ZMP
si:dkey-233p4.1
Ensembl ID:
ZFIN ID:
Description:
Protein broad-minded [Source:UniProtKB/Swiss-Prot;Acc:Q5RHR6]
Human Orthologue:
C6orf170
Human Description:
chromosome 6 open reading frame 170 [Source:HGNC Symbol;Acc:21485]
Mouse Orthologue:
D630037F22Rik
Mouse Description:
RIKEN cDNA D630037F22 gene Gene [Source:MGI Symbol;Acc:MGI:2442827]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45715 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43510 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29433 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16562 | Nonsense | Available for shipment | Available now |
sa16300 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45715
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061168 | Nonsense | 322 | 1298 | 9 | 33 |
ENSDART00000144401 | Nonsense | 322 | 1298 | 10 | 34 |
Genomic Location (Zv9):
Chromosome 20 (position 40809307)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 40880466 |
GRCz11 | 20 | 40777576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATAAATGAGTTTTTTTGTCCTGTGCTCTAGGTACATGGAAGAAATCATT[G/T]AAAACACCCTGTCTCTTCTCGCTCTGCATTCTGAACAGGGCATGAGCAGT
Long Flanking Sequence:
ATCTACGCTAGCATAGGTAATAGTTTAAGCTATAACAGTACTATGCCATATGTTTTAATATTTAATATGTCTGGAATAAACCACTCTGTCAGTTTGTTTTCATGTTTTGTTAACTTTGCTTTTAAGCAAAAACCTTGGAGGCTCATTTCCTTTACCACAAGTTGAGTTTTCCCAGTGGCACTACTAGTATTGATGCAAACAGACCAGATATGGCCCGTCTCCTCAAACAAGTATGTGGCATTTATTTACTCTTTTATATGAATACATTAAAGCTTGCTTGAATATTTTTTCTTTACGGGTCATTCTAGATGCGATTAATGAATGACTTTCAAAAGGAAGTGACTACGTTTTGGATACGGCATCCTGAGAAGTGAGCTTTCACATTTCAAATTCAATTCGCGAGTATTGCATACTATGTTGTGTATCTTGATTATGTCCAATTACTTTAAAAATAAATGAGTTTTTTTGTCCTGTGCTCTAGGTACATGGAAGAAATCATT[G/T]AAAACACCCTGTCTCTTCTCGCTCTGCATTCTGAACAGGGCATGAGCAGTCCCGGCTCAGAGAAATCCCTAGAGCCTATTCACTTAATCTCTCTGCTGGATATCAAAGCCACCTGGTTTAAGAAATGGATGGTGAGCCACATTTTTTTTTTTATCAAAGAATAAATAACCAACACAACACATCAAAACAAACTAAATCTCACACAGACACTATCCTCAAATATTTTGTCTTGCCATAAAACGAGGAATATGTTTTGAAAAACTTTCATACATTTTACATAAAAGTATTGAAATTGATTGTGATAATTGAGGCCTTGAGACGAAGGACCATATAAGTCCATATTTTCTCATTTTGAGTAATACGATTTTTTTCAATTCTATTATGAACATTATGTGACATATTTTTATTTTAATTAAAGATAGACAACAAAAGCTTCTCAATTTATTTCAAGTTTATTATTATTATTATTATTATTATTATTTAAAAACAGAAAATACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43510
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061168 | Nonsense | 409 | 1298 | 11 | 33 |
ENSDART00000144401 | Nonsense | 409 | 1298 | 12 | 34 |
Genomic Location (Zv9):
Chromosome 20 (position 40812037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 40883196 |
GRCz11 | 20 | 40780306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGCATTTATTACTTTGATTCCTGTGATGCATTAAGTGAAGAGACCTTG[G/T]AAATGATCCACAGCCTGGAACATCAGCAGATTGGTACGGCTGAACTTTTG
Long Flanking Sequence:
TGTTTCTCTATGGTTCTGTTCACTTAAAACTGCTTAAAATCTTTTTCTTTGACTTACTATTTCTTCTAGCATGGTTACTATAGCAGAACTGTTGTCTTAAGACTTCTGGAGAGGAAATACAAGTCTTTGGTGAGATATATTTAACTGTTCCATAGACATTTTAAGCAAAATGATGCTACATTGTCATTGGTTGACTTCACATGACATTATCACATTATTTTATTATTTAATATTCATTATTTTTAGTGACAAATATCTAAAAATGGCATAATTTGTTTTTGGCTTAGTAAATTAAGAACACATTTGCATTTTTTTTTACATGAACCATTCCTTTGAATGAAATGGGTAAAATGAACAGCTTTCACCATGACCGCTAACAACATTATGCATTCAAGTGGTTAATTATGGATTTTCTCAATTCTTTCCTTCAGATTGTTAATGCTCTGCAGCAGTGCATTTATTACTTTGATTCCTGTGATGCATTAAGTGAAGAGACCTTG[G/T]AAATGATCCACAGCCTGGAACATCAGCAGATTGGTACGGCTGAACTTTTGCCCAATGTGCACGTGTAGTATCATGCTTTATCTGAAACGTTGGCTTATGTTTTCCCCAGTGTGCTGTTACAGACTGTCCTCTCATGGTCAACTAGTTAGATTATCATTGGCAGAGATAATTCCAAGGGTTTGAGCATTCATACTGAAGAACTTTCCCAGAATTATGGTCCTGTATTGTAGCTAGAAGACTCAAATAGAAAACAAAAAACACCTTCATACATACACAGAGCATTGACTGTTTGCATTATCTTCTGTTGTATACACAAGTCATTGCTACCAGATTTCAGACAAAACCCATACAAAGTTGTCAAACATTCATTACACGGCAGCTCTTTTCAGTAGACGCTTATCTAGTTTCTGTAATCAGACCAAGTTTATGGTTCTTCTATGGAATTGTTCCTTATTTAACATTACTGCTGATTTCAGATGTTTTATATTACCATTGAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29433
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 |
---|---|---|---|---|---|
ENSDART00000061168 | Nonsense | 852 | 1298 | 22 | 33 |
ENSDART00000144401 | Nonsense | 852 | 1298 | 23 | 34 |
Genomic Location (Zv9):
Chromosome 20 (position 40825202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 40896361 |
GRCz11 | 20 | 40793471 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCTCATCATTATTAACTCTGACGCGAAGATTCACTCTCTTTTCAACTA[T/A]GAACAGTCCCACACGTTTGGCCTGAGGTAAGATCAATAGTTCAGTCCTCT
Long Flanking Sequence:
AGATAAACTGTGATCACAAGAATCTCACATCAGTCATGATTTTGAATTTGTTAGTTTGTAATTACACCCTCTATTTTCTTGTGTTTTCAGATAGATAAAATTGTAAAATGAACGACATATAGACAGAAATATACATTTACAGACAGACAGAAAATTATTAAATTAATGATAAACTGACATAGATTGATTGCTTGATTGATTGATTACATAATTTTGACTTAGAGCTGTACCTGTTTCTTTAGCAATACTATTTCTTAGCAAAAATATTAAATATGATATAATTTCCCAGATTCTCTTGCATTGCAGTTCAGATCATGATCATTTGAGGGCAGAGTTTGACCGACAATGTACCAGCCATCTTAGAACCCACTGTGGCCTTGTGTGTCACATTTACTTTGAAATTATGCATGTTTGATAATCACTTGCTCTTCCCGTCAGGACCTGATGGACCGTCTCATCATTATTAACTCTGACGCGAAGATTCACTCTCTTTTCAACTA[T/A]GAACAGTCCCACACGTTTGGCCTGAGGTAAGATCAATAGTTCAGTCCTCTCTACCAGTAAATGGACAGGAAGAGCGCAGAAGTGATAGAGGGTCCTTATAGAGGTTTATTATCTGATTAGCCTTTTTTTTCTCCATTCATTCTTCTCTGGGGATCAATGGCTGATTGATTCAGCTCTTTGTGTTCTCTGGGCTATGATTATCCTGAATTAATACCAGACAGTGTGATACCAGGATATGAAAGAGTTCTAGGGCTCTCAAAGGAAGCAGAAATGACTGGTGTAATCCACCTACTTATTAAAAAGGAACACTTTTGATGCATTTGGTCCACATAAATCAATAAATGATGATAGCTTAAAAATAAATGATGTGTTTTCTTAAATCAGCTTCATGAATTAAAGTTTGTTCAGCCCTTGAGATCACTTACTCGAGGCTAAGATCACATTTACATAGATACACAGTGCTGTGCCAATTATTTCCCCCACCAGTGGCATTTATATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16562
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 |
---|---|---|---|---|---|
ENSDART00000061168 | Nonsense | 957 | 1298 | 25 | 33 |
ENSDART00000144401 | Nonsense | 957 | 1298 | 26 | 34 |
Genomic Location (Zv9):
Chromosome 20 (position 40841636)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 40912795 |
GRCz11 | 20 | 40809905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACCCTTACCCATGGCCAATGGTGWCCACTTATCCTCTGCCWAAGTATTA[T/A]ATATTCGACGTGCCCAAGATTCTCCGCACYAAACAGGGTAAGAACTATCA
Long Flanking Sequence:
CTCTCTCTCTCTATTTCTCTCTCTCACTATTTTATATTGCACTATATATATTGTTTAATATACCATTTATCGCTATATTTAAAAATATTTTAAAGACTGTTAATTTAGAACAGTGCACATTTTAACAATTAATTATGGGTTTTACTATTTTTGTGTGTGTCTGAGTTGTGACATGTATTTTTTATTTTTTGTAACTTCGTCCTATGCTGCCTGTCTTGACCAGGACTCCCTGGTAGAAGAGATCTCAATGGGACATTGCTGTTTAAAAGATTAAGTAATTAAAATTAATAGTTAATTAAACATCATTATAAAAAAAGATTTTGCTTCCTACAGAATCAAGGTAAAATGACATTTTGCTGCCGCCCTCCTGCTTAAAAAAAACAACTGTCAGAAATTTGGAAAAAAATAAAATAAATAAATGTAAATATCTCATCTTTCTTTTAGGGGAATGACCCTTACCCATGGCCAATGGTGTCCACTTATCCTCTGCCTAAGTATTA[T/A]ATATTCGACGTGCCCAAGATTCTCCGCACTAAACAGGGTAAGAACTATCATTTTAAGCATGAAGCATTATACATGTACCATTGTTCTAATATGTGAAAGCAGTTCTTTAAGTTTACTATTTAGTTCAGCAATGGTTTTACTCTGCAGTAACTTCAAGGACACTTTCTCTCTTTATGACAAACTCATTTCTCTTCTTTACTGTCACGGCGATGCATCTTTATTTCAGCTTGACAGCTGTTTCCAGCTCAATAAATAGGGACTAGAGGTTCTTAACGCCTAGTAAACATTCATCCTTTAGGAACAAGCGTCAGCGTGTGGGTAAAGGCCTATTCAGTGTCTGTTTTTTTTTTCTTTAAATGTTTGCTAGGCATGAGTCAGTTTGCAGTCATACTGAAGGCCAAATTGTTGTATAGTATGTATTTTCAAGTGCCATAAACTTTCATAGACTTTGCAGAGGTAAACATAAAGAGTAAATAACTATATATTGTGTTAATTGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16300
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 |
---|---|---|---|---|---|
ENSDART00000061168 | Nonsense | 1188 | 1298 | 31 | 33 |
ENSDART00000144401 | Nonsense | 1188 | 1298 | 32 | 34 |
Genomic Location (Zv9):
Chromosome 20 (position 40854919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 40926078 |
GRCz11 | 20 | 40823188 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AYGTAGAGATGTTGCTCAAGGCTGAGGTTCCTCTGGTKTTTTCTGCCTTC[A/T]GAATGTCWGGCTTYACTCCMTCTCAGGTGCAATATTTTAAGTAYTTMATT
Long Flanking Sequence:
AGTTTAATGTTTTTGTTGTCTAAATGTCATTGAATATAATGGATTTTTGGTTTGTCATTTAAATCATTTCTTTTCATTTATTTTAGCAATATGTAATTCTTCTATACTATTTTTTCAGTGCCGTTTTTTCCTTTCCCACTTGGCAATCACTTAAATCAAATGCTGTCACCAGTCTGCACCTTTTAAATGCTGTCTGTGGTTGTTTTGTGTCTGCTCAGTGCTCAAAACACCAGCTGTCTGTTTTTTCTGTTTATTTTTGGTAATGGAAAGAAGTGTTTATCTCTTAAATTCAATGAAAATCAAGCAAAATTCAGAGATTTTTACATGTGACTTAAAGTAAGCACCATGTCTTCAAAGTTTAATGGATTTTCTTTTTTACGTTATAGGTCCATCTCCCTATAGAGATTGCTCAGTCGGCTATTCATCCAATCTACTCCTGCACCGCTCATTATGTAGAGATGTTGCTCAAGGCTGAGGTTCCTCTGGTTTTTTCTGCCTTC[A/T]GAATGTCTGGCTTCACTCCCTCTCAGGTGCAATATTTTAAGTATTTAATTTTTCATTTTGTTTCACAATTTTAATTGCTCTGTTGTTAAATAATCCAACAGCCCTCCAAACCTGTAGGCATTTTAAAAACAGGTATGCCTGTGTTTGCTGTGCCAACAAAATAAAGCCTTTTTCTGTTGGTTTCCACAAAACGAAAAGCTCTACATTGAAGTTAGTTAATCTTAAGTTATTTTGTCTGATAGCTAAATATATTCTGAATAAACTAAAAACAGATGAGTTTTAAACATAATTGTTTTTCTCTCTATATAGTCTCCCATCACCTGTATAGCTCATTATGCAGGTCTTTATCTTCTTACGTGTAAGGGTGCTTTCACATCTGCTTTATTTAGTTCTGTTGAATCGCACTAGAGTTCGTTTTCTCTTTTGGTGCGGTTCGTTTAGGCAGGTGAGAATGCAGCAATCGTACTCGAGTGCACACCAAAAGCGGACCAAATAAGCGT
Associated Phenotype:
Not determined