGGTTGGAAAGGAATAATGTACTGTACGTGTTTCTGCATGCTCCTCACGTAATCATATGACCAGAAGACATGAAATACAATGTACTGTGTATGTCACATGTACCAGTTTTATGATATTTTATGGTGTTTTGCATTCTGATTTGTAACTTTTAGAAGAATATTATCTTTAACCTTGGAAAAAAATGTTTCTATCAATAGCTGGTCAAAGATCTTGGACCTCTGGAGTTGATCCTAAATACTCCAAGCCACCACAGAGTTCACCACGG[T/C]AAGCATCATTACCCTTTGAAAGTAGATTTGCATTGGTGTGTGTTATCTTTGTGGGTAAAAAGTGAAGAATATTTTGTTTGATTATTTGTCAGTAAGATTTTCTTATCATGTGACATGACTAACACTGTCTATACCCTTATATACTGTAAATAGAGTAATGCTGTAATAATGGCTATCTTTGCAGTAAATTGTTAATATTTGACCATGCACTCACAGGGCGAAATCCATATTGCATTGACAAGAATTATGCAGGAATTCTAATCATATGGGACAGGATGTTTGGTAAGTTTCTGTGTGCTTTTTGCAAAAAAGTGATTTGAAAATAAGCCTTTTCAATGGATTCAGGGCAGCACATTAATCTCTTTCATGTTTTTGTTTTACTGTTTGTTGCATAAAAAAATAAGCCCAAAGTTTAAAGTAGTCGTGTTGTTTATAACTTACTGTAAAACACAAAATGCTGCAGAACAAATAATCTGAAATGCACTTTTATGTTAATTGTA
Associated Phenotype:
Not determined