Busch Lab

ZMP

si:dkeyp-14d3.1

Ensembl ID:
ENSDARG00000075277
ZFIN ID:
ZDB-GENE-081104-459
Description:
Novel protein similar to vertebrate transmembrane protein 132D (TMEM132D) [Source:UniProtKB/TrEMBL;A
Human Orthologues:
TMEM132C, TMEM132D
Human Descriptions:
transmembrane protein 132C [Source:HGNC Symbol;Acc:25436]
transmembrane protein 132D [Source:HGNC Symbol;Acc:29411]
Mouse Orthologues:
Tmem132c, Tmem132d
Mouse Descriptions:
transmembrane protein 132C Gene [Source:MGI Symbol;Acc:MGI:2443061]
transmembrane protein 132D Gene [Source:MGI Symbol;Acc:MGI:3044963]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa34449 Nonsense Mutation detected in F1 DNA Not yet available
sa21341 Nonsense Available for shipment Available now
sa307 Nonsense Confirmed mutation in F2 line Not yet available
sa2456 Nonsense F2 line generated Not yet available

Mutation Details

Allele Name:
sa34449
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111021 Nonsense 48 719 2 8
ENSDART00000143243 Nonsense 23 296 1 1
ENSDART00000144520 None None 665 None 5
Genomic Location (Zv9):
Chromosome 8 (position 36691827)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 35627663
GRCz11 8 35357011
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGAATCTTCAACGCTACGCTTCCCCTACTTACCTACCCGTTAACTA[T/A]CAACTCCTCAACACAGAATCCTCTTTCTTCCTTAAGGAGGCCACCCAGGA
Long Flanking Sequence:
CTTTGGGTGTATGGCCACAAACAGTAAATGCACTATATAATACACATTACATTGCAATCATTTAGCAGATTATAAATTAAGTCAAGATTACAGCATATGTATTGTACCGGCATACAAATGCTTTTAATGTAGAGTTAATGCTTAAACAAGAAACTATTTGCTAAGGCTTAATAAATGATTCATATAGTGCAATTGTTATTAAATGTTACCAAAGTCATTGTTAAAAGTGTGAATTGTTTCTTAAAATAAAGTGTGACCCAACATTTTAATGTCACCTATATGTCATACCTGAAAATAAATATTAGCATTTTGGTATCAGTCAATGCATACTGCGCATACTGATGCATCTGTGCATCTTTCTTCTTTAAATACACCCACCTACATACATGCAACTATCTCAGCTGGATCTGACACCTTTTTTTTTCTCTGTCAGTTACAGACTGTCGAATCCTGGAGAATCTTCAACGCTACGCTTCCCCTACTTACCTACCCGTTAACTA[T/A]CAACTCCTCAACACAGAATCCTCTTTCTTCCTTAAGGAGGCCACCCAGGACTTCATGCGCAACTCTAGTTTCCTTTCCAGAACGGAACTGTTCTTCATCCAGCAGGCAAGGAAGCCTCCTATCATCAATGCCACCTATGGGACCCTCGCTGTGGAAGAGCCTGTACCTTTGGACCTCCTCCAGATGCCCGGTTCCTTTGTGGCATCCACAGAACTCTTCACCTTCAATTGGAAAGTTCAGACCTTTGTTCTTAACGAAAGGATTTTCCTAAACAAACCTAAAGTTCAGGTCTTGTTCTACATTTCTGGAAGAGATTGGGATGACTACAGTGCAGTGGACAAACTCCCCTGCGTACGGATGTTTGCTTTTCATGAAACCCAAGAGGTCCACGGGAGCTGCAGGTTGCGAGGTGACATGGGCGTTTGCGTTGCTGAGCTCGAACCTCTTCCTGGGTGGTTTGCACCTCCTAGCGTCGTTCCTGGTCGACAGAGAAATCCGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21341
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111021 Nonsense 349 719 3 8
ENSDART00000143243 None None 296 None 1
ENSDART00000144520 None None 665 None 5
Genomic Location (Zv9):
Chromosome 8 (position 36811927)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 35747763
GRCz11 8 35477111
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGTGCTCGACCCTGTAACCCCACGCTCTGGATGGTTAGTCAAGACGTC[A/T]GAACAGAAGGACATAGGATTGTGACGCTGCATTGTCGTCGTAAAGAGTCC
Long Flanking Sequence:
TTTTGTGCTGACAGTCTATGTAGTTGATGTTTGCGCTTCAGAAAACCTATAAGGTATAGGTGCTTTGTCAGTTACAGATTTGAAAAGCAAAAAAGGCCGGAAAAAAGAACACGAACCTCACTTTGTATAAAGGACCATTTCAGTATAAAAAGTGTTCTTCAGGACAACTCAATTCTAAACAGAGCTATTGCCATGTAAAGAGTACAGTTAAAAAACTTTTTTAGAGTTTAGGTAGCATAACATTATTTAAAATGATTTGTTTCAGCTATTTTCAATTGAAGTGCAACTCATAATTTCAAAAACACAATTAAATGCTAAGGAGTGTCAAAAAATGCTTAAAGAAATGAATGATTTGTGGGGTTGTGATGTATTTACTGCAGTGCATTGATTTTTTTTCTCTCTCTCTTTCTATATACTGCAGAGTGAAGTTAAAAGATGGAGTGGCGTTTCTTGGTGCTCGACCCTGTAACCCCACGCTCTGGATGGTTAGTCAAGACGTC[A/T]GAACAGAAGGACATAGGATTGTGACGCTGCATTGTCGTCGTAAAGAGTCCAGCTACGGACAGAGGTCAGTTACCATGAACTAACTCAGCTTCAGCGTTGTATTGCAATGTGGCTTCATGGATAATTTACCAAATATAGGCTACTGCATGGTCTGTAAAATATTTGAGTGTTTTGTATGCTGTTGTTGGTGTCAGGTTTGTTGACGAGCATCTACACTTGGTCTTTGGAAACGAATTTTAAATTTTGTCAAAGGTCAATGTTTGAGTCAAAACGAGGATCTTCAATGGTTTGTAAGACATTTCTACATACTGTAAATCTCTCATTCAGTGTAATGCTGGGACTGACCACATAGAGTCAAGAGTCATTTGTACAGTTGATACTCAAGTTCAATTGAGTTCAAATTATGTTTATTTGTGCACTTTTCACAGTAGTTATCATTTCAAAGCAGCTTTATAAATGTGCACAAAATTACATTGCAATCACAATTAGACAGAGTTAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa307
Status:
Confirmed mutation in F2 line
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
ENSDART00000111021 Nonsense 682 719 8 8
ENSDART00000143243 None None 296 None 1
ENSDART00000144520 Nonsense 250 665 4 5
Genomic Location (Zv9):
Chromosome 8 (position 37072514)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 36008350
GRCz11 8 35737698
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCACTGAACTGGGCCTGCAGTTGGTCAGTGGTCTCACACTCAACCTT[C/T]AGCTCAGTACAGGAAGCAACCGAGCCATCAGTGCCACAGCAACCACACAG
Long Flanking Sequence:
TTCATTCTCCGTGAAAGTAGGCTGATATTGCCAGAAACATGTGTCTGCGGAGGTGTTAGTCATCTGGATTTATTTTGTTTTTACTGTCTGCTTTGAGACCAGATACCTAATATGTGCTCGTCTGCAGTGAAAGTGTGGGCAGGCAGGAGACTGTCTGTAACACCTTTTTATTGCATCAATCACTAGATGGGTTTACAGCTCAGTGTTTTTGATATTTCAGTCTGTAATTGCAGGTCGTCCCTGTGGGCAGAACTGTATCCAACAAGCCAGATTGCTTATGATGTTTGTATTTAATAATGCATCTTTTTTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGCTCTACTTCAGGTTCTGTCCCCGCTGTCAGACTCCATCCTGGCGGAGAAGACAGTGGGGGTTGTGGATGATCGAGTGACCATCACTGAACTGGGCCTGCAGTTGGTCAGTGGTCTCACACTCAACCTT[C/T]AGCTCAGTACAGGAAGCAACCGAGCCATCAGTGCCACAGCAACCACACAGGAAGTGCTCAGCAATCCTAAACAGGTACTTTCAGAGTTCATGAGAGGACATTTTCCAATACACTGATAACTCGCAAATATTAGCGTAATGAAATAATTTGTGGTCTTGGTTTACATGGAAACAAATAACCTGGCAATGCAAGTAAACTGAATATACAAGACCTCAGAAAGAAATCTGTTTGTTTCCCGGTAGTGAATTCACTTAATAATTAGCATATCTAACTATGAGTATTGGAAGTTGTGTTCTATTCTTTGTACCTCGCCTAAATTATCTAAGATGATTTGGCAGATCCTGGATCTTTTAATTGTAATAACTGATTTCTGGCTATTTTAGTTCTTTAAACAAGTTCAGATTGAAGCCAGATTAAAATATCTGAATGAATGATCTGATATTACTGCATGTGCTCATGTTTGTTGTGAAGGACAGATCTTTCCAACCTCATCATCATCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa2456
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000111021 None None 719 None 8
ENSDART00000143243 None None 296 None 1
ENSDART00000144520 Nonsense 516 665 5 5
Genomic Location (Zv9):
Chromosome 8 (position 37094570)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 36030406
GRCz11 8 35759754
KASP Assay ID:
554-3281.1 (used for ordering genotyping assays)
KASP Sequence:
TTCTGGTCTTCCTCATCAACTGYATCTCGTACACCCTAAAGTACCGGCAC[A/T]AGGAGATGTCGATCGAGGGCCAGGAGAGCATGAATCACGCACACGATTGG
Long Flanking Sequence:
TTAAGCGCCGAAGCGTCTTGGCGGCTGGAAACTGCAATATTCGTGTAAAGTTTGGTCGCAGTGAAAGCGCCTTGAGGCCCGGAGACTACGGCCAAGATGGAGAAGACATTGACAACAGACCAGGAGACCGCAGACAGAACCCATCTCTCCCTGACAGGACTGGAATGGACAACCACTACTACGGAAGCTCCATCTCAGACATGGAGGATGGTATCATGAGACGAATCACTACCACCACCAAAACTGCAATCATAAGAAGACCCGGTGGAGACAAGCTCTCAGACGATGGAAGCCAGTTGCCTGGCATTCCCATCGACTTCTCAGACTTTCCCGCTCAAGTGGACCTTCCCCGAGGAAATAATGTGGATGAGGATGACCTTCAAATACCTCACGGACTTACTGACCTTGAAATTGGGATGTACGCTTTGTTAGGAGTCTTCTGCTTGGCCATTCTGGTCTTCCTCATCAACTGCATCTCGTACACCCTAAAGTACCGGCAC[A/T]AGGAGATGTCGATCGAGGGCCAGGAGAGCATGAATCACGCACACGATTGGGTGTGGCTTGGAAATGATTCCGAACTGTTGGAGAGCCACGTGAGCCTGTCTCCACAGACTGATGAGCACATCACCATTATGGACTCCAGCTTAGGAGGCTTAGAAGAAGGGAGCCACCTTCTTAATGGCGGGTCTTTGCAGAAAAACGTTCAAGGTCAGGTGCACCGAGGAGCTGACACTGCGACAGTCTGCACCGGGAAGGACAGCAAAGGTGATTCGCCAACCACCAAAAGAAAACGAGTCAAGTTTACCACTTTCACCACCATTCCAGTAGAAAGCATCAGTCCGACTAAGGAAAAGCTGGGAGTTGATCCTGACGATGACATTAAGTGGGTATGTCAGGACGTTGAGCTTGGTGACTCCAAGGAACTACGAAATTACATGGAGCGACTAAATGACAGTGCTTTAAAGGACGTGGCGTAGTCGAATCAGTGTGTGCAGACTGAACTC
Associated Phenotype:
Not determined