ZMP
si:dkeyp-14d3.1
Ensembl ID:
ZFIN ID:
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]
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]
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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.
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