ZMP
tmem67
Ensembl ID:
ZFIN ID:
Human Orthologue:
TMEM67
Human Description:
transmembrane protein 67 [Source:HGNC Symbol;Acc:28396]
Mouse Orthologue:
Tmem67
Mouse Description:
transmembrane protein 67 Gene [Source:MGI Symbol;Acc:MGI:1923928]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42734 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14889 | Nonsense | Available for shipment | Available now |
sa32094 | Nonsense | Available for shipment | Available now |
sa22858 | Nonsense | Available for shipment | Available now |
sa14183 | Nonsense | Available for shipment | Available now |
sa22859 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42734
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111245 | Essential Splice Site | 321 | 991 | 10 | 29 |
ENSDART00000140460 | Essential Splice Site | 314 | 982 | 9 | 28 |
The following transcripts of ENSDARG00000076752 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 29798008)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27635146 |
GRCz11 | 16 | 27569769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGAATGAACCCCTTCCTGTTGGATTCAGCTTTAAAGGGGCACAAAAGG[T/G]AAACACTGGACATTTAAACGTAAACATCAATGTAGTATTTTTTCACCAAT
Long Flanking Sequence:
TTCCTATTGACTATACTTCATCCTAAGAGTAAAATCTTCTTCATTCTGCACTTAAAATGTCCAGATAACTGATAATCTTTGGATTTGATAATCTTTTTTTCTTTCAATCCTATCAACTATTTTAAAAGAGATTTAAACCTGGAGACTGAACTTTAAAAAAACATATTACAGCAATCCTTGATTCTTTAAGGTGATTGTTTGTCTGGATAGTAAAATGATCATTAACCATAGGCATGGCAATTTTTGCCAATGTGGTCTGATTTAAATCCTTGTTGTTCGTACATTTTTCTACTTTCTGCATCCCTATATTCCCTAAATTCTACTTTTGCCCCATTGGTCCATAAAACATGGCAAATTAACCTGCTTTGCTTGACAATGTTGTTATTCTAGGAGGACAAACCTACCTTGGCTGTACTATGGAGATCAACCAGGGATGGCATCACAGGCTCTTCAGAATGAACCCCTTCCTGTTGGATTCAGCTTTAAAGGGGCACAAAAGG[T/G]AAACACTGGACATTTAAACGTAAACATCAATGTAGTATTTTTTCACCAATCGTTCTGCTGCTTTCAGAACACCAACATTGAGTTGCGAGCTGCTGTGTACTCAGTGCGTGGAGAGTTTCTGAGATGGGAAAGCGTTGGTAGAGGCAACCTTCAGGTAGGCAAGCAGGACTGGTTTCTCTTCTGGGGTAAAATCCATGAAACATTCTGAACTGCTGTTTTCTTGATAAGATTATTAAATGATATATACATTTACAATGTTTGTTGTTAATTTTAAGGTGAATAATTAATTTGTGCATGTAAATCCACAAAAAACTGGTTGTTTTGGTCGTCTTTAATGAAAGTCTTGATCATTTTTTTTCTGCTTTTGGAGTGACAGTCCAACCTGAGGGCTTCCATAGCAACCGCATATTAATACTCTTTCTTACGATTAGCTTGCTATGAGGTAGTGATATGCAACATGAAAGAAAGTACATCAACATACTGAAATAAGTCTCAGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14889
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111245 | Nonsense | 328 | 991 | 11 | 29 |
ENSDART00000140460 | Nonsense | 321 | 982 | 10 | 28 |
The following transcripts of ENSDARG00000076752 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 29798094)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27635232 |
GRCz11 | 16 | 27569855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTTWTTCACCAAYCGTTCTGCTGCTTTCAGAACACCAACATTGAGTTG[C/T]GAGCTGCTGTGTACTCAGTGCGTGGRGARTTTCTGAGATGGGAAAGYGTT
Long Flanking Sequence:
GATAATCTTTTTTTCTTTCAATCCTATCAACTATTTTAAAAGAGATTTAAACCTGGAGACTGAACTTTAAAAAAACATATTACAGCAATCCTTGATTCTTTAAGGTGATTGTTTGTCTGGATAGTAAAATGATCATTAACCATAGGCATGGCAATTTTTGCCAATGTGGTCTGATTTAAATCCTTGTTGTTCGTACATTTTTCTACTTTCTGCATCCCTATATTCCCTAAATTCTACTTTTGCCCCATTGGTCCATAAAACATGGCAAATTAACCTGCTTTGCTTGACAATGTTGTTATTCTAGGAGGACAAACCTACCTTGGCTGTACTATGGAGATCAACCAGGGATGGCATCACAGGCTCTTCAGAATGAACCCCTTCCTGTTGGATTCAGCTTTAAAGGGGCACAAAAGGTAAACACTGGACATTTAAACGTAAACATCAATGTAGTATTTTTTCACCAATCGTTCTGCTGCTTTCAGAACACCAACATTGAGTTG[C/T]GAGCTGCTGTGTACTCAGTGCGTGGAGAGTTTCTGAGATGGGAAAGCGTTGGTAGAGGCAACCTTCAGGTAGGCAAGCAGGACTGGTTTCTCTTCTGGGGTAAAATCCATGAAACATTCTGAACTGCTGTTTTCTTGATAAGATTATTAAATGATATATACATTTACAATGTTTGTTGTTAATTTTAAGGTGAATAATTAATTTGTGCATGTAAATCCACAAAAAACTGGTTGTTTTGGTCGTCTTTAATGAAAGTCTTGATCATTTTTTTTCTGCTTTTGGAGTGACAGTCCAACCTGAGGGCTTCCATAGCAACCGCATATTAATACTCTTTCTTACGATTAGCTTGCTATGAGGTAGTGATATGCAACATGAAAGAAAGTACATCAACATACTGAAATAAGTCTCAGATAGTTCTGATACTTTCCAATATGTTACTTTATACAAGTTTCATGTCTCACCAGAATGTTTCATTGATGTTTTAGCTTAAAATACATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32094
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111245 | Nonsense | 352 | 991 | 12 | 29 |
ENSDART00000140460 | Nonsense | 345 | 982 | 11 | 28 |
The following transcripts of ENSDARG00000076752 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 29798889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27636027 |
GRCz11 | 16 | 27570650 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTGTGTTTTAAAGTCTTGTCTTTAATTTATGTATCTTCTAAAGCTCTG[T/A]CCAGACACCCCTACCAGACAACAGTCTGCCTTCAAATTCGGGACAGCCTA
Long Flanking Sequence:
ACCTGAGGGCTTCCATAGCAACCGCATATTAATACTCTTTCTTACGATTAGCTTGCTATGAGGTAGTGATATGCAACATGAAAGAAAGTACATCAACATACTGAAATAAGTCTCAGATAGTTCTGATACTTTCCAATATGTTACTTTATACAAGTTTCATGTCTCACCAGAATGTTTCATTGATGTTTTAGCTTAAAATACATAATGTATAAAGAATTAATATCATTTAACATACTAATCTGATAAAAATATCAAAAACCGACATCAAGCTTATTTTTAAGTTTCTATGTGTCTCTTTAAATGCAAATTAGCTGCTGCTCTTTCCAGAAAGTGAAGCATTTTCAACCCATCTCTTGATCCTCTCACAACAAAATGTCTAAATGTCTGTTGCAATATCAAATGTGCTTATGTGACATTGAAGCTCTTCAATCAGAAGAAAGTTTATTATTTGCTTGTGTTTTAAAGTCTTGTCTTTAATTTATGTATCTTCTAAAGCTCTG[T/A]CCAGACACCCCTACCAGACAACAGTCTGCCTTCAAATTCGGGACAGCCTACAAGCAGAGTGTAAGTCTCATTTATCTTCTGCCTCAACCAGATGGTATTTAGCTATTTGTTTTGTATGTAAATATGTAAATGTGTATTTAATGGCATTTTTCTTTCCACAGTGTGTGCTATCTGTGTCAGAGCTCTTAACTGGTTATCCAGAGCCTTTGTTCTATGATGTGTTCCTGGTCATTCAGAATTCCCAAGACAATCGTCTTCTTGCGGTGCCTCTCCTAAATGCCAATCAGCAGTTTAACGGCCAGTTTGTCAATCAGGGTATAATATCCAATTATATATTTGATCATCAGATGTTAAGGCATTGCTATTTTATTATAGTGTTAACTCCTCATTTATTAGGATCTGACATGAGTAAATGGTTCCTGACCCGAAGGCTGATGCTTGTCGACACATTGAGTGGAAGAGAGAAGTCTATAAGTTCTTCACCCGTAGTTATACGAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22858
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111245 | Nonsense | 390 | 991 | 13 | 29 |
ENSDART00000140460 | Nonsense | 383 | 982 | 12 | 28 |
The following transcripts of ENSDARG00000076752 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 29799104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27636242 |
GRCz11 | 16 | 27570865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTATCTGTGTCAGAGCTCTTAACTGGTTATCCAGAGCCTTTGTTCTA[T/A]GATGTGTTCCTGGTCATTCAGAATTCCCAAGACAATCGTCTTCTTGCGGT
Long Flanking Sequence:
ATTAATATCATTTAACATACTAATCTGATAAAAATATCAAAAACCGACATCAAGCTTATTTTTAAGTTTCTATGTGTCTCTTTAAATGCAAATTAGCTGCTGCTCTTTCCAGAAAGTGAAGCATTTTCAACCCATCTCTTGATCCTCTCACAACAAAATGTCTAAATGTCTGTTGCAATATCAAATGTGCTTATGTGACATTGAAGCTCTTCAATCAGAAGAAAGTTTATTATTTGCTTGTGTTTTAAAGTCTTGTCTTTAATTTATGTATCTTCTAAAGCTCTGTCCAGACACCCCTACCAGACAACAGTCTGCCTTCAAATTCGGGACAGCCTACAAGCAGAGTGTAAGTCTCATTTATCTTCTGCCTCAACCAGATGGTATTTAGCTATTTGTTTTGTATGTAAATATGTAAATGTGTATTTAATGGCATTTTTCTTTCCACAGTGTGTGCTATCTGTGTCAGAGCTCTTAACTGGTTATCCAGAGCCTTTGTTCTA[T/A]GATGTGTTCCTGGTCATTCAGAATTCCCAAGACAATCGTCTTCTTGCGGTGCCTCTCCTAAATGCCAATCAGCAGTTTAACGGCCAGTTTGTCAATCAGGGTATAATATCCAATTATATATTTGATCATCAGATGTTAAGGCATTGCTATTTTATTATAGTGTTAACTCCTCATTTATTAGGATCTGACATGAGTAAATGGTTCCTGACCCGAAGGCTGATGCTTGTCGACACATTGAGTGGAAGAGAGAAGTCTATAAGTTCTTCACCCGTAGTTATACGAGTGGCTTCTGACATTAAGATCGGGTAGGAATTACACACTGCAAACACATTAAATAGATATAGTATTGAGTATGACTTCATTGCACAGTGTTTCATTGAACAGGTTTCAGCTGGTACCAAATACACAGAAGGGACAGGTTTACCCTCCACTGATGAGTGTGGCCTACTCGGATATACAGATCAAAGACCCCAGCACACAGACTGTTACTGTAAGTCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14183
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111245 | Nonsense | 486 | 991 | 15 | 29 |
ENSDART00000140460 | Nonsense | 479 | 982 | 14 | 28 |
The following transcripts of ENSDARG00000076752 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 29799552)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27636690 |
GRCz11 | 16 | 27571313 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAATACACAGAAGGGACAGGTTTACCCTCCACTGATGAGTGTGGCCTA[C/A]TCGGATATACAGATCAAAGACCCCAGCACACAGACTGTTACTGTAAGTCC
Long Flanking Sequence:
GTGTGCTATCTGTGTCAGAGCTCTTAACTGGTTATCCAGAGCCTTTGTTCTATGATGTGTTCCTGGTCATTCAGAATTCCCAAGACAATCGTCTTCTTGCGGTGCCTCTCCTAAATGCCAATCAGCAGTTTAACGGCCAGTTTGTCAATCAGGGTATAATATCCAATTATATATTTGATCATCAGATGTTAAGGCATTGCTATTTTATTATAGTGTTAACTCCTCATTTATTAGGATCTGACATGAGTAAATGGTTCCTGACCCGAAGGCTGATGCTTGTCGACACATTGAGTGGAAGAGAGAAGTCTATAAGTTCTTCACCCGTAGTTATACGAGTGGCTTCTGACATTAAGATCGGGTAGGAATTACACACTGCAAACACATTAAATAGATATAGTATTGAGTATGACTTCATTGCACAGTGTTTCATTGAACAGGTTTCAGCTGGTACCAAATACACAGAAGGGACAGGTTTACCCTCCACTGATGAGTGTGGCCTA[C/A]TCGGATATACAGATCAAAGACCCCAGCACACAGACTGTTACTGTAAGTCCACAATGGTTTCTCTGATTGGCATGCAAAACAACCAATCACGGTTTGTTTATGTGCGTAAATGTCAACATCCCTACAGTAACAGACAGACGGGATTGTTTTTGTTTATGCCAAGTGCTTAAGGAAAACTTTTGCACATATTCTAAAGAGTTTATGACTTCTAGTTGATTATTTGGTAAAGTGACAGTTATTTAAGATGAATCATCTGTTGAACTGCATCACAATCATAACAAATACTGTAGAAGACCTATTGGAACCCACATGGACCAAAAAATCTCACAGAAATCAGTTAAGCTGGTTGAAGAAAAAAATCATGGTTTGGGGTTACAGTCAGTATAGGAGTGTGCGAGAGATCTGCAGAGTGAGTGGCAACATCAATAACCTGGGGTATCAAGACATTTGTGCTGCCCATTAAATTACAAACCACAGGAGAGAGCGAATTCTTCAGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22859
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111245 | Nonsense | 779 | 991 | 24 | 29 |
ENSDART00000140460 | Nonsense | 770 | 982 | 23 | 28 |
The following transcripts of ENSDARG00000076752 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 29806766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27643904 |
GRCz11 | 16 | 27578527 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATTTATATGTGTGTGTCATTTAGATCTCAGTTCTGCTGCTGTCTCAT[C/T]GATGTTTTGGCTACTACATTCATGGGCGCTCTGTTCATGGTCATGCTGAT
Long Flanking Sequence:
TATTAAAGGGAACCTATACAATTGTTAGTTTAATTAACAGTACATATTGTTTTTTTTTTCAGGTTGTAGGCTTCTCAAATTTGGCTCTAAGAGATCCTTCGTCTAACCTGAATCGATCTGCTGAGGAATACACGCCTCCATACAGCCTCATACTCCGCTATGGTGTAGCTACTGCTATGTGGCTCTGCATTGGCTTAATACAGGTACATACGAAAATAGACAAGAGGCATACTAATTGTGTCACCAATTAGATTCCACATGCTCTTCTTTGTGTGATTGTGCTTCAGATGATATTCTTCACAGTGTTCCATGAACGGTTTGTTGAAGACAAGATTCGTCAGTTTGTGGATTTGTGCTCAATCAGTAATGTAAGTATCCGGCTGGAAATCTTGATGATAAATGTAGTTATAAACCACATCTTACATCATGGTTTAATGTTGTTTGTGTTTCTTTATTTATATGTGTGTGTCATTTAGATCTCAGTTCTGCTGCTGTCTCAT[C/T]GATGTTTTGGCTACTACATTCATGGGCGCTCTGTTCATGGTCATGCTGATACTAACATGGATGAGATGAACACTAACCTTAAGAGGGAGGCGGTAAGATTTTGAGGCTTACTGTTTATAGTAGTTTTGAAATAAATAAGTTATTTATTGTATTTTTTATGTGTTTTAGGAGAATCTGTGTGGCCAAAGGGGACTTTTGCCAAACTCTGATACTCAGACGTTTCAGATTTCGATAACTAACCGTCTGCGAGCACAGTATGATCGGATAATCGAGCCAATCAGCAGGGTATAAACACAAGCAAATACTATGTCAAATATTTCCCCCAAAATTAGACATGCCTGTTGAAATTGCCTTTAAAAAAAGAAAAGATGATCAGTCACATTGGTGCTTAAAGAAACACTTTCTTTCTTTCTAAAGAAACAGTTTCACTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTCTTTTTATAAAATACTCATTTTACATGAGCCTAGTGT
Associated Phenotype:
Not determined