ZMP
ift140
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human KIAA0590 [Source:UniProtKB/TrEMBL;Acc:Q7T007]
Human Orthologue:
IFT140
Human Description:
intraflagellar transport 140 homolog (Chlamydomonas) [Source:HGNC Symbol;Acc:29077]
Mouse Orthologue:
Ift140
Mouse Description:
intraflagellar transport 140 homolog (Chlamydomonas) Gene [Source:MGI Symbol;Acc:MGI:2146906]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8632 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37952 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39464 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44183 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa3253 | Nonsense | F2 line generated | Not yet available |
sa24548 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8632
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 |
---|---|---|---|---|---|
ENSDART00000046546 | Nonsense | 229 | 1455 | 5 | 32 |
ENSDART00000129889 | Nonsense | 229 | 774 | 6 | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 39333868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 37942957 |
GRCz11 | 24 | 37830854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGARTGTGTACAGTGTGGATGAGCAGGTGAAGAGTGTGCCTTTGCTGT[C/A]AGTTGAGAGYGCYGTACATAAGATGTGGTACTCCAAGAGAAGATCYGCTC
Long Flanking Sequence:
AAGTTAAAAAATCAGCATTGCATCACACAAATACTTTACATTTGAAAATATATTAACTTAAAAAAACATTTATTTTGAACTGCTGTAATATTTCATTAATTTAATCGAATAAATTTGGATTGGCGAATGTTGAAACTGTGCTACAAGATTTCCTAAACTTTATGCGCACTTCTTTTTCTTAGCTGCTTTATTAGGAAATCTGTCCTAAGCCTCCTCCTGTGTGTTTCATATGTCTGCAGGGATGTAGCGATGCTGGCCCGTGCTGCTGTTAGCGGGGATGAAAATGCTCTGGACATGTTTAACTGGAAGAAGAGCAGTAAAGGAGCAGCGTTTGCTCTGGGATCTCAGGAAGGACTTGCTTTTTACATCAGCACAGCAGATGGTGAGAGACGGTTTACTGACGACCTTCAGTAGCTCAGGGTTTGTTCACACTGTGCATGTGTGTGTTTTAGGGAGTGTGTACAGTGTGGATGAGCAGGTGAAGAGTGTGCCTTTGCTGT[C/A]AGTTGAGAGTGCCGTACATAAGATGTGGTACTCCAAGAGAAGATCTGCTCTCGCTGTAGTTACAGACTCACTGCAGCTTTCACAGTTCAGTCTCGGACCAGAAGGCTTCGCTCAGGAGATCAGCAAGGTAAAAGCCAATCAGAAAACATCTTGCATGTCAGCGGTTTATGAAAGCAGCCAGTTAGATTTCTAAATATGTGTGTGCAGGTGAAGCTGAGTGGCAGAGGAGGGCCGAATGCAGACGTTGTGTGGACAGAAGGCGGTTTGCTTATCACAGCATCAGGAGAACTCCACATCAGGTCTACTAGTTAATAATAATTATAAAAATAATTATAATAGTAGTTTGTGTTAATAGTATATAATATAATATTCTGATGCTGGTGTGTGTCTGTAGGTTGTGGCATGTGGAGCTGGATGATCATTACGCTCTATCACTGGATGAATCTCTGGGCTTTGAGAAAGGAGAACGGCTCAACTGTGTTTCTTTTTGCACTTCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37952
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 |
---|---|---|---|---|---|
ENSDART00000046546 | Nonsense | 990 | 1455 | 25 | 32 |
ENSDART00000129889 | None | None | 774 | None | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 39394365)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38003454 |
GRCz11 | 24 | 37891351 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAGACATGGAGGCTGCGCTGCATTATTACGACTTAGCTCAGGATTACT[T/A]GTCTCAAGTGCGCGTGCACTGCTACCTGGGAAGCATTCAAAAGGTACGTT
Long Flanking Sequence:
TTTAACTTCAGAAAAGCAAAAAAAAAAAAAAAAAAAATGGCCAGTTGTAATTTATTTCTGCTCTAAATGTTGGTGAATCCAGTACCGGTGAATCAACGTCTCTTGTAAATCCAGTACATCCAGAAAAAGTGATAATTTTTTAGTGTTTTCTTAATTTTTTAAGCTAAAAGTAAATAAAAAAATCGAAATGTGGTTGTGATCTTGTTACTTTTTCTTCTTCTTCAGTTTTGAGAAGTCGGACACACATCGGTTTGAAGTTCCACGAATGTTAATGGAGGATAACGTTTCACTGGAGATTTACATCAATAAAATGAGGGACAAGTGAGTCACTCTGCACAGATGATGCATTACTGTGGCCTCTACGGTCTGACTTTTCTTTAATGTTTCCACTCTCTGTTTGTGATTGGTCAGGGATCTGTATAAGTGGTGGGGTCATTATCTAGAGAGCCAATCAGACATGGAGGCTGCGCTGCATTATTACGACTTAGCTCAGGATTACT[T/A]GTCTCAAGTGCGCGTGCACTGCTACCTGGGAAGCATTCAAAAGGTACGTTCAAGTGAATTTCCTTTGTGTCCGAATTAAAGTCCACATGAACTGGAAGCTGTGACCGCTTTTTTTCATATTCTGACGGAGTTCCCAGAGAAACTGAATATTAAATGAGATTTTTTTAAAGTGGGCGGGGCTTGTTTTTGTCTACTGCGAGCTGATTGGATGTAGTAAAGTAGACATTTTATTCAGAAAGATCTAGAAAAGGGTTTGGAAAGAGTTATTACAACCTAACAGACTCCTCCTGCTCACCGTTTCTGTTTGTGGTCAAAACTGAAAGCTGGAGGGGCGTGGTTAATATGTAAGCCACGCCCAATACCTTCAGTTTTATCTAAAAAAACAAATAGGAAGTGCATTTTCAGACTTTGTTTCAAGAATACAAAAGCAAACTAGTAAAGTTCATAGACAAACTTTATGGTGGCTTGAGAAAGCCGTATCTGAAAGTTTGAAGGAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39464
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 |
---|---|---|---|---|---|
ENSDART00000046546 | Nonsense | 1038 | 1455 | 26 | 32 |
ENSDART00000129889 | None | None | 774 | None | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 39396148)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38005237 |
GRCz11 | 24 | 37893134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACGGCAATACGAGGGACAGGATGAAATCAGCCAATCGGTGCACTTCTA[T/A]ACACGCGCACAAGCCTATAATAACGCCATACGACTGTGTAAAGAGAACAA
Long Flanking Sequence:
TAATATGAATTAGCATGTTTGCTAGTATGTTTCCAGTATGGATTGATATGTTAGTCTGCGAGCTGATTGGATGTAGTAAAGTAGACATTTTATTCAGAAAGATCTAGAGAAGGGTTTGGAAAGAGTTATTACAACCTAACAGACTCCTCCTGCTCACCATTTCTGTCTGTTGTCAAAACTGACAGCTGAAAGGGCGTGGTTAATATGTTAGCCACGCCCAATACCTTCAGTTGTAACTGAAAACAAACAGGAAGTGCATTTTCAGACTATAATTCAAGATTACCAAGGCAAACTATATTTTTTTCTTAATGACTTGTACTGATCACCACAAAACTAGCAATATGAGCTAACAAAATCAATATGGCTAGTGTACTTTATTAACACCTTGCTATTTCTCAGGCGAGTGAAATTGCCAATGAAACTGGCAACAGAGCAGCATCTTATCATGTTGCACGGCAATACGAGGGACAGGATGAAATCAGCCAATCGGTGCACTTCTA[T/A]ACACGCGCACAAGCCTATAATAACGCCATACGACTGTGTAAAGAGAACAACCTGGATGACCAGCTTATGAATCTGGCGCTGCTTAGCAATCCAGAGGACATGATGGACACGGCCATGTATTATGAAGAGAAAGGAACGCATATGGACCGAGCTGTTATGCTTTATCATAAGGTACATCTAAATACATGCTGTGTTGATGTTTAACACTAGGTGGTGCTGTTTGCTTGAATAACACCATTCTGCTTCTCCAGGCAGGACATGTCTCCAAGGCTCTGGAACTAGCTTTTGCAACTGAACAGTTTGGAGCCCTGCAGCTGATCGCAGAGGACCTGAATGAAGCCAGCGACCCTGCATTATTAGCACGCTGCTCGGATTTCTTCATAAAACACGCTCAGTACCAGAAAGCTGTGGAATTGCTGGTGGCTGCCAAAAAGGTGAACATGCAACACAAACCGCCTCATATAACATCGGTTCATGTCGCTGTTATTATCATTTCGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44183
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 |
---|---|---|---|---|---|
ENSDART00000046546 | Nonsense | 1135 | 1455 | 27 | 32 |
ENSDART00000129889 | None | None | 774 | None | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 39396518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38005607 |
GRCz11 | 24 | 37893504 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCAGAGGACCTGAATGAAGCCAGCGACCCTGCATTATTAGCACGCTGCT[C/A]GGATTTCTTCATAAAACACGCTCAGTACCAGAAAGCTGTGGAATTGCTGG
Long Flanking Sequence:
TACTTTATTAACACCTTGCTATTTCTCAGGCGAGTGAAATTGCCAATGAAACTGGCAACAGAGCAGCATCTTATCATGTTGCACGGCAATACGAGGGACAGGATGAAATCAGCCAATCGGTGCACTTCTATACACGCGCACAAGCCTATAATAACGCCATACGACTGTGTAAAGAGAACAACCTGGATGACCAGCTTATGAATCTGGCGCTGCTTAGCAATCCAGAGGACATGATGGACACGGCCATGTATTATGAAGAGAAAGGAACGCATATGGACCGAGCTGTTATGCTTTATCATAAGGTACATCTAAATACATGCTGTGTTGATGTTTAACACTAGGTGGTGCTGTTTGCTTGAATAACACCATTCTGCTTCTCCAGGCAGGACATGTCTCCAAGGCTCTGGAACTAGCTTTTGCAACTGAACAGTTTGGAGCCCTGCAGCTGATCGCAGAGGACCTGAATGAAGCCAGCGACCCTGCATTATTAGCACGCTGCT[C/A]GGATTTCTTCATAAAACACGCTCAGTACCAGAAAGCTGTGGAATTGCTGGTGGCTGCCAAAAAGGTGAACATGCAACACAAACCGCCTCATATAACATCGGTTCATGTCGCTGTTATTATCATTTCGCTTTTAATAAATTATTTTCTATTTATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTTTCTGTACATTTTACGTTAGTTTTAGCTTGTTTCGTTAAGGGTTTTTTTAGTTTTAGTTTTTGTTTTGTGGACACATTTCTATTTATTTATTTATTTTTGGAATTTAGTTTACATACAGATAAAAAACGTTTTTGGCGACACGGTGGCTCTGTATTTGGCACTGTTGTCTCACAGCAAGATCAATAATTTGATTCCAGGCTGGGCCGGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTAGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCTCCACAGACCAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3253
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046546 | Nonsense | 1169 | 1455 | 28 | 32 |
ENSDART00000129889 | None | None | 774 | None | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 39398032)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38007121 |
GRCz11 | 24 | 37895018 |
KASP Assay ID:
554-2487.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGTGTTTGTAGTACCATGAGGCGCTCCAGTTGTGTTTGGACCAGAGTT[T/A]GACYATCACAGAAGATCTGGCTGAAAGTCTGACRGTGCCGAAAGACTCAA
Long Flanking Sequence:
CATTCACTCATTGTCCTTCAGCTTAGTCCCTTATTTATCAGGGGTCTCCACAGTGGAATGAACCGCCAGCATATGTTTTACGCCGCGGATGCCAGCAGTATATTTAGTTTACTTTCTTTTTTTTAATTGCAAATGAAGAAAAGATAAAACATTTTATGTTGATATATAAAATATATTTTTGTGTATAACCTTGCACTTGACTGATTCATTTGGCTGTAAAAGCACAATTACAGGTACAAAATGCGAACTTATTATATCTGAAAACCATGACTTATTTTAACGTAATTTTTTGTTTTATTTTTCGCTATTTTTTCAGTGAATGCTTGTTAGTTTTGTTTACTTTTAGTTTTTAATTTGTCAATTTTCCATTTAACAACTAACTTAAATAACTTTCCATAATATCTACATATGCAAACCTTTTTAAATGTTTTGTAAGTATACGCTTATGAATCTGTGTTTGTAGTACCATGAGGCGCTCCAGTTGTGTTTGGACCAGAGTT[T/A]GACCATCACAGAAGATCTGGCTGAAAGTCTGACAGTGCCGAAAGACTCAACTCTTCTGTCTGAGGCCGGGAGGAAAGAGCTGCTGGAGAAAATCGCAGACTGTTGCATGCGACAGGGAAACTACCACCTAGCCACAAAGAAATACACACAAGCTGGAAACAAGATCAAGGTTTGAAAAAATCAACAGCTTAATCAGTCATTTATTTTGTCCTGGCAGATACTTGATTTTCATTGGTCAATCCCTGTATTTTTTATCTTTGATGCAAAACAGTGGAATTAAATTGATCCCATCTTTACCACACACAACTGCTAGTTTCATGTAATTACACGCTCTTTAATTTCTTCTCAGATTAACCCTATAAATCATAATCTATGGGAGTTTTATACATGACATTTTAAGGACTCTTAATGATCAGACTTTACTGAAAAACCTATACAGAGTGTACTATATTTTAAGGAACATTCATTTGTTCATCTCTCAGTCATTATTGTGTTGCATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24548
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 |
---|---|---|---|---|---|
ENSDART00000046546 | Nonsense | 1351 | 1455 | 30 | 32 |
ENSDART00000129889 | None | None | 774 | None | 18 |
Genomic Location (Zv9):
Chromosome 24 (position 39400301)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 38009390 |
GRCz11 | 24 | 37897287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTCATACTGACTCACAGACTCGGCCTTATCAAGAGGTTCATTCAGGCA[C/T]GAAGGTAATGGTGAAATATGAACGGTTTATTTGTGTGTGGTATGTTACAT
Long Flanking Sequence:
AAGGTGTTCTTTTCCATTCTTGTTTTTGACAGGCGATGCGAGCGCTGCTGAAATCAGGAGATACAGAGAAAATAGTCTTTTTCGCTGGCGTTTCCAGACAGAAGGAGATTTATGTAATGGCAGCCAATTACCTGCAGTCACTGGACTGGAGGAACGACGCGGAGATCATGAAGAACATCATTAGCTTTTACACAAAAGGACGGGCGCTCGAGCTGCTCGCTGGTTTCTATGAGGCCTGTGCCGAGGTATGCTGAGAGCACCCCATAGCACTCTTAAAAGTCATACAGGACTCAATACCTCAGTTATGCTTAAATGCAGTCTGTGGTGTATGTGCACAGGTGGAAATTGACGATTATCAGAATTATGAGAAGGCGTACGGCGCTCTGACTGAGGCATGTAAATGTTTAACCAAAGCAAAAGGGCGCAGTGGAGAAGAAGCTGACGGCAAGCTGCTCATACTGACTCACAGACTCGGCCTTATCAAGAGGTTCATTCAGGCA[C/T]GAAGGTAATGGTGAAATATGAACGGTTTATTTGTGTGTGGTATGTTACATCTGTGCATACAACTCAAAAGGTGAGAATACACAGGGCAGGTTTTTGAGTAATGCTGCAGGGCAATAATGTAGTCAGTAGGCAACCAGGTGAGACATTGGGTTACTTATTAGAGGAACTAGATCTACATACAATTCATTCATTCATTCATTTTCTTTTCGGCTTAGTCTTTTTATTAATCTGGGGTCGCCATAGTAGAATGAACCGCCAACTTATCCAGCATATGTTTTACGCAGCGGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAACATCCATACACACTCATACACTACGGACAATTTAGCTTACCCAATTCACCTGTACCACATGTCTTTGGACTGTGGGGAAAACCGGAGCACCCGGAGGAAACCCACGCGCAGGGAGAACATGCAAACTAGAGTTGGGCCGATAGACAATGCCATAGTCCATCGCTGATGGCCAATAGACAA
Associated Phenotype:
Not determined