ZMP

si:ch1073-98b4.1

Ensembl ID:

ENSDARG00000054448

ZFIN ID:

ZDB-GENE-090312-119

Human Orthologue:

KIF1C

Human Description:

kinesin family member 1C [Source:HGNC Symbol;Acc:6317]

Mouse Orthologues:

Gm1305, Kif1c

Mouse Descriptions:

kinesin family member 1C Gene [Source:MGI Symbol;Acc:MGI:1098260]
predicted gene 1305 Gene [Source:MGI Symbol;Acc:MGI:2686151]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa8622	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa37798	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa17181	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa8622

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076647	Essential Splice Site	36	240	None	7
ENSDART00000143054	Essential Splice Site	35	239	None	6

Genomic Location (Zv9):

Chromosome 23 (position 44793242)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	44860691
GRCz11	23	44677211

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AACAACCATGATGCKAAATGTGTCATCCAGATGCAGGGAAACACCACCTG[T/A]GAGTGCACACACCRCATATGACAGTACATAATKTTTGACTGGATRTWCTA

Long Flanking Sequence:

GCAAAGGTGTTTAGTGGCCAAACTGACGCAGGACTTCCAGAGTGAGAATATTTGATGAGATTCTTGTATGTTTGTTATTAGTTCTGCTCAGGTAGATGAAATATTAGACTGATCTCTTCATTAATACTGATTATATGCATCTTTCACGACTTATTAAATTCAGTTTGTCTTGCTAAGTCATTCTCTGTATGATCAGAGCAGCTTCCACGTGCTTTCTCCACAGCATTCAACAGCAGAACAGTGTATTCAGCAGCACATTACCACTGTATAATCTGTCCTGTTGTTTACATCCGATTTTGATTTGATTTCATTGACAGTGTCGCTCTGATGTTGGCTGGCATCTGATTGGTCAGTTTTGCAGTGTGTCTGATCTGTGATTTGCTGTTGTGTTTTAGGATGGCCGCCTCAGTGAAGGTCGCCGTGAGAGTTCGGCCCTTCAACTCCCGGGAAAACAACCATGATGCGAAATGTGTCATCCAGATGCAGGGAAACACCACCTG[T/A]GAGTGCACACACCGCATATGACAGTACATAATGTTTGACTGGATATTCTATATAAGACACTAGTGTTCAGCTTAAAGTGACATTTAAAGGGCCCTATCATACACCCGGTGCAAGGCGCAGTGCAGTAGTCTTTTGGTAGTTTCAGCTTGGTGCAAGAGTGGTTTTGAGGCGTTGCGCTACGCTGCTTAAATAGCAAATGCATTAGCACTCATATGTGCGTCCATAGGCATTCTGGTCTATAAAGGGAGGCGTTCTGAGGCGGACCGCTGGCGTGTTGCTATTTTGAGAAACTAAAATAGATTTTTCATTAGACCAAAACTAACCCGGTCTAAACTCCAGCACAGAGTTGCACCTCGCTTACACACTGCTTAATACACACAAGAGAGCAATAGGCAAATATCTTTACATATGAAAACATCTAAATATTAAGGATATATATAGGATATAATAAGAATAGATATAGGATATAAATATAAAGGATTAAAATATTACAAAACATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37798

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076647	Essential Splice Site	136	240	5	7
ENSDART00000143054	None	None	239	None	6

Genomic Location (Zv9):

Chromosome 23 (position 44786792)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	44854241
GRCz11	23	44670761

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCCTAGCTCAGACCGGGCTGGGTGCAGTAGGATCGATGGGTTATATATA[G/T]ATATCAGTCATTTTCTTTTCGGCTTGCAAACTCCACACAGAAAACTGACC

Long Flanking Sequence:

GACCGCAAAAGCGGTAAAAAAACACTTGCAATAGCGGCATTATCATGATGAACTCATTCAGTAGCGAACTTGAGTTAAATGTGACTTACACTTTTCGTTGAAAAAAGCTCTTTATGTCCACCTTTTTTTTATCGCCATCCTCTCTGGTGCATGTCACACACCTCAGCGCAGTAGTTTTGGCGCTGCTTGTATTTGAAAGCAGTCTGTCACATGATAGCAGAGAAAGGCACAGCCAATCACAATGTTCATATGTGTCTGGGAGGCGGTGCGACTCGAGGAGAGAACGTGATTGAACCCTTTCGGCATGTCTAGGTTTATTGACAGCGCAATGTTTTTTCTGTGAATTAAATTACTGGTGGGGACATTTCAGTAGTTGGTGGTCATCCACCCTAAATCTACGTCCCTATCAAACCGTATATTGTATCGACAGACGTTAGACCAACCGGCTTGATCCTAGCTCAGACCGGGCTGGGTGCAGTAGGATCGATGGGTTATATATA[G/T]ATATCAGTCATTTTCTTTTCGGCTTGCAAACTCCACACAGAAAACTGACCCAGTCGAGGCTCGAACCTGCAACCTTTTTGCTGTGAGGCGATTGTGCTACCCACTGCACCACCGTGACATCACAATATTTAATTTAATATTAAATATGAAAATATTTAAGTATTTTGAGCAAATAGTTTAGCAATGCTTCAACAACAGGTTGAGGAGTTAATTAATTCCAGTTGTAAAGCAGCTCTAGAGTTGATGTTGTGATTTCAGTGTTGTGAAATCCATCAGTTGCGAAAGAGCCCCAGTTTTTAGGGTGTTTTGGTCAAAAGAGTCAAGACGTGCTGTTCTTGGTGAATTCGATCAGTGTGTGTGTGTGTGTGCGTGTGTATTGTATCCCTTGCATTGTGAGGACCAAATGTCCCCACAAATATAGTAATACCAGTTATTTTTGACCTTGTGGAGCCATTTTGTTCTCTGTGATGAAAACGGCTACTAAATGAGGCAAAGTGTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17181

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

C > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000076647	Essential Splice Site	143	240	5	7
ENSDART00000143054	None	None	239	None	6

Genomic Location (Zv9):

Chromosome 23 (position 44786769)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	44854218
GRCz11	23	44670738

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGCAGTAGGATCGATGGGTTATATATANNGATATCAKTCATTTTCTWTTCGG[C/T]TTGCAAACTCCACACAGAAMACTGACCCAGYCGAGGCTYGAACCTGCAAC

Long Flanking Sequence:

ACTTGCAATAGCGGCATTATCATGATGAACTCATTCAGTAGCGAACTTGAGTTAAATGTGACTTACACTTTTCGTTGAAAAAAGCTCTTTATGTCCACCTTTTTTTTATCGCCATCCTCTCTGGTGCATGTCACACACCTCAGCGCAGTAGTTTTGGCGCTGCTTGTATTTGAAAGCAGTCTGTCACATGATAGCAGAGAAAGGCACAGCCAATCACAATGTTCATATGTGTCTGGGAGGCGGTGCGACTCGAGGAGAGAACGTGATTGAACCCTTTCGGCATGTCTAGGTTTATTGACAGCGCAATGTTTTTTCTGTGAATTAAATTACTGGTGGGGACATTTCAGTAGTTGGTGGTCATCCACCCTAAATCTACGTCCCTATCAAACCGTATATTGTATCGACAGACGTTAGACCAACCGGCTTGATCCTAGCTCAGACCGGGCTGGGTGCAGTAGGATCGATGGGTTATATATAGATATCAGTCATTTTCTTTTCGG[C/T]TTGCAAACTCCACACAGAAAACTGACCCAGTCGAGGCTCGAACCTGCAACCTTTTTGCTGTGAGGCGATTGTGCTACCCACTGCACCACCGTGACATCACAATATTTAATTTAATATTAAATATGAAAATATTTAAGTATTTTGAGCAAATAGTTTAGCAATGCTTCAACAACAGGTTGAGGAGTTAATTAATTCCAGTTGTAAAGCAGCTCTAGAGTTGATGTTGTGATTTCAGTGTTGTGAAATCCATCAGTTGCGAAAGAGCCCCAGTTTTTAGGGTGTTTTGGTCAAAAGAGTCAAGACGTGCTGTTCTTGGTGAATTCGATCAGTGTGTGTGTGTGTGTGCGTGTGTATTGTATCCCTTGCATTGTGAGGACCAAATGTCCCCACAAATATAGTAATACCAGTTATTTTTGACCTTGTGGAGCCATTTTGTTCTCTGTGATGAAAACGGCTACTAAATGAGGCAAAGTGTTTTGTGTGAGGGTTGTGTTTAGGGG

Associated Phenotype:

Not determined