ZMP
C3orf63 (2 of 2)
Ensembl ID:
Description:
chromosome 3 open reading frame 63 [Source:HGNC Symbol;Acc:30314]
Human Orthologue:
C3orf63
Human Description:
chromosome 3 open reading frame 63 [Source:HGNC Symbol;Acc:30314]
Mouse Orthologue:
D14Abb1e
Mouse Description:
DNA segment, Chr 14, Abbott 1 expressed Gene [Source:MGI Symbol;Acc:MGI:1921694]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37576 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37577 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24227 | Nonsense | Available for shipment | Available now |
sa10514 | Nonsense | Available for shipment | Available now |
sa43890 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43891 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9869 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37576
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 |
---|---|---|---|---|---|
ENSDART00000129848 | Nonsense | 53 | 1547 | 3 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 42053548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 39021451 |
GRCz11 | 22 | 39008035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTACGTCAGGGTCGGGTGAAGAGCGTGCACGACTGTATATCCCGATA[T/A]CCAGATAACCGCACGTCCAGAGGGATTGATCCCACACCTAAATTTGACAG
Long Flanking Sequence:
GTGTTTGCTCTGCTGCCCGCAGGTCTCTGTGGTGTGTGAGAAAGGTCTGTCTGTTGGCAGCAGCTGGATGAGCATGTTGGGGAATCCATCTAAAGGTGAAGGATCAAACTTTCAGACTAAATCTAATTTCAAAGCACTAGATCTTGAGTTTTGATGGGAAGGAGCCTGCGGGGAATCACAGGCAATGAAATGAGAGATTAATGAAAATGAATGAGTGAAGATTGCTCTTCTCAATTCAGCTGATTGACACTGTGCAGATGTGCATGGAATAAAAGTGTGTTGACTTTGCAGGCGTTTACCTGTGTCAGTTCTCTGATTTACTTCAAATCAACCCGTTTGAGCCTGGAGCTGCAGGAGAGATCATCATCTTCAAAGTGATAAAGGTACATCGGCAGTCTAATGTTTTCACCTGAACACTGCGTTGCTCTTGAGTCTGAGATGGTTTGGTTTTCTGTACGTCAGGGTCGGGTGAAGAGCGTGCACGACTGTATATCCCGATA[T/A]CCAGATAACCGCACGTCCAGAGGGATTGATCCCACACCTAAATTTGACAGCCATTTCTCCAAGAGCTCGACTCGCGTGACGTCCTCACAGTCACACATGGCTTTTGAGTATACGCAGGTAAAAATAAGCAGACTGAATTTAAAGGAAAAGTATTTGAGTGAATCTGTTAGTCAACAACTGCACTGCTGTAATAAACACTGCACTGACTGATTATAGGTTATTGTTAAGATAACTCAAATGTTTACTGGTATATTGCAAACAGTAGGATATCACCCTTCCCCAATGACTTGTTTGCTTTTTGTTGTTGTATTCGCAGCAATACTTCTATGAGTATGTGGATTTCGAGATTTCTTCCAGGCCAAGGCATGTGTGTCCGTATGCTGTGGTCTCTTATTACTTTAAAGGCAAAGAAGCTTCAACGGTCATCCCTAAACCACTGCCTCCTTTCAGGTACCTGACTGTACCCCTGTACTCTCGCTGATGTGGCTTGTAAAACTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37577
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129848 | Nonsense | 82 | 1547 | 3 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 42053634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 39021537 |
GRCz11 | 22 | 39008121 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTAAATTTGACAGCCATTTCTCCAAGAGCTCGACTCGCGTGACGTCCT[C/A]ACAGTCACACATGGCTTTTGAGTATACGCAGGTAAAAATAAGCAGACTGA
Long Flanking Sequence:
CATCTAAAGGTGAAGGATCAAACTTTCAGACTAAATCTAATTTCAAAGCACTAGATCTTGAGTTTTGATGGGAAGGAGCCTGCGGGGAATCACAGGCAATGAAATGAGAGATTAATGAAAATGAATGAGTGAAGATTGCTCTTCTCAATTCAGCTGATTGACACTGTGCAGATGTGCATGGAATAAAAGTGTGTTGACTTTGCAGGCGTTTACCTGTGTCAGTTCTCTGATTTACTTCAAATCAACCCGTTTGAGCCTGGAGCTGCAGGAGAGATCATCATCTTCAAAGTGATAAAGGTACATCGGCAGTCTAATGTTTTCACCTGAACACTGCGTTGCTCTTGAGTCTGAGATGGTTTGGTTTTCTGTACGTCAGGGTCGGGTGAAGAGCGTGCACGACTGTATATCCCGATATCCAGATAACCGCACGTCCAGAGGGATTGATCCCACACCTAAATTTGACAGCCATTTCTCCAAGAGCTCGACTCGCGTGACGTCCT[C/A]ACAGTCACACATGGCTTTTGAGTATACGCAGGTAAAAATAAGCAGACTGAATTTAAAGGAAAAGTATTTGAGTGAATCTGTTAGTCAACAACTGCACTGCTGTAATAAACACTGCACTGACTGATTATAGGTTATTGTTAAGATAACTCAAATGTTTACTGGTATATTGCAAACAGTAGGATATCACCCTTCCCCAATGACTTGTTTGCTTTTTGTTGTTGTATTCGCAGCAATACTTCTATGAGTATGTGGATTTCGAGATTTCTTCCAGGCCAAGGCATGTGTGTCCGTATGCTGTGGTCTCTTATTACTTTAAAGGCAAAGAAGCTTCAACGGTCATCCCTAAACCACTGCCTCCTTTCAGGTACCTGACTGTACCCCTGTACTCTCGCTGATGTGGCTTGTAAAACTCTGTTTGTTTTATTGAAATTGTCTTTGTTTTTCAGGTCCAACAGTCAGCCTGCTGGCACGAGTGTAGGTAGGCATGATTTCTCCTCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24227
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 |
---|---|---|---|---|---|
ENSDART00000129848 | Nonsense | 949 | 1547 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 42069606)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 39037509 |
GRCz11 | 22 | 39024093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAGGTCAGTGGTAGTTCAGTTGCGGAGACTACGGAAGCTGATGAGGGT[C/T]AAACGTCATGCTCAGCTGTCCCTGCTGAAGACACCTCGGTGGACCACACG
Long Flanking Sequence:
ATCAGAGCACACGAGAACCCCCTCAGGCTCCGGTTCCGCCTCTTTCTGATTACATTTCGAACTTTACCACTCCCTTTCCTGTCGGTACCTACGTCAGCTCTTTGCATGATAGCATGATGAGGTTCATTCATGGAAATCAACACCAGGAAGCACAAGAAGATGTGTCGTCTTCCTCTCAACCTACAGAAGATCCTTCAGAAGTCCCTGATACTTCCTCCAGCGTGTGTGCTTCCTCATCCTCAACCACTAAACCCAGCAAAAGCTTCGAGCGCCACCTGACACCATGTTTGCCTTCCAGTGCGCTCCCCGAGCCAGCAACTCAAGCACAGCGTCAGTCAGGTTTGGCTGATGCCCACAAACTGCCCCAAAAGCTTTGGCCATTAGAGCAGGACTCAGTGGCCCAGCAGATTACCGAAGCAAGCACCATGGATGATCGACACCGAGGCTCACATGAGGTCAGTGGTAGTTCAGTTGCGGAGACTACGGAAGCTGATGAGGGT[C/T]AAACGTCATGCTCAGCTGTCCCTGCTGAAGACACCTCGGTGGACCACACGCATTCGGCTATCAGCAGCATCATCCATCAGCTGCAGCCTGAGATGATCACTAACCTGGTGGAGATCCTTAAAGGAGTGCAGAAGAACTCGGTTTACTTCTACATCCATTCCCTGGAGGAGGAGAGTGACGTCTGCTGGGAAATAAAGGTAATGTTTATTTTTATTATGATTTATTATTGCTTTACATGCAAGTTCAGACTAAACATTACCAAAAGTTAATGCTAAATTAATTTGTATAGAGGTTTTTCTTTAATCTAGGTTTATCTCACTGTAATTAATCCAGATTAAAATGGCTGATTTGAATTCTGCTGAAGGCTTTCAGAATGAGTGTGCTACCCGTATAATTAGTCTTCGAGAACAGGCTTCTCCAGCCAGGTGGAGCATTAGACCAGGGGCTCATCTCCTGTTCCCAAAATGCATCACAAACTGCTTAAGGCCAGCAGGGGGCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10514
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 |
---|---|---|---|---|---|
ENSDART00000129848 | Nonsense | 992 | 1547 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 42069735)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 39037638 |
GRCz11 | 22 | 39024222 |
KASP Assay ID:
2261-7149.1 (used for ordering genotyping assays)
KASP Sequence:
AGCTGCAGCCTGAGATGATCACTAACCTGGTGGAGATCCTTAAAGGAGTG[C/T]AGAAGAACTCKGTTTACTTCTACATCCATTCCCTGGAGGAGGAGAGTGAC
Long Flanking Sequence:
ATGGAAATCAACACCAGGAAGCACAAGAAGATGTGTCGTCTTCCTCTCAACCTACAGAAGATCCTTCAGAAGTCCCTGATACTTCCTCCAGCGTGTGTGCTTCCTCATCCTCAACCACTAAACCCAGCAAAAGCTTCGAGCGCCACCTGACACCATGTTTGCCTTCCAGTGCGCTCCCCGAGCCAGCAACTCAAGCACAGCGTCAGTCAGGTTTGGCTGATGCCCACAAACTGCCCCAAAAGCTTTGGCCATTAGAGCAGGACTCAGTGGCCCAGCAGATTACCGAAGCAAGCACCATGGATGATCGACACCGAGGCTCACATGAGGTCAGTGGTAGTTCAGTTGCGGAGACTACGGAAGCTGATGAGGGTCAAACGTCATGCTCAGCTGTCCCTGCTGAAGACACCTCGGTGGACCACACGCATTCGGCTATCAGCAGCATCATCCATCAGCTGCAGCCTGAGATGATCACTAACCTGGTGGAGATCCTTAAAGGAGTG[C/T]AGAAGAACTCGGTTTACTTCTACATCCATTCCCTGGAGGAGGAGAGTGACGTCTGCTGGGAAATAAAGGTAATGTTTATTTTTATTATGATTTATTATTGCTTTACATGCAAGTTCAGACTAAACATTACCAAAAGTTAATGCTAAATTAATTTGTATAGAGGTTTTTCTTTAATCTAGGTTTATCTCACTGTAATTAATCCAGATTAAAATGGCTGATTTGAATTCTGCTGAAGGCTTTCAGAATGAGTGTGCTACCCGTATAATTAGTCTTCGAGAACAGGCTTCTCCAGCCAGGTGGAGCATTAGACCAGGGGCTCATCTCCTGTTCCCAAAATGCATCACAAACTGCTTAAGGCCAGCAGGGGGCGCCCAAACTGTGGTCTGTGTGGGTCCTAATGCCCCAGTATAGTGACAGGGACTCTATACTGCTCAGTGAGCGCCGTCTTTCAGATGAGACGTTAAACCGAGCTCCTGACTCTCTGTGGTCGGTAAAAATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43890
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129848 | Splice Site, Nonsense | 1109 | 1547 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 42073109)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 39041012 |
GRCz11 | 22 | 39027596 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTATTGTGTCAGATGAGGATGTCCTGAATCCGTCCGTCATTACAGCA[G/T]GTAACCTGATTATCCAGTCTGGTGTATTACTAAGATCAGGTTTGATCTGC
Long Flanking Sequence:
ACCTTTCATAGACACACTTCATCATCAAATCAGCAACTAGAAGAGCAGATATTACTTGTGTTCCTAAAACTTGCATAGGCGGCAAGGCTTCAGTCAGGTAGTGTAGGATGTACAATAATACACATTTAATATAATAAGCATATACTGAGATGATAATCATAATAAAAAAGCTTTATATTTTAAATATGAATCATTAATCAAGTTTATATGTTTGTTCTTTATTTATAAAGTCTACATTCCTTTAATAGAGTCAAGAATCAAGTCCTGTGCATGTGACGCTCTCTCTGTTCAGCAGGTCAGTGTGGTTTGCTTGCTCTTGACGTTGTGTTTTACACCCATAGATACCTTCATTAGTTTCCTTGAAGAAGCATCCGTCTGTGAGCTTTGCTGGTGTAGACAACCTGAGTGACATCCAGAACCACACATACAATGAGCTCTTTCAGGCCGGAGGATTTATTGTGTCAGATGAGGATGTCCTGAATCCGTCCGTCATTACAGCA[G/T]GTAACCTGATTATCCAGTCTGGTGTATTACTAAGATCAGGTTTGATCTGCGAACACGTTTCAGCAAGGCTTTGTCTCTGTCTTCAGAAAAACTTCAAGACATCCTCGAGTGCATTGAGCAGCTCAGTTCTCCTCAGAGCCCCTGGAGGTGGAGGGTTCACTTCAAATCTCACAAGAAGCTGCGAGAGCAGAGCAGGTTTGCCACCACTAAACTCTCATCCCAAAGACAAACTGATGCTGTATCGGCTGCAAAAGGATTCCCTACACCACGCGTGTCCAAGCTCGGTCCTGGAGGGCCGGTGTCCTGCAGAGTTTACTTCCAACCTAATCAGACACACCTGGGCTAGCTAATCAAGCTCTTACTAGGCTTTCTAGAAACATCAGCGCAGGTGTGTTGAGGCAAGCTGGAGCTAAACTCTGCAGGACACCGGCCCTCCAGGACTGAGCTTGGACACCCCTGACCTGCAGCATGCTATTGAATTAGTGGTCTAAAACCAGGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43891
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000129848 | Nonsense | 1283 | 1547 | 20 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 42078258)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 39046161 |
GRCz11 | 22 | 39032745 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGACTCCAACCAGGATTCTTCAGATAACACAGTATCTGCCCCCGTATCT[C/T]AGATGACCAGCGCTCTTACAGACCAACAAGCTGACTTCCATCCTTCTGTT
Long Flanking Sequence:
TATCCAAAACAAATATAGCTTAAAGGGGTGAATAATATTGAGCTTAAAATGCTGTTTAAACTATTAAAAACTGCTTTTATTCTAGCCCAAATAAAACAAATCAGACTTTCTCCAGAAGAACAAACATTATCAGACACACTGTGAACATTTCCTCAATCTGCTCAACACCATCTGGAGAATATTTAAATAAAACAGAGTGTGAATAATTGTGAGTTCAGCTGTGAATCCTCAGCTTGGCGTGTGCATCAGGGCATCAGCATTCTCTGTATTCATCTTCTGCAGTGTGATGAGCATGACCGTTTGTCTCTGTAATGCTGTTGTAGAGATGCTGAACCTCTCTTGTAACTGTTGTTTTTGGGCTCAGTTTGGGAGTTTCCCGGTGTTGAACCGTTTCATTGATCGCCTGTAACATTTCTCTTGTGCCTGTAGTGGGAGAGGATAGCATGTCTCTGGACTCCAACCAGGATTCTTCAGATAACACAGTATCTGCCCCCGTATCT[C/T]AGATGACCAGCGCTCTTACAGACCAACAAGCTGACTTCCATCCTTCTGTTCCTGAAGACACTCTTCCAAATCAGGTGCACAGCATTCCTGTGCACACGACAACCTCTGAGCCGCCAAACGCTCTGGACTTTAAAGCTCTCAGCGAAGCGATTTCTCAATTCAAGGCTTCCAAGAAGCTGACAAAGACTTCTGAAACTTCATTTCAGGTGGACCCTCACCAGAGCTTCCTCGCTCACAGTGCTCTGCCAGATTCCTATTGTCTGAGCTCTCCAGAAATCCACAGTCTGCCACAGACGCCAGCCTCGTACAGCTCAAATCAAATGAAGTCTGCGAACACTGAGACGAGCTCCTCTGCTGCATCTCACGCTGAAGCCGGCTGTGAAGCAGACCAGCGAGGAGAAACAGCTGGCAGAATCAAACCAGCCTCGTCTACGCTTGTGGCAATCCCACCAGCCGAGATATCAGACAATCCCGGAGATTGGGAGCAACCCAACACTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9869
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 |
---|---|---|---|---|---|
ENSDART00000129848 | Nonsense | 1368 | 1547 | 20 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 42078515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 39046418 |
GRCz11 | 22 | 39033002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGGACCCTCACCAGAGCTTCCTYGCTCACAGTGCTCTGCCAGATTCCTA[T/A]TGTCTGAGCTCTCCAGAWATCCACAGTCTGCCASAGACGCCAGYCTCGTA
Long Flanking Sequence:
CATTCTCTGTATTCATCTTCTGCAGTGTGATGAGCATGACCGTTTGTCTCTGTAATGCTGTTGTAGAGATGCTGAACCTCTCTTGTAACTGTTGTTTTTGGGCTCAGTTTGGGAGTTTCCCGGTGTTGAACCGTTTCATTGATCGCCTGTAACATTTCTCTTGTGCCTGTAGTGGGAGAGGATAGCATGTCTCTGGACTCCAACCAGGATTCTTCAGATAACACAGTATCTGCCCCCGTATCTCAGATGACCAGCGCTCTTACAGACCAACAAGCTGACTTCCATCCTTCTGTTCCTGAAGACACTCTTCCAAATCAGGTGCACAGCATTCCTGTGCACACGACAACCTCTGAGCCGCCAAACGCTCTGGACTTTAAAGCTCTCAGCGAAGCGATTTCTCAATTCAAGGCTTCCAAGAAGCTGACAAAGACTTCTGAAACTTCATTTCAGGTGGACCCTCACCAGAGCTTCCTCGCTCACAGTGCTCTGCCAGATTCCTA[T/A]TGTCTGAGCTCTCCAGAAATCCACAGTCTGCCACAGACGCCAGCCTCGTACAGCTCAAATCAAATGAAGTCTGCGAACACTGAGACGAGCTCCTCTGCTGCATCTCACGCTGAAGCCGGCTGTGAAGCAGACCAGCGAGGAGAAACAGCTGGCAGAATCAAACCAGCCTCGTCTACGCTTGTGGCAATCCCACCAGCCGAGATATCAGACAATCCCGGAGATTGGGAGCAACCCAACACTAATGCTGAGAGCGGACACGAGCTGAGCAGCGCTCCAGAGACCTCAGCAGCGGACACCGCTCAAGCCTCCACCGCTTCAGTCAAGAACACATACACAAGCGGCGGGTTCCTTCCCAGGCCCAGCACTTCCTCTTACGGCATGGGTAGTTTTTATCCAGCGCTGCAGCAGCAGGGTGGCTTGATGCCAGCTCCACGAGCCTCCATGGGTCTGAGCTACCCTAGATTTGTATCTAACAGCGGTGCTGTTGGACTCAGACATCC
Associated Phenotype:
Not determined