ZMP
LOC796115
Ensembl ID:
Human Orthologue:
KIAA2022
Human Description:
KIAA2022 [Source:HGNC Symbol;Acc:29433]
Mouse Orthologue:
C77370
Mouse Description:
expressed sequence C77370 Gene [Source:MGI Symbol;Acc:MGI:2148050]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14178 | Nonsense | Available for shipment | Available now |
sa42356 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44802 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35647 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28271 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38983 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14178
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 |
---|---|---|---|---|---|
ENSDART00000047816 | Nonsense | 210 | 1232 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 11460177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 10955534 |
GRCz11 | 14 | 11261548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTTCCAGGACAAYATTAGGGAGAAAACCAATGTTCTGCAAGAAGAAACC[C/T]AGTTTAACTTTTTCCCAAGTGTCTTGGTAAACTGCACAAAGAAAGAGAGC
Long Flanking Sequence:
TCAAAATGACTGACATGAACCGAGACTACAGCACCTGCCCTATCTCTGATATTAACATGCAATGCATGAGCACAAGTGAGACAGGAAGTTATGGAGACCAGCTCCTCTCTGATCAGCTTTTGAGCTTTCCTGTCACTAAAACCCAGTTGCTGGAAAAGAAGGACACCGAGAAAATAGACTTAGATGATCCAGCCTCTAAAAACCTGTATGAGAGCCTGTTATTAGACAAGTGCACTGGTGAAGATGGCTTGCTTACTAATCCAAATCAGGACTGGGGCTACTTTGAGTCATTCATTAGCGAGAGTAAAATGGAATTGCTGGATCTTTGCTCCAAGAATGAGCTATCTGTAAATCTCTTCTCCGAGGAGGATGTGGACAATTACATGTTTGATGATGATGATGATTCCACTCTGAGCAGTGATGTGTGCTCGTTAAAAATCCGCTACGAGTCCTTCCAGGACAACATTAGGGAGAAAACCAATGTTCTGCAAGAAGAAACC[C/T]AGTTTAACTTTTTCCCAAGTGTCTTGGTAAACTGCACAAAGAAAGAGAGCGGTGTAGTGAAACGAGTTGTGGATGAGGCACCACCTAAATCAGAGGAGCTTGGATTTCAGAATGACAACAAAGGGGATGTAAACGAATGCTCCGCAGAGCAGATGCCTAGTTACAGCCCTAAAATGAACTACTTCATTGATTCAAGCAACTCGGCTGATGATTCAGGCGAGTATAGTGATGAAAGCTCCTCCACCATTTGCTCTTTTGACACCTTCCAGGACAACAGACCTAAAAACTTGTTCACTCGAAAGAACGCAAGCTGCTCTAACCATCTGAACTACGGATTGCGGGCCAAAAGAAAATTTAGGTTTAGTGACGACTACTTGTATTATGTTGAGTCCACTGATGGAGAAAGAAACGTTGAAAAGCGAGAGAAACCACCGATTGGTCCAAAGCAAGAAGAGGATCTTGACTGGTGCCCTAAAAAGAGACGCAAATATTCTCGCAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42356
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 |
---|---|---|---|---|---|
ENSDART00000047816 | Nonsense | 474 | 1232 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 11460969)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 10956326 |
GRCz11 | 14 | 11262340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCCAGTCCCCCCAAAAGGAAATATAAGCTAGCAAACAGGCTCAGAATT[C/T]AGAGAATTCAAACTGTGGAGCAATCACCCAACATGCAGGGCCCCTTTGCC
Long Flanking Sequence:
TCACTCGAAAGAACGCAAGCTGCTCTAACCATCTGAACTACGGATTGCGGGCCAAAAGAAAATTTAGGTTTAGTGACGACTACTTGTATTATGTTGAGTCCACTGATGGAGAAAGAAACGTTGAAAAGCGAGAGAAACCACCGATTGGTCCAAAGCAAGAAGAGGATCTTGACTGGTGCCCTAAAAAGAGACGCAAATATTCTCGCAAGGATCCACCTGTAATAATCAAATACATTATCGTTAATAGGTTCAAAGGAGATAAATGCATGGCTGTAAAGCTTGGCAGAATTGATTCATCCGACACGACGGTGAGCTTAAATGAGGATACAATCAACAAATATGAGAAGCTTTCACCTCTGAAAGATTTCTGGCAGGAGAAGCAGAGAGAAAGAGAGGAACAGCTTAAGCTGGCAGCAGGAGATAAACACAATTCTCACCATCATGCCTTTAGATCCAGTCCCCCCAAAAGGAAATATAAGCTAGCAAACAGGCTCAGAATT[C/T]AGAGAATTCAAACTGTGGAGCAATCACCCAACATGCAGGGCCCCTTTGCCTCTGATCCCAGGCAGGAGGTTTCTTCTACAGATGAAACTGCCTCCATGGGAATGCCATTAACAATAGCCACCAGCTGTGCAAGCACATTAGACTCAAATGACATCATACACACTGCCGCCCGGAAGAGCAGATCACAAGAGAGGGAGGAAAGGAGAATAGGGAATAAAATATTCAGAATACATAAATTCAGAAGTGAAGCCAGACTTAGAAGCAAGAAAATAAGAGACCTTGTGGAGAATAACGAAAGCATGACAGACCTGACAGAAGTTTGCTCGCTGCAGAAAAATATGGACACAGTAGGAGGTGCAGAAGATAAAAATGTCAGCCCAGCTGCACACATTCCCCATTTGTGTGAAAGTCAAACAGCTAATGCCACTGAAAAATTTGCTTTTGTGTCTAACACCTGCTCCTGTAACAAAGAGTCATCATCGGAGAATGTGGCTGCAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44802
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 |
---|---|---|---|---|---|
ENSDART00000047816 | Nonsense | 734 | 1232 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 11461749)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 10957106 |
GRCz11 | 14 | 11263120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCAAGCCCAGCTTCATTCCAACCAGCAGTTTACCACTGCAGATGTTGCT[G/T]AATCTGCGATTCAACCTAACAGCTTCGATGGAGAGATGGCTTTGCCTATG
Long Flanking Sequence:
TTGTGGAGAATAACGAAAGCATGACAGACCTGACAGAAGTTTGCTCGCTGCAGAAAAATATGGACACAGTAGGAGGTGCAGAAGATAAAAATGTCAGCCCAGCTGCACACATTCCCCATTTGTGTGAAAGTCAAACAGCTAATGCCACTGAAAAATTTGCTTTTGTGTCTAACACCTGCTCCTGTAACAAAGAGTCATCATCGGAGAATGTGGCTGCAAGTGTTTCGGTTATTCCTGGAGGCTACCTTCAAACACTGCTGGATGCCTCTGATTCTTCAGGTAGCACCGGTATCCCGTTTTTCCCCCAGCAGACCCAGCACTCATTGGTACTCTCTTTGGAAAAGCAGCAATTCACCTCAATTCAGCTAGCACAAAGCTGTGTTCTTTCACCACCGTCAGAATCAGAGCTCCAGCAGTCTCCTCAGAATTGCCCGACTCTTACCCAGATGTGGCAAGCCCAGCTTCATTCCAACCAGCAGTTTACCACTGCAGATGTTGCT[G/T]AATCTGCGATTCAACCTAACAGCTTCGATGGAGAGATGGCTTTGCCTATGTCTGAGAGTCTGACTGTGTCAGGATTCAGCCAGCTGAGTCTAGAGAGCAACAGAATGCTTTATGAAAAGAATTACATGCCTGAGCAGCCACTGCCTCCTGATGCTGAGTTTCAGGCATGTCAGAGGCAGCCACAGTTTCAAAGAGCCACACTCCACACCGACAATGGCCGACTCATCAGTTTCGACTCAGTTGGTTCGCTGTCAGCTGCTTCCAGCAATTACAGCTCTCTGAGTCTTAAGTCTTGTGAAAAAGATGGTGAGGATGATGTGAATGAGGACTTTCTGGCCCACTACAGTCCCAAACTTGTTATTCAACAGAGTATTGATGCAATCACACCCCTGAGAGAGTCTACAGACTTGCTAGATATCTCCAACTTCACACCAGATAAATTCAGACACGCATCATTGTCAGAACTTTCTCCTCCGGAGACACCTAATTTATCCCCTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35647
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 |
---|---|---|---|---|---|
ENSDART00000047816 | Nonsense | 738 | 1232 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 11461761)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 10957118 |
GRCz11 | 14 | 11263132 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATTCCAACCAGCAGTTTACCACTGCAGATGTTGCTGAATCTGCGATT[C/T]AACCTAACAGCTTCGATGGAGAGATGGCTTTGCCTATGTCTGAGAGTCTG
Long Flanking Sequence:
ACGAAAGCATGACAGACCTGACAGAAGTTTGCTCGCTGCAGAAAAATATGGACACAGTAGGAGGTGCAGAAGATAAAAATGTCAGCCCAGCTGCACACATTCCCCATTTGTGTGAAAGTCAAACAGCTAATGCCACTGAAAAATTTGCTTTTGTGTCTAACACCTGCTCCTGTAACAAAGAGTCATCATCGGAGAATGTGGCTGCAAGTGTTTCGGTTATTCCTGGAGGCTACCTTCAAACACTGCTGGATGCCTCTGATTCTTCAGGTAGCACCGGTATCCCGTTTTTCCCCCAGCAGACCCAGCACTCATTGGTACTCTCTTTGGAAAAGCAGCAATTCACCTCAATTCAGCTAGCACAAAGCTGTGTTCTTTCACCACCGTCAGAATCAGAGCTCCAGCAGTCTCCTCAGAATTGCCCGACTCTTACCCAGATGTGGCAAGCCCAGCTTCATTCCAACCAGCAGTTTACCACTGCAGATGTTGCTGAATCTGCGATT[C/T]AACCTAACAGCTTCGATGGAGAGATGGCTTTGCCTATGTCTGAGAGTCTGACTGTGTCAGGATTCAGCCAGCTGAGTCTAGAGAGCAACAGAATGCTTTATGAAAAGAATTACATGCCTGAGCAGCCACTGCCTCCTGATGCTGAGTTTCAGGCATGTCAGAGGCAGCCACAGTTTCAAAGAGCCACACTCCACACCGACAATGGCCGACTCATCAGTTTCGACTCAGTTGGTTCGCTGTCAGCTGCTTCCAGCAATTACAGCTCTCTGAGTCTTAAGTCTTGTGAAAAAGATGGTGAGGATGATGTGAATGAGGACTTTCTGGCCCACTACAGTCCCAAACTTGTTATTCAACAGAGTATTGATGCAATCACACCCCTGAGAGAGTCTACAGACTTGCTAGATATCTCCAACTTCACACCAGATAAATTCAGACACGCATCATTGTCAGAACTTTCTCCTCCGGAGACACCTAATTTATCCCCTCAAGTTATGGGCCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28271
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 |
---|---|---|---|---|---|
ENSDART00000047816 | Nonsense | 1021 | 1232 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 11462610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 10957967 |
GRCz11 | 14 | 11263981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCCAAAGCTCCCAAGACAGACAAGGGAAAAATTCCACGTCAGAATTCA[C/T]GAACGTCTAAAAAGCTAAAGACTTTATTGGACGAGAAAGGCAGTAACAGC
Long Flanking Sequence:
TTCAACAGAGTATTGATGCAATCACACCCCTGAGAGAGTCTACAGACTTGCTAGATATCTCCAACTTCACACCAGATAAATTCAGACACGCATCATTGTCAGAACTTTCTCCTCCGGAGACACCTAATTTATCCCCTCAAGTTATGGGCCGTGAGATTAAGATAGTCGGGAAGGCCACTGACCTCCAAGATGGAGTTAAGATGTCATGCACTGAAAACATGGACTGGAAATGCAAGATGATAAAGCAGCAAGATCTAGCTAGATATTCAGTTGAAGGTCACACGTATCAATTGAACGTGTTTAATGGGGAAAACAACTTAAGCTTGGGGACAAAGCAGGAAAATCTATCTAGCATTGATGGCGATATGGTAAATGCAATTAAGGGGACTAAGGCAAAGAGGAGAAATAGCAACAAGCCACCTGCAGGGCAGGGCACCAAAAAAACCAAAGCCCCCAAAGCTCCCAAGACAGACAAGGGAAAAATTCCACGTCAGAATTCA[C/T]GAACGTCTAAAAAGCTAAAGACTTTATTGGACGAGAAAGGCAGTAACAGCCAGACCGAAGGCATTGCATATCTGCTCAAGGACAGTAGCTCTGAGGACTGGACAGGAATAGGTTGTTCAGAGAGCACAAGTCAAGTCCACGATGACCAGAGAGAGTTTGAAGAGCCATCCAACATCTTGTCAAATATCGTCTCAGGGATGGCCGAAGTACAGAGATTCATGATGGCCTCTGTTGAGCCAATTTGGGGCCCTGCAGCAAACGTAAGCCTGCCCTCAGAAGCTAACAGTCTCAAGTTAAAGACTCTGAAAATCCTTGCAGGAACTTCATCTGACCCGAAGAAGAAAGGCACTTTGAGTACAGGGGGCACAAAAGGCAGAAAAGGTGGGACGAAAAGTGTCAAAAATCAGCCAAAGTTCAATGCCTCCTTACCTTTTTTCCCTCAGCTGGCTTTGGGCTGTAACATGTTTGACAAGCCTAACCTTGGCGTTCCAGGTATAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38983
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047816 | Nonsense | 1154 | 1232 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 14 (position 11463009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 10958366 |
GRCz11 | 14 | 11264380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGAGTACAGGGGGCACAAAAGGCAGAAAAGGTGGGACGAAAAGTGTC[A/T]AAAATCAGCCAAAGTTCAATGCCTCCTTACCTTTTTTCCCTCAGCTGGCT
Long Flanking Sequence:
GGAGAAATAGCAACAAGCCACCTGCAGGGCAGGGCACCAAAAAAACCAAAGCCCCCAAAGCTCCCAAGACAGACAAGGGAAAAATTCCACGTCAGAATTCACGAACGTCTAAAAAGCTAAAGACTTTATTGGACGAGAAAGGCAGTAACAGCCAGACCGAAGGCATTGCATATCTGCTCAAGGACAGTAGCTCTGAGGACTGGACAGGAATAGGTTGTTCAGAGAGCACAAGTCAAGTCCACGATGACCAGAGAGAGTTTGAAGAGCCATCCAACATCTTGTCAAATATCGTCTCAGGGATGGCCGAAGTACAGAGATTCATGATGGCCTCTGTTGAGCCAATTTGGGGCCCTGCAGCAAACGTAAGCCTGCCCTCAGAAGCTAACAGTCTCAAGTTAAAGACTCTGAAAATCCTTGCAGGAACTTCATCTGACCCGAAGAAGAAAGGCACTTTGAGTACAGGGGGCACAAAAGGCAGAAAAGGTGGGACGAAAAGTGTC[A/T]AAAATCAGCCAAAGTTCAATGCCTCCTTACCTTTTTTCCCTCAGCTGGCTTTGGGCTGTAACATGTTTGACAAGCCTAACCTTGGCGTTCCAGGTATAAATGGGCCTGCACATAAAAAGATGTACCGTCACAAAACCAGTGCGAAATTCCCTCGGATTGAAAATCTAAAGGGCACGCGACCTGAGCGAGAGCCAAACAAGGACATATCGTTAATGGCTTCTTTTGAGAAACTGAGGTAATATTTTATATCTAGCTGCTGATGCACGTTCCTCACTTTCCCCGATTCCTCTTCATTTCGTACCATACCTACACTGACTCAAGACCAGAGATGCATGGAATTATGTTATGCTTTAGAATCCCCACCTTCTTTTTTGCCCCCCGAAGAGGATATTGATATCTTGCATGAGAAACTTATTGTACTCGCAAACTACCTATTGATTGATTGTGCAAGGCTTGATTGAGATTTGAAATTACCATGGCTGCATTTTTATTCTGCGTTT
Associated Phenotype:
Not determined